Skip to content
2000
image of Nicotine Exposure in Pregnancy and its Link to Autism Spectrum Disorder: A Review on Evidence, Biological Pathways, and Directions for Future Research in Neurological Disorders

Abstract

Pregnancy-related smoking and nicotine exposure by the mother can impact the developing brain of the baby and increase the likelihood that the kid will have autism or other neurodevelopmental disorders. However, conflicting epidemiological evidence links prenatal nicotine exposure to ASD, and the molecular processes involved remain unknown. The data on the impact of the mother smoking during pregnancy on the development of the fetal brain and the likelihood of neurodevelopmental disorders such as ASD are thoroughly reviewed in this paper. Nicotine can enter the developing tissue of the baby through the placenta and build up there. In the developing brain, it attaches itself to nicotinic receptors, impairing chemical equilibrium, growth, communication, and cell division, all essential for the passage of messages between neurons throughout crucial developmental stages. There is conflicting evidence, even though some human studies indicate that smoking during pregnancy raises the risk that the fetus will develop ASD. Some basic biological processes that have been proposed include damage to the placenta, oxygen deprivation, genetic changes, and abnormalities in brain chemistry, including dopamine. Overall, the data now available indicates that smoking during pregnancy is detrimental to the developing brain of the fetus. Consequently, abstaining from smoking and nicotine during pregnancy can reduce the likelihood that the fetus would experience any neurological disorders, including ASD. To fully comprehend the molecular mechanisms involved and establish definitive links between prenatal nicotine exposure and ASD, further studies are still required.

Loading

Article metrics loading...

/content/journals/cprr/10.2174/0126660822328919241212114244
2025-01-21
2025-03-30
Loading full text...

Full text loading...

References

  1. Majerczyk D. Ayad E.G. Brewton K.L. Saing P. Hart P.C. Systemic maternal inflammation promotes ASD via IL-6 and IFN-γ. Biosci. Rep. 2022 42 11 BSR20220713 10.1042/BSR20220713 36300375
    [Google Scholar]
  2. Masini E. Loi E. Vega-Benedetti A.F. Carta M. Doneddu G. Fadda R. Zavattari P. An overview of the main genetic, epigenetic and environmental factors involved in autism spectrum disorder focusing on synaptic activity. Int. J. Mol. Sci. 2020 21 21 8290 10.3390/ijms21218290 33167418
    [Google Scholar]
  3. Liao X. Yang J. Wang H. Li Y. Microglia mediated neuroinflammation in autism spectrum disorder. J. Psychiatr. Res. 2020 130 167 176 10.1016/j.jpsychires.2020.07.013 32823050
    [Google Scholar]
  4. Salari N. Rasoulpoor S. Rasoulpoor S. Shohaimi S. Jafarpour S. Abdoli N. Khaledi-Paveh B. Mohammadi M. The global prevalence of autism spectrum disorder: A comprehensive systematic review and meta-analysis. Ital. J. Pediatr. 2022 48 1 112 10.1186/s13052‑022‑01310‑w 35804408
    [Google Scholar]
  5. Baxter A.J. Brugha T.S. Erskine H.E. Scheurer R.W. Vos T. Scott J.G. The epidemiology and global burden of autism spectrum disorders. Psychol. Med. 2015 45 3 601 613 10.1017/S003329171400172X 25108395
    [Google Scholar]
  6. D’Onofrio B.M. Singh A.L. Iliadou A. Lambe M. Hultman C.M. Grann M. Neiderhiser J.M. Lichtenstein P. Lichtenstein P. Familial confounding of the association between maternal smoking during pregnancy and offspring criminality: A population-based study in Sweden. Arch. Gen. Psychiatry 2010 67 5 529 538 10.1001/archgenpsychiatry.2010.33 20439834
    [Google Scholar]
  7. Ekblad M. Gissler M. Korkeila J. Lehtonen L. Trends and risk groups for smoking during pregnancy in Finland and other Nordic countries. Eur. J. Public Health 2014 24 4 544 551 10.1093/eurpub/ckt128 24025664
    [Google Scholar]
  8. Şengüzel S. Cebeci A.N. Ekici B. Gönen İ. Tatlı B. Impact of eating habits and nutritional status on children with autism spectrum disorder. J. Taibah Univ. Med. Sci. 2021 16 3 413 421 10.1016/j.jtumed.2020.11.010 34140869
    [Google Scholar]
  9. Thielen A. Klus H. Müller L. Tobacco smoke: Unraveling a controversial subject. Exp. Toxicol. Pathol. 2008 60 2-3 141 156 10.1016/j.etp.2008.01.014 18485684
    [Google Scholar]
  10. Lisboa P.C. de Oliveira E. de Moura E.G. Obesity and endocrine dysfunction programmed by maternal smoking in pregnancy and lactation. Front. Physiol. 2012 3 437 10.3389/fphys.2012.00437 23181022
    [Google Scholar]
  11. Becerra T.A. Wilhelm M. Olsen J. Cockburn M. Ritz B. Ambient air pollution and autism in Los Angeles county, California. Environ. Health Perspect. 2013 121 3 380 386 10.1289/ehp.1205827 23249813
    [Google Scholar]
  12. von Ehrenstein O.S. Aralis H. Cockburn M. Ritz B. In utero exposure to toxic air pollutants and risk of childhood autism. Epidemiology 2014 25 6 851 858 10.1097/EDE.0000000000000150 25051312
    [Google Scholar]
  13. Raz R. Roberts A.L. Lyall K. Hart J.E. Just A.C. Laden F. Weisskopf M.G. Autism spectrum disorder and particulate matter air pollution before, during, and after pregnancy: A nested case-control analysis within the Nurses’ Health Study II Cohort. Environ. Health Perspect. 2015 123 3 264 270 10.1289/ehp.1408133 25522338
    [Google Scholar]
  14. Rizwan S. Manning J.T. Brabin B.J. Maternal smoking during pregnancy and possible effects of in utero testosterone: Evidence from the 2D:4D finger length ratio. Early Hum. Dev. 2007 83 2 87 90 10.1016/j.earlhumdev.2006.05.005 16814493
    [Google Scholar]
  15. Nielsen C.H. Larsen A. Nielsen A.L. DNA methylation alterations in response to prenatal exposure of maternal cigarette smoking: A persistent epigenetic impact on health from maternal lifestyle? Arch. Toxicol. 2016 90 2 231 245 10.1007/s00204‑014‑1426‑0 25480659
    [Google Scholar]
  16. Hussain N. Krueger W. Covault J. Walsh S. Kranzler H.R. Oncken C. Effects of prenatal tobacco exposure on gene expression profiling in umbilical cord tissue. Pediatr. Res. 2008 64 2 147 153 10.1203/PDR.0b013e31817c5507 18437100
    [Google Scholar]
  17. Maccani J.Z.J. Koestler D.C. Houseman E.A. Marsit C.J. Kelsey K.T. Placental DNA methylation alterations associated with maternal tobacco smoking at the RUNX3 gene are also associated with gestational age. Epigenomics 2013 5 6 619 630 10.2217/epi.13.63 24283877
    [Google Scholar]
  18. Kovess V. Keyes K.M. Hamilton A. Pez O. Bitfoi A. Koç C. Goelitz D. Kuijpers R. Lesinskiene S. Mihova Z. Otten R. Fermanian C. Pilowsky D.J. Susser E. Maternal smoking and offspring inattention and hyperactivity: Results from a cross-national European survey. Eur. Child Adolesc. Psychiatry 2015 24 8 919 929 10.1007/s00787‑014‑0641‑9 25413602
    [Google Scholar]
  19. Indredavik M.S. Brubakk A.M. Romundstad P. Vik T. Prenatal smoking exposure and psychiatric symptoms in adolescence. Acta Paediatr. 2007 96 3 377 382 10.1111/j.1651‑2227.2006.00148.x 17407460
    [Google Scholar]
  20. Habek D. Kovačević M. Adverse pregnancy outcomes and long-term morbidity after early fetal hypokinesia in maternal smoking pregnancies. Arch. Gynecol. Obstet. 2011 283 3 491 495 10.1007/s00404‑010‑1395‑3 20191283
    [Google Scholar]
  21. Holz N.E. Boecker R. Baumeister S. Hohm E. Zohsel K. Buchmann A.F. Blomeyer D. Jennen-Steinmetz C. Hohmann S. Wolf I. Plichta M.M. Meyer-Lindenberg A. Banaschewski T. Brandeis D. Laucht M. Effect of prenatal exposure to tobacco smoke on inhibitory control: neuroimaging results from a 25-year prospective study. JAMA Psychiatry 2014 71 7 786 796 10.1001/jamapsychiatry.2014.343 24828276
    [Google Scholar]
  22. Tiesler C.M.T. Heinrich J. Prenatal nicotine exposure and child behavioural problems. Eur. Child Adolesc. Psychiatry 2014 23 10 913 929 10.1007/s00787‑014‑0615‑y 25241028
    [Google Scholar]
  23. Agostoni C. Galli C. Riva E. Colombo C. Giovannini M. Marangoni F. Reduced docosahexaenoic acid synthesis may contribute to growth restriction in infants born to mothers who smoke. J. Pediatr. 2005 147 6 854 856 10.1016/j.jpeds.2005.05.040 16356447
    [Google Scholar]
  24. DiPietro J.A. Psychological and psychophysiological considerations regarding the maternal–fetal relationship. Infant Child Dev. 2010 19 1 27 38 10.1002/icd.651 20228872
    [Google Scholar]
  25. Zanardo V. Nicolussi S. Cavallin S. Trevisanuto D. Barbato A. Faggian D. Favaro F. Plebani M. Effect of maternal smoking on breast milk interleukin-1α, β-endorphin, and leptin concentrations and leptin concentrations. Environ. Health Perspect. 2005 113 10 1410 1413 10.1289/ehp.7702 16203256
    [Google Scholar]
  26. Laurberg P. Nøhr S.B. Pedersen K.M. Fuglsang E. Iodine nutrition in breast-fed infants is impaired by maternal smoking. J. Clin. Endocrinol. Metab. 2004 89 1 181 187 10.1210/jc.2003‑030829 14715847
    [Google Scholar]
  27. Levin E.D. Abreu-Villaça Y. Developmental neurotoxicity of nicotine and tobacco. Academic Press 2018 10.1016/B978‑0‑12‑809405‑1.00039‑0
    [Google Scholar]
  28. Banderali G. Martelli A. Landi M. Moretti F. Betti F. Radaelli G. Lassandro C. Verduci E. Short and long term health effects of parental tobacco smoking during pregnancy and lactation: A descriptive review. J. Transl. Med. 2015 13 1 327 10.1186/s12967‑015‑0690‑y 26472248
    [Google Scholar]
  29. Gardener H. Spiegelman D. Buka S.L. Perinatal and neonatal risk factors for autism: A comprehensive meta-analysis. Pediatrics 2011 128 2 344 355 10.1542/peds.2010‑1036 21746727
    [Google Scholar]
  30. Caramaschi D. Taylor A.E. Richmond R.C. Havdahl K.A. Golding J. Relton C.L. Munafò M.R. Davey Smith G. Rai D. Maternal smoking during pregnancy and autism: Using causal inference methods in a birth cohort study. Transl. Psychiatry 2018 8 1 262 10.1038/s41398‑018‑0313‑5 30498225
    [Google Scholar]
  31. Maenner M.J. Warren Z. Williams A.R. Amoakohene E. Bakian A.V. Bilder D.A. Durkin M.S. Fitzgerald R.T. Furnier S.M. Hughes M.M. Ladd-Acosta C.M. McArthur D. Pas E.T. Salinas A. Vehorn A. Williams S. Esler A. Grzybowski A. Hall-Lande J. Nguyen R.H.N. Pierce K. Zahorodny W. Hudson A. Hallas L. Mancilla K.C. Patrick M. Shenouda J. Sidwell K. DiRienzo M. Gutierrez J. Spivey M.H. Lopez M. Pettygrove S. Schwenk Y.D. Washington A. Shaw K.A. Prevalence and characteristics of autism spectrum disorder among children aged 8 years—Autism and developmental disabilities monitoring network, 11 sites, United States, 2020. MMWR Surveill. Summ. 2023 72 2 1 14 10.15585/mmwr.ss7202a1 36952288
    [Google Scholar]
  32. Talbott E.O. Arena V.C. Rager J.R. Clougherty J.E. Michanowicz D.R. Sharma R.K. Stacy S.L. Fine particulate matter and the risk of autism spectrum disorder. Environ. Res. 2015 140 414 420 10.1016/j.envres.2015.04.021 25957837
    [Google Scholar]
  33. Schmidt R.J. Tancredi D.J. Krakowiak P. Hansen R.L. Ozonoff S. Maternal intake of supplemental iron and risk of autism spectrum disorder. Am. J. Epidemiol. 2014 180 9 890 900 10.1093/aje/kwu208 25249546
    [Google Scholar]
  34. Schieve L.A. Clayton H.B. Durkin M.S. Wingate M.S. Drews-Botsch C. Comparison of perinatal risk factors associated with autism spectrum disorder (ASD), intellectual disability (ID), and co-occurring ASD and ID. J. Autism Dev. Disord. 2015 45 8 2361 2372 10.1007/s10803‑015‑2402‑0 25739693
    [Google Scholar]
  35. Williams G. Oliver J.M. Allard A. Sears L. Autism and associated medical and familial factors: A case control study. J. Dev. Phys. Disabil. 2003 15 4 335 349 10.1023/A:1026310216069
    [Google Scholar]
  36. Larsson M. Weiss B. Janson S. Sundell J. Bornehag C.G. Associations between indoor environmental factors and parental-reported autistic spectrum disorders in children 6–8 years of age. Neurotoxicology 2009 30 5 822 831 10.1016/j.neuro.2009.01.011 19822263
    [Google Scholar]
  37. Lee B.K. Gardner R.M. Dal H. Svensson A. Galanti M.R. Rai D. Dalman C. Magnusson C. Brief report: maternal smoking during pregnancy and autism spectrum disorders. J. Autism Dev. Disord. 2012 42 9 2000 2005 10.1007/s10803‑011‑1425‑4 22173844
    [Google Scholar]
  38. Gardener H. Spiegelman D. Buka S.L. Prenatal risk factors for autism: Comprehensive meta-analysis. Br. J. Psychiatry 2009 195 1 7 14 10.1192/bjp.bp.108.051672 19567888
    [Google Scholar]
  39. Rosen B.N. Lee B.K. Lee N.L. Yang Y. Burstyn I. Maternal smoking and autism spectrum disorder: A meta-analysis. J. Autism Dev. Disord. 2015 45 6 1689 1698 10.1007/s10803‑014‑2327‑z 25432101
    [Google Scholar]
  40. Tang S. Wang Y. Gong X. Wang G. A meta-analysis of maternal smoking during pregnancy and autism spectrum disorder risk in offspring. Int. J. Environ. Res. Public Health 2015 12 9 10418 10431 10.3390/ijerph120910418 26343689
    [Google Scholar]
  41. Landau L.I. Parental smoking: Asthma and wheezing illnesses in infants and children. Paediatr. Respir. Rev. 2001 2 3 202 206 10.1053/prrv.2001.0141 12052320
    [Google Scholar]
  42. Aziz Ali S. Khan U. Abrejo F. Vollmer B. Saleem S. Hambidge K.M. Krebs N.F. Westcott J.E. Goldenberg R.L. McClure E.M. Pasha O. Use of smokeless tobacco before conception and its relationship with maternal and fetal outcomes of pregnancy in Thatta, Pakistan: Findings from women first study. Nicotine Tob. Res. 2021 23 8 1291 1299 10.1093/ntr/ntaa215 33084903
    [Google Scholar]
  43. Gallego-Gómez J.I. Campillo-Cano M. Carrión-Martínez A. Balanza S. Rodríguez-González-Moro M.T. Simonelli-Muñoz A.J. Rivera-Caravaca J.M. The COVID-19 pandemic and its impact on homebound nursing students. Int. J. Environ. Res. Public Health 2020 17 20 7383 10.3390/ijerph17207383 33050435
    [Google Scholar]
  44. Wallig M.A. Bolon B. Haschek W.M. Rousseaux C.G. Fundamentals of toxicologic pathology. Academic press 2017
    [Google Scholar]
  45. Strachan D.P. Cook D.G. Parental smoking and childhood asthma: longitudinal and case-control studies. Thorax 1998 53 3 204 212 10.1136/thx.53.3.204 9659358
    [Google Scholar]
  46. Stein R.T. Holberg C.J. Sherrill D. Wright A.L. Morgan W.J. Taussig L. Martinez F.D. Influence of parental smoking on respiratory symptoms during the first decade of life: The tucson children’s respiratory study. Am. J. Epidemiol. 1999 149 11 1030 1037 10.1093/oxfordjournals.aje.a009748 10355379
    [Google Scholar]
  47. Shepherd D. Landon J. Goedeke S. Meads J. Stress and distress in New Zealand parents caring for a child with autism spectrum disorder. Res. Dev. Disabil. 2021 111 103875 10.1016/j.ridd.2021.103875 33549933
    [Google Scholar]
  48. Morishima T. Imanaka Y. Otsubo T. Hayashida K. Watanabe T. Tsuji I. Burden of household environmental tobacco smoke on medical expenditure for Japanese women: A population-based cohort study. J. Epidemiol. 2013 23 1 55 62 10.2188/jea.JE20120072 23183111
    [Google Scholar]
  49. Ebrahim M.T. Alothman A.A. Resilience and social support as predictors of post-traumatic growth in mothers of children with autism spectrum disorder in Saudi Arabia. Res. Dev. Disabil. 2021 113 103943 10.1016/j.ridd.2021.103943 33799234
    [Google Scholar]
  50. Jin C. Rossignol A.M. Effects of passive smoking on respiratory illness from birth to age eighteen months, in Shanghai, People’s Republic of China. J. Pediatr. 1993 123 4 553 558 10.1016/S0022‑3476(05)80949‑7 8410506
    [Google Scholar]
  51. DG C. Parental smoking and prevalence of respiratory symptoms and asthma in school age children. Thorax 1997 52 1081 1084 10.1136/thx.52.12.1081 9516904
    [Google Scholar]
  52. Hanrahan J.P. Tager I.B. Segal M.R. Tosteson T.D. Castile R.G. Van Vunakis H. Weiss S.T. Speizer F.E. The effect of maternal smoking during pregnancy on early infant lung function. Am. Rev. Respir. Dis. 2012 1586058
    [Google Scholar]
  53. Tripathi I. Estabillo J.A. Moody C.T. Laugeson E.A. Long-term treatment outcomes of PEERS® for preschoolers: A parent-mediated social skills training program for children with autism spectrum disorder. J. Autism Dev. Disord. 2022 52 6 2610 2626 10.1007/s10803‑021‑05147‑w 34302574
    [Google Scholar]
  54. Young S. Sherrill D.L. Arnott J. Diepeveen D. LeSouëf P.N. Landau L.I. Parental factors affecting respiratory function during the first year of life. Pediatr. Pulmonol. 2000 29 5 331 340 10.1002/(SICI)1099‑0496(200005)29:5<331::AID‑PPUL1>3.0.CO;2‑A 10790244
    [Google Scholar]
  55. Cross S.J. Linker K.E. Leslie F.M. Sex‐dependent effects of nicotine on the developing brain. J. Neurosci. Res. 2017 95 1-2 422 436 10.1002/jnr.23878 27870426
    [Google Scholar]
  56. Crume T. Tobacco use during pregnancy. Clin. Obstet. Gynecol. 2019 62 1 128 141 10.1097/GRF.0000000000000413 30668557
    [Google Scholar]
  57. Peterson L.A. Hecht S.S. Tobacco, e-cigarettes, and child health. Curr. Opin. Pediatr. 2017 29 2 225 230 10.1097/MOP.0000000000000456 28059903
    [Google Scholar]
  58. Hecht S.S. Carmella S.G. Kotandeniya D. Pillsbury M.E. Chen M. Ransom B.W.S. Vogel R.I. Thompson E. Murphy S.E. Hatsukami D.K. Evaluation of toxicant and carcinogen metabolites in the urine of e-cigarette users versus cigarette smokers. Nicotine Tob. Res. 2015 17 6 704 709 10.1093/ntr/ntu218 25335945
    [Google Scholar]
  59. Yuan M. Cross S.J. Loughlin S.E. Leslie F.M. N icotine and the adolescent brain. J. Physiol. 2015 593 16 3397 3412 10.1113/JP270492 26018031
    [Google Scholar]
  60. Hecht S.S. Research opportunities related to establishing standards for tobacco products under the family smoking prevention and tobacco control act. Nicotine Tob. Res. 2012 14 1 18 28 10.1093/ntr/ntq216 21324834
    [Google Scholar]
  61. Neuspiel D.R. Rush D. Butler N.R. Golding J. Bijur P.E. Kurzon M. Parental smoking and post-infancy wheezing in children: A prospective cohort study. Am. J. Public Health 1989 79 2 168 171 10.2105/AJPH.79.2.168 2783639
    [Google Scholar]
  62. Leeder S.R. Corkhill R. Irwig L.M. Holland W.W. Colley J.R. Influence of family factors on the incidence of lower respiratory illness during the first year of life. J. Epidemiol. Community Health 1976 30 4 203 212 10.1136/jech.30.4.203 1009269
    [Google Scholar]
  63. Amice B. Ho H. Zhang E. Bullen C. Physiologically based pharmacokinetic modelling for nicotine and cotinine clearance in pregnant women. Front. Pharmacol. 2021 12 688597 10.3389/fphar.2021.688597 34354586
    [Google Scholar]
  64. Taghavi T. Arger C.A. Heil S.H. Higgins S.T. Tyndale R.F. Longitudinal influence of pregnancy on nicotine metabolic pathways. J. Pharmacol. Exp. Ther. 2018 364 2 238 245 10.1124/jpet.117.245126 29158210
    [Google Scholar]
  65. Bazylak G. Brózik H. Sabanty W. HPTLC screening assay for urinary cotinine as biomarker of environmental tobacco smoke exposure among male adolescents. J. Pharm. Biomed. Anal. 2000 24 1 113 123 10.1016/S0731‑7085(00)00402‑7 11108545
    [Google Scholar]
  66. Benowitz N.L. Kuyt F. Jacob P. III Jones R.T. Osman A.L. Cotinine disposition and effects. Clin. Pharmacol. Ther. 1983 34 5 604 611 10.1038/clpt.1983.222 6627820
    [Google Scholar]
  67. Benowitz N.L. Jacob P. III Jones R.T. Rosenberg J. Interindividual variability in the metabolism and cardiovascular effects of nicotine in man. J. Pharmacol. Exp. Ther. 1982 221 2 368 372 7077531
    [Google Scholar]
  68. Kovar L. Selzer D. Britz H. Benowitz N. St Helen G. Kohl Y. Bals R. Lehr T. Comprehensive parent–metabolite PBPK/PD modeling insights into nicotine replacement therapy strategies. Clin. Pharmacokinet. 2020 59 9 1119 1134 10.1007/s40262‑020‑00880‑4 32166575
    [Google Scholar]
  69. Feyerabend C. Ings R.M. Russel M.A. Nicotine pharmacokinetics and its application to intake from smoking. Br. J. Clin. Pharmacol. 1985 19 2 239 247 10.1111/j.1365‑2125.1985.tb02637.x 3986082
    [Google Scholar]
  70. Lambers D.S. Clark K.E. The maternal and fetal physiologic effects of nicotine. Semin. Perinatol. 1996 20 2 115 126 10.1016/S0146‑0005(96)80079‑6 8857697
    [Google Scholar]
  71. Gentry P.R. Covington T.R. Clewell H.J. III Evaluation of the potential impact of pharmacokinetic differences on tissue dosimetry in offspring during pregnancy and lactation. Regul. Toxicol. Pharmacol. 2003 38 1 1 16 10.1016/S0273‑2300(03)00047‑3 12878049
    [Google Scholar]
  72. Arcury T.A. Quandt S.A. Health and social impacts of tobacco production. J. Agromed. 2006 11 3-4 71 81 10.1300/J096v11n03_08 19274899
    [Google Scholar]
  73. Luck W. Nau H. Hansen R. Steldinger R. Extent of nicotine and cotinine transfer to the human fetus, placenta and amniotic fluid of smoking mothers. Dev. Pharmacol. Ther. 1985 8 6 384 395 10.1159/000457063 4075937
    [Google Scholar]
  74. Malihi M. Nguyen J. Cardy R.E. Eldon S. Petta C. Kushki A. Short report: Evaluating the safety and usability of head-mounted virtual reality compared to monitor-displayed video for children with autism spectrum disorder. Autism 2020 24 7 1924 1929 10.1177/1362361320934214 32615771
    [Google Scholar]
  75. Mochizuki M. Maruo T. Masuko K. Ohtsu T. Effects of smoking on fetoplacental-maternal system during pregnancy. Am. J. Obstet. Gynecol. 1984 149 4 413 420 10.1016/0002‑9378(84)90156‑X 6203408
    [Google Scholar]
  76. Means S.A. Ho H. A spatial-temporal model for zonal hepatotoxicity of acetaminophen. Drug Metab. Pharmacokinet. 2019 34 1 71 77 10.1016/j.dmpk.2018.09.266 30377056
    [Google Scholar]
  77. Jung Y. Lee A.M. McKee S.A. Picciotto M.R. Maternal smoking and autism spectrum disorder: meta-analysis with population smoking metrics as moderators. Sci. Rep. 2017 7 1 4315 10.1038/s41598‑017‑04413‑1 28659613
    [Google Scholar]
  78. Szapuova Z.J. Argalasova L. Vondrova D. Jansakova K. Belica I. Kopcikova M. Babinska K. Ostatnikova D. Association between environmental tobacco smoke exposure and adaptive behavior in individuals with autism spectrum disorder. Toxics 2022 10 4 189 10.3390/toxics10040189 35448450
    [Google Scholar]
  79. Han C. Liu Y. Gong X. Ye X. Zhou J. Relationship between secondhand smoke exposure and depressive symptoms: A systematic review and dose–response meta-analysis. Int. J. Environ. Res. Public Health 2019 16 8 1356 10.3390/ijerph16081356 30991759
    [Google Scholar]
  80. Benowitz N.L. Nicotine replacement therapy during pregnancy. JAMA 1991 266 22 3174 3177 10.1001/jama.1991.03470220090034 1956108
    [Google Scholar]
  81. Nelson E.A.S. Taylor B.J. ICCPS Study Group International Child Care Practices Study: Infant sleep position and parental smoking. Early Hum. Dev. 2001 64 1 7 20 10.1016/S0378‑3782(01)00165‑7 11408104
    [Google Scholar]
  82. Penn G. Owen L. Factors associated with continued smoking during pregnancy: Analysis of socio‐demographic, pregnancy and smoking‐related factors. Drug Alcohol Rev. 2002 21 1 17 25 10.1080/09595230220119291 12189000
    [Google Scholar]
  83. Russell T. Crawford M. Woodby L. Measurements for active cigarette smoke exposure in prevalence and cessation studies: Why simply asking pregnant women isn’t enough. Nicotine Tob. Res. 2004 6 Suppl. 2 141 151 10.1080/14622200410001669141 15203817
    [Google Scholar]
  84. Gupta P.C. Survey of sociodemographic characteristics of tobacco use among 99,598 individuals in Bombay, India using handheld computers. Tob. Control 1996 5 2 114 120 10.1136/tc.5.2.114 8910992
    [Google Scholar]
  85. Geometric mean lead content in house dust and soil samples in Britain in 1982* and estimated proportions of children aged under 6years with raised blood lead concentrations. BMJ 1995 310 1409
    [Google Scholar]
  86. Benowitz N.L. Lake T. Keller K.H. Lee B.L. Prolonged absorption with development of tolerance to toxic effects after cutaneous exposure to nicotine. Clin. Pharmacol. Ther. 1987 42 1 119 120 10.1038/clpt.1987.119 3595064
    [Google Scholar]
  87. Schneider N.G. Olmstead R.E. Franzon M.A. Lunell E. The nicotine inhaler: Clinical pharmacokinetics and comparison with other nicotine treatments. Clin. Pharmacokinet. 2001 40 9 661 684 10.2165/00003088‑200140090‑00003 11605715
    [Google Scholar]
  88. Tilashalski K. Rodu B. Mayfield C. Assessing the nicotine content of smokeless tobacco products. J. Am. Dent. Assoc. 1994 125 5 590 594, 594 10.14219/jada.archive.1994.0095 8195501
    [Google Scholar]
  89. Fant R.V. Henningfield J.E. Nelson R.A. Pickworth W.B. Pharmacokinetics and pharmacodynamics of moist snuff in humans. Tob. Control 1999 8 4 387 392 10.1136/tc.8.4.387 10629244
    [Google Scholar]
  90. Pichayakorn W. Suksaeree J. Boonme P. Amnuaikit T. Taweepreda W. Ritthidej G.C. Nicotine transdermal patches using polymeric natural rubber as the matrix controlling system: Effect of polymer and plasticizer blends. J. Membr. Sci. 2012 411-412 81 90 10.1016/j.memsci.2012.04.017
    [Google Scholar]
  91. Jacob P. III Yu L. Shulgin A.T. Benowitz N.L. Minor tobacco alkaloids as biomarkers for tobacco use: comparison of users of cigarettes, smokeless tobacco, cigars, and pipes. Am. J. Public Health 1999 89 5 731 736 10.2105/AJPH.89.5.731 10224986
    [Google Scholar]
  92. Hukkanen J. Jacob P. III Benowitz N.L. Metabolism and disposition kinetics of nicotine. Pharmacol. Rev. 2005 57 1 79 115 10.1124/pr.57.1.3 15734728
    [Google Scholar]
  93. Dempsey D. Jacob P. III Benowitz N.L. Accelerated metabolism of nicotine and cotinine in pregnant smokers. J. Pharmacol. Exp. Ther. 2002 301 2 594 598 10.1124/jpet.301.2.594 11961061
    [Google Scholar]
  94. Pastrakuljic A. Schwartz R. Simone C. Derewlany L.O. Knie B. Koren G. Transplacental transfer and biotransformation studies of nicotine in the human placental cotyledon perfused in vitro. Life Sci. 1998 63 26 2333 2342 10.1016/S0024‑3205(98)00522‑0 9877223
    [Google Scholar]
  95. Giannotti M. Bonatti S.M. Tanaka S. Kojima H. de Falco S. Parenting stress and social style in mothers and fathers of children with autism spectrum disorder: A cross-cultural investigation in Italy and Japan. Brain Sci. 2021 11 11 1419 10.3390/brainsci11111419 34827418
    [Google Scholar]
  96. Hickson C. Lewis S. Campbell K.A. Cooper S. Berlin I. Claire R. Oncken C. Coleman-Haynes T. Coleman T. Comparison of nicotine exposure during pregnancy when smoking and abstinent with nicotine replacement therapy: Systematic review and meta‐analysis. Addiction 2019 114 3 406 424 10.1111/add.14473 30315598
    [Google Scholar]
  97. Polónyiová K. Belica I. Celušáková H. Janšáková K. Kopčíková M. Szapuová Ž. Ostatníková D. Comparing the impact of the first and second wave of COVID-19 lockdown on Slovak families with typically developing children and children with autism spectrum disorder. Autism 2022 26 5 1046 1055 10.1177/13623613211051480 34657487
    [Google Scholar]
  98. Leonardi-Bee J. Jere M.L. Britton J. Exposure to parental and sibling smoking and the risk of smoking uptake in childhood and adolescence: A systematic review and meta-analysis. Thorax 2011 66 10 847 855 10.1136/thx.2010.153379 21325144
    [Google Scholar]
  99. Berlin I. Grangé G. Jacob N. Tanguy M.L. Nicotine patches in pregnant smokers: Randomised, placebo controlled, multicentre trial of efficacy. BMJ 2014 348 mar11 2 g1622 10.1136/bmj.g1622 24627552
    [Google Scholar]
  100. Bricker J.B. Peterson A.V. Jr Leroux B.G. Andersen M.R. Rajan K.B. Sarason I.G. Prospective prediction of children’s smoking transitions: Role of parents’ and older siblings’ smoking. Addiction 2006 101 1 128 136 10.1111/j.1360‑0443.2005.01297.x 16393199
    [Google Scholar]
  101. den Exter Blokland E.A.W. Engels R.C.M.E. Hale W.W. III Meeus W. Willemsen M.C. Lifetime parental smoking history and cessation and early adolescent smoking behavior. Prev. Med. 2004 38 3 359 368 10.1016/j.ypmed.2003.11.008 14766120
    [Google Scholar]
  102. Bauman K.E. Carver K. Gleiter K. Trends in parent and friend influence during adolescence. Addict. Behav. 2001 26 3 349 361 10.1016/S0306‑4603(00)00110‑6 11436927
    [Google Scholar]
  103. Patel Y.M. Park S.L. Carmella S.G. Paiano V. Olvera N. Stram D.O. Haiman C.A. Le Marchand L. Hecht S.S. Metabolites of the polycyclic aromatic hydrocarbon phenanthrene in the urine of cigarette smokers from five ethnic groups with differing risks for lung cancer. PLoS One 2016 11 6 e0156203 10.1371/journal.pone.0156203 27275760
    [Google Scholar]
  104. Grazuleviciene R. Danileviciute A. Nadisauskiene R. Vencloviene J. Maternal smoking, GSTM1 and GSTT1 polymorphism and susceptibility to adverse pregnancy outcomes. Int. J. Environ. Res. Public Health 2009 6 3 1282 1297 10.3390/ijerph6031282 19440446
    [Google Scholar]
  105. Yuen R.K.C. Avila L. Peñaherrera M.S. von Dadelszen P. Lefebvre L. Kobor M.S. Robinson W.P. Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes. PLoS One 2009 4 10 e7389 10.1371/journal.pone.0007389 19838307
    [Google Scholar]
  106. Wang X. Zuckerman B. Pearson C. Kaufman G. Chen C. Wang G. Niu T. Wise P.H. Bauchner H. Xu X. Maternal cigarette smoking, metabolic gene polymorphism, and infant birth weight. JAMA 2002 287 2 195 202 10.1001/jama.287.2.195 11779261
    [Google Scholar]
  107. Aagaard-Tillery K. Spong C.Y. Thom E. Sibai B. Wendel G. Jr Wenstrom K. Samuels P. Simhan H. Sorokin Y. Miodovnik M. Meis P. O’Sullivan M.J. Conway D. Wapner R.J. Pharmacogenomics of maternal tobacco use: Metabolic gene polymorphisms and risk of adverse pregnancy outcomes. Obstet. Gynecol. 2010 115 3 568 577 10.1097/AOG.0b013e3181d06faf 20177288
    [Google Scholar]
  108. Morales-Suárez-Varela M. Puig B.M. Kaerlev L. Peraita-Costa I. Perales-Marín A. Safety of nicotine replacement therapy during pregnancy: A narrative review. Int. J. Environ. Res. Public Health 2022 20 1 250 10.3390/ijerph20010250 36612572
    [Google Scholar]
  109. Bowker K. Lewis S. Coleman T. Cooper S. Changes in the rate of nicotine metabolism across pregnancy: A longitudinal study. Addiction 2015 110 11 1827 1832 10.1111/add.13029 26119134
    [Google Scholar]
  110. Benowitz N.L. Hukkanen J. Jacob P. III Nicotine chemistry, metabolism, kinetics and biomarkers. Handb. Exp. Pharmacol. 2009 192 192 29 60 10.1007/978‑3‑540‑69248‑5_2 19184645
    [Google Scholar]
  111. Park H. Kim U.J. Choi E.J. Jun S. Park B. Lee H.A. Kim H.S. Park H. The association between urinary cotinine level and metabolic syndrome profiles among adolescents: Findings from the Ewha Birth and growth study. BMC Public Health 2023 23 1 732 10.1186/s12889‑023‑15458‑5 37085791
    [Google Scholar]
  112. Tan X. Vrana K. Ding Z.M. Cotinine: Pharmacologically active metabolite of nicotine and neural mechanisms for its actions. Front. Behav. Neurosci. 2021 15 758252 10.3389/fnbeh.2021.758252 34744656
    [Google Scholar]
  113. Bernardo H Cesar V Long-term effects of breastfeeding: A systematic review. 2013 Available from: https://iris.who.int/bitstream/handle/10665/79198/9789241505307_eng.pdf;jsessionid=787EA76CE140929AB83007A782C66FB7?sequence=1
  114. Resstel L.B.M. Corrêa F.M.A. Involvement of the medial prefrontal cortex in central cardiovascular modulation in the rat. Auton. Neurosci. 2006 126-127 130 138 10.1016/j.autneu.2006.02.022 16603420
    [Google Scholar]
  115. Brindle R.C. Ginty A.T. Phillips A.C. Carroll D. A tale of two mechanisms: A meta‐analytic approach toward understanding the autonomic basis of cardiovascular reactivity to acute psychological stress. Psychophysiology 2014 51 10 964 976 10.1111/psyp.12248 24924500
    [Google Scholar]
  116. Chida Y. Steptoe A. Greater cardiovascular responses to laboratory mental stress are associated with poor subsequent cardiovascular risk status: A meta-analysis of prospective evidence. Hypertension 2010 55 4 1026 1032 10.1161/HYPERTENSIONAHA.109.146621 20194301
    [Google Scholar]
  117. Gianaros P.J. Wager T.D. Brain-body pathways linking psychological stress and physical health. Curr. Dir. Psychol. Sci. 2015 24 4 313 321 10.1177/0963721415581476 26279608
    [Google Scholar]
  118. Li Y.F. Gilliland F.D. Berhane K. McCONNELL R.O.B. James Gauderman W. Rappaport E.B. Peters J.M. Effects of in utero and environmental tobacco smoke exposure on lung function in boys and girls with and without asthma. Am. J. Respir. Crit. Care Med. 2000 162 6 2097 2104 10.1164/ajrccm.162.6.2004178 11112121
    [Google Scholar]
  119. Breton C.V. Vora H. Salam M.T. Islam T. Wenten M. Gauderman W.J. Van Den Berg D. Berhane K. Peters J.M. Gilliland F.D. Variation in the GST mu locus and tobacco smoke exposure as determinants of childhood lung function. Am. J. Respir. Crit. Care Med. 2009 179 7 601 607 10.1164/rccm.200809‑1384OC 19151192
    [Google Scholar]
  120. Gagliardi L. Rusconi F. Bellù R. Zanini R. Association of maternal hypertension and chorioamnionitis with preterm outcomes. Pediatrics 2014 134 1 e154 e161 10.1542/peds.2013‑3898 24913788
    [Google Scholar]
  121. McEvoy C.T. Spindel E.R. Pulmonary effects of maternal smoking on the fetus and child: effects on lung development, respiratory morbidities, and life long lung health. Paediatr. Respir. Rev. 2017 21 27 33 27639458
    [Google Scholar]
  122. Schneider S. Huy C. Schütz J. Diehl K. Smoking cessation during pregnancy: A systematic literature review. Drug Alcohol Rev. 2010 29 1 81 90 10.1111/j.1465‑3362.2009.00098.x 20078687
    [Google Scholar]
  123. Baker R.R. Massey E.D. Smith G. An overview of the effects of tobacco ingredients on smoke chemistry and toxicity. Food Chem. Toxicol. 2004 42 Suppl. 53 83 10.1016/j.fct.2004.01.001 15072838
    [Google Scholar]
  124. Suzuki K. Horiguchi T. Comas-urrutia A.C. Mueller-Heubach E. Morishima H.O. Adamsons K. Pharmacologic effects of nicotine upon the fetus and mother in the rhesus monkey. Am. J. Obstet. Gynecol. 1971 111 8 1092 1101 10.1016/0002‑9378(71)90109‑8 5001981
    [Google Scholar]
  125. Gaither K.H. Huber L.R.B. Thompson M.E. Huet-Hudson Y.M. Does the use of nicotine replacement therapy during pregnancy affect pregnancy outcomes? Matern. Child Health J. 2009 13 4 497 504 10.1007/s10995‑008‑0361‑1 18478321
    [Google Scholar]
  126. Naeye R.L. Effects of maternal cigarette smoking on the fetus and placenta. BJOG 1978 85 10 732 737 10.1111/j.1471‑0528.1978.tb15593.x 708656
    [Google Scholar]
  127. Spinillo A. Nicola S. Piazzi G. Ghazal K. Colonna L. Baltaro F. Epidemiological correlates of preterm premature rupture of membranes. Int. J. Gynaecol. Obstet. 1994 47 1 7 15 10.1016/0020‑7292(94)90454‑5 7813758
    [Google Scholar]
  128. Cnattingius S. The epidemiology of smoking during pregnancy: Smoking prevalence, maternal characteristics, and pregnancy outcomes. Nicotine Tob. Res. 2004 6 Suppl. 2 125 140 10.1080/14622200410001669187 15203816
    [Google Scholar]
  129. Haebig E. Jiménez E. Cox C.R. Hills T.T. Characterizing the early vocabulary profiles of preverbal and minimally verbal children with autism spectrum disorder. Autism 2021 25 4 958 970 10.1177/1362361320973799 33246365
    [Google Scholar]
  130. Wu S.T. Lin C.H. Lin Y.H. Hsu Y.C. Hsu C.T. Lin M.C. Maternal risk factors for preterm birth in Taiwan, a nationwide population-based cohort study. Pediatr. Neonatol. 2024 65 1 38 47 10.1016/j.pedneo.2023.03.014 37517971
    [Google Scholar]
  131. Kendle A.M. Buhimschi C.S. Lockwood C.J. Pathogenesis and prediction of preterm delivery. Queenan’s management of high‐risk pregnancy. An Evidence‐Based Approach. 2024 2 344 360
    [Google Scholar]
  132. Qi M. Zhu P. Wang H. He Q. Huo C. Abnormalities in behavior relevant to schizophrenia in embryonic day 17 MAM-exposed rodent models: A systematic review and meta-analysis. Pharmacol. Biochem. Behav. 2024 245 173888 10.1016/j.pbb.2024.173888 39384086
    [Google Scholar]
  133. Vakilzadeh G. Maseko B.C. Bartely T.D. McLennan Y.A. Martínez-Cerdeño V. Increased number of excitatory synapsis and decreased number of inhibitory synapsis in the prefrontal cortex in autism. Cereb. Cortex 2024 34 13 121 128 10.1093/cercor/bhad268 38696601
    [Google Scholar]
  134. Genkel V. Domozhirova E. Malinina E. Multimorbidity in severe mental illness as part of the neurodevelopmental continuum: Physical health-related endophenotypes of schizophrenia—A narrative review. Brain Sci. 2024 14 7 725 10.3390/brainsci14070725 39061465
    [Google Scholar]
  135. Capal J.K. Jeste S.S. Autism and epilepsy. Pediatr. Clin. North Am. 2024 71 2 241 252 10.1016/j.pcl.2024.01.004 38423718
    [Google Scholar]
  136. Nóbrega I.S. Teles e Silva A.L. Yokota-Moreno B.Y. Sertié A.L. The importance of large-scale genomic studies to unravel genetic risk factors for autism. Int. J. Mol. Sci. 2024 25 11 5816 10.3390/ijms25115816 38892002
    [Google Scholar]
  137. Saleem S. Habib S.H. Implications of genetic factors and modifiers in autism spectrum disorders: A systematic review. Rev. J. Autism Dev. Disord. 2024 11 1 172 183 10.1007/s40489‑022‑00333‑7
    [Google Scholar]
  138. Bicks L.K. Geschwind D.H. Functional neurogenomics in autism spectrum disorders: A decade of progress. Curr. Opin. Neurobiol. 2024 86 102858 10.1016/j.conb.2024.102858 38547564
    [Google Scholar]
  139. Voglewede M.M. Ozsen E.N. Ivak N. Bernabucci M. Tang R. Sun M. Pang Z.P. Zhang H. Loss of the polarity protein Par3 promotes dendritic spine neoteny and enhances learning and memory. iScience 2024 27 7 110308 10.1016/j.isci.2024.110308 39045101
    [Google Scholar]
  140. Bosetti C. Ferrini L. Ferrari A.R. Bartolini E. Calderoni S. Children with autism spectrum disorder and abnormalities of clinical eeg: A qualitative review. J. Clin. Med. 2024 13 1 279 10.3390/jcm13010279 38202286
    [Google Scholar]
  141. Yang Y. Zheng T. Tang Q. Xiang B. Yang M. Zeng J. Zhou F. Xie X. Developmental dyslexia genes are selectively targeted by diverse environmental pollutants. BMC Psychiatry 2024 24 1 509 10.1186/s12888‑024‑05952‑4 39020327
    [Google Scholar]
  142. Banks W.A. Rhea E.M. Reed M.J. Erickson M.A. The penetration of therapeutics across the blood-brain barrier: Classic case studies and clinical implications. Cell Rep. Med. 2024 101760 10.1016/j.xcrm.2024.101760 39383873
    [Google Scholar]
  143. Yesildemir O. Celik M.N. Association between pre- and postnatal exposure to endocrine-disrupting chemicals and birth and neurodevelopmental outcomes: An extensive review. Clinical and Experimental Pediatrics 2024 67 7 328 346 10.3345/cep.2023.00941 37986566
    [Google Scholar]
  144. Iannuccelli M. Vitriolo A. Licata L. Lo Surdo P. Contino S. Cheroni C. Capocefalo D. Castagnoli L. Testa G. Cesareni G. Perfetto L. Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders. Mol. Psychiatry 2024 29 1 186 196 10.1038/s41380‑023‑02317‑3 38102483
    [Google Scholar]
  145. Toledano J.M. Puche-Juarez M. Moreno-Fernandez J. Gonzalez-Palacios P. Rivas A. Ochoa J.J. Diaz-Castro J. Implications of prenatal exposure to endocrine-disrupting chemicals in offspring development: A narrative review. Nutrients 2024 16 11 1556 10.3390/nu16111556 38892490
    [Google Scholar]
  146. Moch J. Radtke M. Liehr T. Eggermann T. Gilissen C. Pfundt R. Astuti G. Hentschel J. Schumann I. Automatized detection of uniparental disomies in a large cohort. Hum. Genet. 2024 143 8 955 964 10.1007/s00439‑024‑02687‑w 39012485
    [Google Scholar]
  147. Valeeva E.V. Sabirov I.S. Safiullina L.R. Nikitin D.O. Semina I.I. Rees T. Fesenko D.O. Ahmetov I.I. The role of the CNTNAP2 gene in the development of autism spectrum disorder. Res. Autism Spectr. Disord. 2024 114 102409 10.1016/j.rasd.2024.102409
    [Google Scholar]
  148. Kovacheva E. Gevezova M. Maes M. Sarafian V. Mast cells in autism spectrum disorder—The enigma to be solved? Int. J. Mol. Sci. 2024 25 5 2651 10.3390/ijms25052651 38473898
    [Google Scholar]
  149. Kumar S. Garg N.K. Jain A. Pandey P. Khopade A. Sawant K.K. Emerging therapeutic landscape on delivery of oxytocin to brain for treating neurological disorders. J. Drug Deliv. Sci. Technol. 2024 92 105370 10.1016/j.jddst.2024.105370
    [Google Scholar]
  150. Caria A. A hypothalamic perspective of human socioemotional behavior. Neuroscientist 2024 30 4 399 420 10.1177/10738584221149647 36703298
    [Google Scholar]
  151. Moerkerke M. Daniels N. Tibermont L. Tang T. Evenepoel M. Van der Donck S. Debbaut E. Prinsen J. Chubar V. Claes S. Vanaudenaerde B. Willems L. Steyaert J. Boets B. Alaerts K. Chronic oxytocin administration stimulates the oxytocinergic system in children with autism. Nat. Commun. 2024 15 1 58 10.1038/s41467‑023‑44334‑4 38167302
    [Google Scholar]
  152. McCrae C.S. Chan W.S. Curtis A.F. Nair N. Deroche C.B. Munoz M. Takamatsu S. McLean D. Davenport M. Muckerman J.E. Takahashi N. McCann D. McGovney K. Sahota P. Mazurek M.O. Telehealth cognitive behavioral therapy for insomnia in children with autism spectrum disorder: A pilot examining feasibility, satisfaction, and preliminary findings. Autism 2021 25 3 667 680 10.1177/1362361320949078 32838539
    [Google Scholar]
  153. Sallis H.M. Wootton R.E. Davey Smith G. Munafò M.R. Proxy gene-by-environment Mendelian randomization study of the association between cigarette smoking during pregnancy and offspring mental health. Int. J. Epidemiol. 2023 52 5 1350 1359 10.1093/ije/dyad022 36860174
    [Google Scholar]
  154. Ku J Asuri P Stem cell-based approaches for developmental neurotoxicity testing. Front Toxicol 2024 6 1402630 10.3389/ftox.2024.1402630
    [Google Scholar]
  155. Settivari RS Martini A Wijeyesakere S Toltin A LeBaron MJ Application of Evolving New Approach Methodologies for Chemical Safety Assessment. Academic Press 2024 10.1016/B978‑0‑323‑85704‑8.00026‑8
    [Google Scholar]
  156. Nussinov R. Yavuz B.R. Demirel H.C. Arici M.K. Jang H. Tuncbag N. Review: Cancer and neurodevelopmental disorders: multi-scale reasoning and computational guide. Front. Cell Dev. Biol. 2024 12 1376639 10.3389/fcell.2024.1376639 39015651
    [Google Scholar]
  157. Guerra M. Medici V. La Sala G. Farini D. Unravelling the cerebellar involvement in autism spectrum disorders: Insights into genetic mechanisms and developmental pathways. Cells 2024 13 14 1176 10.3390/cells13141176 39056758
    [Google Scholar]
  158. Sanford B.T. Brownstein N.C. Baker N.L. Palmer A.M. Smith T.T. Rojewski A.M. Toll B.A. Shift from smoking cigarettes to vaping nicotine in young adults. JAMA Intern. Med. 2024 184 1 106 108 10.1001/jamainternmed.2023.5239 37955869
    [Google Scholar]
  159. Chaudhary R Steinson E. Genes and their involvement in the pathogenesis of autism spectrum disorder: Insights from earlier genetic studies. Neurobiology of Autism Spectrum Disorders Springer Cham 2024
    [Google Scholar]
  160. Sun Q. Jin C. Cell signaling and epigenetic regulation of nicotine-induced carcinogenesis. Environ. Pollut. 2024 345 123426 10.1016/j.envpol.2024.123426 38295934
    [Google Scholar]
  161. Banoji V. Kumar Angajala K. Vianala S. Manne S. rao Ravulapelly K. Vannada J. Synthesis, characterization, cytotoxic evaluation, and molecular docking studies of novel 1,2,3-triazole-based chalcones for potential anticancer applications. Results in Chemistry 2024 7 101294 10.1016/j.rechem.2023.101294
    [Google Scholar]
  162. Chen Y. Yang Z. Zhou Z. Liu E.J. Luo W. He Z. Han W. Liu Y. Metabolism-dependent mutagenicity of two structurally similar tobacco-specific nitrosamines (N-nitrosonornicotine and N-nitrosoanabasine) in human cells, partially different CYPs being activating enzymes. Toxicology 2024 504 153774 10.1016/j.tox.2024.153774 38490321
    [Google Scholar]
  163. Deshmukh R. Sethi P. Singh B. Shiekmydeen J. Salave S. Patel R.J. Ali N. Rashid S. Elossaily G.M. Kumar A. Recent review on biological barriers and host–Material interfaces in precision drug delivery: advancement in biomaterial engineering for better treatment therapies. Pharmaceutics 2024 16 8 1076 10.3390/pharmaceutics16081076 39204421
    [Google Scholar]
  164. Borkar N.A. Thompson M.A. Bartman C.M. Khalfaoui L. Sine S. Sathish V. Prakash Y.S. Pabelick C.M. Nicotinic receptors in airway disease. Am. J. Physiol. Lung Cell. Mol. Physiol. 2024 326 2 L149 L163 10.1152/ajplung.00268.2023 38084408
    [Google Scholar]
  165. Marti F. Faure P. Le Borgne T. Nguyen C. Vicq E. Jehl J. Solie C. Guyon N. Daussy L. Gulmez A. Reynolds L. Nicotine engages a VTA-NAc feedback loop to inhibit amygdala-projecting dopamine neurons and induce anxiety. bioRxiv 2024
    [Google Scholar]
  166. Wells A.C. Mojica C. Lotfipour S. Hypersensitivity of the nicotinic acetylcholine receptor subunit (CHRNA2 ) in female adolescent mice produces deficits in nicotine-induced facilitation of hippocampal-dependent learning and memory. Neurobiol. Learn. Mem. 2024 213 107959 10.1016/j.nlm.2024.107959 38964600
    [Google Scholar]
  167. Alatawi A. Ajarem J. Alarifi S. Al-Shaebi E. Khadrawy S. Wang C. Maodaa S. Teucrium polium extract ameliorates neurobehavioral, neurochemical induced by nicotine in brain of mice. Indian J. Anim. Res. 2024 58 Of 982 990 10.18805/IJAR.BF‑1777
    [Google Scholar]
  168. Penman S.L. Roeder N.M. Wang J. Richardson B.J. Pareek O. Freeman-Striegel L. Mohr P. Khan A. Eiden R.D. Chakraborty S. Thanos P.K. Vaporized nicotine in utero results in reduced birthweight, increased locomotion, and decreased voluntary exercise, dependent on sex and diet in offspring. Psychopharmacology (Berl.) 2024 241 9 1857 1882 10.1007/s00213‑024‑06602‑z 38733527
    [Google Scholar]
  169. Frie J.A. McCunn P. Eed A. Hassan A. Luciani K.R. Chen C. Tyndale R.F. Khokhar J.Y. Factors influencing JUUL e-cigarette nicotine vapour-induced reward, withdrawal, pharmacokinetics and brain connectivity in rats: Sex matters. Neuropsychopharmacology 2024 49 5 782 795 10.1038/s41386‑023‑01773‑3 38057369
    [Google Scholar]
  170. Gotti C. Clementi F. Zoli M. Special issue “The multifaceted activities of nervous and non-nervous neuronal nicotinic acetylcholine receptors in physiology and pathology”. Pharmacol. Res. 2024 205 107239 10.1016/j.phrs.2024.107239 38801984
    [Google Scholar]
  171. Ketata I. Ellouz E. Mizouri R. Impact of prenatal, neonatal, and postnatal factors on epilepsy risk in children and adolescents: A systematic review and meta-analysis. Acta Epileptologica 2024 6 1 1 10.1186/s42494‑023‑00143‑2
    [Google Scholar]
  172. Karatayev O. Collier A.D. Targoff S.R. Leibowitz S.F. Neurological disorders induced by drug use: effects of adolescent and embryonic drug exposure on behavioral neurodevelopment. Int. J. Mol. Sci. 2024 25 15 8341 10.3390/ijms25158341 39125913
    [Google Scholar]
  173. Greenwood P.B. DeSerisy M. Koe E. Rodriguez E. Salas L. Perera F.P. Herbstman J. Pagliaccio D. Margolis A.E. Combined and sequential exposure to prenatal second hand smoke and postnatal maternal distress is associated with cingulo-opercular global efficiency and attention problems in school-age children. Neurotoxicol. Teratol. 2024 102 107338 10.1016/j.ntt.2024.107338 38431065
    [Google Scholar]
  174. Shenassa E.D. Gleason J.L. Hirabayashi K. Fetal exposure to tobacco metabolites and depression during adulthood: Beyond binary measures. Epidemiology 2024 35 5 602 609 10.1097/EDE.0000000000001757 38967976
    [Google Scholar]
  175. Fekom M. Nguyen T.L. Lepeule J. Nakamura A. Keyes K. Martins S. Strandberg-Larsen K. Melchior M. Intergenerational transmission of tobacco smoking: The role of the child’s behavioral difficulties. Data from the Danish National Birth cohort (DNBC). Drug Alcohol Depend. 2024 255 111056 10.1016/j.drugalcdep.2023.111056 38128363
    [Google Scholar]
  176. Carreño D. Facundo A. Nguyen M.T.T. Lotfipour S. Dopamine and norepinephrine tissue levels in the developing limbic brain are impacted by the human CHRNA6 3′-UTR single-nucleotide polymorphism (rs2304297) in rats. Int. J. Mol. Sci. 2024 25 7 3676 10.3390/ijms25073676 38612487
    [Google Scholar]
  177. Aldridge C. Keene K.L. Normeshie C.A. Mychaleckyi J.C. Hauck F.R. Metabolomic profiles of children with sudden infant death syndrome: A case-control analysis. SSRN 4885142 10.2139/ssrn.4885142
    [Google Scholar]
  178. Lafta M.S. Mwinyi J. Affatato O. Rukh G. Dang J. Andersson G. Schiöth H.B. Exploring sex differences: insights into gene expression, neuroanatomy, neurochemistry, cognition, and pathology. Front. Neurosci. 2024 18 1340108 10.3389/fnins.2024.1340108 38449735
    [Google Scholar]
  179. Hanusrichterova J. Mokry J. Al-Saiedy M.R. Koetzler R. Amrein M.W. Green F.H.Y. Calkovska A. Factors influencing airway smooth muscle tone: A comprehensive review with a special emphasis on pulmonary surfactant. Am. J. Physiol. Cell Physiol. 2024 327 3 C798 C816 10.1152/ajpcell.00337.2024 39099420
    [Google Scholar]
  180. Gupta N. Mukhi S. Singhal V. Basics of neurosciences [anatomy, physiology and pharmacology]. Academic Press 2024 5 31
    [Google Scholar]
  181. Nygren G. Linnsand P. Hermansson J. Dinkler L. Johansson M. Gillberg C. Feeding problems including avoidant restrictive food intake disorder in young children with autism spectrum disorder in a multiethnic population. Front Pediatr. 2021 9 780680 10.3389/fped.2021.780680 34966704
    [Google Scholar]
  182. Kaur B. The Association between Autism Spectrum Disorders and Secondhand Tobacco Exposure. 2014 Available from: https://corescholar.libraries.wright.edu/cgi/viewcontent.cgi?article=1119&context=mph#:~:text=In%20univariate%20logistic%20regression%20analysis,parents%20smoked%20inside%20the%20house.
  183. Tran P.L. Lehti V. Lampi K.M. Helenius H. Suominen A. Gissler M. Brown A.S. Sourander A. Smoking during Pregnancy and Risk of A utism S pectrum D isorder in a F innish N ational B irth C ohort. Paediatr. Perinat. Epidemiol. 2013 27 3 266 274 10.1111/ppe.12043 23574415
    [Google Scholar]
  184. Hertz-Picciotto I. Korrick S.A. Ladd-Acosta C. Karagas M.R. Lyall K. Schmidt R.J. Dunlop A.L. Croen L.A. Dabelea D. Daniels J.L. Duarte C.S. Fallin M.D. Karr C.J. Lester B. Leve L.D. Li Y. McGrath M. Ning X. Oken E. Sagiv S.K. Sathyanaraya S. Tylavsky F. Volk H.E. Wakschlag L.S. Zhang M. O’Shea T.M. Musci R.J. Maternal tobacco smoking and offspring autism spectrum disorder or traits in ECHO cohorts. Autism Res. 2022 15 3 551 569 10.1002/aur.2665 35199959
    [Google Scholar]
  185. Hahad O. Kuntic M. Kuntic I. Daiber A. Münzel T. Tobacco smoking and vascular biology and function: Evidence from human studies. Pflugers Arch. 2023 475 7 797 805 10.1007/s00424‑023‑02805‑z 36961561
    [Google Scholar]
  186. Liu X. Lin J. Zhang H. Khan N.U. Zhang J. Tang X. Cao X. Shen L. Oxidative stress in autism spectrum disorder—current progress of mechanisms and biomarkers. Front. Psychiatry 2022 13 813304 10.3389/fpsyt.2022.813304 35299821
    [Google Scholar]
  187. Caliri A.W. Tommasi S. Besaratinia A. Relationships among smoking, oxidative stress, inflammation, macromolecular damage, and cancer. Mutat. Res. Rev. Mutat. Res. 2021 787 108365 10.1016/j.mrrev.2021.108365 34083039
    [Google Scholar]
  188. Isik B. Ceylan A. Isik R. Oxidative stress in smokers and non-smokers. Inhal. Toxicol. 2007 19 9 767 769 10.1080/08958370701401418 17613085
    [Google Scholar]
  189. Castro E.M. Lotfipour S. Leslie F.M. Nicotine on the developing brain. Pharmacol. Res. 2023 190 106716 10.1016/j.phrs.2023.106716 36868366
    [Google Scholar]
  190. Goriounova N.A. Mansvelder H.D. Short- and long-term consequences of nicotine exposure during adolescence for prefrontal cortex neuronal network function. Cold Spring Harb. Perspect. Med. 2012 2 12 a012120 10.1101/cshperspect.a012120 22983224
    [Google Scholar]
  191. Social L. Social, environmental, cognitive, and genetic influences on the use of tobacco among youth. Preventing Tobacco Use Among Youth and Young Adults: A Report of the Surgeon General. Centers for Disease Control and Prevention Atlanta (GA) 2012
    [Google Scholar]
  192. Garrett B.E. Martell B.N. Caraballo R.S. King B.A. Peer reviewed: Socioeconomic differences in cigarette smoking among sociodemographic groups. Prev. Chronic Dis. 2019 ••• 16
    [Google Scholar]
  193. Nargis N. Yong H.H. Driezen P. Mbulo L. Zhao L. Fong G.T. Thompson M.E. Borland R. Palipudi K.M. Giovino G.A. Thrasher J.F. Siahpush M. Socioeconomic patterns of smoking cessation behavior in low and middle-income countries: Emerging evidence from the global adult tobacco surveys and international tobacco control surveys. PLoS One 2019 14 9 e0220223 10.1371/journal.pone.0220223 31490958
    [Google Scholar]
  194. Sharma H. Chandra P. Pathak R. Bhandari M. Arushi S.V. Advancements in the therapeutic approaches to treat neurological disorders. Cah Magellanes-NS. 2024 6 2 4328 4389
    [Google Scholar]
  195. Chandra P. Sharma H. Phosphodiesterase inhibitors for treatment of alzheimer’s disease. INDIAN DRUGS 2024 61 7 7 22 10.53879/id.61.07.14382
    [Google Scholar]
  196. Pathak R. Sharma S. Bhandari M. Nogai L. Mishra R. Saxena A. Reena Km S.H. Neuroinflammation at the crossroads of metabolic and neurodegenerative diseases: Causes, consequences and interventions. J. Exp. Zool. India 2024 21 2 2447 2461 10.59467/jez.2024.27.2.2447
    [Google Scholar]
  197. Pathak R. Sharma H. Chandra P. Halagali P. Ali Z. A compressive review: Mechanisms underlying the use of diuretics in the treatment of hypertension. Indian J Nat Sci. 2024 15 85 78063 78075
    [Google Scholar]
  198. Singh A. Kumar P. Sharma H. Breakthrough opportunities of nanotheranostics in psoriasis: From pathogenesis to management strategy. Infect. Disord. Drug Targets 2024 24 1 20 10.2174/0118715265298802240603120251 39075964
    [Google Scholar]
  199. Sharma H. Tyagi S.J. Varshney P. Pathak N. Pathak R. A review on Mpox: Diagnosis, prevention and treatments. Coronaviruses 2024 5 1 17 10.2174/0126667975301557240604113752
    [Google Scholar]
  200. Sharma H. Halagali P. Majumder A. Sharma V. Pathak R. Natural compounds targeting signaling pathways in breast cancer therapy. African J Biol Sci 2024 6 10 5430 5479 10.33472/AFJBS.6.10.2024.5430‑5479
    [Google Scholar]
  201. Sharma H. Pathak R. Biswas D. Unveiling the therapeutic potential of modern probiotics in addressing neurodegenerative disorders: A comprehensive exploration, review and future perspectives on intervention strategies. Curr. Psychiatry Res. Rev. 2024 20 10.2174/0126660822304321240520075036
    [Google Scholar]
  202. Pathak R. Kaur V. Sharma S. Bhandari M. Mishra R. Saxena A. Pazopanib: Effective monotherapy for precise cancer treatment, targeting specific mutations and tumors. Afr.J.Bio.Sc. 2024 6 9 1311 1330 10.33472/AFJBS.6.9.2024.1311‑1330
    [Google Scholar]
  203. Kapoor D.U. Sharma H. Maheshwari R. Pareek A. Gaur M. Prajapati B.G. Castro G.R. Thanawuth K. Suttiruengwong S. Sriamornsak P. Konjac glucomannan: A comprehensive review of its extraction, health benefits, and pharmaceutical applications. Carbohydr. Polym. 2024 339 122266 10.1016/j.carbpol.2024.122266 38823930
    [Google Scholar]
  204. Chandra P. Ali Z. Fatima N. Sharma H. Sachan N. Sharma K.K. Verma A. Shankhpushpi (Convolvulus pluricaulis): Exploring its cognitive enhancing mechanisms and therapeutic potential in neurodegenerative disorders. Curr. Bioact. Compd. 2024 20 10.2174/0115734072292339240416095600
    [Google Scholar]
  205. Kumar P. Sharma H. Singh A. Durgapal S. Kukreti G. Bhowmick M. Bhowmick P. Ashique S. Targeting the interplay of proteins through PROTACs for management cancer and associated disorders. Curr. Cancer Ther. Rev. 2024 20 [Internet]. 10.2174/0115733947304806240417092449
    [Google Scholar]
  206. Sharma H. Chandra P. Effects of natural remedies on memory loss and alzheimer’s disease. Afr.J.Bio.Sc. 2024 6 7 187 211 10.33472/AFJBS.6.7.2024.187‑211
    [Google Scholar]
  207. Halagali P. Inamdar A. Singh J. Anand A. Sadhu P. Pathak R. Sharma H. Biswas D. Phytochemicals, herbal extracts, and dietary supplements for metabolic disease management. Endocr. Metab. Immune Disord. Drug Targets 2024 24 10.2174/0118715303287911240409055710 38676520
    [Google Scholar]
  208. Das S. Mukherjee T. Mohanty S. Nayak N. Mal P. Ashique S. Pal R. Mohanto S. Sharma H. Impact of NF-κB signaling and Sirtuin-1 protein for targeted inflammatory intervention. Curr. Pharm. Biotechnol. 2024 25 10.2174/0113892010301469240409082212 38638042
    [Google Scholar]
  209. Sharma H. Kaushik M. Goswami P. Sreevani S. Chakraborty A. Ashique S. Pal R. Role of miRNAs in brain development. MicroRNA 2024 13 2 96 109 10.2174/0122115366287127240322054519 38571343
    [Google Scholar]
  210. Ashique S. Bhowmick M. Pal R. Khatoon H. Kumar P. Sharma H. Garg A. Kumar S. Das U. Multi drug resistance in Colorectal Cancer- Approaches to overcome, advancements and future success. Advances in Cancer Biology - Metastasis 2024 10 100114 10.1016/j.adcanc.2024.100114
    [Google Scholar]
  211. Ashique S. Pal R. Sharma H. Mishra N. Garg A. Unraveling the emerging niche role of extracellular vesicles (EVs) in traumatic brain injury (TBI). CNS Neurol. Disord. Drug Targets 2024 23 11 1357 1370 10.2174/0118715273288155240201065041 38351688
    [Google Scholar]
  212. Kumar P. Pandey S. Ahmad F. Verma A. Sharma H. Ashique S. Carbon nanotubes: A targeted drug delivery against cancer cell. Curr. Nanosci. 2023 9 1 31 10.2174/0115734137271865231105070727
    [Google Scholar]
  213. Sharma H. Chandra P. Verma A. Pandey S.N. Kumar P. Sigh A. Therapeutic approaches of nutraceuticals in the prevention of neurological disorders. Eur. Chem. Bull. 2023 12 5 1575 1596
    [Google Scholar]
  214. Sharma H. Chandra P. Challenges and future prospects: A benefaction of phytoconstituents on molecular targets pertaining to alzheimer’s disease. Int. J. Pharm. Investig. 2023 14 1 117 126 10.5530/ijpi.14.1.15
    [Google Scholar]
  215. Sharma H. Pathak R. Jain S. Bhandari M. Mishra R. Reena K. Varshney P. Ficus racemosa L: A review on its important medicinal uses, phytochemicals and biological activities. J. Popul. Ther. Clin. Pharmacol. 2023 30 17 213 227 10.47750/jptcp.2023.30.17.018
    [Google Scholar]
  216. Singh L.P. Gugulothu S. Perusomula R. Mishra A. Bhavani P.D. Singh S. Sharma H. Dwivedi M. Synthesis of some tetrazole and thiazolidine-4-One derivatives of schiff base by using ionic liquids as catalyst and evaluation of their antifungal and antibacterial activity. Eur. Chem. Bull. 2023 12 8 281 297
    [Google Scholar]
  217. Pathak Rashmi A brief review on pathogenesis, transmission and management of monkeypox virus outbreaks. Bull. Environ. Pharmacol. Life Sci. 2023 12 4 244 256
    [Google Scholar]
  218. Sharma H. Bhattacharya V. Bhatt A. Garg S. Chaurasia G. Akram W. Sharma K. Mandal S. Optimization of formulation by box Behnken and in-vitro studies of emulsified gel containing zaltoprofen for the management of arthritis. Eur. Chem. Bull. 2023 12 4 11734 11744
    [Google Scholar]
  219. Manju Koli Nogai L. Bhandari M. Mishra R. Pathak R. Sharma H. Formulation and evaluation of berberine hydrochloride film coated tablet. J. Pharm. Negat. Results 2023 ••• 3439 3449 10.47750/pnr.2023.14.02.403
    [Google Scholar]
  220. Dwivedi M. Jha K.K. Pandey S. Sachan A. Sharma H. Dwivedi S.K. Formulation and evaluation of herbal medicated chocolate in treatment of intestinal worms and related problems. IJFANS 2022 11 2 1426 1439
    [Google Scholar]
  221. Sharma H. Pathak R. Kumar N. Nogai L. Mishra R. Bhandari M. Koli M. Pandey P. Endocannabinoid system: Role in depression, recompense, and pain control. Journal of Survey in Fisheries Sciences. 2023 10 4S 2743 2751 10.17762/sfs.v10i4S.1655
    [Google Scholar]
  222. Sharma H. Pathak R. Saxena D. Kumar N. Emerging role of non-coding RNA’S: Human health and diseases. GIS 2022 9 7 2022 2050
    [Google Scholar]
  223. Sharma H. Rani T. Khan S. An insight into neuropathic pain: A systemic and up-to-date review. Int. J. Pharm. Sci. Res. 2023 14 2 607 621 10.13040/IJPSR.0975‑8232.14(2).607‑21
    [Google Scholar]
  224. Pandey P. Kumar N. Kaur T. Saini S. Sharma H. Antidiabetic activity of caesalpinia bonducella leaves of hydro alcoholic extracts in albino rats. YMER Digital 2022 21 7 840 846 10.37896/YMER21.07/67
    [Google Scholar]
  225. Pathak R. Sharma H. Kumar N. A brief review on anthocephalus cadamba. Acta Scientific Pharmacology. 2022 3 5
    [Google Scholar]
  226. Sharma S. Dinda S.C.S.H. Matrix types drug delivery system for sustained release : A review. 2022 https://doi-ds.org/doilink/03.2022-65678198/ASIO-JDD/10.2016-21915953/2022/V6I1/920
    [Google Scholar]
  227. Sharma H. Pathak R. A review on prelimenary phytochemical screening of curcuma longa linn. J Pharma Herbal Med Res 2021 7 2 24 27
    [Google Scholar]
  228. Pathak R. Sharma H. A review on medicinal uses of Cinnamomum verum (Cinnamon). J. Drug Deliv. Ther. 2021 11 6-S 161 166 10.22270/jddt.v11i6‑S.5145
    [Google Scholar]
  229. Sharma H. Pande M. Jha K.K. 2020 Hyperuricemia: a risk factor beyond gout. ASIO-JPHMR 2020 6 1 42 49
    [Google Scholar]
  230. Sharma H. Singh S. Jha K.K. Treatment and recommendations for homeless patients with hypertension, hyperlipidemia & heart failure-a review. ASIO-JEPCR 2020 6 1 24 32
    [Google Scholar]
  231. Sharma H. Pathak R. Sachan N. Chandra P. Role of Tumor Antigens for Cancer Vaccine Development. Cancer Vaccination and Challenges. Apple Academic Press New York 2024 57 94 10.1201/9781003501718‑3
    [Google Scholar]
  232. Sharma H. Anand A. Halagali P. Inamdar A. Pathak R. Taghizadeh‐Hesary F. Ashique S. Advancement of nanoengineered flavonoids for chronic metabolic diseases. Role Flavonoids Chronic Metab. Dis.: Bench to Clinic. 2024 18 459 510 10.1002/9781394238071.ch13
    [Google Scholar]
  233. Datta D. Colaco V. Bandi S.P. Sharma H. Dhas N. Giram P.S. Classes/types of polymers used in oral delivery (natural, semisynthetic, synthetic), their chemical structure and general functionalities. Polymers for Oral Drug Delivery Technologies Elsevier 2025 263 333 10.1016/B978‑0‑443‑13774‑7.00007‑4
    [Google Scholar]
  234. Sharma H. Jai Tyagi S. Pathak N. Keshari A. Varshney P. Pathak R. Social, Economic, and Environmental Justifications for 3D Printing of Pharmaceutical Products. Handbook of 3D Printing in Pharmaceutics. CRC Press Boca Raton 2024 179 194 10.1201/9781003439509‑17
    [Google Scholar]
  235. Cano S. González C.S. Gil-Iranzo R.M. Albiol-Pérez S. Affective communication for socially assistive robots (sars) for children with autism spectrum disorder: A systematic review. Sensors 2021 21 15 5166 10.3390/s21155166 34372402
    [Google Scholar]
  236. Kaushik M. Kumar S. Singh M. Sharma H. Bhowmick M. Bhowmick P. Bio-inspired Nanomaterials in Cancer Theranostics. Nanotheranostics for Diagnosis and Therapy. Springer Nature Singapore 2024 95 123 10.1007/978‑981‑97‑3115‑2_5
    [Google Scholar]
  237. Pathak R. Sachan N. Chandra P. Mechanistic approach towards diabetic neuropathy screening techniques and future challenges: A review. Biomed. Pharmacother. 2022 150 113025 10.1016/j.biopha.2022.113025 35658222
    [Google Scholar]
  238. Bhandari M. Sharma S. Mishra R. Nogai L. Bajaj M. Pathak R. Geography and the therapeutic effect of matcha tea in drinks. J. Pharm. Negat. Results 2022 ••• 5094 5099
    [Google Scholar]
  239. Pathak R. Sachan N. Kabra A. Alanazi A.S. Alanazi M.M. Alsaif N.A. Chandra P. Isolation, characterization, development and evaluation of phytoconstituent based formulation for diabetic neuropathy. Saudi Pharm. J. 2023 31 8 101687 10.1016/j.jsps.2023.06.020 37448840
    [Google Scholar]
  240. Pathak R. Pandey S.P. Chandra P. Gastroprotective effects of biological macromolecule: Polysaccharides. Macromol. Symp. 2024 413 1 2300122 10.1002/masy.202300122
    [Google Scholar]
  241. Chandra P. Sachan N. Pathak R. Pal D. Medicinal Plants Against Vesicular Stomatitis Virus (VSV) Infections: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies. Anti-Viral Metabolites from Medicinal Plants Springer International Publishing Cham 2023 603 638
    [Google Scholar]
  242. Chandra P. Kaleem M. Sachan N. Pathak R. Alanazi A.S. Alsaif N.A. Alsanea S. Alsuwayt B. Alanazi M.M. Kabra A. Gastroprotective evaluation of Medicago sativa L. (Fabaceae) on diabetic rats. Saudi Pharm. J. 2023 31 11 101815 10.1016/j.jsps.2023.101815 37860685
    [Google Scholar]
  243. Chandra P Sachan N Pathak R Pal D. Role of pistachio, cashew, and almond seeds in prevention and treatment of abnormal proliferation. Anti-proliferative Storehouse for Bioactive Secondary Metabolites Springer Singapore 2024 727 727
    [Google Scholar]
  244. Chandra P Sachan N Pathak R Patel AK Pal D Camellia and lotus seeds: Plant made subunit in prevention and treatment of malignant diseases. Seeds: Anti-proliferative Storehouse for Bioactive Secondary Metabolites Springer Singapore 2024 869 900
    [Google Scholar]
  245. Sharma H. Rachamalla H.K. Mishra N. Chandra P. Pathak R. Ashique S. Mishra N. Ashique S. Garg A. Chithravel V. Anand K. Introduction to exosome and its role in brain disorders BT. Exosomes Based Drug Delivery Strategies for Brain Disorders. Springer Nature Singapore Singapore 2024 1 35 10.1007/978‑981‑99‑8373‑5_1
    [Google Scholar]
  246. Kumar P. Ashique S. Kumar N. Jain A. Sharma H. Pandey S.N. Regulation of plant hormones under abiotic stress conditions in plants. Plant Secondary Metabolites and Abiotic Stress. Wiley 2024 243 276 10.1002/9781394186457.ch10
    [Google Scholar]
  247. Sharma H. Tyagi S.J. Chandra P. Verma A. Kumar P. Ashique S. Mishra N. Ashique S. Garg A. Chithravel V. Anand K. Role of exosomes in parkinson’s and alzheimer’s diseases BT. Exosomes Based Drug Delivery Strategies for Brain Disorders. Springer Nature Singapore Singapore 2024 147 182 10.1007/978‑981‑99‑8373‑5_6
    [Google Scholar]
  248. Kumar P. Sharma H. Singh A. Pandey S.N. Chandra P. Mishra N. Ashique S. Garg A. Chithravel V. Anand K. Correlation between exosomes and neuro-inflammation in various brain disorders BT. Exosomes Based Drug Delivery Strategies for Brain Disorders. Springer Nature Singapore 2024 273 302 10.1007/978‑981‑99‑8373‑5_11
    [Google Scholar]
  249. Al Noman A. Afrosa H. Lihu I.K. Sarkar O. Nabin N.R. Datta M. Pathak R. Sharma H. Vitamin D and neurological health: Unraveling risk factors, disease progression, and treatment potential. CNS Neurol. Disord. Drug Targets 2024 24 1 12 10.2174/0118715273330972241009092828 39440730
    [Google Scholar]
  250. Chandra P. Porwal M. Rastogi V. Tyagi S.J. Sharma H. Verma A. Carb‐loaded passion: A comprehensive exploration of carbohydrates in shaping aphrodisiac effects. Macromol. Symp. 2024 413 5 2400064 10.1002/masy.202400064
    [Google Scholar]
  251. Sarkar S. Bhui U. Kumar B. Ashique S. Kumar P. Sharma H. Correlation between cognitive impairment and peripheral biomarkers - Significance of phosphorylated Tau and Amyloid-β in alzheimer’s Disease : A new insight. Curr Psychiatry Res Rev 2024 1 25
    [Google Scholar]
/content/journals/cprr/10.2174/0126660822328919241212114244
Loading
/content/journals/cprr/10.2174/0126660822328919241212114244
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test