PMID- 35338387 OWN - NLM STAT- MEDLINE DCOM- 20220518 LR - 20220910 IS - 1432-2072 (Electronic) IS - 0033-3158 (Linking) VI - 239 IP - 5 DP - 2022 May TI - The effects of prenatal nicotine and THC E-cigarette exposure on motor development in rats. PG - 1579-1591 LID - 10.1007/s00213-022-06095-8 [doi] AB - RATIONALE: In the USA, nicotine and cannabis are the most common licit and illicit drugs used among pregnant women. Importantly, nicotine and cannabis are now being combined for consumption via e-cigarettes, an increasingly popular delivery device. Both nicotine and tetrahydrocannabinol (THC), the primary psychoactive component of cannabis, cross the placenta barrier. However, the consequences of prenatal cannabis use are not well understood, and less is known about potential combination effects when consumed with nicotine, especially via e-cigarettes. OBJECTIVE: The present study used a rodent model to examine how prenatal e-cigarette exposure to nicotine, THC, and the combination impacts motor development among offspring. METHODS: Pregnant Sprague-Dawley rats were exposed to nicotine (36 mg/mL), THC (100 mg/mL), the combination, or vehicle via e-cigarette inhalation from gestational days (GD) 5-20. One sex pair per litter was tested on an early sensorimotor development task (postnatal days [PD] 12-20) and a parallel bar motor coordination task (PD 30-32). RESULTS: Combined prenatal exposure to nicotine and THC delayed sensorimotor development, even though neither drug produced impairments on their own. In contrast, prenatal exposure to either nicotine or THC impaired motor coordination, whereas combined exposure exacerbated these effects, particularly among females. CONCLUSIONS: These data illustrate that prenatal exposure to either nicotine or THC may alter motor development, and that the combination may produce more severe effects. These findings have important implications for pregnant women as we better understand the teratogenic effects of these drugs consumed via e-cigarettes. CI - (c) 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. FAU - Hussain, S AU - Hussain S AD - Center for Behavioral Teratology, Department of Psychology, San Diego State University, CA, San Diego, USA. FAU - Breit, K R AU - Breit KR AD - Center for Behavioral Teratology, Department of Psychology, San Diego State University, CA, San Diego, USA. AD - Department of Psychology, West Chester University of Pennsylvania, West Chester, PA, USA. FAU - Thomas, J D AU - Thomas JD AD - Center for Behavioral Teratology, Department of Psychology, San Diego State University, CA, San Diego, USA. Thomas3@sdsu.edu. LA - eng GR - R21 AA025425/AA/NIAAA NIH HHS/United States GR - 28IP-0026/Tobacco-Related Disease Research Program/ GR - T32AA007456-38/AA/NIAAA NIH HHS/United States PT - Journal Article DEP - 20220326 PL - Germany TA - Psychopharmacology (Berl) JT - Psychopharmacology JID - 7608025 RN - 0 (Cannabinoid Receptor Agonists) RN - 0 (Hallucinogens) RN - 6M3C89ZY6R (Nicotine) RN - 7J8897W37S (Dronabinol) SB - IM MH - Animals MH - Cannabinoid Receptor Agonists/pharmacology MH - Dronabinol/toxicity MH - *Electronic Nicotine Delivery Systems MH - Female MH - *Hallucinogens MH - Humans MH - Nicotine/toxicity MH - Pregnancy MH - *Prenatal Exposure Delayed Effects MH - Rats MH - Rats, Sprague-Dawley OTO - NOTNLM OT - Behavior OT - Cannabis OT - E-cigarette OT - Motor OT - Nicotine OT - Prenatal OT - THC EDAT- 2022/03/27 06:00 MHDA- 2022/05/19 06:00 CRDT- 2022/03/26 05:31 PHST- 2021/10/22 00:00 [received] PHST- 2022/02/13 00:00 [accepted] PHST- 2022/03/27 06:00 [pubmed] PHST- 2022/05/19 06:00 [medline] PHST- 2022/03/26 05:31 [entrez] AID - 10.1007/s00213-022-06095-8 [pii] AID - 10.1007/s00213-022-06095-8 [doi] PST - ppublish SO - Psychopharmacology (Berl). 2022 May;239(5):1579-1591. doi: 10.1007/s00213-022-06095-8. Epub 2022 Mar 26.