Javadi-Paydar Mehrak, Kerr Tony M, Taffe Michael A
Department of Neuroscience; The Scripps Research Institute; La Jolla, CA, USA.
Department of Psychiatry, University of California, San Diego; La Jolla, CA, USA.
bioRxiv. 2024 Feb 14:2024.02.12.579996. doi: 10.1101/2024.02.12.579996.
Preclinical models of electronic nicotine delivery system (ENDS; "e-cigarette") use have been rare, so there is an urgent need to develop experimental approaches to evaluate their effects.
To contrast the impact of inhaled nicotine across sex.
Male and female Wistar rats were exposed to vapor from a propylene glycol vehicle (PG), nicotine (NIC; 1-30 mg/mL in PG), or were injected with NIC (0.1-0.8 mg/kg, s.c.), and then assessed for changes in temperature and activity. The antagonist mecamylamine (2 mg/kg) was administered prior to NIC to verify pharmacological specificity. Plasma levels of nicotine and cotinine were determined after inhalation and injection.
Activity increased in females for ~60 minutes after nicotine inhalation, and this was blocked by mecamylamine. A similar magnitude of hyperlocomotion was observed after s.c. administration. Body temperature was reduced after nicotine inhalation by female rats but mecamylamine increased this hypothermia. Increased locomotor activity was observed in male rats if inhalation was extended to 40 minutes or when multiple inhalation epochs were used per session. The temperature of male rats was not altered by nicotine. Plasma nicotine concentrations were slightly lower in male rats than in female rats after 30-minute nicotine vapor inhalation and slightly higher after nicotine injection (1.0 mg/kg, s.c.).
Nicotine inhalation increases locomotor activity in male and female rats to a similar or greater extent than by subcutaneous injection. Sex differences were observed, which may be related to lower nicotine plasma levels, lower baseline activity and/or a higher vehicle response in males.
电子尼古丁传送系统(ENDS;“电子烟”)使用的临床前模型很少见,因此迫切需要开发实验方法来评估其效果。
对比吸入尼古丁对不同性别的影响。
将雄性和雌性Wistar大鼠暴露于丙二醇载体(PG)、尼古丁(NIC;在PG中为1 - 30mg/mL)的蒸汽中,或皮下注射NIC(0.1 - 0.8mg/kg),然后评估体温和活动的变化。在给予NIC之前给予拮抗剂美加明(2mg/kg)以验证药理学特异性。吸入和注射后测定血浆中尼古丁和可替宁的水平。
尼古丁吸入后,雌性大鼠的活动增加约60分钟,这被美加明阻断。皮下给药后观察到类似程度的运动亢进。雌性大鼠吸入尼古丁后体温降低,但美加明加剧了这种体温过低。如果将吸入时间延长至40分钟或每次使用多个吸入时段,则雄性大鼠的运动活动增加。尼古丁未改变雄性大鼠的体温。吸入尼古丁30分钟后,雄性大鼠的血浆尼古丁浓度略低于雌性大鼠,皮下注射尼古丁(1.0mg/kg)后略高。
吸入尼古丁使雄性和雌性大鼠的运动活动增加,程度与皮下注射相似或更大。观察到了性别差异,这可能与雄性大鼠较低的血浆尼古丁水平、较低的基线活动和/或较高的载体反应有关。