Behavioral Pharmacology Research Unit, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Addict Biol. 2021 Jul;26(4):e12968. doi: 10.1111/adb.12968. Epub 2020 Sep 28.
Policy changes have increased access to cannabis for individuals with little or no prior exposure. Few studies have examined sex differences in cannabis effects among individuals with sporadic cannabis use or for nonsmoked routes of cannabis administration. Data from four double-blind, placebo-controlled studies were pooled to compare the acute pharmacodynamic effects of vaporized and oral cannabis in male (n = 27) and female (n = 23) participants who used cannabis infrequently (no use ≥30 days prior to randomization). Analyses compared peak change-from-baseline scores between male and female participants for subjective drug effects, cognitive/psychomotor performance, cardiovascular effects, and blood concentrations of Δ9-tetrahydrocannabinol (THC) and its primary metabolites (11-OH-THC, THC-COOH) after exposure to placebo cannabis or cannabis containing low-dose (5 or 10 mg) or high-dose THC (20 or 25 mg). Overall, cannabis elicited dose-orderly increases in subjective effects, impairment of cognitive/psychomotor performance, heart rate, and blood cannabinoid concentrations. Females exhibited greater peak blood 11-OH-THC concentrations and reported greater peak subjective ratings of "drug effect" that remained when controlling for body weight. When controlling for both body weight and peak blood cannabinoid concentrations, ratings of "anxious/nervous," "heart racing," and "restless" were significantly higher for females than males. Although additional research is needed to elucidate sex differences in responses to cannabis at a wider range of THC doses, other routes of administration, and products with diverse chemical composition, the current data indicate that public health messaging and clinical decision making around the use of cannabinoids should recommend lower starting doses for females and warnings about acute anxiogenic reactions.
政策的改变增加了那些以前接触过很少或没有接触过大麻的个人获取大麻的机会。很少有研究调查过在偶尔使用大麻或非吸烟途径使用大麻的个体中,大麻效应的性别差异。四项双盲、安慰剂对照研究的数据被汇总,以比较男性(n=27)和女性(n=23)参与者在使用大麻不频繁(在随机分组前≥30 天无使用)时,吸入式和口服大麻的急性药效学效应。分析比较了男性和女性参与者在接受安慰剂大麻或含有低剂量(5 或 10mg)或高剂量 THC(20 或 25mg)大麻时,从基线的主观药物效应、认知/心理运动表现、心血管效应以及血液中 Δ9-四氢大麻酚(THC)及其主要代谢物(11-羟基-THC、THC-COOH)浓度的峰值变化。总的来说,大麻引起了剂量有序的主观效应增加、认知/心理运动表现受损、心率和血液大麻素浓度增加。女性表现出更高的峰值血液 11-羟基-THC 浓度,并报告了更高的峰值主观“药物效应”评分,在控制体重后仍然存在。当同时控制体重和峰值血液大麻素浓度时,女性比男性报告的“焦虑/紧张”、“心跳加速”和“不安”的评分明显更高。尽管需要进一步的研究来阐明在更广泛的 THC 剂量、其他给药途径和具有不同化学成分的产品中对大麻的反应中的性别差异,但目前的数据表明,在大麻素使用方面的公共卫生信息和临床决策应该建议女性使用较低的起始剂量,并警告急性焦虑反应。