Festa Eugene D, Russo Scott J, Gazi Farhad M, Niyomchai Tipyamol, Kemen Lynne M, Lin Shen-Nan, Foltz Rodger, Jenab Shirzad, Quinones-Jenab Vanya
Department of Psychology, Hunter College, The City University of New York, 695 Park Avenue, New York, NY 10021, USA.
Neuropharmacology. 2004 Apr;46(5):672-87. doi: 10.1016/j.neuropharm.2003.11.017.
Female rats display a more robust behavioral response to acute cocaine administration than do male rats. However, a clear understanding of the biological mechanisms underlying these differences remains elusive. The present study investigated whether sexual dimorphisms in cocaine-induced motor behavior might be based on monoaminergic levels and/or cocaine pharmacokinetics. An acute injection of cocaine (5, 15, 20 or 30 mg/kg) or saline was administered to male and female rats, and behavioral activity was monitored for 3 h. Following acute cocaine or saline administration motor behavior varied according to dose and sex; overall, female rats displayed greater rearing counts and stereotypic scores, greater total locomotor counts at 15, 20, and 30 mg/kg of cocaine, and greater ambulatory counts at 20 and 30 mg/kg of cocaine than did male rats. Neurochemical determinations in post-mortem tissue showed that both male and female rats had increases in total dopamine (DA) in the caudate putamen (CPu) 15 min following cocaine administration. Additionally, male rats had a decrease in dihydroxyphenylacetic acid (DOPAC)/DA turnover. Female rats showed significant reductions in total levels of DA, DOPAC, HVA, serotonin (5-HT), 5-hydroxyindole acetic acid (5-HIAA), and DOPAC/DA turnover in the nucleus accumbens (NAc). Male rats displayed a reduction only in DOPAC/DA turnover and increases in 5-HT in the NAc following cocaine administration. Furthermore, sex differences in cocaine metabolism were observed where females had greater brain/blood levels of norcocaine and ecgonine methyl ester while male rats had higher blood levels of benzoylecgonine. These results suggest that sex differences in the behavioral responses to cocaine administration could be explained in part by intrinsic differences in both monoaminergic levels and metabolic processes.
与雄性大鼠相比,雌性大鼠对急性给予可卡因表现出更强的行为反应。然而,对于这些差异背后的生物学机制仍缺乏清晰的认识。本研究调查了可卡因诱导的运动行为中的性别差异是否可能基于单胺能水平和/或可卡因的药代动力学。对雄性和雌性大鼠急性注射可卡因(5、15、20或30 mg/kg)或生理盐水,并监测3小时的行为活动。急性给予可卡因或生理盐水后,运动行为因剂量和性别而异;总体而言,与雄性大鼠相比,雌性大鼠在15、20和30 mg/kg可卡因剂量下表现出更多的竖毛次数和刻板行为评分、更多的总运动次数,以及在20和30 mg/kg可卡因剂量下表现出更多的行走次数。死后组织的神经化学测定表明,给予可卡因15分钟后,雄性和雌性大鼠尾壳核(CPu)中的总多巴胺(DA)均增加。此外,雄性大鼠的二羟基苯乙酸(DOPAC)/DA周转率降低。雌性大鼠伏隔核(NAc)中的DA、DOPAC、高香草酸(HVA)、5-羟色胺(5-HT)、5-羟吲哚乙酸(5-HIAA)和DOPAC/DA周转率的总水平显著降低。给予可卡因后,雄性大鼠仅表现出DOPAC/DA周转率降低,而NAc中的5-HT增加。此外,观察到可卡因代谢存在性别差异,雌性大鼠脑/血中的去甲可卡因和芽子碱甲酯水平较高,而雄性大鼠血中的苯甲酰芽子碱水平较高。这些结果表明,可卡因给药行为反应中的性别差异可能部分由单胺能水平和代谢过程的内在差异所解释。