Castelli Maria Paola, Fadda Paola, Casu Angelo, Spano Maria Sabrina, Casti Alberto, Fratta Walter, Fattore Liana
CNR National Research Council of Italy, Neuroscience Institute - Cagliari, @ Department of Biomedical Sciences, Division of Neuroscience and Clinical Pharmacology, University of Cagliari, Cittadella Universitaria di Monserrato, 09042 Monserrato (Cagliari), Italy.
Curr Pharm Des. 2014;20(13):2100-13. doi: 10.2174/13816128113199990430. Epub 2013 Jul 9.
Sex-dependent differences are frequently observed in the biological and behavioural effects of substances of abuse, including cannabis. We recently demonstrated a modulating effect of sex and oestrous cycle on cannabinoid-taking and seeking behaviours. Here, we investigated the influence of sex and oestrogen in the regulation of cannabinoid CB1 receptor density and function, measured by [(3)H]CP55940 and CP55940-stimulated [(35)S]GTPγS binding autoradiography, respectively, in the prefrontal cortex (Cg1 and Cg3), caudate- putamen, nucleus accumbens, amygdala and hippocampus of male and cycling female rats, as well as ovariectomised (OVX) rats and OVX rats primed with oestradiol (10 µg/rat) (OVX+E). CB1 receptor density was significantly lower in the prefrontal cortex and amygdala of cycling females than in males and in OVX females, a difference that appeared to be oestradiol-dependent, because it was no more evident in the OVX+E group. CP55940-stimulated [(35)S]GTPγS binding was significantly higher in the Cg3 of OVX rats relative to cycling and OVX+E rats. No difference was observed in CB1 receptor density or function in any of the other brain areas analysed. Finally, sex and oestradiol were also found to affect motor activity, social behaviour and sensorimotor gating in rats tested in locomotor activity boxes, social interaction and prepulse inhibition tasks, respectively. Our findings provide biochemical evidence for sex- and hormone- dependent differences in the density and function of CB1 receptors in selected brain regions, and in behaviours associated with greater vulnerability to drug addiction, revealing a more vulnerable behavioural phenotype in female than in male rats.
在包括大麻在内的滥用物质的生物学和行为效应中,经常观察到性别依赖性差异。我们最近证明了性别和发情周期对大麻素摄取和觅药行为的调节作用。在此,我们分别通过[(3)H]CP55940和CP55940刺激的[(35)S]GTPγS结合放射自显影技术,研究了性别和雌激素对雄性和处于发情周期的雌性大鼠以及卵巢切除(OVX)大鼠和用雌二醇(10μg/只)预处理的OVX大鼠(OVX+E)前额叶皮质(Cg1和Cg3)、尾状壳核、伏隔核、杏仁核和海马中大麻素CB1受体密度和功能的影响。与雄性和OVX雌性大鼠相比,处于发情周期的雌性大鼠前额叶皮质和杏仁核中的CB1受体密度显著降低,这种差异似乎依赖于雌二醇,因为在OVX+E组中不再明显。相对于处于发情周期的大鼠和OVX+E大鼠,OVX大鼠Cg3中CP55940刺激的[(35)S]GTPγS结合显著更高。在所分析的任何其他脑区中,未观察到CB1受体密度或功能的差异。最后,还发现性别和雌二醇分别影响在运动活动箱、社会互动和前脉冲抑制任务中测试的大鼠运动活动、社会行为和感觉运动门控。我们的研究结果为选定脑区中CB1受体密度和功能以及与药物成瘾易感性增加相关的行为中的性别和激素依赖性差异提供了生化证据,揭示了雌性大鼠比雄性大鼠更易受影响的行为表型。