D'Souza D N, Harlan R E, Garcia M M
Department of Anatomy, Tulane University School of Medicine, New Orleans, LA 70112, USA.
Neuroscience. 1999;93(4):1539-47. doi: 10.1016/s0306-4522(99)00229-8.
It has been suggested that there are sex differences in the neural response to drugs of abuse. Previous studies have shown that, upon administration of morphine, the immediate early gene c-Fos is induced in the striatum, nucleus accumbens and cortex of the rat brain. This induction of c-Fos is reduced by administration of the N-methyl-D-aspartate receptor antagonist dizocilpine maleate. However, in studies using immunocytochemistry, we found that the pattern of this expression differed markedly between the sexes. In male rats treated with morphine (10 mg/kg, s.c.) and killed 2 h later, there was an induction of c-Fos in the dorsomedial caudate-putamen, the nucleus accumbens and in the intralaminar nuclei of the thalamus. Administration of dizocilpine maleate (0.2 mg/kg, i.p.; 30 min before morphine) partially blocked the response in the caudate-putamen, but not in the thalamus. In females, morphine induced c-Fos in the caudate-putamen, but with more inter-animal variability than in males. In the midline intralaminar thalamic nuclei, female rats showed less induction than males. In male rats, dizocilpine maleate alone caused negligible induction of c-Fos, whereas in female rats, it caused a large induction in the rhomboid, reuniens and central medial nuclei of the thalamus, and in the cortex. Whereas dizocilpine maleate partially blocked the morphine-induced c-Fos expression in the caudate-putamen of males, it completely blocked this response in females. With dizocilpine maleate alone, there was little or no effect on behavior in male rats, whereas in female rats, it caused head bobbing, thrashing, hyperactivity and uncoordinated movements. These behavioral sex differences were not seen on treatment of rats with the competitive N-methyl-D-aspartate receptor antagonist 2R,4R,5S-2-amino-4,5-(1,2-cyclohexyl)-7-phosphoheptanoic acid (NPC-17742; 10 mg/kg, i.p.) and this drug did not induce c-Fos expression in either sex. In the caudate-putamen, morphine-induced c-Fos expression was significantly reduced by NPC-17742 (30 min before morphine) in males and completely blocked in females. These results suggest that the responses to both morphine and N-methyl-D-aspartate receptor antagonists differ between the sexes and emphasize that glutamate is involved in morphine-induced immediate early gene expression in the brain. These studies thus have important implications for gender differences in drug addiction.
有人提出,在对滥用药物的神经反应方面存在性别差异。先前的研究表明,给大鼠脑部注射吗啡后,即刻早期基因c-Fos会在纹状体、伏隔核和大脑皮层中被诱导表达。给予N-甲基-D-天冬氨酸受体拮抗剂马来酸氯氮平可降低这种c-Fos的诱导表达。然而,在使用免疫细胞化学的研究中,我们发现这种表达模式在两性之间存在显著差异。在用吗啡(10毫克/千克,皮下注射)处理并在2小时后处死的雄性大鼠中,背内侧尾状核-壳核、伏隔核和丘脑板内核中出现了c-Fos的诱导表达。给予马来酸氯氮平(0.2毫克/千克,腹腔注射;在吗啡注射前30分钟)可部分阻断尾状核-壳核中的反应,但对丘脑中的反应没有影响。在雌性大鼠中,吗啡可诱导尾状核-壳核中c-Fos的表达,但与雄性大鼠相比,动物个体间的变异性更大。在丘脑的中线板内核中,雌性大鼠的诱导表达比雄性大鼠少。在雄性大鼠中,单独给予马来酸氯氮平引起的c-Fos诱导表达可忽略不计,而在雌性大鼠中,它可在丘脑的菱形核、连合核和中央内侧核以及皮层中引起大量诱导表达。虽然马来酸氯氮平可部分阻断雄性大鼠尾状核-壳核中吗啡诱导的c-Fos表达,但它可完全阻断雌性大鼠中的这种反应。单独使用马来酸氯氮平对雄性大鼠的行为几乎没有影响,而在雌性大鼠中,它会引起点头、翻滚、多动和不协调运动。在用竞争性N-甲基-D-天冬氨酸受体拮抗剂2R,4R,5S-2-氨基-4,5-(1,2-环己基)-7-磷酸庚酸(NPC-17742;10毫克/千克,腹腔注射)处理大鼠时,未观察到这些行为上的性别差异,并且这种药物在两性中均未诱导c-Fos表达。在尾状核-壳核中,NPC-17742(在吗啡注射前30分钟)可显著降低雄性大鼠中吗啡诱导的c-Fos表达,并完全阻断雌性大鼠中的表达。这些结果表明,两性对吗啡和N-甲基-D-天冬氨酸受体拮抗剂的反应不同,并强调谷氨酸参与了大脑中吗啡诱导的即刻早期基因表达。因此,这些研究对药物成瘾中的性别差异具有重要意义。