Canonaco M, Tavolaro R, Facciolo R M
Ecology Department, University of Calabria, Cosenza, Italy.
J Comp Neurol. 1997 Apr 21;380(4):423-34.
Labeling of the two more important gamma-aminobutyric acidA (GABA(A)) supramolecular sites with [3H] muscimol (GABA(A)) and [3H] flunitrazepam (benzodiazepine) provided saturable, stable, and dimorphic binding activities in cortical and limbic regions of the wood mouse Apodemus sylvaticus. Of the cortical layers, which contained the highest [3H] muscimol binding levels, only the female lamina V supplied a greater (51%; P <0.01) receptor density than in the male. Areas of the limbic system instead proved to be the more favorable targets for differential GABA(A) binding levels. The highest (P <0.001) and higher levels were found in the oriens-pyramidalis CA1 layer of the hippocampus (65%) and in the vertical limb diagonal band-medial septal nucleus (48%), basolateral amygdala nucleus (45%), and ventromedial hypothalamic nucleus (43%), respectively, of the female. A similar pattern was obtained for [3H]flunitrazepam binding activity, especially in the presence of GABA. The highest and higher binding activities were obtained in the female central amygdala nucleus (78%) and in the ventromedial hypothalamic nucleus (52%), basolateral amygdala nucleus (48%), and oriens-pyramidalis CA1 layer of the hippocampus (47%), respectively, whereas higher levels were observed only in the male vertical limb diagonal band-medial septal nucleus (56%). Even in the cortical regions, the female exhibited higher (42%; cortex lamina V) and moderately higher (38%; cortex lamina VI) levels, with binding differences in the latter site plus in the basolateral amygdala nucleus occurring in a GABA-nondependent manner. From the saturation binding analyses it was possible to reveal that both maximal number of binding sites (Bmax) and mean dissociation constant (K(D)) modifications were responsible for receptor differences of the two GABAergic sites. These findings tend to suggest that dimorphic variations of the GABA(A) supramolecular sites, in some cortical and limbic regions, are strongly involved in sex-specific aggressive and reproductive activities of rodents living in their natural habitats.
用[³H]蝇蕈醇(GABA(A))和[³H]氟硝西泮(苯二氮卓类)标记两个更重要的γ-氨基丁酸A(GABA(A))超分子位点,在森林小鼠(Apodemus sylvaticus)的皮质和边缘区域提供了可饱和、稳定且呈二态性的结合活性。在含有最高[³H]蝇蕈醇结合水平的皮质层中,只有雌性的第V层提供了比雄性更高(51%;P<0.01)的受体密度。相反,边缘系统的区域被证明是GABA(A)结合水平差异更有利的靶点。在雌性中,最高(P<0.001)和较高水平分别出现在海马体的梨状细胞层CA1(65%)、垂直支斜角带-内侧隔核(48%)、基底外侧杏仁核(45%)和腹内侧下丘脑核(43%)。对于[³H]氟硝西泮结合活性也获得了类似的模式,尤其是在存在GABA的情况下。最高和较高的结合活性分别出现在雌性的中央杏仁核(78%)、腹内侧下丘脑核(52%)、基底外侧杏仁核(48%)和海马体的梨状细胞层CA1(47%),而仅在雄性的垂直支斜角带-内侧隔核(56%)观察到较高水平。即使在皮质区域,雌性也表现出较高(42%;皮质第V层)和中等较高(38%;皮质第VI层)水平,后者位点以及基底外侧杏仁核的结合差异以不依赖GABA的方式出现。从饱和结合分析中可以揭示,结合位点的最大数量(Bmax)和平均解离常数(K(D))的改变都导致了两个GABA能位点的受体差异。这些发现倾向于表明,在一些皮质和边缘区域,GABA(A)超分子位点的二态性变化强烈参与了生活在自然栖息地的啮齿动物的性别特异性攻击和生殖活动。