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首页> 外文期刊>Psychopharmacology >In the ventral tegmental area picrotoxin blocks FGIN 1-27-induced increases in sexual behavior of rats and hamsters
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In the ventral tegmental area picrotoxin blocks FGIN 1-27-induced increases in sexual behavior of rats and hamsters

机译:在腹侧被膜区,微毒素阻断FGIN 1-27诱导的大鼠和仓鼠性行为增加

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摘要

There are two types of benzodiazepine receptors, mitochondrial benzodiazepine receptors (MBRs), and γ-aminobutyric acid (GABAA)/benzodiazepine receptor complexes (GBRs). MBR activation increases neurosteroidogenesis. Ventral tegmental area (VTA) infusions of the MBR agonist, FGIN 1-27, increase midbrain levels of the progesterone metabolite 5α-pregnan-3α-ol-20-one (3α,5α-THP) and lordosis of rats and hamsters. Activation of GBRs leads to membrane hyperpolarization. In the VTA, infusions of GBR agonists enhance 3α,5α-THP-facilitated lordosis. Thus, if, in the VTA, MBR-mediated increases in 3α,5α-THP enhance sexual responses via actions at GBRs, then blocking GBRs with picrotoxin will reduce FGIN 1-27-induced increases in sexual behavior of female rodents.
机译:苯并二氮杂receptor受体有两种类型,线粒体苯并二氮杂receptor受体(MBR)和γ-氨基丁酸(GABAA )/苯并二氮杂receptor受体复合物(GBR)。 MBR激活会增加神经甾体生成。 MBR激动剂FGIN 1-27的腹侧被盖区(VTA)输注会增加孕酮代谢物5α-pregnan-3α-ol-20-one(3α,5α-THP)的中脑水平,并导致大鼠和仓鼠的脊柱前凸。 GBR的激活导致膜超极化。在VTA中,输注GBR激动剂可增强3α,5α-THP促进的脊柱前凸。因此,如果在VTA中,MBR介导的3α,5α-THP的增加通过对GBR的作用增强了性反应,那么用微毒素阻断GBR将减少FGIN 1-27诱导的雌性啮齿动物性行为的增加。

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