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γ-氨基丁酸能系统对雌激素给药反应中的性别二态性。

Sexual dimorphism in the response of the GABAergic system to estrogen administration.

作者信息

Perez J, Zucchi I, Maggi A

出版信息

J Neurochem. 1986 Dec;47(6):1798-803. doi: 10.1111/j.1471-4159.1986.tb13091.x.

DOI:10.1111/j.1471-4159.1986.tb13091.x
PMID:3021905
Abstract

Administration of estradiol benzoate to gonadectomized female rats results in up-regulation of CNS gamma-aminobutyric acid (GABA) receptors. The increase of [3H]muscimol binding activity is observed in six of the seven brain areas examined. The same treatment, performed in castrated male or androgenized female rats, induced an increase of [3H]muscimol binding only in the striatum. Evidence is provided suggesting that the dimorphic sensitivity of GABA receptor is not correlated with the difference in spontaneous motor activity reported between male and female rats.

摘要

给去性腺的雌性大鼠注射苯甲酸雌二醇会导致中枢神经系统γ-氨基丁酸(GABA)受体上调。在所检测的七个脑区中的六个中观察到了[³H]蝇蕈醇结合活性的增加。在去势雄性大鼠或雄激素化雌性大鼠中进行相同处理,仅在纹状体中诱导[³H]蝇蕈醇结合增加。有证据表明,GABA受体的两性敏感性差异与雄性和雌性大鼠之间报道的自发运动活动差异无关。

相似文献

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Sexual dimorphism in the response of the GABAergic system to estrogen administration.γ-氨基丁酸能系统对雌激素给药反应中的性别二态性。
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Estrogen-induced up-regulation of gamma-aminobutyric acid receptors in the CNS of rodents.雌激素诱导啮齿动物中枢神经系统中γ-氨基丁酸受体上调。
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Delayed but not immediate effects of estrogen curtail gamma-aminobutyric acid-mediated feeding responses elicited from the nucleus accumbens shell.雌激素延迟而非即刻抑制从伏隔核壳部引出的γ-氨基丁酸介导的摄食反应。
Behav Neurosci. 2022 Jun;136(3):219-229. doi: 10.1037/bne0000511. Epub 2022 Apr 7.
2
Estradiol and testosterone modulate the anesthetic action of the GABA-A agonist THIP, but not of the neurosteroid 3alpha,5beta-pregnanolone in the rat.雌二醇和睾酮可调节大鼠体内GABA-A激动剂THIP的麻醉作用,但不调节神经甾体3α,5β-孕烷醇酮的麻醉作用。
Psychopharmacology (Berl). 2004 Mar;172(3):283-90. doi: 10.1007/s00213-003-1649-x. Epub 2003 Dec 17.
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Steroid and barbiturate modulation of the GABAa receptor. Possible mechanisms.
类固醇和巴比妥类药物对GABAa受体的调节作用。可能的机制。
Mol Neurobiol. 1989 Winter;3(4):275-304. doi: 10.1007/BF02740608.
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Sex differences in GABAA receptor binding in rat brain measured by an improved in vitro binding assay.
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