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前列腺素E2介导甲氧明对去卵巢雌性恒河猴体内促黄体生成激素释放激素(LH-RH)释放的刺激作用。

Prostaglandin E2 mediates the stimulatory effect of methoxamine on in vivo luteinizing hormone-releasing hormone (LH-RH) release in the ovariectomized female rhesus monkey.

作者信息

Gearing M, Terasawa E

机构信息

Wisconsin Regional Primate Research Center, Madison 53715.

出版信息

Brain Res. 1991 Sep 27;560(1-2):276-81. doi: 10.1016/0006-8993(91)91243-t.

Abstract

Previously, we found that noradrenergic input through alpha 1-receptors modulates pulsatile release of luteinizing hormone-releasing hormone (LH-RH) in ovariectomized rhesus monkeys in the absence of estrogen. In the present study, the role of prostaglandin E2 (PGE2) in mediating alpha-adrenergic stimulation of LH-RH release is investigated. In the first experiment the effects of the alpha 1-adrenergic agonist methoxamine (MTX) on LH-RH and PGE2 release were examined. Push-pull perfusion of the stalk-median eminence (S-ME) was performed in conscious, ovariectomized monkeys, and perfusate samples were collected on ice. MTX (10(-5) M) was infused into the S-ME through the push cannula for 10 min at 90-min intervals, and LH-RH and PGE2 in aliquots of the same perfusate samples were measured by radioimmunoassay. Infusion of MTX significantly stimulated LH-RH release (n = 12; P less than 0.01) and PGE2 release (P less than 0.05). In the second experiment, the effect of PGE2 infusion on LH-RH release was tested. PGE2 (10(-7) M) was infused using the same protocol as above, and LH-RH was measured in the perfusates. Infusion of PGE2 through the push cannula significantly stimulated LH-RH release (n = 23; P less than 0.05). These results suggest that the stimulatory effect of MTX on LH-RH release is at least partly mediated by PGE2, since MTX stimulated not only LH-RH but also PGE2 release, and since PGE2 itself stimulated LH-RH release. Therefore, PGE2 may be an important endogenous mediator of alpha 1-adrenergic input stimulating pulsatile LH-RH release.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

此前,我们发现,在切除卵巢的恒河猴体内,在缺乏雌激素的情况下,通过α1受体的去甲肾上腺素能输入调节促黄体生成激素释放激素(LH-RH)的脉冲式释放。在本研究中,研究了前列腺素E2(PGE2)在介导α-肾上腺素能刺激LH-RH释放中的作用。在第一个实验中,检测了α1-肾上腺素能激动剂甲氧明(MTX)对LH-RH和PGE2释放的影响。对清醒的、切除卵巢的猴子进行推挽式正中隆起(S-ME)灌注,并将灌注液样本收集在冰上。MTX(10(-5) M)通过推注套管以90分钟的间隔注入S-ME 10分钟,通过放射免疫测定法测量同一灌注液样本等分中的LH-RH和PGE2。注入MTX显著刺激了LH-RH释放(n = 12;P < 0.01)和PGE2释放(P < 0.05)。在第二个实验中,测试了注入PGE2对LH-RH释放的影响。使用与上述相同的方案注入PGE2(10(-7) M),并在灌注液中测量LH-RH。通过推注套管注入PGE2显著刺激了LH-RH释放(n = 23;P < 0.05)。这些结果表明,MTX对LH-RH释放的刺激作用至少部分由PGE2介导,因为MTX不仅刺激了LH-RH,还刺激了PGE2释放,并且因为PGE2本身刺激了LH-RH释放。因此,PGE2可能是刺激LH-RH脉冲式释放的α1-肾上腺素能输入的重要内源性介质。(摘要截短为250字)

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