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蛋白质合成抑制剂可防止孕酮对雌性大鼠性接受能力的顺序抑制,且这种抑制与下丘脑孕激素受体水平降低无因果关系。

Sequential inhibition of sexual receptivity by progesterone is prevented by a protein synthesis inhibitor and is not causally related to decreased levels of hypothalamic progestin receptors in the female rat.

作者信息

Parsons B, McEwen B S

出版信息

J Neurosci. 1981 May;1(5):527-31. doi: 10.1523/JNEUROSCI.01-05-00527.1981.

Abstract

In the estrogen-primed ovariectomized female rat, the administration of progesterone facilitates sexual receptivity and activates proceptivity for many hours. If the progesterone dose is large (e.g., 2.5 mg), a refractory period follows, during which time animals are less sensitive to additional progesterone. This refractory period has been termed "sequential inhibition" and has been correlated previously with decreased levels of cytosol progestin receptors in the mediobasal hypothalamus-preoptic area (MBH-POA). Our present results indicate that the "sequential inhibition" of mating behavior by progesterone appears to involve a protein synthetic step that is not related causally to decreased levels of cytosol progestin receptors in the MBH-POA. Animals which received subcutaneous injections of the protein synthesis inhibitor, anisomycin (100 mg/kg in saline), 15 min prior to and again 3 hr after progesterone (2.5 mg in propylene glycol) treatment, displayed greater sexual receptivity at 24 hr than did animals which received subcutaneous saline injections. However, cytosol progestin receptor levels in the MBH-POA of animals which received anisomycin plus progesterone were decreased at 24 hr, relative to animals which received saline plus progesterone. Anisomycin did not produce positive or negative behavioral effects at 24 hr when administered 15 min prior to and again 3 hr after propylene glycol, suggesting that the behavioral effects of anisomycin appear to be related to selective blockade of progesterone action. In separate experiments, we administered single subcutaneous injections of anisomycin at various times relative to progesterone (2.5 mg) treatment. According to the time course of effective anisomycin application, the presumed protein synthesis which is responsible for the inhibition of mating behavior occurs between 3 and 13 hr after the administration of progesterone.

摘要

在经雌激素预处理的去卵巢雌性大鼠中,给予孕酮可促进性接受能力,并在数小时内激活求偶行为。如果孕酮剂量较大(例如2.5毫克),随后会出现不应期,在此期间动物对额外的孕酮不太敏感。这种不应期被称为“顺序抑制”,此前已与中基底下丘脑-视前区(MBH-POA)中胞质孕酮受体水平的降低相关。我们目前的结果表明,孕酮对交配行为的“顺序抑制”似乎涉及一个蛋白质合成步骤,这与MBH-POA中胞质孕酮受体水平的降低没有因果关系。在孕酮(2.5毫克丙二醇溶液)处理前15分钟和处理后3小时,皮下注射蛋白质合成抑制剂茴香霉素(100毫克/千克盐水溶液)的动物,在24小时时比皮下注射盐水的动物表现出更高的性接受能力。然而,与接受盐水加孕酮的动物相比,接受茴香霉素加孕酮的动物在24小时时MBH-POA中的胞质孕酮受体水平降低。在丙二醇溶液处理前15分钟和处理后3小时给予茴香霉素,在24小时时未产生阳性或阴性行为影响,这表明茴香霉素的行为影响似乎与孕酮作用的选择性阻断有关。在单独的实验中,我们在相对于孕酮(2.5毫克)处理的不同时间给予单次皮下注射茴香霉素。根据有效应用茴香霉素的时间进程,推测负责抑制交配行为的蛋白质合成发生在给予孕酮后的3至13小时之间。

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Oestradiol, sexual receptivity and cytosol progestin receptors in rat hypothalamus.
Nature. 1981 Jul 2;292(5818):58-9. doi: 10.1038/292058a0.

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