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性腺激素调节雄性和雌性大鼠的脱氧皮质酮-盐性高血压。

Gonadal hormones modulate deoxycorticosterone-salt hypertension in male and female rats.

作者信息

Crofton J T, Share L

机构信息

Department of Physiology and Biophysics, University of Tennessee, Memphis 38163, USA.

出版信息

Hypertension. 1997 Jan;29(1 Pt 2):494-9. doi: 10.1161/01.hyp.29.1.494.

Abstract

We have shown previously that, in rats with deoxycorticosterone (DOC)-salt hypertension, arterial blood pressure rises more rapidly and reaches a higher level in male than in female rats and that the course of the hypertension was ameliorated by gonadectomy in male rats and exacerbated by gonadectomy in female rats. The present investigation was undertaken to examine the role of the gonadal steroid hormones in modulating the course of DOC-salt hypertension in the rat. Our previous findings with respect to the effects of gender and gonadectomy on DOC-salt hypertension were confirmed in this study. Chronic treatment with gonadal steroids was begun 1 week before the start of the DOC-salt protocol. 17 beta-Estradiol attenuated the course of the hypertension in intact male rats and in gonadectomized females. Testosterone exacerbated the development of the hypertension in gonadectomized male rats but was without effect in intact females. Progesterone alone had no effect on the hypertension in ovariectomized rats but when given to ovariectomized rats in combination with estradiol transiently prevented the ameliorating effect of the estradiol. These effects of the gonadal steroid hormones could not be attributed to effects of saline intake. Thus, these findings demonstrate that the gonadal steroid hormones play an important role in modulating the pathogenesis of DOC-salt hypertension in the rat. It is suggested that the effects of the gonadal hormones on the course of the hypertension may be due to modulation of the cardiovascular and renal actions of vasopressin, since vasopressin is required for this model of hypertension.

摘要

我们之前已经表明,在脱氧皮质酮(DOC)-盐性高血压大鼠中,雄性大鼠的动脉血压升高更快且达到的水平高于雌性大鼠,并且雄性大鼠去势可改善高血压病程,而雌性大鼠去势则会加剧高血压病程。本研究旨在探讨性腺类固醇激素在调节大鼠DOC-盐性高血压病程中的作用。本研究证实了我们之前关于性别和去势对DOC-盐性高血压影响的发现。在开始DOC-盐方案前1周开始用性腺类固醇进行慢性治疗。17β-雌二醇可减轻完整雄性大鼠和去势雌性大鼠的高血压病程。睾酮会加剧去势雄性大鼠的高血压发展,但对完整雌性大鼠无影响。单独使用孕酮对去卵巢大鼠的高血压无影响,但与雌二醇联合给予去卵巢大鼠时,会短暂阻止雌二醇的改善作用。性腺类固醇激素的这些作用不能归因于盐摄入量的影响。因此,这些发现表明性腺类固醇激素在调节大鼠DOC-盐性高血压发病机制中起重要作用。有人提出,性腺激素对高血压病程的影响可能是由于对血管加压素心血管和肾脏作用的调节,因为该高血压模型需要血管加压素。

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