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皮质酮调节小鼠肝脏糖皮质激素受体的水平。

Corticosterone regulates the level of hepatic glucocorticoid receptors in mice.

作者信息

Svec F

机构信息

Department of Medicine, Louisiana State University Medical Center, New Orleans 70112.

出版信息

Proc Soc Exp Biol Med. 1988 Sep;188(4):474-9. doi: 10.3181/00379727-188-42763.

Abstract

The effect of exogenous corticosterone on the level of mouse hepatic glucocorticoid receptor was monitored to ascertain whether agonist-induced glucocorticoid receptor regulation takes place in living animals as it does in isolated cell systems. Adrenalectomized male Swiss-Webster mice were given 1 mg of corticosterone ip and 24 hr later the glucocorticoid receptor binding capacity of a high-speed cytosolic extract of liver was measured. It was shown that at this time point the administered steroid had been totally cleared and thus, the decrease in binding capacity was a reflection of downregulation. Receptor binding capacity was decreased by 25%. Downregulation was not permanent; 48-72 hr after the injection receptor content returned to baseline. Multiple daily injections of corticosterone were no more effective at causing downregulation than a single injection. It is concluded that glucocorticoid agonists downregulate their own receptors in the glucocorticoid target organs of intact animals as they do in cloned cell models.

摘要

监测外源性皮质酮对小鼠肝脏糖皮质激素受体水平的影响,以确定激动剂诱导的糖皮质激素受体调节是否如在分离的细胞系统中那样在活体动物中发生。对肾上腺切除的雄性瑞士-韦伯斯特小鼠腹腔注射1毫克皮质酮,24小时后测量肝脏高速胞质提取物的糖皮质激素受体结合能力。结果显示,在这个时间点,所给予的类固醇已完全清除,因此,结合能力的下降反映了下调。受体结合能力下降了25%。下调不是永久性的;注射后48 - 72小时,受体含量恢复到基线水平。每日多次注射皮质酮在引起下调方面并不比单次注射更有效。得出的结论是,糖皮质激素激动剂在完整动物的糖皮质激素靶器官中下调其自身受体,这与在克隆细胞模型中的情况相同。

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