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海蟾蜍精干扰盐皮质激素受体的功能。

Marinobufagenin interferes with the function of the mineralocorticoid receptor.

作者信息

Smith Carolyn L, He Qiang, Huang Luping, Foster Estrella, Puschett Jules B

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.

出版信息

Biochem Biophys Res Commun. 2007 May 18;356(4):930-4. doi: 10.1016/j.bbrc.2007.03.085. Epub 2007 Mar 26.

Abstract

Marinobufagenin (MBG) is a cardiotonic steroid of the bufadienolide class of compounds which has the ability to inhibit the ubiquitous enzyme, Na+/K+-ATPase, resulting in natriuresis. The involvement of MBG in the pathogenesis of volume expansion-mediated forms of hypertension has been suggested for some time, and we have proposed that MBG participates in the hypertension noted in preeclampsia. We examined the hypothesis that MBG might contribute to these forms of hypertension by promoting the activity of the mineralocorticoid receptor (MR). However, our data demonstrate that instead, MBG interferes with the functioning of the MR by inhibiting the transcriptional activity of the receptor, and this is reflected in a reduced interaction between the SRC-3 coactivator and the MR. Thus, the ability of MBG to cause a natriuresis may be due, not only to inhibition of Na+/K+-ATPase activity, but also to its ability to interfere with MR-dependent expression of the Na/K/H exchanger in the late distal nephron.

摘要

海蟾蜍精(MBG)是一种蟾蜍二烯羟酸内酯类强心甾体化合物,能够抑制普遍存在的酶——钠钾ATP酶,从而导致利钠作用。一段时间以来,人们一直认为MBG参与容量扩张介导型高血压的发病机制,并且我们已经提出MBG参与子痫前期出现的高血压。我们检验了这样一个假说,即MBG可能通过促进盐皮质激素受体(MR)的活性而导致这些类型的高血压。然而,我们的数据表明,MBG反而通过抑制该受体的转录活性来干扰MR的功能,这表现为SRC - 3共激活因子与MR之间的相互作用减少。因此,MBG导致利钠作用的能力可能不仅归因于对钠钾ATP酶活性的抑制,还归因于其干扰远曲小管晚期钠/钾/氢交换体的MR依赖性表达的能力。

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