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慢性肾功能衰竭时心脏中甲状旁腺激素-甲状旁腺激素相关蛋白受体的下调:细胞内钙浓度的作用

Down-regulation of PTH-PTHrP receptor of heart in CRF: role of [Ca2+]i.

作者信息

Smogorzewski M, Tian J, Massry S G

机构信息

Division of Nephrology, University of Southern California School of Medicine, Los Angeles, USA.

出版信息

Kidney Int. 1995 Apr;47(4):1182-6. doi: 10.1038/ki.1995.168.

Abstract

The mRNA of PTH-PTHrP receptor in the kidney and liver of CRF rats is down-regulated. It is not known whether this is a generalized phenomenon and the signals that mediate such down-regulation are not evident. Excess PTH in CRF induces a rise in basal levels of cytosolic calcium ([Ca2+]i), and the high [Ca2+]i is implicated in the genesis of cell dysfunction in CRF. Therefore, it is reasonable to propose that the PTH-induced rise in [Ca2+]i provides a negative feedback control system for the down-regulation of the mRNA of the PTH-PTHrP in order to protect the cells from the harmful effects of progressive rise in blood levels of PTH in CRF. The heart contains the mRNA for this receptor and it is a target organ for PTH action. We examined whether the message of the PTH-PTHrP receptor is down-regulated in the heart of CRF animals and evaluated the role of [Ca2+]i in this process. The expression of the mRNA of the PTH-PTHrP was significantly reduced in the heart of CRF rats as compared to normal animals. Also, the CRF rats had elevated blood levels of PTH and high [Ca2+]i of cardiac myocytes. The parathyroidectomy of CRF rats prevented the rise in blood PTH levels and normalized [Ca2+]i of cardiac myocytes and returned the mRNA of their PTH-PTHrP receptor towards normal levels. The treatment of CRF rats with verapamil normalized [Ca2+]i of cardiac myocytes and returned the mRNA of their PTH-PTHrP receptor towards normal levels, despite marked elevation of blood levels of PTH.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

慢性肾功能衰竭(CRF)大鼠肾脏和肝脏中甲状旁腺激素-甲状旁腺激素相关蛋白(PTH-PTHrP)受体的信使核糖核酸(mRNA)表达下调。目前尚不清楚这是否为普遍现象,介导这种下调的信号也不明确。CRF中过量的甲状旁腺激素(PTH)会导致细胞溶质钙([Ca2+]i)基础水平升高,而高[Ca2+]i与CRF中的细胞功能障碍发生有关。因此,有理由认为PTH诱导的[Ca2+]i升高为PTH-PTHrP的mRNA下调提供了一个负反馈控制系统,以保护细胞免受CRF中PTH血水平逐渐升高的有害影响。心脏含有该受体的mRNA,是PTH作用的靶器官。我们研究了CRF动物心脏中PTH-PTHrP受体的信使是否下调,并评估了[Ca2+]i在此过程中的作用。与正常动物相比,CRF大鼠心脏中PTH-PTHrP的mRNA表达显著降低。此外,CRF大鼠的PTH血水平升高,心肌细胞的[Ca2+]i也升高。CRF大鼠的甲状旁腺切除术可防止血PTH水平升高,使心肌细胞的[Ca2+]i恢复正常,并使它们的PTH-PTHrP受体的mRNA恢复到正常水平。用维拉帕米治疗CRF大鼠可使心肌细胞的[Ca2+]i恢复正常,并使它们的PTH-PTHrP受体的mRNA恢复到正常水平,尽管PTH血水平显著升高。(摘要截短至250字)

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