D3 dopamine receptor regulation of D5 receptor expression and function in renal proximal tubule cells
D3 dopamine receptor regulation of D5 receptor expression and function in renal proximal tubule cells
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D3 多巴胺受体对肾近曲小管细胞 D5 受体表达和功能的调节
DOI:
10.1038/hr.2012.11
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发表时间:
2012-06
影响因子:
5.4
通讯作者:
Jose PA
中科院分区:
文献类型:
--
作者:
Zeng C;Ren H;Chen C;Yang J;Han Y;He D;Zhou L;Asico LD;Jose PA
Dopamine receptor, via D 1-like and D 2-like receptors, increases sodium excretion in kidney. We have reported positive interactions between D 3 and D 1 receptors in renal proximal tubule (RPT) cells. These reports, however do not preclude that there may be also interaction between D 3 and D 5 receptors, because of the lack of selective D 1 and D 5 receptor agonists or antagonists. We hypothesize that D 3 receptors can regulate D 5 receptors, and that D 3 receptor regulation of D 5 receptors in RPTs is impaired in spontaneously hypertensive rats (SHRs). It showed that a D 3 receptor agonist, PD128907, by the activation of protein kinase C activity, increased the expression of D 5 receptors in a concentration-and time-dependent manner in RPT cells from Wistar-Kyoto (WKY) rats. The stimulatory effect of the D 3 receptor on D 5 receptor expression was impaired in RPT cells from SHRs. The effect of D 3 receptor on D 5 receptor is functionally relevant; stimulation of D 5 receptor decreases Na+–K+ adenosine triphosphatase (ATPase) activity in WKY cells. Pretreatment with D 3 receptor agonist for 24 h enhances the D 5 receptor expression and D 5 receptor-mediated inhibitory effect on Na+–K+ ATPase activity in WKY cells, but decreases them in SHR cells. The effect of D 3 receptor on D 5 receptor expression and function was also confirmed in the D 5 receptor-transfected HEK293 cells. It indicates that activation of D 3 receptor increases D 5 receptor expression and function. Altered regulation of D 3 receptor on D 5 receptors may have a role in the pathogenesis of hypertension.
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DOI:
10.1152/ajpregu.00600.2005
发表时间:
2006-03
期刊:
American journal of physiology. Regulatory, integrative and comparative physiology
影响因子:
--
作者:
R. Khalil
通讯作者:
R. Khalil
影响因子:
8.3
作者:
C. Zeng;Z. Wang;Hewang Li;P. Yu;S. Zheng;Li-juan Wu;L. Asico;U. Hopfer;G. Eisner;R. Felder;P. Jose
通讯作者:
C. Zeng;Z. Wang;Hewang Li;P. Yu;S. Zheng;Li-juan Wu;L. Asico;U. Hopfer;G. Eisner;R. Felder;P. Jose
DOI:
10.2174/187152507781058708
发表时间:
2007-06
影响因子:
--
作者:
C. Zeng;Zhiwei Yang;L. Asico;P. Jose
通讯作者:
C. Zeng;Zhiwei Yang;L. Asico;P. Jose
DOI:
10.1152/ajpregu.00434.2005
发表时间:
2006
期刊:
American journal of physiology. Regulatory, integrative and comparative physiology
影响因子:
--
作者:
Zhiwei Yang;L. Asico;P. Yu;Z. Wang;J. Jones;C. Escano;Xiaoyan Wang;M. Quinn;D. Sibley;G. R
通讯作者:
Zhiwei Yang;L. Asico;P. Yu;Z. Wang;J. Jones;C. Escano;Xiaoyan Wang;M. Quinn;D. Sibley;G. R
DOI:
10.1152/ajpheart.01036.2007
发表时间:
2008-02
期刊:
American journal of physiology. Heart and circulatory physiology
影响因子:
--
作者:
C. Zeng;I. Armando;Yingjin Luo;G. Eisner;R. Felder;P. Jose
通讯作者:
C. Zeng;I. Armando;Yingjin Luo;G. Eisner;R. Felder;P. Jose