Uh M, White B H, Sidhu A
Department of Pediatrics, Georgetown University Medical Center, Washington DC 20007, USA.
J Hypertens. 1998 Sep;16(9):1307-13. doi: 10.1097/00004872-199816090-00012.
Defective D1A dopamine receptor-G protein coupling has been identified in renal proximal tubules of the spontaneously hypertensive rat (SHR).
To determine whether association of D1A dopamine receptors with the alpha subunits of G proteins in kidney of SHR is normal.
We analyzed the association of agonist-activated [1251]-labeled D1A dopamine receptors in kidneys of SHR and the normotensive Wistar-Kyoto (WKY) rat through immunoprecipitation, using highly specific antipeptide antibodies directed against alpha subunits of G proteins.
We have shown for the first time that the D1A receptors of renal proximal tubules are associated with the adenylyl cyclase inhibitory G proteins G(i)alpha. The association of WKY rat proximal tubule D1A receptors with Gi1alpha and Gi2alpha in the presence of agonist is significantly (P<0.01) greater (2.4-fold and 3.1-fold greater, respectively) than it is without agonist D1A receptors of WKY rat also exhibit (twofold greater) association with G(s)alpha, consistently with the ability of these receptors to mediate stimulation of adenylyl cyclase. The WKY rat D1A receptors do not associate either with G(o)alpha or with G(q)alpha. The D1A receptors of SHR proximal tubule membranes appear to be resistant to activation by agonist and do not associate with G(s)alpha, G(o)alpha and any of the subunits of G(i)alpha. However, the SHR D1A sites exhibit a modestly (1.7-fold) greater association with G(q)alpha, which was not statistically significant. The differences among associations of the D1A receptors of WKY rat and SHR with these Galpha proteins may be important in understanding renal dopaminergic functions in normal and pathophysiologic states.
在自发性高血压大鼠(SHR)的肾近端小管中已发现D1A多巴胺受体 - G蛋白偶联存在缺陷。
确定SHR肾脏中D1A多巴胺受体与G蛋白α亚基的结合是否正常。
我们通过免疫沉淀分析了SHR和血压正常的Wistar - Kyoto(WKY)大鼠肾脏中激动剂激活的[125I]标记的D1A多巴胺受体的结合情况,使用针对G蛋白α亚基的高度特异性抗肽抗体。
我们首次表明肾近端小管的D1A受体与腺苷酸环化酶抑制性G蛋白G(i)α相关联。在激动剂存在的情况下,WKY大鼠近端小管D1A受体与Gi1α和Gi2α的结合显著(P<0.01)增强(分别增强2.4倍和3.1倍),而在没有激动剂时则不然。WKY大鼠的D1A受体与G(s)α的结合也增强(两倍),这与这些受体介导腺苷酸环化酶刺激的能力一致。WKY大鼠的D1A受体既不与G(o)α也不与G(q)α结合。SHR近端小管膜的D1A受体似乎对激动剂激活有抗性,并且不与G(s)α、G(o)α以及G(i)α的任何亚基结合。然而,SHR的D1A位点与G(q)α的结合略有增强(1.7倍),但无统计学意义。WKY大鼠和SHR的D1A受体与这些Gα蛋白结合的差异可能对理解正常和病理生理状态下的肾多巴胺能功能很重要。