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连接蛋白模拟肽无法抑制肾小动脉中的血管传导性钙反应。

Connexin mimetic peptides fail to inhibit vascular conducted calcium responses in renal arterioles.

作者信息

Sorensen Charlotte Mehlin, Salomonsson Max, Braunstein Thomas Hartig, Nielsen Morten Schak, Holstein-Rathlou Niels-Henrik

机构信息

Univ. of Copenhagen, Dept. of Biomedical Sciences, The Panum Institute, Bldg. 10.5, Blegdamsvej 3, DK-2200 Copenhagen N, Denmark.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2008 Sep;295(3):R840-7. doi: 10.1152/ajpregu.00491.2007. Epub 2008 Jul 9.

DOI:10.1152/ajpregu.00491.2007
PMID:18614765
Abstract

Vascular conducted responses are believed to play a central role in controlling the microcirculatory blood flow. The responses most likely spread through gap junctions in the vascular wall. At present, four different connexins (Cx) have been detected in the renal vasculature, but their role in transmission of conducted vasoconstrictor signals in the preglomerular arterioles is unknown. Connexin mimetic peptides were previously reported to target and inhibit specific connexins. We, therefore, investigated whether conducted vasoconstriction in isolated renal arterioles could be blocked by the use of mimetic peptides directed against one or more connexins. Preglomerular resistance vessels were microdissected from kidneys of Sprague-Dawley rats and loaded with fura 2. The vessels were stimulated locally by applying electrical current through a micropipette, and the conducted calcium response was measured 500 mum from the site of stimulation. Application of connexin mimetic peptides directed against Cx40, 37/43, 45, or a cocktail with equimolar amounts of each, did not inhibit the propagated response, whereas the nonselective gap junction uncoupler carbenoxolone completely abolished the propagated response. However, the connexin mimetic peptides were able to reduce dye coupling between rat aorta endothelial cells shown to express primarily Cx40. In conclusion, we did not observe any attenuating effects on conducted calcium responses in isolated rat interlobular arteries when exposed to connexin mimetic peptides directed against Cx40, 37/43, or 45. Further studies are needed to determine whether conducted vasoconstriction is mediated via previously undescribed pathways.

摘要

血管传导反应被认为在控制微循环血流中起核心作用。这些反应很可能通过血管壁中的缝隙连接传播。目前,已在肾血管系统中检测到四种不同的连接蛋白(Cx),但它们在肾小球前小动脉中传导血管收缩信号的作用尚不清楚。此前有报道称连接蛋白模拟肽可靶向并抑制特定的连接蛋白。因此,我们研究了使用针对一种或多种连接蛋白的模拟肽是否能阻断离体肾小动脉中的传导性血管收缩。从Sprague-Dawley大鼠的肾脏中显微分离出肾小球前阻力血管,并加载fura 2。通过微量移液器施加电流对血管进行局部刺激,并在距刺激部位500μm处测量传导性钙反应。应用针对Cx40、37/43、45的连接蛋白模拟肽或每种等摩尔量的混合物,均未抑制传播反应,而非选择性缝隙连接解偶联剂羧苄青霉素完全消除了传播反应。然而,连接蛋白模拟肽能够减少主要表达Cx40的大鼠主动脉内皮细胞之间的染料偶联。总之,当暴露于针对Cx40、37/43或45的连接蛋白模拟肽时,我们未观察到对离体大鼠小叶间动脉中传导性钙反应有任何减弱作用。需要进一步研究以确定传导性血管收缩是否通过先前未描述的途径介导。

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