首页> 外文期刊>The Journal of Physiology >Angiotensin II inhibition of ATP-sensitive K+ currents in rat arterial smooth muscle cells through protein kinase C.
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Angiotensin II inhibition of ATP-sensitive K+ currents in rat arterial smooth muscle cells through protein kinase C.

机译:血管紧张素II通过蛋白激酶C抑制大鼠动脉平滑肌细胞中ATP敏感的K +电流。

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摘要

1. The effects of the vasoconstrictor angiotensin II (Ang II) on whole-cell ATP-sensitive K+ currents (IK,ATP) of smooth muscle cells isolated enzymatically from rat mesenteric arteries were investigated using the patch clamp technique. 2. Ang II, at a physiological concentration (100 nM), reduced IK,ATP activated by 0.1 mM internal ATP and 10 microM levcromakalim by 36.4 +/- 2.3%. 3. The protein kinase C (PKC) activator 1-oleoyl-2-acetyl-sn-glycerol (OAG, 1 microM) reduced IK,ATP by 44.1 +/- 2.7%. GDP beta S (1 mM), included in the pipette solution, abolished the inhibition by Ang II, while that by OAG was unaffected. 4. Pretreatment with the PKC inhibitors staurosporine (100 nM) or calphostin C (500 nM) prevented the Ang II-induced inhibition of IK,ATP. 5. Ang II inhibition was unaffected by cell dialysis with PKA inhibitor peptide (5 microM), and the PKA inhibitor Rp-cAMPS (100 microM) did not reduce IK,ATP. 6. Our results suggest that Ang II modulates KATP channels through activation of PKC but notthrough inhibition of PKA.
机译:1.使用膜片钳技术研究了通过酶法分离大鼠肠系膜动脉的血管收缩血管紧张素II(Ang II)对全细胞ATP敏感性K +电流(IK,ATP)的影响。 2.在生理浓度(100 nM)的Ang II,IK,ATP被0.1 mM内部ATP和10 microM左克马卡林激活的程度降低了36.4 +/- 2.3%。 3.蛋白激酶C(PKC)激活剂1-油酰基-2-乙酰基-sn-甘油(OAG,1 microM)使IK,ATP降低44.1 +/- 2.7%。移液器中包含的GDP beta S(1 mM)取消了Ang II的抑制作用,而OAG的抑制作用不受影响。 4.用PKC抑制剂星形孢菌素(100 nM)或钙磷蛋白C(500 nM)预处理可防止Ang II诱导的IK,ATP抑制。 5.用PKA抑制剂肽(5 microM)进行细胞透析不会影响Ang II抑制,并且PKA抑制剂Rp-cAMPS(100 microM)不会降低IK,ATP。 6.我们的结果表明,Ang II通过激活PKC而不是通过抑制PKA来调节KATP通道。

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