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蛋白激酶A抑制剂H-89可直接抑制兔冠状动脉平滑肌细胞中的ATP敏感性钾通道和内向整流钾通道。

The protein kinase A inhibitor, H-89, directly inhibits KATP and Kir channels in rabbit coronary arterial smooth muscle cells.

作者信息

Sun Park Won, Kyoung Son Youn, Kim Nari, Boum Youm Jae, Joo Hyun, Warda Mohamad, Ko Jae-Hong, Earm Yung E, Han Jin

机构信息

Mitochondrial Signaling Laboratory, Department of Physiology and Biophysics, College of Medicine, Biohealth Products Research Center, Cardiovascular and Metabolic disease Center, Inje University, Busan, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2006 Feb 24;340(4):1104-10. doi: 10.1016/j.bbrc.2005.12.116. Epub 2005 Dec 28.

Abstract

The effects of the protein kinase A (PKA) inhibitor H-89 on ATP-sensitive K+ (KATP) and inward rectifier K+ (Kir) currents were examined in rabbit coronary arterial smooth muscle cells using the patch clamp technique. The H-89, in a dose-dependent manner, inhibited KATP and Kir currents with apparent Kd values of 1.19+/-0.18 and 3.78+/-0.37 microM, respectively. H-85, which is considered as an inactive form of H-89, inhibited KATP and Kir currents, similar to the result of H-89. KATP and Kir currents were not affected by either Rp-8-CPT-cAMPs, which is a membrane-permeable selective PKA inhibitor, or KT 5720, which is also known as a PKA inhibitor. Also, these two drugs did not significantly alter the effects of H-89 on the KATP and Kir currents. These results suggest that H-89 directly inhibits the KATP and Kir currents of rabbit coronary arterial smooth muscle cells independently of PKA inhibition.

摘要

采用膜片钳技术,在兔冠状动脉平滑肌细胞中研究了蛋白激酶A(PKA)抑制剂H - 89对ATP敏感性钾通道(KATP)电流和内向整流钾通道(Kir)电流的影响。H - 89呈剂量依赖性抑制KATP电流和Kir电流,其表观解离常数(Kd)值分别为1.19±0.18 μM和3.78±0.37 μM。被认为是H - 89无活性形式的H - 85,对KATP电流和Kir电流的抑制作用与H - 89的结果相似。KATP电流和Kir电流既不受膜通透性选择性PKA抑制剂Rp - 8 - CPT - cAMPs的影响,也不受同样作为PKA抑制剂的KT 5720的影响。此外,这两种药物并未显著改变H - 89对KATP电流和Kir电流的作用。这些结果表明,H - 89可直接抑制兔冠状动脉平滑肌细胞的KATP电流和Kir电流,且与抑制PKA无关。

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