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过氧化物和超氧化物对冠状动脉的影响:血管紧张素II反应和肌浆网Ca2+泵

Effects of peroxide and superoxide on coronary artery: ANG II response and sarcoplasmic reticulum Ca2+ pump.

作者信息

Grover A K, Samson S E, Fomin V P, Werstiuk E S

机构信息

Department of Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.

出版信息

Am J Physiol. 1995 Sep;269(3 Pt 1):C546-53. doi: 10.1152/ajpcell.1995.269.3.C546.

Abstract

The sarcoplasmic reticulum (SR) Ca2+ pump in membranes isolated from arterial smooth muscle is damaged by reactive oxygen species (ROS). Because angiotensin II (ANG II) contracts arterial smooth muscle by mobilizing intracellular Ca2+ concentrations ([Ca2+])i, we determined the effects of ROS pretreatment on ANG II-induced contractions in coronary artery rings and [Ca2+]i transients in smooth muscle cells (SMC) cultured from them. This experimental design eliminates direct ROS interference in assay solutions, thus monitoring only the tissue damage. Pretreating the arteries with peroxide inhibited the ANG II contractions with the concentration for half-maximal activation (K0.5) = 74 +/- 5 microM. Peroxide (250 microM) inhibited the contractions to ANG II and cyclopiazonic acid (CPA, SR Ca(2+)-pump inhibitor) by 78.3 +/- 5.1 and 67.4 +/- 6.3%, respectively, but did not significantly affect the contractions by 60 mM KCl. Pretreating SMC with peroxide inhibited the ANG II-induced increase in [Ca2+]i with K0.5 = 24 +/- 3 microM for peroxide. Peroxide (100 microM) inhibited the increase in [Ca2+]i in response to ANG II and CPA by 78.9 +/- 5.1 and 38.3 +/- 4.9%, respectively. The SR Ca(2+)-pump activity was also measured as the Ca(2+)-dependent formation of 115-kDa acylphosphate. Pretreating SMC with 100 microM peroxide inhibited the acylphosphate levels by 36.3 +/- 3.2%. Peroxide (100 microM) pretreatment of SMC did not significantly affect their ANG II binding.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

从动脉平滑肌分离的细胞膜中的肌浆网(SR)Ca2+泵会被活性氧(ROS)破坏。由于血管紧张素II(ANG II)通过动员细胞内Ca2+浓度([Ca2+])i使动脉平滑肌收缩,我们测定了ROS预处理对冠状动脉环中ANG II诱导的收缩以及从中培养的平滑肌细胞(SMC)中[Ca2+]i瞬变的影响。这种实验设计消除了测定溶液中ROS的直接干扰,从而仅监测组织损伤。用过氧化物预处理动脉可抑制ANG II收缩,其半最大激活浓度(K0.5)= 74±5微摩尔。过氧化物(250微摩尔)分别抑制对ANG II和环匹阿尼酸(CPA,SR Ca(2+)-泵抑制剂)的收缩达78.3±5.1%和67.4±6.3%,但对60毫摩尔氯化钾引起的收缩无显著影响。用过氧化物预处理SMC可抑制ANG II诱导的[Ca2+]i增加,过氧化物的K0.5 = 24±3微摩尔。过氧化物(100微摩尔)分别抑制对ANG II和CPA的[Ca2+]i增加达78.9±5.1%和38.3±4.9%。SR Ca(2+)-泵活性也以Ca(2+)-依赖性形成115-kDa酰基磷酸来测定。用100微摩尔过氧化物预处理SMC可使酰基磷酸水平降低36.3±3.2%。用100微摩尔过氧化物预处理SMC对其ANG II结合无显著影响。(摘要截短于250字)

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