Suppr超能文献

过氧化氢:一种将心肌代谢与冠状动脉血流相耦合的前馈性扩张剂。

Hydrogen peroxide: a feed-forward dilator that couples myocardial metabolism to coronary blood flow.

作者信息

Saitoh Shu-ichi, Zhang Cuihua, Tune Johnathan D, Potter Barry, Kiyooka Takahiko, Rogers Paul A, Knudson Jarrod D, Dick Gregory M, Swafford Albert, Chilian William M

机构信息

Department of Physiology, LSU Health Sciences Center, 1901 Perdido St, New Orleans, LA 70112, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2614-21. doi: 10.1161/01.ATV.0000249408.55796.da. Epub 2006 Oct 5.

Abstract

OBJECTIVE

We tested the hypothesis that hydrogen peroxide (H2O2), the dismutated product of superoxide (O2*-), couples myocardial oxygen consumption to coronary blood flow. Accordingly, we measured O2*- and H2O2 production by isolated cardiac myocytes, determined the role of mitochondrial electron transport in the production of these species, and determined the vasoactive properties of the produced H2O2.

METHODS AND RESULTS

The production of O2*- is coupled to oxidative metabolism because inhibition of complex I (rotenone) or III (antimycin) enhanced the production of O2*- during pacing by about 50% and 400%, respectively; whereas uncoupling oxidative phosphorylation by decreasing the protonmotive force with carbonylcyanide-p-trifluoromethoxyphenyl-hydrazone (FCCP) decreased pacing-induced O2*- production. The inhibitor of cytosolic NAD(P)H oxidase assembly, apocynin, did not affect O2*- production by pacing. Aliquots of buffer from paced myocytes produced vasodilation of isolated arterioles (peak response 67+/-8% percent of maximal dilation) that was significantly reduced by catalase (5+/-0.5%, P<0.05) or the antagonist of Kv channels, 4-aminopyridine (18+/-4%, P<0.05). In intact animals, tissue concentrations of H2O2 are proportionate to myocardial oxygen consumption and directly correlated to coronary blood flow. Intracoronary infusion of catalase reduced tissue levels of H2O2 by 30%, and reduced coronary flow by 26%. Intracoronary administration of 4-aminopyridine also shifted the relationship between myocardial oxygen consumption and coronary blood flow or coronary sinus pO2.

CONCLUSIONS

Taken together, our results demonstrate that O2*- is produced in proportion to cardiac metabolism, which leads to the production of the vasoactive reactive oxygen species, H2O2. Our results further suggest that the production of H2O2 in proportion to metabolism couples coronary blood flow to myocardial oxygen consumption.

摘要

目的

我们检验了如下假设,即超氧化物(O2*-)的歧化产物过氧化氢(H2O2)使心肌耗氧量与冠状动脉血流量相匹配。因此,我们测量了分离的心肌细胞产生O2*-和H2O2的情况,确定了线粒体电子传递在这些物质产生中的作用,并确定了所产生的H2O2的血管活性特性。

方法与结果

O2*-的产生与氧化代谢相关,因为抑制复合体I(鱼藤酮)或复合体III(抗霉素)分别使起搏期间O2*-的产生增加约50%和400%;而用羰基氰化物-对-三氟甲氧基苯基腙(FCCP)降低质子动力势来解偶联氧化磷酸化,则会减少起搏诱导的O2*-产生。胞质NAD(P)H氧化酶组装抑制剂阿朴吗啡对起搏产生O2*-没有影响。来自起搏心肌细胞的缓冲液等分试样可使分离的小动脉舒张(峰值反应为最大舒张的67±8%),而过氧化氢酶(5±0.5%,P<0.05)或钾通道拮抗剂4-氨基吡啶(18±4%,P<0.05)可使其显著降低。在完整动物中,组织中H2O2的浓度与心肌耗氧量成比例,并与冠状动脉血流量直接相关。冠状动脉内注入过氧化氢酶可使组织中H2O2水平降低30%,并使冠状动脉血流量减少26%。冠状动脉内给予4-氨基吡啶也改变了心肌耗氧量与冠状动脉血流量或冠状窦pO2之间的关系。

结论

综上所述,我们的结果表明,O2*-的产生与心脏代谢成比例,这导致了具有血管活性的活性氧物质H2O2的产生。我们的结果进一步表明,与代谢成比例的H2O2产生使冠状动脉血流量与心肌耗氧量相匹配。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验