Department of Cardiology and Hematology, Fukushima Medical University, Fukushima, Japan.
Eur J Pharmacol. 2010 Oct 25;645(1-3):127-34. doi: 10.1016/j.ejphar.2010.07.025. Epub 2010 Jul 27.
Metabolic regulation plays an important role in modifying coronary vascular tone. We hypothesized that hydrogen peroxide, purinergic components, and angiotensin, produced by cardiac myocytes control coronary vascular tone in proportion to metabolism. We measured changes in the diameter of isolated, pressurized coronary arterioles in response to supernatant from isolated cardiac myocytes in rats (stimulated for 20-, 60-, and 120-min at 400 bpm). Changes in the diameter of arterioles were determined under control conditions following treatment of arterioles with an adenosine receptor antagonist, 8-PSPT, a P2Y1 receptor antagonist, MRS-2179, or an angiotensin II receptor antagonist, olmesartan. A supernatant (500 microl to a 2 ml bath) from myocytes stimulated for 20-, 60- and 120-min caused graded vasodilation (14.1+/-0.4, 20.2+/-1.6, 53.8+/-6.2%, P<0.01 vs. non-stimulated, respectively). In 20-min stimulation, catalase with myocyte supernatants eliminated vasodilation. Following 60-min stimulation, catalase converted myocyte supernatant-induced vasodilation to a vasoconstriction (-15.1+/-1.0%), and this vasoconstriction was eliminated by olmesartan. Upon 120-min stimulation, catalase partially reduced the vasodilation by myocyte supernatants (37.2+/-3.8%). The remaining vasodilation was converted to a vasoconstriction with 8-PSPT and MRS-2179, and this vasoconstriction was completely eliminated with olmesartan. Cardiac myocytes modulate vascular tone through the net effects of hydrogen peroxide, purinergic components (adenosine and ADP), and angiotensin in proportion to ischemia.
代谢调节在调节冠状动脉张力中起着重要作用。我们假设心肌细胞产生的过氧化氢、嘌呤能成分和血管紧张素,与代谢成正比控制冠状动脉张力。我们测量了大鼠分离的加压冠状动脉小动脉对心肌细胞上清液(400 次/分钟刺激 20、60 和 120 分钟)的反应的直径变化。在使用腺苷受体拮抗剂 8-PSPT、P2Y1 受体拮抗剂 MRS-2179 或血管紧张素 II 受体拮抗剂奥美沙坦处理小动脉后,在对照条件下确定小动脉直径的变化。来自刺激 20、60 和 120 分钟的心肌细胞的上清液(500 微升至 2 毫升浴液)引起逐渐的血管扩张(分别为 14.1+/-0.4、20.2+/-1.6 和 53.8+/-6.2%,与非刺激相比,P<0.01)。在 20 分钟刺激中,过氧化氢酶与心肌细胞上清液一起消除了血管扩张。在 60 分钟刺激后,过氧化氢酶将心肌细胞上清液诱导的血管扩张转化为血管收缩(-15.1+/-1.0%),并且这种血管收缩被奥美沙坦消除。在 120 分钟刺激后,过氧化氢酶部分减少了心肌细胞上清液引起的血管扩张(37.2+/-3.8%)。剩余的血管扩张与 8-PSPT 和 MRS-2179 一起转化为血管收缩,这种血管收缩被奥美沙坦完全消除。心肌细胞通过过氧化氢、嘌呤能成分(腺苷和 ADP)和血管紧张素的净效应调节血管张力,与缺血成正比。