Matsumoto Takayuki, Takayanagi Keisuke, Katome Tomoki, Kojima Mihoka, Taguchi Kumiko, Kobayashi Tsuneo
Department of Physiology and Morphology, Institute of Medicinal Chemistry, Hoshi University.
Biol Pharm Bull. 2021;44(10):1530-1535. doi: 10.1248/bpb.b21-00437.
We investigated the vascular response to nucleobase adenine using freshly isolated superior mesenteric arteries of spontaneously hypertensive rats (SHR) and its control, Wistar Kyoto (WKY) rats. Endothelium-dependent and endothelium-independent relaxations were assessed in isolated segments in an organ bath. The releases of the metabolites of thromboxane A and prostaglandin I were also detected. Adenine induced vasorelaxation in both the endothelium-intact and endothelium-denuded arteries in a concentration-dependent manner. In the SHR group, the adenine-induced relaxation was slightly but significantly reduced in the endothelium-intact rings when compared with that in the WKY group. However, the relaxation in the endothelium-denuded rings were similar between the two groups. The difference in the adenine-mediated relaxation in the superior mesenteric arteries between the SHR and WKY groups was eliminated by endothelial denudation and a nitric oxide (NO) synthase inhibitor. In the absence and presence of adenine, SHR tended to have higher levels of metabolites of thromboxane A and prostaglandin I compared with WKY. However, adenine did not induce the release of these substances in the arteries in both the SHR and WKY groups. These results suggest that the reduced adenine-mediated relaxation in the superior mesenteric arteries in SHR is due to a lack of contribution from the endothelium-derived NO and not from the release of prostanoids.
我们使用新鲜分离的自发性高血压大鼠(SHR)及其对照Wistar Kyoto(WKY)大鼠的肠系膜上动脉,研究了血管对核碱基腺嘌呤的反应。在器官浴中对分离的动脉段进行内皮依赖性和非内皮依赖性舒张功能评估。还检测了血栓素A和前列腺素I代谢产物的释放情况。腺嘌呤以浓度依赖性方式诱导内皮完整和内皮剥脱的动脉血管舒张。在SHR组中,与WKY组相比,内皮完整环中腺嘌呤诱导的舒张作用略有但显著降低。然而,两组内皮剥脱环中的舒张作用相似。SHR组和WKY组之间肠系膜上动脉中腺嘌呤介导的舒张差异通过内皮剥脱和一氧化氮(NO)合酶抑制剂消除。在不存在和存在腺嘌呤的情况下,与WKY相比,SHR的血栓素A和前列腺素I代谢产物水平往往更高。然而,腺嘌呤并未在SHR组和WKY组的动脉中诱导这些物质的释放。这些结果表明,SHR肠系膜上动脉中腺嘌呤介导的舒张作用降低是由于内皮源性NO缺乏,而非前列腺素释放所致。
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