Chang K S, Zhong M Z, Davis R F
Department of Anesthesiology, Oregon Health Sciences University, Portland 97201, USA.
Hypertension. 1996 Feb;27(2):228-34. doi: 10.1161/01.hyp.27.2.228.
To investigate the potential mechanisms by which indigo carmine produces hypertension, we tested the hypothesis that indigo carmine inhibits endothelium-dependent vasodilation and determined the possible site of the inhibition (endothelium versus smooth muscle). Using isolated rat thoracic aortic rings that were precontracted with phenylephrine, we examined vasodilatory responses to acetylcholine, histamine, and Ca2+ ionophore A23187 (in endothelium-intact rings) and sodium nitroprusside and isoproterenol (in endothelium-denuded rings) in the presence and absence of indigo carmine. In addition, the effects of methylene blue on the acetylcholine- and sodium nitroprusside-induced vasodilation were compared with those of indigo carmine. Indigo carmine (10(-6), 10(-5), and 10(-4) mol/L) significantly inhibited receptor- and non-receptor-mediated endothelium-dependent vasorelaxation. Indigo carmine (10(-4) mol/L) also inhibited endothelium-independent vasorelaxation induced by sodium nitroprusside (an activator of vascular smooth muscle soluble guanylyl cyclase), although to a lesser extent than vasodilation from acetylcholine, histamine, and Ca2+ ionophore A23187. In contrast, indigo carmine (10(-4) mol/L) had no effect on the vasodilation induced by isoproterenol (an activator of adenylyl cyclase), indicating that indigo carmine selectively inhibits nitric oxide-mediated responses. Methylene blue, a known inhibitor of soluble guanylyl cyclase, inhibited both acetylcholine- and sodium nitroprusside-induced vasorelaxation. The inhibition was also greater in the acetylcholine- than the sodium nitroprusside-induced vasodilation. These results suggest that indigo carmine, like methylene blue, may inhibit endothelium-dependent relaxation by a mechanism that involves two levels. The major action of indigo carmine appears to be at the level of nitric oxide generation and/or release from the endothelial cell. In addition, indigo carmine appears to inhibit vascular smooth muscle guanylyl cyclase. Thus, indigo carmine may elevate blood pressure by interfering with these nitric oxide-mediated vasodilatory mechanisms.
为了研究靛胭脂导致高血压的潜在机制,我们检验了以下假设:靛胭脂抑制内皮依赖性血管舒张,并确定了抑制的可能部位(内皮细胞与平滑肌)。我们使用预先用去氧肾上腺素预收缩的离体大鼠胸主动脉环,在存在和不存在靛胭脂的情况下,检测了对乙酰胆碱、组胺和Ca2+离子载体A23187(在内皮完整的血管环中)以及硝普钠和异丙肾上腺素(在内皮剥脱的血管环中)的血管舒张反应。此外,比较了亚甲蓝对乙酰胆碱和硝普钠诱导的血管舒张的影响与靛胭脂的影响。靛胭脂(10(-6)、10(-5)和10(-4) mol/L)显著抑制受体介导和非受体介导的内皮依赖性血管舒张。靛胭脂(10(-4) mol/L)也抑制硝普钠(血管平滑肌可溶性鸟苷酸环化酶的激活剂)诱导的非内皮依赖性血管舒张,尽管程度小于乙酰胆碱、组胺和Ca2+离子载体A23187引起的血管舒张。相比之下,靛胭脂(10(-4) mol/L)对异丙肾上腺素(腺苷酸环化酶的激活剂)诱导的血管舒张没有影响,表明靛胭脂选择性抑制一氧化氮介导的反应。亚甲蓝是一种已知的可溶性鸟苷酸环化酶抑制剂,它抑制乙酰胆碱和硝普钠诱导的血管舒张。乙酰胆碱诱导的血管舒张中的抑制作用也大于硝普钠诱导的血管舒张。这些结果表明,靛胭脂与亚甲蓝一样,可能通过涉及两个层面的机制抑制内皮依赖性舒张。靛胭脂的主要作用似乎在于一氧化氮从内皮细胞生成和/或释放的层面。此外,靛胭脂似乎抑制血管平滑肌鸟苷酸环化酶。因此,靛胭脂可能通过干扰这些一氧化氮介导的血管舒张机制来升高血压。