格列本脲
血管舒张
苯肾上腺素
胸主动脉
主动脉
钾通道
药理学
医学
四乙基铵
一氧化氮
内皮
化学
环氧合酶
钾通道阻滞剂
四乙基氯化铵
一氧化氮合酶
麻醉
钾
氯化钡
内科学
内分泌学
生物化学
酶
血压
糖尿病
有机化学
作者
Wei Zhou,Ran Zhou,Nan Li,Yefeng Chen,Yanmin Pei,Liangjuan Han,Jun Ren
标识
DOI:10.4103/cjp.cjp_60_21
摘要
Oxysophoridine (OSR) is a main active alkaloid extracted from Sophora alopecuroides, which is a traditional Chinese herbal medicine that has been used widely. In this study, we used thoracic aorta rings isolated from Sprague-Dawley rats to explore the vasodilative activity of OSR and its potential mechanisms. The isolated rat thoracic aorta rings were used to observe the effects of different concentrations of OSR (0.4-2.0 g·L-1) on the resting normal rings and the phenylephrine precontracted endothelium-intact or endothelium-denudedisolated thoracic aorta rings, respectively. The interactions among OSR and barium chloride (BaCl2), tetraethylamine, 4-aminopyridine, glibenclamide (Gli), L-nitroarginine methyl ester (L-NAME), and cyclooxygenase (COX) inhibitor indomethacin (INDO) were evaluated. The experimental results show that OSR had no effect on the tension of resting vascular rings, but the vasodilating effect could be confirmed in a concentration-dependent manner on both endothelium-intact and endothelium-denuded vascular rings. This vasodilation effect of OSR on thoracic aorta vascular rings could be inhibited significantly by potassium channel blockers glibenclamide (Gli, 10 μmol·L-1) and 4-aminopyridine (4-AP, 5 mmol·L-1). In addition, vasodilatory effects of OSR were not inhibited in the presence of potassium channel blockers barium chloride (BaCl2, 1 mmol·L-1) and tetraethylamine (TEA, 10 mmol·L-1), nitric oxide synthase inhibitor (L-NAME, 0.1 mmol·L-1) and COX inhibitor (INDO, 10 μmol·L-1). In conclusion, the vasodilatory effects of OSR on thoracic aorta rings is associated with KV and KATP.
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