Laboratoire des molécules bioactives, Faculté des sciences et techniques, Université Sidi Mohamed Ben Abdellah, Fès, Morocco.
Can J Physiol Pharmacol. 2012 May;90(5):607-16. doi: 10.1139/y2012-035. Epub 2012 Apr 24.
The vasodilatory effect of Globularia alypum L. (GA) extract was evaluated in rat mesenteric arterial bed pre-contracted by continuous infusion of phenylephrine (2-4 ng/mL). Bolus injections of GA elicited dose-response vasodilation, which was abolished after endothelium removal. Addition of a nitric oxide synthase inhibitor, N(G)-nitro-l-arginine methyl ester (100 µmol/L), alone or in the presence of a cyclooxygenase inhibitor, indomethacin (10 µmol/L), did not significantly affect the vasodilation of the mesenteric arterial bed in response to GA extract. These results suggest that GA-induced vasodilation is endothelium dependent but nitric oxide and prostacyclin independent. In the presence of high K(+) (60 mmol/L), the GA vasodilatory effect was completely abolished, suggesting that the vasodilation effect is mediated by hyperpolarization of the vascular cells. Also, pre-treatment with atropine (a muscarinic receptors antagonist) antagonized the GA-induced vasodilation, suggesting that the vasodilatory effect is mainly mediated by the endothelium-derived hyperpolarizing factor through activation of endothelial muscarinic receptors.
我们评价了圆叶牵牛(GA)提取物对预先用持续滴注苯肾上腺素(2-4ng/ml)收缩的大鼠肠系膜动脉床的血管舒张作用。GA 的单次注射引起了剂量依赖性的血管舒张,而内皮去除后这种作用被消除。单独加入一氧化氮合酶抑制剂 N(G)-硝基-L-精氨酸甲酯(100μmol/L)或在环氧化酶抑制剂吲哚美辛(10μmol/L)存在的情况下,对 GA 提取物引起的肠系膜动脉床舒张作用没有显著影响。这些结果表明,GA 诱导的血管舒张是内皮依赖性的,但与一氧化氮和前列环素无关。在高钾(60mmol/L)存在的情况下,GA 的血管舒张作用完全被消除,表明血管舒张作用是通过血管细胞的超极化介导的。此外,用阿托品(毒蕈碱受体拮抗剂)预处理可拮抗 GA 引起的血管舒张,表明血管舒张作用主要是通过内皮衍生的超极化因子通过激活内皮毒蕈碱受体来介导的。