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作 者:薛文鑫[1] 张明升[1] 牛龙刚[1] 刘宇[1] 梁月琴[1]
机构地区:[1]山西医科大学药理学教研室,山西太原030001
出 处:《中国药理学与毒理学杂志》2007年第1期23-27,共5页Chinese Journal of Pharmacology and Toxicology
摘 要:目的 研究牛磺酸舒血管作用的可能机制。方法 记录苯肾上腺素(PE)和KCl预收缩的离体大鼠主动脉环张力变化,观察牛磺酸的舒血管作用及不同工具药对其作用的影响。结果 牛磺酸(20~80mmol·L^-1)对PE(1μmol·L^-1)或KCl(60mmol·L^-1)预收缩的大鼠主动脉环均有非内皮依赖的、浓度依赖性的舒张作用。在内皮完整的血管环,左旋硝基精氨酸甲酯(0.1mmol·L^-1)对牛磺酸的舒血管作用无明显影响;β-丙氨酸(60mmol·L^-1)在PE预收缩的血管环增强牛磺酸的舒血管作用,而在KCl预收缩的血管环则降低牛磺酸的舒血管作用;在KCl预收缩基础上,钾通道阻断剂格列本脲(10μmol·L^-1)和四乙胺(10mmol·L^-1)明显抑制牛磺酸的舒血管作用,而4-氨基吡啶(1mmol·L^-1)和BaCl2(1mmol·L^-1)无影响。结论 牛磺酸有浓度依赖性的血管舒张作用,此作用不依赖血管内皮,可能与其跨细胞膜转运有关,可能有钙依赖性钾通道和ATP敏感性钾通道的参与。AIM To investigate the vasodilative roles and the possible mechanisms of taurine on thoracic aorta of rats. METHODS Isotonic tension of thoracic aortic rings precontracted by phenylephrine ( PE, 1 μmol .L^-1 ) or KCl (60 mmol.L^-1) was recorded. The vasorelaxing action of taurine and the influence of various drugs on it were observed in the rings with endothelium intact or endothelium denuded. RESULTS Taurine ( 20 - 80 mmol . L^-1) caused concentration-dependent relaxation in thoracic aortas with or without endothelium, and there was no significant difference between them. NG-nitro-L-arginine methyl ester (0.1 mmol.L^-1) had no effect on the vasorelaxing action of taurine on thoracic aortas precontracted by PE or KCl. β-Alanine (60 mmol. L^- 1 ) diminished the vasorelaxing action of taurine in KCl-precontracted rings, but enhanced the action in PE-precontracted rings. Tetraethylamine, an antagonist of calcium activated potassium channels ( KBCa ) , and glibenclamide,an antagonist of ATP sensitive potassium channels ( KATP ) attenuated the vasorelaxing effect of taurine, but 4-aminopyridine and BaCl2 had no significant effect on the vasorelaxing action of taurine. CONCLUSION The vasorelaxing action of taurine is endothelium-independent and associated with taurine transmembrane transportation; KBCa and KATP may be involved in the action of taurine.
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