首页> 外文期刊>Vascular pharmacology >Relaxant effects of danshen aqueous extract and its constituent danshensu on rat coronary artery are mediated by inhibition of calcium channels.
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Relaxant effects of danshen aqueous extract and its constituent danshensu on rat coronary artery are mediated by inhibition of calcium channels.

机译:丹参水提物及其成分丹参素对大鼠冠状动脉的松弛作用是通过抑制钙通道介导的。

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摘要

In this study, we have investigated the actions of danshensu, an active, water-extractable component of the medicinal herb danshen (Salvia miltiorrhiza), on rat isolated coronary artery rings precontracted with 1 microM 5-hydroxytryptamine (5-HT) and its action compared to the water-extractable fraction of the herb. Extraction of the water-soluble fraction from danshen (S. miltiorrhiza) provided yield of 17.5% (35 g/200 g). The amount of danshensu determined in the crude danshen herb and in its aqueous fraction was 0.45 mg/g (0.045%) and 3.28 mg/g (0.33%). The danshen aqueous extract was 13 times less potent than danshensu in relaxing 5-HT-precontracted coronary artery rings; IC50 values were 930.3+/-133.5 microg/ml and 71.5+/-11.0 microg/ml. Removal of the endothelium did not significantly affect their vasodilator potencies; IC50 values were 842.1+/-123.8 microg/ml and 84.8+/-8.8 microg/ml. On the other hand, a potassium channel inhibitor tetraethylammonium (TEA, 10 mM) shifted their concentration-response curves by 1.7 and 2.2 folds. The possible involvement of Ca2+ channels was investigated in artery rings incubated with Ca2+-free buffer and primed with 1 microM 5-HT or 60 mM KCl for 5 min prior to addition of CaCl2 to elicit contraction. In 5-HT-primed preparations, the CaCl2-induced vasoconstriction was abolished by 2 mg/ml danshen aqueous extract and 200 microg/ml danshensu, whereas, in KCl-primed preparations, 10 mg/ml danshen aqueous extract and 600 microg/ml danshensu were required to abrogate the vasoconstriction. These findings suggest the vasorelaxant actions of danshen aqueous extract and danshensu were produced by inhibition of Ca2+ influx in the vascular smooth muscle cells. The opening of K+ channels had a minor contribution to the response, but endothelium-dependent mechanisms were not involved.
机译:在这项研究中,我们研究了丹参素(丹参,丹参)的活性,水可萃取成分对预分离有1 microM 5-羟色胺(5-HT)的大鼠离体冠状动脉环的作用及其作用与草药的水提取物相比。从丹参(S. miltiorrhiza)中提取水溶性级分,收率为17.5%(35 g / 200 g)。在粗制丹参药草及其水溶液中测定的丹参素含量为0.45 mg / g(0.045%)和3.28 mg / g(0.33%)。在松弛的5-HT预收缩冠状动脉环中,丹参水提物的功效比丹参素低13倍。 IC50值为930.3 +/- 133.5微克/毫升和71.5 +/- 11.0微克/毫升。去除内皮并没有显着影响其血管扩张药的效力。 IC50值为842.1 +/- 123.8微克/毫升和84.8 +/- 8.8微克/毫升。另一方面,钾通道抑制剂四乙铵(TEA,10 mM)将其浓度-响应曲线移动了1.7和2.2倍。在加入无Ca2 +的缓冲液孵育的动脉环中研究了Ca2 +通道的可能参与,并在加入CaCl2引起收缩之前,先用1 microM 5-HT或60 mM KCl灌注5分钟。在5-HT引发的制剂中,CaCl2诱导的血管收缩被2 mg / ml的丹参水提取物和200 microg / ml的丹参素消除,而在KCl引发的制品中,10 mg / ml的丹参水提取物和600 microg / ml丹参素被要求取消血管收缩。这些发现表明,丹参水提物和丹参素的血管舒张作用是通过抑制血管平滑肌细胞中Ca 2+流入而产生的。 K +通道的开放对反应的贡献很小,但不涉及内皮依赖性机制。

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