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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings
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Vasorelaxant Effect of Osterici Radix Ethanol Extract on Rat Aortic Rings

机译:Osterici adranol提取物对大鼠主动脉戒指的血管瘤效应

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摘要

The root of Ostericum koreanum Maximowicz has been used as a traditional medicine called "Kanghwal" in Korea (or "Qianghuo" in China). The purpose of this study was to investigate the vasorelaxant activity and mechanism of action of an ethanol extract of the O. koreanum root (EOK). We used isolated rat aortic rings to assess the effects of EOK on various vasorelaxant or vasoconstriction factors. EOK induced vasorelaxation in phenylephrine hydrochloride (PE) or KCl precontracted aortic rings in a concentration-dependent manner. However, the vasorelaxant effects of EOK on endothelium-intact aortic rings were reduced by pretreatment with l-NAME or methylene blue. In Ca~(2+)-free Krebs-Henseleit solution, pretreatment with EOK (0.3 mg/mL) completely inhibited PE-induced constriction. In addition, EOK (0.3 mg/mL) also completely inhibited vasoconstriction induced by supplemental Ca~(2+) in aortic rings that were precontracted with PE or KCl. Furthermore, the EOK-induced vasorelaxation in PE-contracted aortic rings was inhibited by preincubation with nifedipine. These results indicate that the vasorelaxant effects of EOK are responsible for the induction of NO formation from L-Arg and NO-cGMP pathways, blockage of the extracellular Ca~(2+) entry via the receptor-operative Ca~(2+) channel and voltage-dependent calcium channel, and blockage of sarcoplasmic reticulum Ca~(2+) release via the inositol triphosphate pathway.
机译:Ostericum Koreanum Maximowicz的根源被用作韩国叫“康沃尔”的传统医学(或“中国Qianuo”)。本研究的目的是探讨O. oreanum Root(Eok)的乙醇提取物的血管克莱克兰活性和作用机制。我们使用了分离的大鼠主动脉戒指来评估Eok对各种血管内或血管收割机的影响。 EOK诱导盐酸苯肾上腺素(PE)或KCL以浓度依赖性的方式进行血管藻。然而,通过用L-NAME或亚甲基蓝预处理降低了Eok对内皮完整主动脉环的血管交延效应。在CA〜(2 +) - 免费克雷斯 - Henseleit解决方案,用EOK(0.3mg / ml)的预处理完全抑制PE诱导的收缩。此外,EOK(0.3mg / ml)还完全抑制由PE或KCl预生育的主动脉环中由辅助Ca〜(2+)引起的血管收缩。此外,通过与硝苯地平预孵育来抑制体积凝聚的主动脉环中的Eok诱导的血管插入。这些结果表明,Eok的血管内抑制效应负责从L-Arg和No-CGMP途径,通过受体操作Ca〜(2+)通道的细胞外Ca〜(2+)进入的诱导诱导。和电压依赖性钙通道,并通过肌醇三磷酸途径释放肌肉网状术Ca〜(2+)裂缝。

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