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Vasorelaxation and Superoxide Scavenging Activities of Orotic Acid

机译:乳清酸的血管舒张和超氧化物清除活性

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The aim of study is to investigate effects of orotic acid (OA) on phenylephrine-induced contraction of rat thoracic aorta and its antioxidative activity. Results showed that the OA exhibited maximal vasorelaxation in dose-dependent manner with ED50 of 3.16x10-7 M, but the effect was less than those of acetylcholine (ACh)-induced nitric oxide (NO) vasorelaxation. Significant reductions of the vasorelaxations were found in the presence of either NG-nitro-L-arginine methyl ester (L-NAME) or indomethacin (INDO). Synergistic effects were observed in the presence of L-NAME plus INDO that led to loss of vasorelaxation of both the ACh and the OA. In addition, complete loss of the vasorelaxation was manifested under removal of endothelial cells. This implies that the vasorelaxations are mediated by partially endothelium-induced NO and prostacyclin. The OA exhibited antioxidative activity in both DPPH and SOD assays. The significant results reveal novel actions of the OA as vasorelaxants and superoxide scavenger which are benefits as therapeutic uses and health supplements.
机译:研究的目的是研究乳清酸(OA)对去氧肾上腺素诱导的大鼠胸主动脉收缩及其抗氧化活性的影响。结果表明,OA具有剂量依赖性的最大舒张作用,ED 50 为3.16x10 -7 M,但作用小于乙酰胆碱(ACh)-诱发一氧化氮(NO)血管舒张。在N G -硝基-L-精氨酸甲酯(L-NAME)或消炎痛(INDO)的存在下,血管舒张作用明显减少。在存在L-NAME和INDO的情况下观察到协同作用,导致ACh和OA的血管舒张功能丧失。另外,在去除内皮细胞的情况下,血管舒张完全丧失。这暗示血管舒张由部分内皮诱导的NO和前列环素介导。 OA在DPPH和SOD分析中均表现出抗氧化活性。显着的结果揭示了OA作为血管舒张剂和超氧化物清除剂的新作用,这些作用可作为治疗用途和健康补品。

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