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首页> 外文期刊>Phytomedicine : >Gastroprotective effect of epoxy clerodane diterpene isolated from Tinospora cordifolia Miers (Guduchi) on indomethacin-induced gastric ulcer in rats
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Gastroprotective effect of epoxy clerodane diterpene isolated from Tinospora cordifolia Miers (Guduchi) on indomethacin-induced gastric ulcer in rats

机译:豚草中环氧环戊二烯二萜对吲哚美辛诱导的大鼠胃溃疡的胃保护作用

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摘要

The present study evaluated the gastroprotective effect of epoxy clerodane diterpene (ECD), isolated from Tinospora cordifolia on indomethacin-induced gastric ulcer in rats. Administration of indomethacin exhibits extreme levels of ulcer index (UI) and myeloperoxidase (MPO) activity. Indomethacin down regulated PGE2, anti-inflammatory cytokines (IL-4, IL-10) and pro-angiogenic factors (VEGF and EGF). The ECD pretreatment considerably increased the levels of PGE2, anti-inflammatory cytokines and pro-angiogenic factors. The ulcer-healing activity of ECD was inhibited by pre-administration of the specific COX-1 inhibitor (SC560) and nonspecific NOS inhibitor (l-NAME), which indicates the involvement of PGE2 and NOS in ECD induced ulcer healing activity. These findings suggest that ECD exerts its antiulcer activity by reinforcement of defensive elements and diminishing the offensive elements.
机译:本研究评估了从心叶成虫中分离出的环氧双环戊二烯(ECD)对消炎痛诱导的大鼠胃溃疡的胃保护作用。消炎痛的给药表现出极高水平的溃疡指数(UI)和髓过氧化物酶(MPO)活性。消炎痛下调PGE2,抗炎细胞因子(IL-4,IL-10)和促血管生成因子(VEGF和EGF)。 ECD预处理可大大提高PGE2,抗炎细胞因子和促血管生成因子的水平。预先施用特异性COX-1抑制剂(SC560)和非特异性NOS抑制剂(1-NAME)可抑制ECD的溃疡愈合活性,这表明PGE2和NOS参与了ECD诱导的溃疡愈合活性。这些发现表明,ECD通过增强防御元素并减少攻击元素来发挥其抗溃疡活性。

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