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首页> 外文期刊>Journal of Pharmacy and Pharmacology >In-vitro and in-vivo anti-inflammatory and antinociceptive effects of the methanol extract of the roots of Morinda officinalis.
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In-vitro and in-vivo anti-inflammatory and antinociceptive effects of the methanol extract of the roots of Morinda officinalis.

机译:巴戟天根的甲醇提取物的体外和体内抗炎和镇痛作用。

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摘要

The anti-inflammatory effects of the methanol extract of the roots of Morinda officinalis (MEMO) (Rubiaceae) were evaluated in-vitro and in-vivo. The effects of MEMO on lipopolysaccharide (LPS)induced responses in the murine macrophage cell line RAW 264.7 were examined. MEMO potently inhibited the production of nitric oxide (NO), prostaglandin E2 and tumour necrosis factor-alpha (TNF-alpha) in LPS-stimulated RAW 264.7 macrophages. Consistent with these results, the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at the protein level, and of iNOS, COX-2 and TNF-alpha at the mRNA level, was also inhibited by MEMO in a concentration-dependent manner. Furthermore, MEMO inhibited the nuclear factor kappa B (NF-kappaB) activation induced by LPS, and this was associated with the prevention of degradation of the inhibitor kappaB (IkappaB), and subsequently with attenuated p65 protein in the nucleus. The anti-inflammatory effect of MEMO was examined in rats using the carrageenan-induced oedema model. The antinociceptive effects of MEMO were assessed in mice using the acetic acid-induced abdominal constriction test and the hot-plate test. MEMO (100, 200 mg kg-1 per day, p.o.) exhibited anti-inflammatory and antinociceptive effects in these animal models. Taken together, the data demonstrate that MEMO has anti-inflammatory and antinociceptive activity, inhibiting iNOS, COX-2 and TNF-alpha expression by down-regulating NF-kappaB binding activity.
机译:在体外和体内评价了巴戟天的根的甲醇提取物(MEMO)(茜草科)的抗炎作用。检查了MEMO对脂多糖(LPS)诱导的小鼠巨噬细胞RAW 264.7细胞系应答的影响。 MEMO有效抑制LPS刺激的RAW 264.7巨噬细胞中一氧化氮(NO),前列腺素E2和肿瘤坏死因子-α(TNF-alpha)的产生。与这些结果一致,MEMO也抑制了蛋白质水平的诱导型一氧化氮合酶(iNOS)和环氧合酶-2(COX-2)的表达,以及mRNA水平的iNOS,COX-2和TNF-α的表达。以浓度依赖的方式。此外,MEMO抑制了LPS诱导的核因子kappa B(NF-kappaB)的激活,这与防止抑制剂kappaB(IkappaB)降解以及随后抑制核中p65蛋白的降解有关。使用角叉菜胶诱导的水肿模型检查了MEMO的抗炎作用。使用乙酸诱导的腹部收缩试验和热板试验评估了MEMO在小鼠中的镇痛作用。在这些动物模型中,MEMO(每天100,200 mg kg-1,p.o.)表现出抗炎和镇痛作用。两者合计,数据表明MEMO具有抗炎和抗伤害感受的活性,通过下调NF-κB的结合活性来抑制iNOS,COX-2和TNF-α的表达。

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