首页> 外文期刊>Biochemical and Biophysical Research Communications >N-(2-mercaptopropionyl)-glycine, a diffusible antioxidant, activates HIF-1 by inhibiting HIF prolyl hydroxylase-2: Implication in amelioration of rat colitis by the antioxidant
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N-(2-mercaptopropionyl)-glycine, a diffusible antioxidant, activates HIF-1 by inhibiting HIF prolyl hydroxylase-2: Implication in amelioration of rat colitis by the antioxidant

机译:N-(2-巯基丙酰基)-甘氨酸是一种可扩散的抗氧化剂,可通过抑制HIF脯氨酰羟化酶-2激活HIF-1:抗氧化剂在改善大鼠结肠炎中的作用

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We investigated anti-colitic effects of N-(2-mercaptopropionyl)-glycine (NMPG), a diffusible antioxidant, in TNBS-induced rat colitis model and a potential molecular mechanism underlying the pharmacologic effect of the antioxidant. NMPG alleviated colonic injury and effectively lowered myeloperoxidase activity. Moreover, NMPG substantially attenuated expression of pro-inflammatory mediators in the inflamed colon. NMPG induced hypoxia-inducible factor-1α (HIF-1α) in human colon carcinoma cells, leading to elevated secretion of vascular endothelial growth factor (VEGF), a target gene product of HIF-1 involved in ulcer healing of gastrointestinal mucosa. NMPG induction of HIF-1α occurred by inhibiting HIF prolyl hydroxylase-2 (HPH-2), an enzyme that plays a major role in negatively regulating HIF-1α protein stability. In in vitro Von Hippel-Lindau protein binding assay, the inhibitory effect of NMPG on HPH-2 was attenuated by escalating dose of ascorbate but not 2-ketoglutarate, cofactors of the enzyme. Consistent with this, cell-permeable ascorbate significantly attenuated NMPG induction of HIF-1α in cells. Our data suggest that NMPG is an anti-colitic antioxidant that exerts its pharmacologic effects at least partly through activation of an ulcer healing pathway, HIF-1-VEGF.
机译:我们调查了可扩散的抗氧化剂N-(2-巯基丙酰基)-甘氨酸(NMPG)在TNBS诱导的大鼠结肠炎模型中的抗结肠炎作用以及潜在的分子机制,该潜在的分子机制是抗氧化剂的药理作用。 NMPG减轻了结肠损伤并有效降低了髓过氧化物酶活性。而且,NMPG大大减弱了发炎结肠中促炎介质的表达。 NMPG诱导人结肠癌细胞中的缺氧诱导因子-1α(HIF-1α),导致血管内皮生长因子(VEGF)的分泌增加,血管内皮生长因子是参与胃肠道粘膜溃疡愈合的HIF-1的目标基因产物。 NMPG对HIF-1α的诱导是通过抑制HIF脯氨酰羟化酶2(HPH-2)而产生的,该酶在负调控HIF-1α蛋白的稳定性中起主要作用。在体外Von Hippel-Lindau蛋白结合试验中,NMPG对HPH-2的抑制作用通过增加酶的抗坏血酸而不是2-酮戊二酸的剂量而减弱。与此相一致,细胞可渗透的抗坏血酸盐显着减弱了细胞中HIF-1α的NMPG诱导。我们的数据表明NMPG是一种抗结肠炎的抗氧化剂,至少部分通过激活溃疡愈合途径HIF-1-VEGF发挥其药理作用。

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