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首页> 外文期刊>The Journal of Nutritional Biochemistry >Quercetin supplementation suppresses the secretion of pro-inflammatory cytokines in the lungs of Mongolian gerbils and in A549 cells exposed to benzo[a]pyrene alone or in combination with beta -carotene: in vivo and ex vivo studies.
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Quercetin supplementation suppresses the secretion of pro-inflammatory cytokines in the lungs of Mongolian gerbils and in A549 cells exposed to benzo[a]pyrene alone or in combination with beta -carotene: in vivo and ex vivo studies.

机译:槲皮素补充剂可抑制蒙古沙土鼠肺脏和暴露于单独或与β-胡萝卜素联用的苯并[a]]暴露的A549细胞中促炎性细胞因子的分泌:体内和离体研究。

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In vitro studies have shown that quercetin modulates the effects of beta -carotene induced by stimulants. Whether these reactions happen in vivo, however, is unclear. Thus, we investigated whether quercetin supplementation suppresses the harmful effects of benzo[a]pyrene (BaP) alone or combined with beta -carotene in the lungs of Mongolian gerbils. The gerbils were given quercetin (100 mg/kg body wt, 3 times/week), beta -carotene (10 mg/kg body wt, 3 times/week), and BaP (8 mmol, 2 times/week) alone or in combination by gavage for 6 months. beta -Carotene supplementation enhanced the pro-inflammatory effects of BaP in the lungs of gerbils. In contrast, quercetin supplementation significantly decreased the infiltration of inflammatory cells as well as the levels of TNF- alpha and IL-1 beta in the bronchoalveolar lavage fluid and plasma of gerbils exposed to BaP or BaP+ beta -carotene (P<.05). Such effects of quercetin supplementation were accompanied by a down-regulation of the expression of phospho-c-Jun and phospho-JNK induced by BaP or BaP+ beta -carotene in the lungs of gerbils. Furthermore, in the ex vivo study, we found that quercetin-metabolite-enriched plasma (QP) obtained from gerbils acted like a JNK inhibitor to significantly suppress the secretion of pro-inflammatory cytokines induced by BaP or BaP+ beta -carotene in A549 cells (P<.05). QP also suppressed the activation of the JNK pathway in the A549 cells. These results suggest that supplemental quercetin suppress the pro-inflammatory effect of beta -carotene induced by BaP in vivo and ex vivo. The regulation of the JNK pathway by the metabolites of quercetin contributes, at least in part, to such effects of quercetin in vivo.
机译:体外研究表明,槲皮素调节兴奋剂诱导的β-胡萝卜素的作用。但是,这些反应是否在体内发生尚不清楚。因此,我们研究了槲皮素补充剂是否单独或结合β-胡萝卜素抑制了蒙古沙土鼠肺部的苯并[a] i re(BaP)的有害作用。单独或在沙鼠中给予槲皮素(100 mg / kg体重,3次/周),β-胡萝卜素(10 mg / kg体重,3次/周)和BaP(8 mmol,2次/周)。连续灌胃6个月。 β-胡萝卜素的补充增强了沙土鼠肺中BaP的促炎作用。相比之下,槲皮素的补充显着降低了暴露于BaP或BaP +β-胡萝卜素( P i> <。05)。槲皮素补充剂的这种作用伴随下沙土鼠肺中BaP或BaP +β-胡萝卜素诱导的磷酸化c-Jun和磷酸化JNK的表达下调。此外,在离体研究中,我们发现从沙鼠获得的富含槲皮素-代谢物的血浆(QP)就像JNK抑制剂一样,可显着抑制BaP或BaP +β-胡萝卜素诱导的A549细胞促炎性细胞因子的分泌( P <。05)。 QP还抑制了A549细胞中JNK途径的激活。这些结果表明补充槲皮素在体内和体外抑制了BaP诱导的β-胡萝卜素的促炎作用。槲皮素的代谢产物对JNK途径的调节至少部分有助于槲皮素在体内的这种作用。

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