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首页> 外文期刊>The Journal of Experimental Biology >The effects of L-arginine and L-NAME supplementation on redox-regulation and thermogenesis in interscapular brown adipose tissue
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The effects of L-arginine and L-NAME supplementation on redox-regulation and thermogenesis in interscapular brown adipose tissue

机译:L-精氨酸和L-NAME的添加对肩inter间褐色脂肪组织氧化还原调节和生热的影响

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Changes in inducible nitric oxide synthase (iNOS) protein levels and its relationship with the hyperplasia and uncoupling protein 1 (UCP1) levels were examined in interscapular brown adipose tissue (IBAT) of adult rat males receiving L-arginine (L-Arg; 2.25%) or N-nitro-L-arginine methyl ester (L-NAME; 0.01%) as a drinking liquid and maintained at low (4+/-1 degrees C) or room (22+/-1 degrees C) temperature for 45 days. Cold generally diminished both iNOS immunopositivity and protein level in IBAT, as well as the rate of apoptosis. Among groups acclimated to cold, higher iNOS immunopositivity and protein levels were detected only in the L-Arg-treated group. Furthermore, chronic L-Arg treatment increased IBAT mass and UCP1 protein content, while L-NAME had an opposite effect, decreasing both IBAT mass and UCP1 protein level, as compared to the control maintained at 4+/-1 degrees C. These data suggest that nitric oxide (NO) produced by iNOS could also contribute to overall NO-associated regulation of thermogenesis in IBAT. Namely, that iNOS, i.e. NO, in correlation with enhanced thermogenesis, additionally induced IBAT hyperplasia and UCP1 level compared to that induced by low temperature. Cooperative action of decreased apoptosis accompanied by increased tissue hyperplasia and UCP1 level, observed in IBAT of cold-acclimated rats, would be a way of meeting the metabolic requirements for increased thermogenesis.
机译:在接受L-精氨酸(L-Arg; 2.25%)的成年大鼠雄性肩s间棕色脂肪组织(IBAT)中检查了诱导型一氧化氮合酶(iNOS)蛋白水平的变化及其与增生和解偶联蛋白1(UCP1)水平的关系。 )或N-硝基-L-精氨酸甲酯(L-NAME; 0.01%)作为饮用液,并在低温(4 +/- 1摄氏度)或室温(22 +/- 1摄氏度)下保持45天。感冒通常会降低IBAT中的iNOS免疫阳性和蛋白质水平以及细胞凋亡率。在适应寒冷的组中,仅在L-Arg治疗组中检测到更高的iNOS免疫阳性和蛋白质水平。此外,与维持在4 +/- 1摄氏度的对照组相比,慢性L-Arg治疗增加了IBAT质量和UCP1蛋白含量,而L-NAME具有相反的作用,降低了IBAT质量和UCP1蛋白水平。提示iNOS产生的一氧化氮(NO)也可能有助于IBAT热生成的整体NO相关调节。即,与低温诱导的iNOS,即NO,与生热增强相关,还额外诱导了IBAT增生和UCP1水平。在冷驯化的大鼠的IBAT中观察到,凋亡减少的协同作用伴随组织增生和UCP1水平的增加,将是满足增加热生成的代谢要求的一种方式。

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