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首页> 外文期刊>Journal of dietary supplements >An Improvement of Oxidative Stress in Diabetic Rats by Ubiquinone-10 and Ubiquinol-10 and Bioavailability after Short- and Long-Term Coenzyme Q10 Supplementation
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An Improvement of Oxidative Stress in Diabetic Rats by Ubiquinone-10 and Ubiquinol-10 and Bioavailability after Short- and Long-Term Coenzyme Q10 Supplementation

机译:补充短期和长期辅酶Q10后,Ubiquinone-10和Ubiquinol-10对糖尿病大鼠氧化应激的改善及其生物利用度

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摘要

This study explored effects of ubiquinol-10 and ubiquinone-10, two different forms of coenzyme Q10, in diabetic rats. Oxidative stress is characterized by the depletion of antioxidant defenses and overproduction of free radicals that might contributeto, and even accelerate, the development of diabetes mellitus (DM) complications. Coenzyme Qio was administered orally to diabetic rats and oxidative stress markers were then assessed. Bioavailability in normal rats was additionally assessed in various tissues and subcellular fractions after short-term and long-term coenzyme Qio supplementation. Elevated nonfasting blood glucose and blood pressure in diabetic rats were decreased by ubiquinone-10. Both ubiquinol-10 and ubiquinone-10 ameliorated oxidativestress, based on assays for reactive oxygen metabolites and malondi-aldehyde. Coenzyme Qio levels increased with both treatments and liver nicotinamide adenine dinucleotide phosphate (NADPH) coenzyme 0 reductase with ubiquinone-10. Ubiquinol-10 was better absorbed in the liver and pancreas than ubiquinone-10, though both were similarly effective. In bioavailability study, a longer period of coenzyme Qio supplementation did not lead to its accumulation in tissues or organelles. Both forms of coenzyme Qio reduced oxidative stress in diabetic rats. Long-term supplementation of coenzyme Qio appeared to be safe.
机译:这项研究探讨了两种不同形式的辅酶Q10泛醇10和泛醌10在糖尿病大鼠中的作用。氧化应激的特征是抗氧化剂防御能力的丧失和自由基的过度产生,这些自由基可能有助于甚至加速糖尿病(DM)并发症的发展。将辅酶Qio口服给予糖尿病大鼠,然后评估其氧化应激标志物。在短期和长期补充辅酶Qio后,还评估了正常大鼠的生物利用度,包括各种组织和亚细胞部分。泛醌10可以降低糖尿病大鼠的非空腹血糖和血压升高。基于活性氧代谢产物和丙二醛的测定,泛醇10和泛醌10均改善了氧化应激。辅酶Qio水平随着两种处理以及肝烟酰胺腺嘌呤二核苷酸磷酸(NADPH)辅酶0还原酶与泛醌10的增加而增加。泛醌10在肝脏和胰腺中的吸收要比泛醌10更好,尽管两者的效果相似。在生物利用度研究中,补充辅酶Qio的时间较长并未导致其在组织或细胞器中的积累。两种形式的辅酶Qio均可降低糖尿病大鼠的氧化应激。长期补充辅酶Qio似乎是安全的。

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