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控制小鼠体内L-色氨酸-烟酰胺转化以及尿排泄率(N(1)-甲基-2-吡啶酮-5-甲酰胺 + N(1)-甲基-4-吡啶酮-3-甲酰胺)/N(1)-甲基烟酰胺的酶。

Enzymes that control the conversion of L-tryptophan-nicotinamide and the urinary excretion ratio (N(1)-methyl-2-pyridone-5-carboxamide + N(1)-methyl-4-pyridone-3-carboxamide)/N(1)-methylnicotinamide in mice.

作者信息

Shibata Katsumi, Morita Nobuya, Shibata Yoshika, Fukuwatari Tsutomu

机构信息

Department of Nutrition, School of Human Cultures, The University of Shiga Prefecture.

出版信息

Biosci Biotechnol Biochem. 2013;77(10):2105-11. doi: 10.1271/bbb.130467. Epub 2013 Oct 7.

Abstract

There is little information on L-tryptophan→nicotinamide metabolism in mice. In the present study, we investigated the two important nutritional factors involved in metabolism L-tryptophan→nicotinamide; one is the amount of nicotinamide synthesized from L-tryptophan, and the other is the urine ratio (N(1)-methyl-2-pyridone-5-carboxamide + N(1)-methyl-4-pyridone-3-carboxamide)/N(1)-methylnicotinamide. The order of the percentages of nicotinamide synthesized from L-tryptophan was as follows: CBA strain mice (conversion percentage 0.41%) < BALB strain mice (0.82%) < C57BL/6 strain mice (1.13%) < ICR strain mice (1.70%). Urinary excretion of quinolinic acid was correlated with urinary excretion of the sum of nicotinamide and its catabolites (p<0.0001). The urine sum, which reflects the conversion of L-tryptophan→nicotinamide, correlated well with the activity of 3-hydroxyanthranilic acid dioxygenase (p=0.040). A nutritional indicator, the urine ratio (N(1)-methyl-2-pyridone-5-carboxamide + N(1)-methyl-4-pyridone-3-carboxamide)/N(1)-methylnicotinamide, was controlled by the activity of N(1)-methyl-2-pyridone-5-carboxamide-forming N(1)-methylnicotinamide oxidase.

摘要

关于小鼠体内L-色氨酸→烟酰胺代谢的信息很少。在本研究中,我们调查了参与L-色氨酸→烟酰胺代谢的两个重要营养因素;一个是由L-色氨酸合成的烟酰胺量,另一个是尿液比值(N(1)-甲基-2-吡啶酮-5-甲酰胺 + N(1)-甲基-4-吡啶酮-3-甲酰胺)/N(1)-甲基烟酰胺。由L-色氨酸合成烟酰胺的百分比顺序如下:CBA品系小鼠(转化率0.41%)< BALB品系小鼠(0.82%)< C57BL/6品系小鼠(1.13%)< ICR品系小鼠(1.70%)。喹啉酸的尿排泄量与烟酰胺及其分解代谢产物总和的尿排泄量相关(p<0.0001)。反映L-色氨酸→烟酰胺转化的尿液总和与3-羟基邻氨基苯甲酸双加氧酶的活性密切相关(p=0.040)。一种营养指标,即尿液比值(N(1)-甲基-2-吡啶酮-5-甲酰胺 + N(1)-甲基-4-吡啶酮-3-甲酰胺)/N(1)-甲基烟酰胺,受形成N(1)-甲基-2-吡啶酮-5-甲酰胺的N(1)-甲基烟酰胺氧化酶活性的控制。

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