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雄性C57BL/6小鼠硫氨基酸代谢的年龄相关变化

Age-Related Changes in Sulfur Amino Acid Metabolism in Male C57BL/6 Mice.

作者信息

Jeon Jang Su, Oh Jeong-Ja, Kwak Hui Chan, Yun Hwi-Yeol, Kim Hyoung Chin, Kim Young-Mi, Oh Soo Jin, Kim Sang Kyum

机构信息

College of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.

Bio-Evaluation Center, KRIBB, Ochang 28116, Republic of Korea.

出版信息

Biomol Ther (Seoul). 2018 Mar 1;26(2):167-174. doi: 10.4062/biomolther.2017.054.

Abstract

Alterations in sulfur amino acid metabolism are associated with an increased risk of a number of common late-life diseases, which raises the possibility that metabolism of sulfur amino acids may change with age. The present study was conducted to understand the age-related changes in hepatic metabolism of sulfur amino acids in 2-, 6-, 18- and 30-month-old male C57BL/6 mice. For this purpose, metabolite profiling of sulfur amino acids from methionine to taurine or glutathione (GSH) was performed. The levels of sulfur amino acids and their metabolites were not significantly different among 2-, 6- and 18-month-old mice, except for plasma GSH and hepatic homocysteine. Plasma total GSH and hepatic total homocysteine levels were significantly higher in 2-month-old mice than those in the other age groups. In contrast, 30-month-old mice exhibited increased hepatic methionine and cysteine, compared with all other groups, but decreased hepatic S-adenosylmethionine (SAM), S-adenosylhomocysteine and homocysteine, relative to 2-month-old mice. No differences in hepatic reduced GSH, GSH disulfide, or taurine were observed. The hepatic changes in homocysteine and cysteine may be attributed to upregulation of cystathionine β-synthase and down-regulation of γ-glutamylcysteine ligase in the aged mice. The elevation of hepatic cysteine levels may be involved in the maintenance of hepatic GSH levels. The opposite changes of methionine and SAM suggest that the regulatory role of SAM in hepatic sulfur amino acid metabolism may be impaired in 30-month-old mice.

摘要

硫氨基酸代谢的改变与许多常见的老年疾病风险增加有关,这增加了硫氨基酸代谢可能随年龄变化的可能性。本研究旨在了解2个月、6个月、18个月和30个月大的雄性C57BL/6小鼠肝脏中硫氨基酸代谢的年龄相关变化。为此,对从蛋氨酸到牛磺酸或谷胱甘肽(GSH)的硫氨基酸进行了代谢物谱分析。除血浆GSH和肝脏同型半胱氨酸外,2个月、6个月和18个月大的小鼠中硫氨基酸及其代谢物的水平没有显著差异。2个月大的小鼠血浆总GSH和肝脏总同型半胱氨酸水平显著高于其他年龄组。相比之下,与所有其他组相比,30个月大的小鼠肝脏蛋氨酸和半胱氨酸增加,但相对于2个月大的小鼠,肝脏S-腺苷甲硫氨酸(SAM)、S-腺苷同型半胱氨酸和同型半胱氨酸减少。未观察到肝脏还原型GSH、GSH二硫化物或牛磺酸的差异。老年小鼠肝脏中同型半胱氨酸和半胱氨酸的变化可能归因于胱硫醚β-合酶的上调和γ-谷氨酰半胱氨酸连接酶的下调。肝脏半胱氨酸水平的升高可能参与维持肝脏GSH水平。蛋氨酸和SAM的相反变化表明,SAM在30个月大的小鼠肝脏硫氨基酸代谢中的调节作用可能受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73e/5839495/fd3d321c1ae5/bt-26-167f1.jpg

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