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限制蛋氨酸摄入会导致高同型半胱氨酸血症,并改变 Fischer-344 大鼠肝脏 HS 的产生能力。

Methionine restriction leads to hyperhomocysteinemia and alters hepatic HS production capacity in Fischer-344 rats.

机构信息

Department of Biological Sciences, University of Manitoba, Winnipeg, MB, Canada.

Department of Food and Human Nutritional Sciences, University of Manitoba, Winnipeg, MB, Canada.

出版信息

Mech Ageing Dev. 2018 Dec;176:9-18. doi: 10.1016/j.mad.2018.10.004. Epub 2018 Oct 25.

DOI:10.1016/j.mad.2018.10.004
PMID:30367932
Abstract

Dietary methionine restriction (MR) increases lifespan in several animal models. Despite low dietary intake of sulphur amino acids, rodents on MR develop hyperhomocysteinemia. On the contrary, MR has been reported to increase HS production in mice. Enzymes involved in homocysteine metabolism also take part in HS production and hence, in this study, the impact of MR on hyperhomocysteinemia and HS production capacity were investigated using Fischer-344 rats assigned either a control or a MR diet for 8 weeks. The MR animals showed elevated plasma homocysteine accompanied with a reduction in liver cysteine content and methylation potential. It was further found that MR decreased cystathionine-β-synthase (CBS) activity in the liver, however, MR increased hepatic cystathionine-γ-lyase (CGL) activity which is the second enzyme in the transsulfuration pathway and also participates in regulating HS production. The relative contribution of CGL in HS production increased concomitantly with the increased CGL activity. Additionally, hepatic mercaptopyruvate-sulphur-transferase (MPST) activity also increased in response to MR. Taken together, our results suggest that reduced CBS activity and S-Adenosylmethionine availability contributes to hyperhomocysteinimia in MR animals. Elevated CGL and MPST activities may provide a compensatory mechanism for maintaining hepatic HS production capacity in response to the decreased CBS activity.

摘要

饮食蛋氨酸限制(MR)可延长几种动物模型的寿命。尽管硫氨基酸的饮食摄入量低,但 MR 组的啮齿动物会发生高同型半胱氨酸血症。相反,据报道 MR 可增加小鼠的 HS 产生。参与同型半胱氨酸代谢的酶也参与 HS 的产生,因此,在这项研究中,使用 Fischer-344 大鼠进行了研究,这些大鼠被分配接受对照或 MR 饮食 8 周。MR 动物表现出血浆同型半胱氨酸升高,伴随着肝半胱氨酸含量和甲基化潜力降低。进一步发现,MR 降低了肝脏胱硫醚-β-合酶(CBS)的活性,然而,MR 增加了肝胱硫醚-γ-裂合酶(CGL)的活性,CGL 是转硫途径中的第二种酶,也参与调节 HS 的产生。CGL 在 HS 产生中的相对贡献随着 CGL 活性的增加而增加。此外,肝脏巯基丙酮酸-硫转移酶(MPST)的活性也随着 MR 而增加。总之,我们的结果表明,CBS 活性降低和 S-腺苷甲硫氨酸可用性导致 MR 动物的高同型半胱氨酸血症。CGL 和 MPST 活性的升高可能为维持肝脏 HS 产生能力提供了一种补偿机制,以应对 CBS 活性的降低。

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