Richie John P, Komninou Despina, Leutzinger Yvonne, Kleinman Wayne, Orentreich Norman, Malloy Virginia, Zimmerman Jay A
Division of Epidemiology and Cancer Susceptibility, American Health Foundation Cancer Center, Institute for Cancer Prevention, Valhalla, NY 10595, USA.
Nutrition. 2004 Sep;20(9):800-5. doi: 10.1016/j.nut.2004.05.009.
Previously, we demonstrated that lifelong methionine (Met) restriction (MR) increases lifespan, decreases the incidence of aging-related diseases, increases blood glutathione (GSH) levels, and prevents loss of GSH during aging in rats. Our present objective was to elucidate the effects of MR on GSH metabolism and transport by determining the time course and nature of GSH and cysteine changes in blood and other tissues in young and mature rats.
Male F-344 rats were placed on control (0.86% Met) or MR (0.17% Met) defined amino acid diets at age 7 wk and killed at different times thereafter. MR was also initiated in adult (12-mo-old) rats.
Throughout the first 2 mo of MR, blood GSH levels increased 84% and liver GSH decreased 66% in relation to controls. After this period, liver GSH levels remained constant through at least 6 mo. GSH levels also decreased in the pancreas (80%) and kidney (22%) but remained unchanged in other tissues examined after 11 wk of MR. The increase in blood GSH was evident as soon as 1 wk after initiating MR and reached a plateau by 6 wk. A similar increase in erythrocyte GSH levels was observed when MR was administered to mature adult rats. Fasting decreased liver GSH in controls but had no further effect in MR animals. By 1 mo, cysteine levels had decreased in all tissues except brain.
These results suggest that adaptive changes occur in the metabolism of Met, cysteine, and/or GSH as a result of MR in young and adult rats. These early metabolic changes lead to conservation of GSH levels in most extrahepatic tissues and increased GSH in erythrocytes by depleting liver GSH to a critical level.
此前,我们证明终身蛋氨酸(Met)限制(MR)可延长寿命,降低与衰老相关疾病的发病率,提高血液谷胱甘肽(GSH)水平,并防止大鼠衰老过程中GSH的流失。我们目前的目标是通过确定年轻和成熟大鼠血液及其他组织中GSH和半胱氨酸变化的时间进程和性质,阐明MR对GSH代谢和转运的影响。
7周龄雄性F-344大鼠被置于对照(0.86% Met)或MR(0.17% Met)的限定氨基酸饮食中,并在之后的不同时间处死。成年(12月龄)大鼠也开始进行MR。
在MR的前2个月,与对照组相比,血液GSH水平增加84%,肝脏GSH水平降低66%。在此之后,肝脏GSH水平至少在6个月内保持恒定。胰腺(80%)和肾脏(22%)中的GSH水平也降低,但在MR 11周后检查的其他组织中保持不变。开始MR后1周,血液GSH的增加就很明显,并在6周时达到平台期。对成熟成年大鼠进行MR时,红细胞GSH水平也有类似增加。禁食降低了对照组肝脏中的GSH,但对MR动物没有进一步影响。到1个月时,除大脑外的所有组织中半胱氨酸水平均下降。
这些结果表明,由于年轻和成年大鼠的MR,Met、半胱氨酸和/或GSH的代谢发生了适应性变化。这些早期代谢变化通过将肝脏GSH消耗到临界水平,导致大多数肝外组织中GSH水平的保守以及红细胞中GSH的增加。