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饮食限制对长寿突变小鼠胰岛素信号相关基因表达的影响。

Effects of dietary restriction on the expression of insulin-signaling-related genes in long-lived mutant mice.

作者信息

Bartke Andrzej, Masternak Michal M, Al-Regaiey Khalid A, Bonkowski Michael S

机构信息

Geriatrics Research, Departments of Internal Medicine and Physiology, Southern Illinois University School of Medicine, PO Box 19628, Springfield, IL 62794, USA.

出版信息

Interdiscip Top Gerontol. 2007;35:69-82. doi: 10.1159/000096556.

Abstract

Hypopituitary Ames dwarf mice and growth-hormone-resistant (growth hormone receptor knockout, GHRKO) mice have reduced plasma levels of insulin-like growth factor 1 and insulin, enhanced insulin sensitivity and a remarkably increased life span. This resembles the phenotypic characteristics of genetically normal animals subjected to dietary restriction (DR). Interestingly, DR leads to further increases in insulin sensitivity and longevity in Ames dwarfs but not in GHRKO mice. It was therefore of interest to examine the effects of DR on the expression of insulin-related genes in these two types of long-lived mutant mice. The effects of DR partially overlapped but did not duplicate the effects of Ames dwarfism or GHR deletion on the expression of genes related to insulin signaling and cell responsiveness to insulin. Moreover, the effects of DR on the expression of the examined genes in different insulin target organs were not identical. Some of the insulin-related genes were similarly affected by DR in both GHRKO and normal mice, some were affected only in GHRKO mice and some only in normal animals. This last category is of particular interest since genes affected in normal but not GHRKO mice may be related to mechanisms by which DR extends longevity.

摘要

垂体功能减退的艾姆斯侏儒小鼠和生长激素抵抗(生长激素受体敲除,GHRKO)小鼠的血浆胰岛素样生长因子1和胰岛素水平降低,胰岛素敏感性增强,寿命显著延长。这类似于饮食限制(DR)的基因正常动物的表型特征。有趣的是,DR导致艾姆斯侏儒小鼠的胰岛素敏感性和寿命进一步增加,但在GHRKO小鼠中并非如此。因此,研究DR对这两种长寿突变小鼠中胰岛素相关基因表达的影响很有意义。DR的影响部分重叠,但并未重复艾姆斯侏儒症或GHR缺失对胰岛素信号相关基因表达和细胞对胰岛素反应性的影响。此外,DR对不同胰岛素靶器官中所检测基因表达的影响并不相同。一些胰岛素相关基因在GHRKO小鼠和正常小鼠中受DR的影响相似,一些仅在GHRKO小鼠中受影响,而一些仅在正常动物中受影响。最后这一类特别有趣,因为在正常但非GHRKO小鼠中受影响的基因可能与DR延长寿命的机制有关。

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