Health Nutrition, Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Biomedical Gerontology Laboratory, Faculty of Human Sciences, Waseda University, 2-579-1 Mikajima, Tokorozawa, Saitama 359-1164, Japan.
Nutrients. 2021 Jun 30;13(7):2277. doi: 10.3390/nu13072277.
Many studies have shown the beneficial effects of calorie restriction (CR) on rodents' aging; however, the molecular mechanism explaining these beneficial effects is still not fully understood. Previously, we conducted transcriptomic analysis on rat liver with short-term and mild-to-moderate CR to elucidate its early response to such diet. Here, we expanded transcriptome analysis to muscle, adipose tissue, intestine, and brain and compared the gene expression profiles of these multiple organs and of our previous dataset. Several altered gene expressions were found, some of which known to be related to CR. Notably, the commonly regulated genes by CR include nicotinamide phosphoribosyltransferase and heat shock protein 90, which are involved in declining the aging process and thus potential therapeutic targets for aging-related diseases. The data obtained here provide information on early response markers and key mediators of the CR-induced delay in aging as well as on age-associated pathological changes in mammals.
许多研究表明热量限制(CR)对啮齿动物衰老有有益影响;然而,解释这些有益效果的分子机制仍不完全清楚。此前,我们对短期和轻度至中度 CR 的大鼠肝脏进行了转录组分析,以阐明其对这种饮食的早期反应。在这里,我们将转录组分析扩展到肌肉、脂肪组织、肠道和大脑,并比较了这些多个器官和我们之前数据集的基因表达谱。发现了一些改变的基因表达,其中一些已知与 CR 有关。值得注意的是,CR 共同调节的基因包括烟酰胺磷酸核糖基转移酶和热休克蛋白 90,它们参与了衰老过程的下降,因此是与衰老相关疾病的潜在治疗靶点。这里获得的数据提供了有关 CR 诱导的衰老延迟的早期反应标志物和关键介质以及哺乳动物与年龄相关的病理变化的信息。