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年轻老鼠骨骼肌对热量限制的反应存在性别特异性差异。

Sex Specific Differences in Response to Calorie Restriction in Skeletal Muscle of Young Rats.

机构信息

Translational Research in Aging and Longevity (TRIAL) Group, Health Research Institute of the Balearic Islands (IdISBa), 07120 Palma de Mallorca, Spain.

Department of Health & Exercise Science, Center for Healthy Aging, Colorado State University, Fort Collins, CO 80521, USA.

出版信息

Nutrients. 2022 Oct 28;14(21):4535. doi: 10.3390/nu14214535.

Abstract

Calorie restriction (CR), defined as a reduction of the total calorie intake of 30% to 60% without malnutrition, is the only nutritional strategy that has been shown to extend lifespan, prevent or delay the onset of age-associated diseases, and delay the functional decline in a wide range of species. However, little is known about the effects of CR when started early in life. We sought to analyze the effects of CR in the skeletal muscle of young Wistar rats. For this, 3-month-old male and female rats were subjected to 40% CR or fed ad libitum for 3 months. Gastrocnemius muscles were used to extract RNA and total protein. Western blot and RT-qPCR were performed to evaluate the expression of key markers/pathways modulated by CR and affected by aging. CR decreased body and skeletal muscle weight in both sexes. No differences were found in most senescence, antioxidant, and nutrient sensing pathways analyzed. However, we found a sexual dimorphism in markers of oxidative stress, inflammation, apoptosis, and mitochondrial function in response to CR. Our data show that young female rats treated with CR exhibit similar expression patterns of key genes/pathways associated with healthy aging when compared to old animals treated with CR, while in male rats these effects are reduced. Additional studies are needed to understand how early or later life CR exerts positive effects on healthspan and lifespan.

摘要

热量限制(CR),定义为总热量摄入减少 30%至 60%而不造成营养不良,是唯一被证明能延长寿命、预防或延缓与年龄相关疾病的发生、并延缓多种物种功能下降的营养策略。然而,对于早期开始 CR 的影响知之甚少。我们试图分析 CR 对年轻 Wistar 大鼠骨骼肌的影响。为此,将 3 月龄雄性和雌性大鼠进行 40%的 CR 或自由进食 3 个月。使用比目鱼肌提取 RNA 和总蛋白。进行 Western blot 和 RT-qPCR 以评估受 CR 调节和受衰老影响的关键标志物/途径的表达。CR 降低了两性的体重和骨骼肌重量。在分析的大多数衰老、抗氧化和营养感应途径中未发现差异。然而,我们发现 CR 对氧化应激、炎症、细胞凋亡和线粒体功能的标志物存在性别二态性。我们的数据表明,与接受 CR 治疗的老年动物相比,接受 CR 治疗的年轻雌性大鼠表现出与健康衰老相关的关键基因/途径的相似表达模式,而在雄性大鼠中,这些影响则降低。需要进一步的研究来了解早期或晚期 CR 如何对健康寿命和寿命产生积极影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea45/9658986/89c23992538c/nutrients-14-04535-g001.jpg

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