Vatner Dorothy E, Zhang Jie, Vatner Stephen F
Department of Cell Biology and Molecular Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.
Aging (Albany NY). 2024 Dec 18;16(22):13442-13451. doi: 10.18632/aging.206179.
Brown adipose tissue (BAT), a major subtypes of adipose tissues, is known for thermogenesis and promoting healthful longevity. Our hypothesis is that BAT protects against impaired healthful longevity, i.e., obesity, diabetes, cardiovascular disorders, cancer, Alzheimer's disease, and reduced exercise tolerance. While most prior studies have shown that exercise regulates BAT activation and improves BAT density, relatively few have shown that BAT increases exercise performance. In contrast, our recent studies with the regulator of G protein signaling 14 (RGS14) knockout (KO) model of extended longevity showed that it enhances exercise performance, mediated by its more potent BAT, compared with BAT from wild type mice. For example, when the BAT from RGS14 KO mice is transplanted to WT mice, their exercise capacity is enhanced at 3 days after BAT transplantation, whereas BAT transplantation from WT to WT mice increased exercise performance, but only at 8 weeks after transplantation. The goal of this research perspective is to review the role of BAT in mediating healthful longevity, specifically exercise capacity. In view of the ability of BAT to mediate healthful longevity and enhance exercise performance, it is likely that a pharmaceutical analog of BAT will become a novel therapeutic modality.
棕色脂肪组织(BAT)是脂肪组织的一种主要亚型,以产热和促进健康长寿而闻名。我们的假设是,BAT可预防健康长寿受损,即预防肥胖、糖尿病、心血管疾病、癌症、阿尔茨海默病以及运动耐力下降。虽然大多数先前的研究表明运动可调节BAT的激活并提高BAT密度,但相对较少的研究表明BAT能提高运动表现。相比之下,我们最近对具有延长寿命作用的G蛋白信号调节因子14(RGS14)基因敲除(KO)模型的研究表明,与野生型小鼠的BAT相比,该模型更有效的BAT介导了运动表现的增强。例如,将RGS14基因敲除小鼠的BAT移植到野生型小鼠后,在BAT移植后3天其运动能力增强,而野生型小鼠之间的BAT移植虽能提高运动表现,但仅在移植后8周出现。本研究视角的目标是综述BAT在介导健康长寿,特别是运动能力方面的作用。鉴于BAT具有介导健康长寿和提高运动表现的能力,BAT的药物类似物很可能会成为一种新型治疗方式。