Fischer Kathleen E, Gelfond Jonathan A L, Soto Vanessa Y, Han Chul, Someya Shinichi, Richardson Arlan, Austad Steven N
Barshop Institute for Longevity & Aging Studies, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America; Department of Physiology, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.
Department of Epidemiology & Biostatistics, University of Texas Health Science Center San Antonio, San Antonio, Texas, United States of America.
PLoS One. 2015 May 15;10(5):e0126644. doi: 10.1371/journal.pone.0126644. eCollection 2015.
Rapamycin, an mTOR inhibitor, has been shown to extend lifespan in a range of model organisms. It has been reported to extend lifespan in multiple strains of mice, administered chronically or acutely early or late in life. The ability of rapamycin to extend health (healthspan) as opposed to life is less well documented. To assess the effects chronic rapamycin treatment on healthspan, enteric rapamycin was given to male and female C57BL/6J mice starting at 4 months of age and continued throughout life. Repeated, longitudinal assessments of health in individual animals were made starting at 16 months of age (=12 months of treatment) until death. A number of health parameters were improved (female grip strength, female body mass and reduced sleep fragmentation in both sexes), others showed no significant difference, while at least one (male rotarod performance) was negatively affected. Rapamycin treatment affected many measures of health in a highly sex-specific manner. While sex-specific phenotypic effects of rapamycin treatment have been widely reported, in this study we document sex differences in the direction of phenotypic change. Rapamycin-fed males and females were both significantly different from controls; however the differences were in the opposite direction in measures of body mass, percent fat and resting metabolic rate, a pattern not previously reported.
雷帕霉素是一种mTOR抑制剂,已被证明可延长多种模式生物的寿命。据报道,在多种品系的小鼠中,无论是在生命早期还是晚期长期或短期给药,雷帕霉素都能延长其寿命。与延长寿命相比,雷帕霉素延长健康期(健康寿命)的能力的相关记录较少。为了评估长期使用雷帕霉素治疗对健康寿命的影响,从4月龄开始对雄性和雌性C57BL/6J小鼠进行肠道内雷帕霉素给药,并持续终生。从16月龄(即治疗12个月后)开始对个体动物进行重复的纵向健康评估,直至死亡。一些健康参数得到改善(雌性握力、雌性体重以及两性睡眠片段化减少),其他参数无显著差异,而至少有一项(雄性转棒试验表现)受到负面影响。雷帕霉素治疗对许多健康指标的影响具有高度性别特异性。虽然雷帕霉素治疗的性别特异性表型效应已被广泛报道,但在本研究中,我们记录了表型变化方向上的性别差异。喂食雷帕霉素的雄性和雌性与对照组均有显著差异;然而,在体重、脂肪百分比和静息代谢率方面,差异方向相反,这是此前未报道过的一种模式。