Metabolic consequences of long-term rapamycin exposure on common marmoset monkeys (Callithrix jacchus)

Rapamycin has been shown to extend lifespan in rodent models, but the effects on metabolic health and function have been widely debated in both clinical and translational trials. Prior to rapamycin being used as a treatment to extend both lifespan and healthspan in the human population, it is vital to assess the side effects of the treatment on metabolic pathways in animal model systems, including a closely related non-human primate model. In this study, we found that long-term treatment of marmoset monkeys with orally-administered encapsulated rapamycin resulted in no overall effects on body weight and only a small decrease in fat mass over the first few months of treatment. Rapamycin treated subjects showed no overall changes in daily activity counts, blood lipids, or significant changes in glucose metabolism including oral glucose tolerance. Adipose tissue displayed no differences in gene expression of metabolic markers following treatment, while liver tissue exhibited suppressed G6Pase activity with increased PCK and GPI activity. Overall, the marmosets revealed only minor metabolic consequences of chronic treatment with rapamycin and this adds to the growing body of literature that suggests that chronic and/or intermittent rapamycin treatment results in improved health span and metabolic functioning. The marmosets offer an interesting alternative animal model for future intervention testing and translational modeling.

[1]  S. Tardif,et al.  Testing efficacy of administration of the antiaging drug rapamycin in a nonhuman primate, the common marmoset. , 2015, The journals of gerontology. Series A, Biological sciences and medical sciences.

[2]  W. Fok,et al.  Rapamycin and dietary restriction induce metabolically distinctive changes in mouse liver. , 2015, The journals of gerontology. Series A, Biological sciences and medical sciences.

[3]  J. Praestgaard,et al.  mTOR inhibition improves immune function in the elderly , 2014, Science Translational Medicine.

[4]  M. Blagosklonny,et al.  Comparison of rapamycin schedules in mice on high-fat diet , 2014, Cell cycle.

[5]  Dudley Lamming,et al.  Rapamycin-induced metabolic defects are reversible in both lean and obese mice , 2014, Aging.

[6]  N. Barnard,et al.  You are what you eat, or are you? The challenges of translating high-fat-fed rodents to human obesity and diabetes , 2014, Nutrition & Diabetes.

[7]  Y. Deshaies,et al.  PPARγ activation attenuates glucose intolerance induced by mTOR inhibition with rapamycin in rats. , 2014, American journal of physiology. Endocrinology and metabolism.

[8]  M. Blagosklonny,et al.  Weekly administration of rapamycin improves survival and biomarkers in obese male mice on high-fat diet , 2014, Aging cell.

[9]  Z. D. Sharp,et al.  Rapamycin-mediated lifespan increase in mice is dose and sex dependent and metabolically distinct from dietary restriction , 2014, Aging cell.

[10]  S. Austad,et al.  Rapamycin extends life and health in C57BL/6 mice. , 2014, The journals of gerontology. Series A, Biological sciences and medical sciences.

[11]  B. Vergès,et al.  Endocrine side effects of anti-cancer drugs: effects of anti-cancer targeted therapies on lipid and glucose metabolism. , 2014, European journal of endocrinology.

[12]  W. Wood,et al.  Mice Fed Rapamycin Have an Increase in Lifespan Associated with Major Changes in the Liver Transcriptome , 2014, PloS one.

[13]  M. Blagosklonny TOR-centric view on insulin resistance and diabetic complications: perspective for endocrinologists and gerontologists , 2013, Cell Death and Disease.

[14]  TL Jensen,et al.  Fasting of mice: a review , 2013, Laboratory animals.

[15]  Dudley Lamming,et al.  A Central role for mTOR in lipid homeostasis. , 2013, Cell metabolism.

[16]  Dudley Lamming,et al.  Rapamycin doses sufficient to extend lifespan do not compromise muscle mitochondrial content or endurance , 2013, Aging.

[17]  S. Tardif,et al.  Metabolic consequences of the early onset of obesity in common marmoset monkeys , 2013, Obesity.

[18]  Dudley Lamming,et al.  Young and old genetically heterogeneous HET3 mice on a rapamycin diet are glucose intolerant but insulin sensitive , 2013, Aging cell.

[19]  R. Colman,et al.  Development of Metabolic Function Biomarkers in the Common Marmoset, Callithrix jacchus , 2013, American journal of primatology.

[20]  Yimin Fang,et al.  Prolonged Rapamycin treatment led to beneficial metabolic switch , 2013, Aging.

[21]  S. Tardif,et al.  Relation of food intake behaviors and obesity development in young common marmoset monkeys , 2013, Obesity.

[22]  Jie Chen,et al.  Duration of rapamycin treatment has differential effects on metabolism in mice. , 2013, Cell metabolism.

[23]  M. Blagosklonny,et al.  Resveratrol potentiates rapamycin to prevent hyperinsulinemia and obesity in male mice on high fat diet , 2013, Cell Death and Disease.

[24]  S. Austad,et al.  Chronic inhibition of mammalian target of rapamycin by rapamycin modulates cognitive and non-cognitive components of behavior throughout lifespan in mice , 2012, Neuroscience.

[25]  Dudley Lamming,et al.  Rapamycin has a biphasic effect on insulin sensitivity in C2C12 myotubes due to sequential disruption of mTORC1 and mTORC2 , 2012, Front. Gene..

[26]  Maria A. Woodward,et al.  Rapamycin slows aging in mice , 2012, Aging cell.

[27]  M. Blagosklonny Once again on rapamycin-induced insulin resistance and longevity: despite of or owing to , 2012, Aging.

[28]  J. Hjelmesæth,et al.  New‐Onset Diabetes After Kidney Transplantation—Changes and Challenges , 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

[29]  S. Tardif,et al.  Aging Phenotypes of Common Marmosets (Callithrix jacchus) , 2012, Journal of aging research.

[30]  Dudley Lamming,et al.  Rapamycin-Induced Insulin Resistance Is Mediated by mTORC2 Loss and Uncoupled from Longevity , 2012, Science.

[31]  S. Tardif,et al.  The Development of Obesity Begins at an Early Age in Captive Common Marmosets (Callithrix jacchus) , 2012, American journal of primatology.

[32]  M. Blagosklonny Rapamycin-induced glucose intolerance: Hunger or starvation diabetes , 2011, Cell cycle.

[33]  K. Mansfield,et al.  Differential Contribution of Dietary Fat and Monosaccharide to Metabolic Syndrome in the Common Marmoset (Callithrix jacchus) , 2011, Obesity.

[34]  E. Boyland,et al.  Pharmacological management of appetite expression in obesity , 2010, Nature Reviews Endocrinology.

[35]  Y. Deshaies,et al.  Chronic Rapamycin Treatment Causes Glucose Intolerance and Hyperlipidemia by Upregulating Hepatic Gluconeogenesis and Impairing Lipid Deposition in Adipose Tissue , 2010, Diabetes.

[36]  S. Tardif,et al.  Characterization of Obese Phenotypes in a Small Nonhuman Primate, the Common Marmoset (Callithrix jacchus) , 2009, Obesity.

[37]  Marco Pahor,et al.  Rapamycin fed late in life extends lifespan in genetically heterogeneous mice , 2009, Nature.

[38]  L. Gesualdo,et al.  Management of Side Effects of Sirolimus Therapy , 2009, Transplantation.

[39]  A. Webster,et al.  Sirolimus is associated with new-onset diabetes in kidney transplant recipients. , 2008, Journal of the American Society of Nephrology : JASN.

[40]  C. Warden,et al.  Comparisons of diets used in animal models of high-fat feeding. , 2008, Cell metabolism.

[41]  S. Estrem,et al.  Assessment of Diet‐induced Obese Rats as an Obesity Model by Comparative Functional Genomics , 2008, Obesity.

[42]  Christophe Magnan,et al.  mTOR Inhibition by Rapamycin Prevents β-Cell Adaptation to Hyperglycemia and Exacerbates the Metabolic State in Type 2 Diabetes , 2008, Diabetes.

[43]  A. Vigé,et al.  C57BL/6J and A/J Mice Fed a High‐Fat Diet Delineate Components of Metabolic Syndrome , 2007, Obesity.

[44]  Niels Grarup,et al.  Gene–environment interactions in the pathogenesis of type 2 diabetes and metabolism , 2007, Current opinion in clinical nutrition and metabolic care.

[45]  G. Perdomo,et al.  Rapamycin-mediated inhibition of mammalian target of rapamycin in skeletal muscle cells reduces glucose utilization and increases fatty acid oxidation. , 2006, Metabolism: clinical and experimental.

[46]  M. W. Schwartz,et al.  Central nervous system control of food intake and body weight , 2006, Nature.

[47]  S. di Paolo,et al.  Glucose metabolism in renal transplant recipients: effect of calcineurin inhibitor withdrawal and conversion to sirolimus. , 2005, Journal of the American Society of Nephrology : JASN.

[48]  A. Tzakis,et al.  A Retrospective Review of Liver Transplant Patients Treated with Sirolimus from a Single Center: An Analysis of Sirolimus-Related Complications , 2004, Transplantation.

[49]  R. Power,et al.  Husbandry, handling, and nutrition for marmosets. , 2003, Comparative medicine.

[50]  O. Ezaki,et al.  High-fat diet-induced hyperglycemia and obesity in mice: differential effects of dietary oils. , 1996, Metabolism: clinical and experimental.

[51]  S. Tardif,et al.  The marmoset as a model of aging and age-related diseases. , 2011, ILAR journal.

[52]  Mackenzie Hs,et al.  Diabetes after Transplantation and Sirolimus: What's the Connection? , 2008 .

[53]  G. Bray,et al.  Obesity , 2008, Annals of Internal Medicine.