Mitochondrially targeted tamoxifen alleviates markers of obesity and type 2 diabetes mellitus in mice

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作者
Eliska Vacurova
Jaroslava Trnovska
Petr Svoboda
Vojtech Skop
Vendula Novosadova
David Pajuelo Reguera
Silvia Petrezselyová
Benoit Piavaux
Berwini Endaya
Frantisek Spoutil
Dagmar Zudova
Jan Stursa
Magdalena Melcova
Zuzana Bielcikova
Lukas Werner
Jan Prochazka
Radislav Sedlacek
Martina Huttl
Sona Stemberkova Hubackova
Martin Haluzik
Jiri Neuzil
机构
[1] Czech Academy of Sciences,Institute of Biotechnology
[2] Charles University,Faculty of Science
[3] Institute for Clinical and Experimental Medicine,Centre for Experimental Medicine
[4] University of Chemistry and Technology Prague,Department of Biochemistry and Microbiology
[5] National Institute of Diabetes and Digestive and Kidney Diseases,Diabetes, Endocrinology, and Obesity Branch
[6] NIH,Institute of Molecular Genetics
[7] Czech Academy of Sciences,Diabetes Centre
[8] General University Hospital,School of Pharmacy and Medical Science
[9] Institute for Clinical and Experimental Medicine,undefined
[10] Griffith University,undefined
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摘要
Type 2 diabetes mellitus represents a major health problem with increasing prevalence worldwide. Limited efficacy of current therapies has prompted a search for novel therapeutic options. Here we show that treatment of pre-diabetic mice with mitochondrially targeted tamoxifen, a potential anti-cancer agent with senolytic activity, improves glucose tolerance and reduces body weight with most pronounced reduction of visceral adipose tissue due to reduced food intake, suppressed adipogenesis and elimination of senescent cells. Glucose-lowering effect of mitochondrially targeted tamoxifen is linked to improvement of type 2 diabetes mellitus-related hormones profile and is accompanied by reduced lipid accumulation in liver. Lower senescent cell burden in various tissues, as well as its inhibitory effect on pre-adipocyte differentiation, results in lower level of circulating inflammatory mediators that typically enhance metabolic dysfunction. Targeting senescence with mitochodrially targeted tamoxifen thus represents an approach to the treatment of type 2 diabetes mellitus and its related comorbidities, promising a complex impact on senescence-related pathologies in aging population of patients with type 2 diabetes mellitus with potential translation into the clinic.
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