The accumulation of senescent cells in white adipose tissue (WAT) is closely associated with the functional decline of WAT and plays a causal role...
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[title] => Homoharringtonine exhibits senotherapeutic activity that mitigates diet- and age
[paragraph] => Homoharringtonine exhibits senotherapeutic activity that mitigates diet- and age-associated obesity and insulin resistance and extends lifespan in mice
[content] => Authors
Kim, Eok-Cheon, Jung, Han-Byul, Park, Yu-kyoung, Son, Youlim, Cha, Hye-Na, Patel, Yash, Lee, Ju Hee, Choi, Minah, Park, Soyoung, Kim, Il-Kug, Pickel, Lauren, Lee, Seungju, Ha, Yuna, Shin, Min-Gyeong, Zhang, Qiwei, Yang, Jielin, de Oliveira, Bruno Rodrigues, Vo, Nathaniel, Yew, Annie, Togo, Jacques, Ealey, Kafi N., Jung, Su-Ryun, Moon, Sunjin, Yoon, Hye-Jin, Lee, Jee-Young, Sung, Hoon-Ki, Kim, Jae-Ryong, Park, So-Young
Lab
Journal
Nature Communications
Abstract
The accumulation of senescent cells in white adipose tissue (WAT) is closely associated with the functional decline of WAT and plays a causal role in the pathogenesis of metabolic diseases. Therefore, the elimination of senescent cells in WAT holds promise for the treatment and prevention of age-related metabolic diseases. Using a drug-repositioning strategy for 2150 clinically applied compounds, we discover that homoharringtonine (HHT), an FDA-approved anti-leukemic drug, manifests senotherapeutic activity in vitro in multiple cell types including human preadipocytes, while inflicting minimal cytotoxicity to non-senescent cells. HHT treatment prevents diet- or age-induced metabolic abnormalities in male mice targeting senescent adipocytes and preadipocytes to improve WAT function and reduce WAT inflammation. Moreover, HHT treatment attenuates age-associated phenotypes of human adipose tissue. Mechanistically, the senotherapeutic effects of HHT are mediated through the direct interaction of HHT with heat shock protein family A member 5 (HSPA5). Importantly, we found that HHT treatment delays aging and extends the lifespan in progeroid and aged mice. Our study demonstrates the novel senotherapeutic potential of HHT to mitigate age- and obesity-related metabolic dysfunction and extend longevity in mice. This study identifies an FDA-approved leukemia drug, Homoharringtonine, that can eliminate aged fat cells, improve metabolic health, reduce inflammation and extend lifespan in mice, revealing a potential approach to treat age- and obesity-related metabolic disease.
Keywords/Topics
Molecular medicine; Obesity; Phenotypic screening; Senescence
BIOSEB Instruments Used:
Grip strength test (BIO-GS4)
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[name] => Grip strength test
[description_short] => An easy way to objectively quantify the muscular strength of mice and rats, and to assess the effect of drugs, toxins, muscular (i.e. myopathy) and neurodegenerative diseases on muscular degeneration. It is widely used in conjunction with the ROTAROD motor coordination test: a normally coordinated rodent will show a decreased latency to fall off the rotating rod if its muscular strength is low. The Grip Strength Test is a must for your research on activity, motor control & coordination, and is particularly well suited for studies on Parkinson's & Huntington's disease.
New features GS4 - 2023: Color display with permanent backlight screen for easier reading, reset by footswitch, Improved battery time, Larger data memory of 500 values, Animal counter, USB port (charging/data transfer)


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