Open Access
Aging, volume 12, issue 23, pages 23497-23508
Pharmacological blockade of TNFα prevents sarcopenia and prolongs survival in aging mice
Clara Sciorati
1
,
Riccardo Gamberale
1
,
Antonella Monno
1
,
L. Citterio
2
,
Chiara Lanzani
2
,
Rebecca De Lorenzo
1, 3
,
Giuseppe A. Ramirez
1, 3
,
Ernesto Di Cesare
3, 4
,
P. Manunta
2, 3
,
A. A. Manfredi
1, 3
,
Patrizia Rovere-Querini
1, 3
4
Experimental Imaging Centre, San Raffaele Scientific Institute, Milan, Italy
|
Publication type: Journal Article
Publication date: 2020-11-26
Cell Biology
Aging
Abstract
Sarcopenia is a hallmark of aging. Inflammation due to increased generation of cytokines such as TNFα, IL-1β and IL-6 has been implicated in the pathogenesis of sarcopenia. In skeletal muscle of C57BL/6 mice from 12 until 28 months of age, we observed a progressive reduction of myofiber cross sectional area, loss of type II fibers and infiltration by inflammatory cells. Muscle strength decreased in parallel. Pharmacological TNFα blockade by weekly subcutaneous injection of Etanercept from 16 to 28 months of age prevented atrophy and loss of type II fibers, with significant improvements in muscle function and mice lifespan. The effects on leukocyte recruitment were limited. These results provide a proof of principle that endogenous TNFα is sufficient to cause sarcopenia and to reduce animal survival, and open a novel perspective on novel potential pharmacological treatment strategies based on TNFα blockade to prevent the noxious events associated with aging.
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