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Two types of mouse models for sarcopenia research: Senescence acceleration and genetic modification modelsopen access

Authors
Baek, K.-W.Jung, Y.-K.Park, J.S.Kim, J.-S.Hah, Y.-S.Kim, S.-J.Yoo, J.-I.
Issue Date
Aug-2021
Publisher
Korean Society for Bone and Mineral Research
Keywords
Aging; Mice; Muscle; Sarcopenia; Skeletal
Citation
Journal of Bone Metabolism, v.28, no.3, pp 179 - 191
Pages
13
Indexed
SCOPUS
KCI
Journal Title
Journal of Bone Metabolism
Volume
28
Number
3
Start Page
179
End Page
191
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/5634
DOI
10.11005/JBM.2021.28.3.179
ISSN
2287-6375
2287-7029
Abstract
Sarcopenia leads to loss of skeletal muscle mass, quality, and strength due to aging; it was recently given a disease code (International Classification of Diseases, Tenth Revision, Clinical Modification, M62.84). As a result, in recent years, sarcopenia-related research has increased. In addition, various studies seeking to prevent and treat sarcopenia by identifying the various mechanisms related to the reduction of skeletal muscle properties have been conducted. Previous studies have identified muscle synthesis and breakdown; investigating them has generated evidence for preventing and treating sarcopenia. Mouse models are still the most useful ones for determining mechanisms underlying sarcopenia through correlations and interventions involving specific genes and their phenotypes. Mouse models used to study sarcopenia often induce muscle atrophy by hindlimb unloading, denervation, or immobilization. Though it is less frequently used, the senescence-accelerated mouse can also be useful for sarcopenia research. Herein, we discuss cases where senescence-accelerated and genetically engineered mouse models were used in sarcopenia research and different perspectives to use them. ? 2021 The Korean Society for Bone and Mineral Research
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사범대학 (체육교육과)
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