Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy

Sarcopenia has been defined as a progressive decline of skeletal muscle mass, strength, and functions in elderly people. It is accompanied by physical frailty, functional disability, falls, hospitalization, and mortality, and is becoming a major geriatric disorder owing to the increasing life expect...

Full description

Bibliographic Details
Main Authors: Sakulrat Mankhong, Sujin Kim, Sohee Moon, Hyo-Bum Kwak, Dong-Ho Park, Ju-Hee Kang
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/9/6/1385
_version_ 1827715693279182848
author Sakulrat Mankhong
Sujin Kim
Sohee Moon
Hyo-Bum Kwak
Dong-Ho Park
Ju-Hee Kang
author_facet Sakulrat Mankhong
Sujin Kim
Sohee Moon
Hyo-Bum Kwak
Dong-Ho Park
Ju-Hee Kang
author_sort Sakulrat Mankhong
collection DOAJ
description Sarcopenia has been defined as a progressive decline of skeletal muscle mass, strength, and functions in elderly people. It is accompanied by physical frailty, functional disability, falls, hospitalization, and mortality, and is becoming a major geriatric disorder owing to the increasing life expectancy and growing older population worldwide. Experimental models are critical to understand the pathophysiology of sarcopenia and develop therapeutic strategies. Although its etiologies remain to be further elucidated, several mechanisms of sarcopenia have been identified, including cellular senescence, proteostasis imbalance, oxidative stress, and “inflammaging.” In this article, we address three main aspects. First, we describe the fundamental aging mechanisms. Next, we discuss both in vitro and in vivo experimental models based on molecular mechanisms that have the potential to elucidate the biochemical processes integral to sarcopenia. The use of appropriate models to reflect sarcopenia and/or its underlying pathways will enable researchers to understand sarcopenia and develop novel therapeutic strategies for sarcopenia. Lastly, we discuss the possible molecular targets and the current status of drug candidates for sarcopenia treatment. In conclusion, the development of experimental models for sarcopenia is essential to discover molecular targets that are valuable as biochemical biomarkers and/or therapeutic targets for sarcopenia.
first_indexed 2024-03-10T19:24:29Z
format Article
id doaj.art-1f4f49ba35614fc0aeff1324860f24d7
institution Directory Open Access Journal
issn 2073-4409
language English
last_indexed 2024-03-10T19:24:29Z
publishDate 2020-06-01
publisher MDPI AG
record_format Article
series Cells
spelling doaj.art-1f4f49ba35614fc0aeff1324860f24d72023-11-20T02:39:46ZengMDPI AGCells2073-44092020-06-0196138510.3390/cells9061385Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic StrategySakulrat Mankhong0Sujin Kim1Sohee Moon2Hyo-Bum Kwak3Dong-Ho Park4Ju-Hee Kang5Department of Pharmacology, Hypoxia-related Disease Research Center, College of Medicine, Inha University, Incheon 22212, KoreaDepartment of Pharmacology, Hypoxia-related Disease Research Center, College of Medicine, Inha University, Incheon 22212, KoreaDepartment of Pharmacology, Hypoxia-related Disease Research Center, College of Medicine, Inha University, Incheon 22212, KoreaDepartment of Kinesiology, Inha University, Incheon 22212, KoreaDepartment of Kinesiology, Inha University, Incheon 22212, KoreaDepartment of Pharmacology, Hypoxia-related Disease Research Center, College of Medicine, Inha University, Incheon 22212, KoreaSarcopenia has been defined as a progressive decline of skeletal muscle mass, strength, and functions in elderly people. It is accompanied by physical frailty, functional disability, falls, hospitalization, and mortality, and is becoming a major geriatric disorder owing to the increasing life expectancy and growing older population worldwide. Experimental models are critical to understand the pathophysiology of sarcopenia and develop therapeutic strategies. Although its etiologies remain to be further elucidated, several mechanisms of sarcopenia have been identified, including cellular senescence, proteostasis imbalance, oxidative stress, and “inflammaging.” In this article, we address three main aspects. First, we describe the fundamental aging mechanisms. Next, we discuss both in vitro and in vivo experimental models based on molecular mechanisms that have the potential to elucidate the biochemical processes integral to sarcopenia. The use of appropriate models to reflect sarcopenia and/or its underlying pathways will enable researchers to understand sarcopenia and develop novel therapeutic strategies for sarcopenia. Lastly, we discuss the possible molecular targets and the current status of drug candidates for sarcopenia treatment. In conclusion, the development of experimental models for sarcopenia is essential to discover molecular targets that are valuable as biochemical biomarkers and/or therapeutic targets for sarcopenia.https://www.mdpi.com/2073-4409/9/6/1385sarcopeniaagingskeletal musclecellular senescenceexperimental model
spellingShingle Sakulrat Mankhong
Sujin Kim
Sohee Moon
Hyo-Bum Kwak
Dong-Ho Park
Ju-Hee Kang
Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy
Cells
sarcopenia
aging
skeletal muscle
cellular senescence
experimental model
title Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy
title_full Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy
title_fullStr Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy
title_full_unstemmed Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy
title_short Experimental Models of Sarcopenia: Bridging Molecular Mechanism and Therapeutic Strategy
title_sort experimental models of sarcopenia bridging molecular mechanism and therapeutic strategy
topic sarcopenia
aging
skeletal muscle
cellular senescence
experimental model
url https://www.mdpi.com/2073-4409/9/6/1385
work_keys_str_mv AT sakulratmankhong experimentalmodelsofsarcopeniabridgingmolecularmechanismandtherapeuticstrategy
AT sujinkim experimentalmodelsofsarcopeniabridgingmolecularmechanismandtherapeuticstrategy
AT soheemoon experimentalmodelsofsarcopeniabridgingmolecularmechanismandtherapeuticstrategy
AT hyobumkwak experimentalmodelsofsarcopeniabridgingmolecularmechanismandtherapeuticstrategy
AT donghopark experimentalmodelsofsarcopeniabridgingmolecularmechanismandtherapeuticstrategy
AT juheekang experimentalmodelsofsarcopeniabridgingmolecularmechanismandtherapeuticstrategy