Skip to main navigation Skip to main content
  • KSBMR

JBM : Journal of Bone Metabolism

OPEN ACCESS
ABOUT
BROWSE ARTICLES
EDITORIAL POLICIES
FOR CONTRIBUTORS

Page Path

3
results for

"Jin Sung Park"

Article category

Keywords

Publication year

Authors

Funded articles

"Jin Sung Park"

Review Article

Two Types of Mouse Models for Sarcopenia Research: Senescence Acceleration and Genetic Modification Models
Kyung-Wan Baek, Youn-Kwan Jung, Jin Sung Park, Ji-Seok Kim, Young-Sool Hah, So-Jeong Kim, Jun-Il Yoo
J Bone Metab 2021;28(3):179-191.
Published online August 31, 2021
DOI: https://doi.org/10.11005/jbm.2021.28.3.179
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.

Citations

Citations to this article as recorded by  Crossref logo
  • 1. CD9, a novel potential biomarker of sarcopenia
    Lin Yin, Na Li, Peirong Bai, Shasha Wu, Xuena Wang, Bin Lu
    Scientific Reports.2025;[Epub]     CrossRef
  • 2. Changes in aquaporins expression due to acute water restriction in naturally aging mice
    So-Jeong Kim, Kyung-Wan Baek, Youn-Kwan Jung, Ji-Seok Kim, Bo-Gyu Kim, Hak Sun Yu, Jin Sung Park, Jun-Il Yoo
    Journal of Physiology and Biochemistry.2023; 79(1): 71.     CrossRef
  • 3. Preclinical assessment of rodent jumping power with a novel electrical stimulation-assisted device
    Seung-Rok Kim, Ey-In Lee, Yongnyun Kim, Sang Wouk Cho, Namki Hong, Yumie Rhee, Jin-Woo Park
    Scientific Reports.2023;[Epub]     CrossRef
  • 4. Higher Plasma Stromal Cell-Derived Factor 1 Is Associated with Lower Risk for Sarcopenia in Older Asian Adults
    Sunghwan Ji, Kyunggon Kim, So Jeong Park, Jin Young Lee, Hee-Won Jung, Hyun Ju Yoo, Il-Young Jang, Eunju Lee, Ji Yeon Baek, Beom-Jun Kim
    Endocrinology and Metabolism.2023; 38(6): 701.     CrossRef
  • 5. Differential Gene Expression in Cell Types of the Human Skeletal Muscle: A Bioinformatics-Based Meta-Review
    Kyung-Wan Baek, So-Jeong Kim, Ji-Seok Kim, Sun-Ok Kwon
    Exercise Science.2021; 30(4): 444.     CrossRef
  • 11,315 View
  • 257 Download
  • Crossref

Original Article

Validation of Dual Energy X-Ray Absorptiometry and Nuclear Magnetic Resonance in the Analysis of Body Composition in Mice
Kyung-Wan Baek, Ji-Seok Kim, Jin Sung Park, So-Jeong Kim, Yong-Chan Ha, Ok-Yi Jeong, Jun-Il Yoo
J Bone Metab 2020;27(4):291-299.
Published online November 30, 2020
DOI: https://doi.org/10.11005/jbm.2020.27.4.291
Background
As an instrument for measuring body composition in experimental animals, dual energy X-ray absorptiometry (DXA) is ideal for accuracy, cost, and measurement efficiency. However, there is too little insight into the effectiveness of the various aspects of applying DXA to experimental animals. We investigated whether to compare and verify the precision and accuracy of DXA and nuclear magnetic resonance (NMR) animal body composition analyzers.
Methods
We used 30 Institution of Cancer Research mice in the study. First, in order to evaluate the reproducibility of DXA and NMR, we did repeated measurements by repositioning each mouse in anesthesia and euthanasia states. Subsequently, the accuracy of each device was evaluated by comparing the weight measured before the experiment, the weight of the tissue extracted from the mice after the experiment, and the measured DXA and NMR. In addition, when measuring the body composition of animals, we compared the time and the measurable body composition parameters and summarized the advantages and disadvantages of the 2 devices.
Results
Compared to NMR, DXA had the advantage of a fast measurement of bone composition and rapid image analysis. In addition, DXA showed a higher correlation (>95%) with fat mass, lean mass baseline than did NMR (>85%).
Conclusions
In conclusion, DXA was confirmed to have higher precision and measurement accuracy than did NMR. Therefore, DXA is an effective method for evaluating the body composition of experimental animals.

Citations

Citations to this article as recorded by  Crossref logo
  • 1. Small animal DXA instrument comparison and validation
    Jennifer C. Coulombe, David E. Maridas, Jarred L. Chow, Mary L. Bouxsein
    Bone.2024; 178: 116923.     CrossRef
  • 2. Changes in aquaporins expression due to acute water restriction in naturally aging mice
    So-Jeong Kim, Kyung-Wan Baek, Youn-Kwan Jung, Ji-Seok Kim, Bo-Gyu Kim, Hak Sun Yu, Jin Sung Park, Jun-Il Yoo
    Journal of Physiology and Biochemistry.2023; 79(1): 71.     CrossRef
  • 3. Antiobesity Effects of Lactobacillus paracasei Subsp. paracasei, L. casei 431 on High-Fat Diet-Induced Obese Rats
    Yun Jeong Shin, Jung-Min Bae, Hye-Rin Cho, Patience Mahoro, Hye Hyun Kim, Seon Hwa Kim, Tae Hoon Kim, Min-Jung Bae
    Journal of Medicinal Food.2023; 26(7): 445.     CrossRef
  • 4. Impact of Two Whole-Body Vibration Exercise Protocols on Body Composition of Patients with Metabolic Syndrome: A Randomized Controlled Trial
    Aline Reis-Silva, Ana C. Coelho-Oliveira, Elzi Martins-Anjos, Márcia Cristina Moura-Fernandes, Alessandra Mulder, Vinicius Layter Xavier, Vanessa A. Mendonça, Ana C. R. Lacerda, Laisa Liane Paineiras-Domingos, Redha Taiar, Alessandro Sartorio, Mario Berna
    International Journal of Environmental Research and Public Health.2022; 20(1): 436.     CrossRef
  • 5. Screening for Sarcopenia (Physical Frailty) in the COVID-19 Era
    Amira Mohammed Ali, Hiroshi Kunugi, Gerardo Garcia-Rivas
    International Journal of Endocrinology.2021; 2021: 1.     CrossRef
  • 15,894 View
  • 140 Download
  • Crossref

Review Article

Rodent Model of Muscular Atrophy for Sarcopenia Study
Kyung-Wan Baek, Youn-Kwan Jung, Ji-Seok Kim, Jin Sung Park, Young-Sool Hah, So-Jeong Kim, Jun-Il Yoo
J Bone Metab 2020;27(2):97-110.
Published online May 31, 2020
DOI: https://doi.org/10.11005/jbm.2020.27.2.97

The hallmark symptom of sarcopenia is the loss of muscle mass and strength without the loss of overall body weight. Sarcopenia patients are likely to have worse clinical outcomes and higher mortality than do healthy individuals. The sarcopenia population shows an annual increase of ~0.8% in the population after age 50, and the prevalence rate is rapidly increasing with the recent worldwide aging trend. Based on International Classification of Diseases, Tenth Revision, a global classification of disease published by the World Health Organization, issued the disease code (M62.84) given to sarcopenia in 2016. Therefore, it is expected that the study of sarcopenia will be further activated based on the classification of disease codes in the aging society. Several epidemiological studies and meta-analyses have looked at the correlation between the prevalence of sarcopenia and several environmental factors. In addition, studies using cell lines and rodents have been done to understand the biological mechanism of sarcopenia. Laboratory rodent models are widely applicable in sarcopenia studies because of the advantages of time savings, cost saving, and various analytical applications that could not be used for human subjects. The rodent models that can be applied to the sarcopenia research are diverse, but a simple and fast method that can cause atrophy or aging is preferred. Therefore, we will introduce various methods of inducing muscular atrophy in rodent models to be applied to the study of sarcopenia.

Citations

Citations to this article as recorded by  Crossref logo
  • 1. Integrated cross-species translation and biophysical multi-scale modeling links molecular signatures and locomotory phenotypes in spaceflight-induced sarcopenia
    Brendan K. Ball, Hammad F. Khan, Jee Hyun Park, Krishna Jayant, Deva D. Chan, Douglas K. Brubaker
    npj Microgravity.2026;[Epub]     CrossRef
  • 2. Propionibacterium freudenreichii MJ2 Improves Dexamethasone-Induced Muscle Atrophy in Rats by Increasing Muscle Mass and Muscle Fiber Area
    Sang-Hun Kim, Hee-Eun Woo, Mirae An, Young- Hee Lim
    Journal of Microbiology and Biotechnology.2026;[Epub]     CrossRef
  • 3. Centella asiatica , Daucus carota , and Brassica oleracea Extracts Protect Against Dexamethasone-Induced Muscle Atrophy Through the Activation of the AKT/mTOR Pathway
    Eunju Jang, Tae-Baek Lee, Soobin Choi, Lisa Tonini, Da-Ye Nam, Ji-Youl Jung, Hyuk-Joon Choi, Changhwan Ahn
    Journal of Medicinal Food.2026; 29(3): 147.     CrossRef
  • 4. Alcohol Consumption During Muscle Disuse Causes Differential Signaling Responses in a Muscle-Specific Manner in Mice
    Jinseok Lee, Deokhwa Jeong, Rudy J. Valentine
    International Journal of Molecular Sciences.2026; 27(4): 1870.     CrossRef
  • 5. Effects of platelet-rich plasma on recovery process following hindlimb unloading-induced atrophy of gastrocnemius muscle in mice
    Keying Cheng, Yung-Li Hung, Jie Zhou, Shuichi Machida, Hisashi Naito
    Japanese Journal of Physical Fitness and Sports Medicine.2026; 75(2): 133.     CrossRef
  • 6. Effect of Combining Exercise with Adipose-Derived Mesenchymal Stem Cells in Muscle Atrophy Model of Sarcopenia
    Dong-Hwa Jeong, Min-Jeong Kim, Chul-Hyun Park
    International Journal of Molecular Sciences.2025; 26(2): 451.     CrossRef
  • 7. FRET‐Based Sensor Zebrafish Reveal Muscle Cells Do Not Undergo Apoptosis in Starvation or Natural Aging‐Induced Muscle Atrophy
    Hao Jia, Renfei Wu, Hongmei Yang, Kathy Qian Luo
    Advanced Science.2025;[Epub]     CrossRef
  • 8. Effect of Curcumin Supplementation on Rat Skeletal Muscle Morphology and AMPK Levels: Study Protocol for a Randomized Controlled Trial
    Maria Grace A De Guzman, Veatrix Myrtle P Cruz, Raymond L Rosales
    Journal of Medicine, University of Santo Tomas.2025; 9(1): 1623.     CrossRef
  • 9. Physical Activity Attenuates Brain Irradiation-Associated Skeletal Muscle Damage in the Rat
    Julie Bécam, Gwenn Ropars, Fatima-Azzahra Dwiri, Carole Brunaud, Jérôme Toutain, Laurent Chazalviel, Mikaël Naveau, Samuel Valable, Myriam Bernaudin, Omar Touzani, Elodie Anne Pérès
    International Journal of Radiation Oncology*Biology*Physics.2024; 118(4): 1081.     CrossRef
  • 10. Mentha rotundifolia (L.) Huds. and Salvia officinalis L. hydrosols mitigate aging related comorbidities in rats
    Khadija Boualam, Hind Ibork, Zakaria Lahboub, Mansour Sobeh, Khalid Taghzouti
    Frontiers in Aging Neuroscience.2024;[Epub]     CrossRef
  • 11. The role of TGF-β signaling in muscle atrophy, sarcopenia and cancer cachexia
    Xin-Qiang Lan, Cheng-Jie Deng, Qi-Quan Wang, Li-Min Zhao, Bao-Wei Jiao, Yang Xiang
    General and Comparative Endocrinology.2024; 353: 114513.     CrossRef
  • 12. Reliability and Agreement Assessment of Sarcopenia Diagnosis through Comparison of Bioelectrical Impedance Analysis and Dual-Energy X-ray Absorptiometry
    Jung Hun Lee, Hee Jin Kim, Sanghun Han, Seong Jun Park, Myongheon Sim, Kang Hyun Lee
    Diagnostics.2024; 14(9): 899.     CrossRef
  • 13. 6′-sialyllactose prevents dexamethasone-induced muscle atrophy by controlling the muscle protein degradation pathway
    Hiroe Go, Nam Ji Sung, Jaeil Choi, Lila Kim, Eun Jung Park
    Biochemical and Biophysical Research Communications.2024; 736: 150892.     CrossRef
  • 14. Incretin-Based Therapies: A Promising Approach for Modulating Oxidative Stress and Insulin Resistance in Sarcopenia
    Raniah I. Alnaser, Fawaz A. Alassaf, Mohammed N. Abed
    Journal of Bone Metabolism.2024; 31(4): 251.     CrossRef
  • 15. Changes in aquaporins expression due to acute water restriction in naturally aging mice
    So-Jeong Kim, Kyung-Wan Baek, Youn-Kwan Jung, Ji-Seok Kim, Bo-Gyu Kim, Hak Sun Yu, Jin Sung Park, Jun-Il Yoo
    Journal of Physiology and Biochemistry.2023; 79(1): 71.     CrossRef
  • 16. Exploring the Role of Oxidative Stress in Skeletal Muscle Atrophy: Mechanisms and Implications
    Suyash Agrawal, Swarupa Chakole, Nidhi Shetty, Roshan Prasad, Tejaswee Lohakare, Mayur Wanjari
    Cureus.2023;[Epub]     CrossRef
  • 17. Cold-induced muscle atrophy in zebrafish: Insights from swimming activity and gene expression analysis
    Daisuke Ikeda, Seina Fujita, Kaito Toda, Yuma Yaginuma, Nobuhiro Kan-no, Shugo Watabe
    Biochemistry and Biophysics Reports.2023; 36: 101570.     CrossRef
  • 18. KeyPathwayMineR: De Novo Pathway Enrichment in the R Ecosystem
    Konstantinos Mechteridis, Michael Lauber, Jan Baumbach, Markus List
    Frontiers in Genetics.2022;[Epub]     CrossRef
  • 19. Secreted Protein Acidic and Rich in Cysteine as an Exercise-Induced Gene: Towards Novel Molecular Therapies for Immobilization-Related Muscle Atrophy in Elderly Patients
    Abdelaziz Ghanemi, Mayumi Yoshioka, Jonny St-Amand
    Genes.2022; 13(6): 1014.     CrossRef
  • 20. Body Composition and Metabolic Changes in a Lyon Hypertensive Congenic Rat and Identification of Ercc6l2 as a Positional Candidate Gene
    Karen C. Clark, Valerie A. Wagner, Katie L. Holl, John J. Reho, Monika Tutaj, Jennifer R. Smith, Melinda R. Dwinell, Justin L. Grobe, Anne E. Kwitek
    Frontiers in Genetics.2022;[Epub]     CrossRef
  • 21. Targeting Hydrogen Sulfide Modulates Dexamethasone-Induced Muscle Atrophy and Microvascular Rarefaction, through Inhibition of NOX4 and Induction of MGF, M2 Macrophages and Endothelial Progenitors
    Mohamed Adel, Hassan Reda Hassan Elsayed, Mohammad El-Nablaway, Shereen Hamed, Amira Eladl, Samah Fouad, Eman Mohamad El Nashar, Mohammed Lafi Al-Otaibi, Mohammed R. Rabei
    Cells.2022; 11(16): 2500.     CrossRef
  • 22. Effects of lifelong spontaneous exercise on skeletal muscle and angiogenesis in super-aged mice
    Kyung-Wan Baek, So-Jeong Kim, Bo-Gyu Kim, Youn-Kwan Jung, Young-Sool Hah, Hyo Youl Moon, Jun-Il Yoo, Jin Sung Park, Ji-Seok Kim, Jun Yu
    PLOS ONE.2022; 17(8): e0263457.     CrossRef
  • 23. Untargeted muscle tissue metabolites profiling in young, adult, and old rats supplemented with tocotrienol-rich fraction
    Siti Liyana Saud Gany, Jen Kit Tan, Kok Yong Chin, Nur Haleeda Hakimi, Nazirah Ab Rani, Nurhazirah Ihsan, Suzana Makpol
    Frontiers in Molecular Biosciences.2022;[Epub]     CrossRef
  • 24. Zebrafish Models for Skeletal Muscle Senescence: Lessons from Cell Cultures and Rodent Models
    Shogo Ichii, Izumi Matsuoka, Fumiyoshi Okazaki, Yasuhito Shimada
    Molecules.2022; 27(23): 8625.     CrossRef
  • 25. Effect of 40 Hz Magnetic Field Application in Posttraumatic Muscular Atrophy Development on Muscle Mass and Contractions in Rats
    Figen Cicek, Bora Tastekin, Ilknur Baldan, Murat Tokus, Aykut Pelit, Isil Ocal, Ismail Gunay, Hasan U. Ogur, Hakan Cicek
    Bioelectromagnetics.2022; 43(8): 453.     CrossRef
  • 26. Early Lipid Raft-Related Changes: Interplay between Unilateral Denervation and Hindlimb Suspension
    Irina G. Bryndina, Maria N. Shalagina, Vladimir A. Protopopov, Alexey V. Sekunov, Andrey L. Zefirov, Guzalia F. Zakirjanova, Alexey M. Petrov
    International Journal of Molecular Sciences.2021; 22(5): 2239.     CrossRef
  • 27. Profiling age-related muscle weakness and wasting: neuromuscular junction transmission as a driver of age-related physical decline
    Carlos J. Padilla, Markus E. Harrigan, Hallie Harris, Jan M. Schwab, Seward B. Rutkove, Mark M. Rich, Brian C. Clark, W. David Arnold
    GeroScience.2021; 43(3): 1265.     CrossRef
  • 28. Mouse models of sarcopenia: classification and evaluation
    Wen‐qing Xie, Miao He, Deng‐jie Yu, Yu‐xiang Wu, Xiu‐hua Wang, Shan Lv, Wen‐feng Xiao, Yu‐sheng Li
    Journal of Cachexia, Sarcopenia and Muscle.2021; 12(3): 538.     CrossRef
  • 29. Mechanical load regulates bone growth via periosteal Osteocrin
    Haruko Watanabe-Takano, Hiroki Ochi, Ayano Chiba, Ayaka Matsuo, Yugo Kanai, Shigetomo Fukuhara, Naoki Ito, Keisuke Sako, Takahiro Miyazaki, Kazuki Tainaka, Ichiro Harada, Shingo Sato, Yasuhiro Sawada, Naoto Minamino, Shu Takeda, Hiroki R. Ueda, Akihiro Ya
    Cell Reports.2021; 36(2): 109380.     CrossRef
  • 30. Natural Compounds Attenuate Denervation-Induced Skeletal Muscle Atrophy
    Tomohiko Shirakawa, Aki Miyawaki, Tatsuo Kawamoto, Shoichiro Kokabu
    International Journal of Molecular Sciences.2021; 22(15): 8310.     CrossRef
  • 31. Two Types of Mouse Models for Sarcopenia Research: Senescence Acceleration and Genetic Modification Models
    Kyung-Wan Baek, Youn-Kwan Jung, Jin Sung Park, Ji-Seok Kim, Young-Sool Hah, So-Jeong Kim, Jun-Il Yoo
    Journal of Bone Metabolism.2021; 28(3): 179.     CrossRef
  • 32. Differential Gene Expression in Cell Types of the Human Skeletal Muscle: A Bioinformatics-Based Meta-Review
    Kyung-Wan Baek, So-Jeong Kim, Ji-Seok Kim, Sun-Ok Kwon
    Exercise Science.2021; 30(4): 444.     CrossRef
  • 18,850 View
  • 452 Download
  • Crossref