1. Academic Validation
  2. Integration of Transcriptomic Analysis, Network Pharmacology, and Experimental Validation Demonstrates Enhanced Muscle-Protective Effects of Ethanol Extract of Jakyak-Gamcho-Tang

Integration of Transcriptomic Analysis, Network Pharmacology, and Experimental Validation Demonstrates Enhanced Muscle-Protective Effects of Ethanol Extract of Jakyak-Gamcho-Tang

  • Antioxidants (Basel). 2025 Jun 27;14(7):795. doi: 10.3390/antiox14070795.
Aeyung Kim 1 Minh Nhat Tran 2 3 A Yeong Lee 4 Heerim Yeo 2 Su-Jin Baek 4 No Soo Kim 5 Seongwon Cha 4 Sang-Min Park 2
Affiliations

Affiliations

  • 1 KM Application Center, Korea Institute of Oriental Medicine, Daegu 41062, Republic of Korea.
  • 2 College of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.
  • 3 Faculty of Traditional Medicine, Hue University of Medicine and Pharmacy, Hue University, Hue 530000, Vietnam.
  • 4 KM Data Division, Korea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
  • 5 KM Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon 34054, Republic of Korea.
Abstract

Muscle atrophy, characterized by progressive loss of skeletal muscle mass and strength, remains a significant therapeutic challenge. Jakyak-gamcho-tang (JGT) is a traditional herbal formulation that has demonstrated promising muscle-protective effects; however, the key bioactive constituents and the influence of different extraction methods have not yet been fully elucidated. This study compared the muscle-protective effects of the ethanol and water extracts of JGT (JGT-E and JGT-W, respectively), while also identifying the principal bioactive compounds that contribute to the enhanced efficacy of JGT-E. An integrative methodological approach was adopted, incorporating transcriptomic profiling, network pharmacology analysis, antioxidant activity assays, and in vitro validation using C2C12 myoblasts and myotubes. This comprehensive investigation enabled a detailed assessment of the biological activities of both JGT-E and JGT-W. Transcriptomic analysis revealed that JGT-E significantly modulates key pathways involved in Oxidative Phosphorylation, mitochondrial biogenesis, and signaling cascades related to PGC-1α, mTORC1, and ERRα, while simultaneously inhibiting TGF-β-mediated muscle atrophic signaling. Functional assays demonstrated that under oxidative stress conditions, JGT-E preserved mitochondrial content more effectively, reduced Reactive Oxygen Species levels, and enhanced both myoblast viability and myotube integrity. Network pharmacology analysis identified isoliquiritigenin, catechin, and glabridin as major bioactive compounds enriched in JGT-E, all of which play critical roles in mitigating oxidative stress and supporting mitochondrial function. These findings were further substantiated by antioxidant assays that confirmed the contribution of these compounds to the observed muscle-protective effects of JGT-E. Overall, JGT-E exhibited superior efficacy in preventing muscle atrophy compared to JGT-W, likely due to its enriched profile of potent bioactive constituents. These results highlight the critical role of extraction methods in herbal medicine research and support the potential of JGT-E as a promising candidate for the treatment of muscle atrophy.

Keywords

Jakyak-gamcho-tang; muscle atrophy; network pharmacology; oxidative stress; transcriptome analysis.

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