Evidence map›Paper›PMID 41281601›Full record

ArticleCurrent research in toxicology2025

Areca nut extract exposure disrupts myogenesis and metabolism in C2C12 cells.

Chi-Wei Chen, Tsung-Teng Huang, Yan-Ru Chen, Chin-Hung Liu, Chia-Hsun Hsieh, Tai-Lin Chen, Kuo-Chu Lai

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Article in Current research in toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Chi-Wei ChenDepartment of Biology, College of Arts and Sciences, Appalachian State University, Boone, NC, USA.
Tsung-Teng HuangDepartment of Physiology and Pharmacology, College of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Yan-Ru ChenMaster's Program in Pharmacology and Toxicology, Department of Medicine, School of Medicine, Tzu Chi University, Hualien, Taiwan.
Chin-Hung LiuDepartment of Pharmacology, School of Medicine, Tzu Chi University, Hualien, Taiwan.
Chia-Hsun HsiehDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou Medical Center, Taoyuan, Taiwan.
Tai-Lin ChenDepartment of Post-Baccalaureate Medicine, National Chung Hsing University, Taichung, Taiwan.
Kuo-Chu LaiDepartment of Physiology and Pharmacology, College of Medicine, Chang Gung University, Taoyuan City, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Areca nut (AN), which is commonly consumed in Southeast Asia, contains bioactive compounds that may influence cellular functions. Accumulating evidence has revealed several health impacts of AN consumption, but the toxicological effects of areca nut extract (ANE) on muscle cells remain largely unexplored. Myogenesis, a critical process for muscle development and regeneration, is closely tied to metabolic activity, which governs the differentiation and function of myocytes. This study aimed to evaluate the effects of ANE on myogenesis in murine C2C12 myoblasts and differentiated myotubes. In ANE-treated C2C12 myoblasts, we observed a significant decrease in the intracellular glutamine level that was accompanied by decreased GSH levels, decreased mTOR signaling, and increased autophagy in myoblasts but not in differentiated myotubes. ANE treatment decreased glutamine and 6-phosphogluconate levels in both myoblasts and myotubes, suggesting the widespread suppression of amino acid and redox-related metabolic pathways. Moreover, ANE significantly altered the metabolomic profile, upregulating the levels of glycolysis and TCA cycle intermediates but reducing ATP levels, indicating impaired energy metabolism in differentiated myotubes. ANE also downregulated the expression of key metabolic genes, including those involved in glycolysis (AKR1B3 and LDHA), glycerol metabolism (GPD1 and GPD2), and nitrogen metabolism (GLUD1, ARG1, GS, and GLS1), indicating that ANE disrupts critical pathways involved in muscle cell metabolism and myogenesis. This study provides new insights into the mechanisms by which AN consumption affects muscle development, emphasizing the need for further research into the dietary and environmental factors influencing myogenesis.

Indexed as

Areca nut extractAutophagyC2C12 myoblastsDifferentiated myotubesMetabolomicsMuscle atrophy

Identifiers

PMID41281601
PMCPMC12634855

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.