ZERO WORLD RESEARCHアミノ酸・有機酸の学術文献データベース

Skeletal Muscle and Circulating microRNAs Adaptations to 12-Week HIIT With or Without L-Citrulline in Obese Older Adults.

肥満高齢者における12週間のHIITとL-シトルリン併用または非併用による骨格筋および循環microRNAの適応 (機械翻訳の邦題)

Journal of cachexia, sarcopenia and muscle2026Mercier-Guery A, Millet M, Croset M, et al.
研究デザインランダム化比較試験
対象ヒト

記録の確認項目

研究デザイン
ランダム化比較試験
対象
ヒト
出版年
2026
出典
doi.org
抄録の表示
表示あり
出版状態
有効な記録
状態確認日
2026/08/17
収集日
2026/08/03
鮮度
確認期限内
確認段階
自動処理
記録状態
公開

日本語要約(機械生成)

肥満高齢者を対象に、12週間の高強度インターバルトレーニング(HIIT)が骨格筋および血清中のmicroRNA発現に及ぼす影響を検討した。二重盲検ランダム化試験の副次解析として、HIITにL-シトルリン(CIT)を併用した群とプラセボ群で比較した。その結果、筋特異的マイクロRNA(myo-miRNA)の発現は変化しなかったが、筋非特異的miRNA(miR-504-5p、miR-744-5pなど)や血清中miRNA(miR-151a-3p、miR-4433b-5pなど)の発現変化が、体組成や機能的能力、代謝指標の改善と関連した。特に、CIT併用は筋miR-504-5pを低下させ、体脂肪減少や機能改善と関連した。これらのmiRNAはHIIT効果のバイオマーカー候補となる可能性が示唆された。

この要約は公開抄録のみを根拠にAIが機械的に生成したものです。正確な内容は原文を確認してください。

抄録

Background: High-intensity interval training (HIIT) with or without L-citrulline (CIT) oral supplementation improves body composition, functional capacities and muscle health in obese older adults, potentially through microRNA-driven regulation. We aimed to (1) investigate the impact of a 12-week HIIT on the expression level of microRNAs in vastus lateralis muscle biopsies and serum of obese older adults and (2) assess whether the differential expression level of microRNAs was associated with clinico-biological adaptations to HIIT and provide potential biomarkers of HIIT response.Methods: In this secondary exploratory analysis of a double-blind randomized trial, 36 women and 32 men (67.2 ± 5.2 years) following 12 weeks HIIT randomized in two groups were supplemented daily with CIT (HIIT-CIT, n = 37) or with placebo (HIIT-PLA, n = 31). Phenotypic variables, serum parameters, muscle biopsies and subcutaneous abdominal adipose tissue outcomes were collected pre-intervention and postintervention. To assess the microRNA profile, the miRNome of muscle biopsy and serum was analysed using next generation sequencing in participants' subsets (n = 13). The microRNAs' differential expression level was analysed pre-intervention and postintervention by TaqMan-real-time qPCR in 68 participants.Results: The expression of myo-microRNAs (miR-133a, b, -1, -206) and muscle-related-microRNAs (miR-499, -208) was not altered following HIIT with or without CIT. In HIIT-PLA, HIIT-CIT and subgroups (based on sex, age, body mass index, dynapenic status), the change in muscle (miR-504-5p, -744-5p, -151a-3p, -106b-5p, -127-5p) and circulating (miR-4433b-5p, 151a-3p, -744-5p, 483-3p, -106b-5p, -484) microRNA levels was associated with changes of clinico-biological parameters. Supplementing HIIT with CIT decreased the muscle miR-504-5p level (p = 0.022), correlating with lower body fat, improved functional capacities, muscle power and increased IGF-1 level (r = -0.6, p < 0.05). MiR-744-5p expression increased in dynapenic participants (p = 0.04), associated with lean mass gain (r = 0.50, p < 0.05), while miR-151a-3p downregulation in men's muscle (p = 0.01) was associated with better insulin sensitivity (HOMA-IR, r = 0.57, p = 0.05). In serum, miR-151a-3p upregulation in women (p = 0.01) correlated with improved muscle power and lower circulating leptin levels, while miR-4433b-5p downregulation (p = 0.001) was linked to reduced fat mass, lean mass gain and enhanced functional capacity. The downregulation of miR-106b-5p (p = 0.05) was associated with a higher adiponectin level and a better score of the 4-m walking test (p = 0.05).Conclusion: HIIT did not impact the expression level of myo-microRNAs and muscle-related microRNAs but induced changes in muscle-nonspecific microRNAs in muscle biopsy and serum. Modulations of microRNAs in muscle (miR-504-5p, -744-5p) and serum (miR-151a-3p, -4433b-5p, -106b-5p) were associated with HIIT's beneficial effects, suggesting their role in the HIIT effects and their potential as candidate biomarkers for response.

MeSH

Adaptation, PhysiologicalAgedBiomarkersCirculating MicroRNACitrullineDouble-Blind MethodFemaleHigh-Intensity Interval TrainingHumansMaleMicroRNAsMuscle, SkeletalObesity

DOI 10.1002/jcsm.70267

PMID 41933456

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