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( A ) Dot plot showing the top 15 enriched pathways in Mrep (Ly6C hi PDPN + subcluster). ( B ) GSEA plots of the KEGG TLR signaling pathway in 3 MDM subclusters. NES, normalized enrichment score. ( C ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with 100 ng/mL LPS for 1 day. BMDMs were derived from different mice. n = 5 for each group. ( D and E ) RT-qPCR results showing the relative Inhba expression in the Mrep sorted from WT ( n = 9) and Tlr4 –/– ( n = 4) mice at 1 dpi ( D ) and muscles from WT ( n = 3) and Tlr4 –/– ( n = 10) mice at 4 dpi ( E ). ( F ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with muscle lysates and heated muscle lysates for 1 day. To inactivate protein, muscle lysates were subjected to 95°C for 5 minutes. BMDMs and muscle lysates were from different mice ( n = 3). ( G ) Heatmap showing the relative expression of genes encoding DAMPs in the uninjured muscles and muscles at 1 dpi ( n = 2 for each). ( H ) RT-qPCR results showing the relative Inhba mRNA expression in BMDMs treated with 1 μg/mL of indicated DAMPs for 24 hours. ( I ) RT-qPCR results showing the relative Inhba mRNA expression in muscles at 1 dpi of the mice injected with vehicle ( n = 7), 10 mg/kg S100A8/A9 inhibitor (paquinimod) ( n = 6), and <t>HMGB1</t> inhibitor (glycyrrhizin) ( n = 5). The P values were calculated using unpaired 2-tailed t test ( C – E ) and 1-way ANOVA with Tukey’s multiple-comparison test ( F , H , and I ). A P value or q value < 0.05 was considered significant. Data are shown as the mean ± SEM, and symbols represent individual mice.
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( A ) Dot plot showing the top 15 enriched pathways in Mrep (Ly6C hi PDPN + subcluster). ( B ) GSEA plots of the KEGG TLR signaling pathway in 3 MDM subclusters. NES, normalized enrichment score. ( C ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with 100 ng/mL LPS for 1 day. BMDMs were derived from different mice. n = 5 for each group. ( D and E ) RT-qPCR results showing the relative Inhba expression in the Mrep sorted from WT ( n = 9) and Tlr4 –/– ( n = 4) mice at 1 dpi ( D ) and muscles from WT ( n = 3) and Tlr4 –/– ( n = 10) mice at 4 dpi ( E ). ( F ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with muscle lysates and heated muscle lysates for 1 day. To inactivate protein, muscle lysates were subjected to 95°C for 5 minutes. BMDMs and muscle lysates were from different mice ( n = 3). ( G ) Heatmap showing the relative expression of genes encoding DAMPs in the uninjured muscles and muscles at 1 dpi ( n = 2 for each). ( H ) RT-qPCR results showing the relative Inhba mRNA expression in BMDMs treated with 1 μg/mL of indicated DAMPs for 24 hours. ( I ) RT-qPCR results showing the relative Inhba mRNA expression in muscles at 1 dpi of the mice injected with vehicle ( n = 7), 10 mg/kg S100A8/A9 inhibitor (paquinimod) ( n = 6), and <t>HMGB1</t> inhibitor (glycyrrhizin) ( n = 5). The P values were calculated using unpaired 2-tailed t test ( C – E ) and 1-way ANOVA with Tukey’s multiple-comparison test ( F , H , and I ). A P value or q value < 0.05 was considered significant. Data are shown as the mean ± SEM, and symbols represent individual mice.
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Effects of HMB-FA supplementation after four bouts of simulated Olympic judo competition on creatine kinase (CK) levels in elite judokas.

Journal: Journal of the International Society of Sports Nutrition

Article Title: Effects of acute HMB-FA supplementation on antioxidant status and muscle damage in Elite Judoka: a randomized pilot trial

doi: 10.1080/15502783.2026.2665962

Figure Lengend Snippet: Effects of HMB-FA supplementation after four bouts of simulated Olympic judo competition on creatine kinase (CK) levels in elite judokas.

Article Snippet: HMB-FA group capsules each contained 500 mg of β -hydroxy- β -methylbutyrate free acid (BetaTOR®, Metabolic Technologies Inc.), for a total acute dose of 1000 mg.

Techniques:

Effects of HMB-FA supplementation after four bouts of simulated Olympic judo competition on lactate dehydrogenase (LDH) levels in elite judokas. *Indicates statistically significant difference at p = 0.001.

Journal: Journal of the International Society of Sports Nutrition

Article Title: Effects of acute HMB-FA supplementation on antioxidant status and muscle damage in Elite Judoka: a randomized pilot trial

doi: 10.1080/15502783.2026.2665962

Figure Lengend Snippet: Effects of HMB-FA supplementation after four bouts of simulated Olympic judo competition on lactate dehydrogenase (LDH) levels in elite judokas. *Indicates statistically significant difference at p = 0.001.

Article Snippet: HMB-FA group capsules each contained 500 mg of β -hydroxy- β -methylbutyrate free acid (BetaTOR®, Metabolic Technologies Inc.), for a total acute dose of 1000 mg.

Techniques:

Effects of HMB-FA supplementation after four bouts of simulated Olympic judo competition on malondialdehyde (MDA) levels in elite judokas.

Journal: Journal of the International Society of Sports Nutrition

Article Title: Effects of acute HMB-FA supplementation on antioxidant status and muscle damage in Elite Judoka: a randomized pilot trial

doi: 10.1080/15502783.2026.2665962

Figure Lengend Snippet: Effects of HMB-FA supplementation after four bouts of simulated Olympic judo competition on malondialdehyde (MDA) levels in elite judokas.

Article Snippet: HMB-FA group capsules each contained 500 mg of β -hydroxy- β -methylbutyrate free acid (BetaTOR®, Metabolic Technologies Inc.), for a total acute dose of 1000 mg.

Techniques:

Effect of HMB-FA supplementation after four bouts of simulated Olympic judo competition on total antioxidant capacity (TAC) levels in elite judokas.

Journal: Journal of the International Society of Sports Nutrition

Article Title: Effects of acute HMB-FA supplementation on antioxidant status and muscle damage in Elite Judoka: a randomized pilot trial

doi: 10.1080/15502783.2026.2665962

Figure Lengend Snippet: Effect of HMB-FA supplementation after four bouts of simulated Olympic judo competition on total antioxidant capacity (TAC) levels in elite judokas.

Article Snippet: HMB-FA group capsules each contained 500 mg of β -hydroxy- β -methylbutyrate free acid (BetaTOR®, Metabolic Technologies Inc.), for a total acute dose of 1000 mg.

Techniques:

( A ) Dot plot showing the top 15 enriched pathways in Mrep (Ly6C hi PDPN + subcluster). ( B ) GSEA plots of the KEGG TLR signaling pathway in 3 MDM subclusters. NES, normalized enrichment score. ( C ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with 100 ng/mL LPS for 1 day. BMDMs were derived from different mice. n = 5 for each group. ( D and E ) RT-qPCR results showing the relative Inhba expression in the Mrep sorted from WT ( n = 9) and Tlr4 –/– ( n = 4) mice at 1 dpi ( D ) and muscles from WT ( n = 3) and Tlr4 –/– ( n = 10) mice at 4 dpi ( E ). ( F ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with muscle lysates and heated muscle lysates for 1 day. To inactivate protein, muscle lysates were subjected to 95°C for 5 minutes. BMDMs and muscle lysates were from different mice ( n = 3). ( G ) Heatmap showing the relative expression of genes encoding DAMPs in the uninjured muscles and muscles at 1 dpi ( n = 2 for each). ( H ) RT-qPCR results showing the relative Inhba mRNA expression in BMDMs treated with 1 μg/mL of indicated DAMPs for 24 hours. ( I ) RT-qPCR results showing the relative Inhba mRNA expression in muscles at 1 dpi of the mice injected with vehicle ( n = 7), 10 mg/kg S100A8/A9 inhibitor (paquinimod) ( n = 6), and HMGB1 inhibitor (glycyrrhizin) ( n = 5). The P values were calculated using unpaired 2-tailed t test ( C – E ) and 1-way ANOVA with Tukey’s multiple-comparison test ( F , H , and I ). A P value or q value < 0.05 was considered significant. Data are shown as the mean ± SEM, and symbols represent individual mice.

Journal: The Journal of Clinical Investigation

Article Title: Activin A secretion by muscle-repairing macrophages induces heterotopic ossification in mice

doi: 10.1172/JCI193797

Figure Lengend Snippet: ( A ) Dot plot showing the top 15 enriched pathways in Mrep (Ly6C hi PDPN + subcluster). ( B ) GSEA plots of the KEGG TLR signaling pathway in 3 MDM subclusters. NES, normalized enrichment score. ( C ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with 100 ng/mL LPS for 1 day. BMDMs were derived from different mice. n = 5 for each group. ( D and E ) RT-qPCR results showing the relative Inhba expression in the Mrep sorted from WT ( n = 9) and Tlr4 –/– ( n = 4) mice at 1 dpi ( D ) and muscles from WT ( n = 3) and Tlr4 –/– ( n = 10) mice at 4 dpi ( E ). ( F ) RT-qPCR results showing the relative Inhba expression in BMDMs stimulated with muscle lysates and heated muscle lysates for 1 day. To inactivate protein, muscle lysates were subjected to 95°C for 5 minutes. BMDMs and muscle lysates were from different mice ( n = 3). ( G ) Heatmap showing the relative expression of genes encoding DAMPs in the uninjured muscles and muscles at 1 dpi ( n = 2 for each). ( H ) RT-qPCR results showing the relative Inhba mRNA expression in BMDMs treated with 1 μg/mL of indicated DAMPs for 24 hours. ( I ) RT-qPCR results showing the relative Inhba mRNA expression in muscles at 1 dpi of the mice injected with vehicle ( n = 7), 10 mg/kg S100A8/A9 inhibitor (paquinimod) ( n = 6), and HMGB1 inhibitor (glycyrrhizin) ( n = 5). The P values were calculated using unpaired 2-tailed t test ( C – E ) and 1-way ANOVA with Tukey’s multiple-comparison test ( F , H , and I ). A P value or q value < 0.05 was considered significant. Data are shown as the mean ± SEM, and symbols represent individual mice.

Article Snippet: BMDMs were stimulated with 100 ng/mL LPS (Sigma-Aldrich), recombinant S100A8/A9 (1 μg/mL) (BioLegend), recombinant HMGB1 (1 μg/mL) (R&D Systems), heparan sulfate (1 μg/mL) (Sigma-Aldrich), low molecular weight hyaluronan (1 μg/mL) (R&D Systems), or muscle lysates.

Techniques: Quantitative RT-PCR, Expressing, Derivative Assay, Muscles, Injection, Comparison