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Representative Western blot analyses reveal (A-D) decreased catalase and superoxide dismutase type 2 (SOD2) levels with no significant change in superoxide dismutase type 1 (SOD1) levels. (E-G) Increased apoptotic protein expression was observed. (H-K) Decreased expression of major proteins in the electron transport chain and (L-O) proteins governing mitochondrial biogenesis was presented. All data are presented as mean ± SEM. RCR, regular circadian rhythm; ICR, irregular circadian rhythm; Bcl2, B-cell lymphoma 2; Bax, Bcl2 associated X; NADH, reduced nicotinamide adenine dinucleotide; SDHB, succinate dehydrogenase subunit B; COX-I, cytochrome oxidase (COX) subunit I; AMPK, AMP-activated protein kinase; PGC-1α, <t>peroxisome</t> <t>proliferator-activated</t> receptor-gamma coactivator (PGC)-1alpha; Tfam, mitochondrial transcription factor A. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 as determined using two-way ANOVA and Tukey’s post-hoc analyses (n = 6).
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Representative Western blot analyses reveal (A-D) decreased catalase and superoxide dismutase type 2 (SOD2) levels with no significant change in superoxide dismutase type 1 (SOD1) levels. (E-G) Increased apoptotic protein expression was observed. (H-K) Decreased expression of major proteins in the electron transport chain and (L-O) proteins governing mitochondrial biogenesis was presented. All data are presented as mean ± SEM. RCR, regular circadian rhythm; ICR, irregular circadian rhythm; Bcl2, B-cell lymphoma 2; Bax, Bcl2 associated X; NADH, reduced nicotinamide adenine dinucleotide; SDHB, succinate dehydrogenase subunit B; COX-I, cytochrome oxidase (COX) subunit I; AMPK, AMP-activated protein kinase; PGC-1α, peroxisome proliferator-activated receptor-gamma coactivator (PGC)-1alpha; Tfam, mitochondrial transcription factor A. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 as determined using two-way ANOVA and Tukey’s post-hoc analyses (n = 6).

Journal: The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology

Article Title: Exercise improves muscle mitochondrial dysfunction-associated lipid profile under circadian rhythm disturbance

doi: 10.4196/kjpp.2024.28.6.515

Figure Lengend Snippet: Representative Western blot analyses reveal (A-D) decreased catalase and superoxide dismutase type 2 (SOD2) levels with no significant change in superoxide dismutase type 1 (SOD1) levels. (E-G) Increased apoptotic protein expression was observed. (H-K) Decreased expression of major proteins in the electron transport chain and (L-O) proteins governing mitochondrial biogenesis was presented. All data are presented as mean ± SEM. RCR, regular circadian rhythm; ICR, irregular circadian rhythm; Bcl2, B-cell lymphoma 2; Bax, Bcl2 associated X; NADH, reduced nicotinamide adenine dinucleotide; SDHB, succinate dehydrogenase subunit B; COX-I, cytochrome oxidase (COX) subunit I; AMPK, AMP-activated protein kinase; PGC-1α, peroxisome proliferator-activated receptor-gamma coactivator (PGC)-1alpha; Tfam, mitochondrial transcription factor A. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 as determined using two-way ANOVA and Tukey’s post-hoc analyses (n = 6).

Article Snippet: The membranes were incubated with primary antibodies for two hours to overnight as follows: β-actin (Invitrogen, MA1-140); p-AMPK α1/2 (Millipore, #07-681); AMPK α1/2 (SCBT, sc-25792); peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1α; GenTex, GTX37356); mitochondrial transcription factor A (Tfam; SCBT, sc-166965); NADH:ubiquinone oxidoreductase subunit A9 (NADH; Abcam, ab110242); succinate dehydrogenase (SDH) subunits B (SDHB; ab14714, Abcam); cytochrome oxidase (COX) subunit I (COX-I; ab14705, Abcam); superoxide dismutase type 1 (SOD1; SCBT, sc-8637); superoxide dismutase type 2 (SOD2; SCBT, sc-18503); Catalase (SCBT, sc-271358); p-P53 (SCBT, sc-51690); P53 (SCBT, sc-55476); Bcl2 associated X (Bax; SCBT, sc-7480); B-cell lymphoma 2 (Bcl2; SCBT, sc-7382); brain and muscle ARNT-like 1 (BMAL1; SCBT, sc-365645); period circadian regulator 2 (PER2; Invitrogen, #PA5-100107).

Techniques: Western Blot, Expressing

Western blot analyses reveal (A-D) increased antioxidant levels stimulated a (E-G) decrease in apoptotic protein expression. (H-K) Results exhibit heightened expression of proteins involved in the electron transport chain and (L-O) proteins governing mitochondrial biogenesis. All data are presented as mean ± SEM. EXT, endurance exercise training; SED, sedentary; RCR, regular circadian rhythm; ICR, irregular circadian rhythm; SOD1 & 2, superoxide dismutase type 1 & 2; Bcl2, B-cell lymphoma 2; Bax, Bcl2 associated X; NADH, reduced nicotinamide adenine dinucleotide; SDHB, succinate dehydrogenase subunit B; COX-I, cytochrome oxidase (COX) subunit I; AMPK, AMP-activated protein kinase; PGC-1α, peroxisome proliferator-activated receptor-gamma coactivator (PGC)-1alpha; Tfam, mitochondrial transcription factor A. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 as determined using two-way ANOVA and Tukey’s post-hoc analyses (n = 6).

Journal: The Korean Journal of Physiology & Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology

Article Title: Exercise improves muscle mitochondrial dysfunction-associated lipid profile under circadian rhythm disturbance

doi: 10.4196/kjpp.2024.28.6.515

Figure Lengend Snippet: Western blot analyses reveal (A-D) increased antioxidant levels stimulated a (E-G) decrease in apoptotic protein expression. (H-K) Results exhibit heightened expression of proteins involved in the electron transport chain and (L-O) proteins governing mitochondrial biogenesis. All data are presented as mean ± SEM. EXT, endurance exercise training; SED, sedentary; RCR, regular circadian rhythm; ICR, irregular circadian rhythm; SOD1 & 2, superoxide dismutase type 1 & 2; Bcl2, B-cell lymphoma 2; Bax, Bcl2 associated X; NADH, reduced nicotinamide adenine dinucleotide; SDHB, succinate dehydrogenase subunit B; COX-I, cytochrome oxidase (COX) subunit I; AMPK, AMP-activated protein kinase; PGC-1α, peroxisome proliferator-activated receptor-gamma coactivator (PGC)-1alpha; Tfam, mitochondrial transcription factor A. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 as determined using two-way ANOVA and Tukey’s post-hoc analyses (n = 6).

Article Snippet: The membranes were incubated with primary antibodies for two hours to overnight as follows: β-actin (Invitrogen, MA1-140); p-AMPK α1/2 (Millipore, #07-681); AMPK α1/2 (SCBT, sc-25792); peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1α; GenTex, GTX37356); mitochondrial transcription factor A (Tfam; SCBT, sc-166965); NADH:ubiquinone oxidoreductase subunit A9 (NADH; Abcam, ab110242); succinate dehydrogenase (SDH) subunits B (SDHB; ab14714, Abcam); cytochrome oxidase (COX) subunit I (COX-I; ab14705, Abcam); superoxide dismutase type 1 (SOD1; SCBT, sc-8637); superoxide dismutase type 2 (SOD2; SCBT, sc-18503); Catalase (SCBT, sc-271358); p-P53 (SCBT, sc-51690); P53 (SCBT, sc-55476); Bcl2 associated X (Bax; SCBT, sc-7480); B-cell lymphoma 2 (Bcl2; SCBT, sc-7382); brain and muscle ARNT-like 1 (BMAL1; SCBT, sc-365645); period circadian regulator 2 (PER2; Invitrogen, #PA5-100107).

Techniques: Western Blot, Expressing