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Effects of RSV on mitochondrial function–related indicators exposed to TCS. (A, B) Protein expression and quantitative analysis of SIRT1, <t>PGC–1α,</t> NRF1, and mRNA expression levels (C) mRNA expression levels of SIRT1, PGC–1α, NRF1, and TFAM (D) mRNA expression levels of MFN2, OPA1, MFN1, DRP1, FIS1, and MFF. Data were analyzed using one–way ANOVA. Inter–group differences are indicated by different letters ( P < 0.05). Groups with the same letter were considered not to have significant differences (mean ± SD, n = 6).
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Effects of RSV on mitochondrial function–related indicators exposed to TCS. (A, B) Protein expression and quantitative analysis of SIRT1, <t>PGC–1α,</t> NRF1, and mRNA expression levels (C) mRNA expression levels of SIRT1, PGC–1α, NRF1, and TFAM (D) mRNA expression levels of MFN2, OPA1, MFN1, DRP1, FIS1, and MFF. Data were analyzed using one–way ANOVA. Inter–group differences are indicated by different letters ( P < 0.05). Groups with the same letter were considered not to have significant differences (mean ± SD, n = 6).
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( A to Db ) Cross sections through the Gas muscle of Pax +/+ , Myh7 fl/+ (A to Bb) and Pax7 icre/+ , Myh7 Δ/fl (C to Db) mice at 2 and 12 months, respectively, labeled by immunofluorescence for MyHC-slow (green), troponin T1 (red), and DAPI (blue). Scale bars, 100 μm (Cb and Db). ( E to H ) SDH staining on Gas muscle sections of Pax +/+ , Myh7 fl/+ (E and G) and Pax7 icre/+ , Myh7 Δ/fl (Ea and Ga) mice and quantification of the percentage SDH activity (F and H) at 2 and 12 months of age, respectively ( n = 5). Scale bars, 100 μm (Ea and Ga). ( I to L ) Representative Western blots for troponin T1, <t>PGC-1α,</t> and α-tubulin (loading control) using Gas muscle protein lysates of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 2 and 6 months (I) and their densitometric quantification (J to L) ( n = 4). ( M to P ) Representative Western blots for mitochondrial complexes and α-tubulin (loading control) using protein lysates from the Gas muscle of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 6 months (M and O) and their densitometric quantification (N to P) ( n = 4 to 6). ( Q to T ) Representative Western blots for FIS1, pDRP1, DRP1, OPA1, Mitofusin 1, Mitofusin 2, and α-tubulin (loading control) using protein lysates from the Gas muscle of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 2 and 6 months (Q) and densitometric quantification (R to T) ( n = 4). ( U and V ) Quantification of ATP levels in the Gas muscle of Pax +/+ , Myh7 fl/+ and Pax7 icre/+ , Myh7 Δ/fl mice at 2 and 12 months of age ( n = 5). Data are presented as means ± SEM. * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001, and **** P ≤ 0.0001.
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Effects of RSV on mitochondrial function–related indicators exposed to TCS. (A, B) Protein expression and quantitative analysis of SIRT1, PGC–1α, NRF1, and mRNA expression levels (C) mRNA expression levels of SIRT1, PGC–1α, NRF1, and TFAM (D) mRNA expression levels of MFN2, OPA1, MFN1, DRP1, FIS1, and MFF. Data were analyzed using one–way ANOVA. Inter–group differences are indicated by different letters ( P < 0.05). Groups with the same letter were considered not to have significant differences (mean ± SD, n = 6).

Journal: Poultry Science

Article Title: Resveratrol protects against triclosan–induced impairment of colonic barrier function in chickens

doi: 10.1016/j.psj.2026.106946

Figure Lengend Snippet: Effects of RSV on mitochondrial function–related indicators exposed to TCS. (A, B) Protein expression and quantitative analysis of SIRT1, PGC–1α, NRF1, and mRNA expression levels (C) mRNA expression levels of SIRT1, PGC–1α, NRF1, and TFAM (D) mRNA expression levels of MFN2, OPA1, MFN1, DRP1, FIS1, and MFF. Data were analyzed using one–way ANOVA. Inter–group differences are indicated by different letters ( P < 0.05). Groups with the same letter were considered not to have significant differences (mean ± SD, n = 6).

Article Snippet: PGC-1α , 1:600 , WANLEIBIO.

Techniques: Expressing

( A to Db ) Cross sections through the Gas muscle of Pax +/+ , Myh7 fl/+ (A to Bb) and Pax7 icre/+ , Myh7 Δ/fl (C to Db) mice at 2 and 12 months, respectively, labeled by immunofluorescence for MyHC-slow (green), troponin T1 (red), and DAPI (blue). Scale bars, 100 μm (Cb and Db). ( E to H ) SDH staining on Gas muscle sections of Pax +/+ , Myh7 fl/+ (E and G) and Pax7 icre/+ , Myh7 Δ/fl (Ea and Ga) mice and quantification of the percentage SDH activity (F and H) at 2 and 12 months of age, respectively ( n = 5). Scale bars, 100 μm (Ea and Ga). ( I to L ) Representative Western blots for troponin T1, PGC-1α, and α-tubulin (loading control) using Gas muscle protein lysates of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 2 and 6 months (I) and their densitometric quantification (J to L) ( n = 4). ( M to P ) Representative Western blots for mitochondrial complexes and α-tubulin (loading control) using protein lysates from the Gas muscle of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 6 months (M and O) and their densitometric quantification (N to P) ( n = 4 to 6). ( Q to T ) Representative Western blots for FIS1, pDRP1, DRP1, OPA1, Mitofusin 1, Mitofusin 2, and α-tubulin (loading control) using protein lysates from the Gas muscle of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 2 and 6 months (Q) and densitometric quantification (R to T) ( n = 4). ( U and V ) Quantification of ATP levels in the Gas muscle of Pax +/+ , Myh7 fl/+ and Pax7 icre/+ , Myh7 Δ/fl mice at 2 and 12 months of age ( n = 5). Data are presented as means ± SEM. * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001, and **** P ≤ 0.0001.

Journal: Science Advances

Article Title: The skeletal muscle slow myosin heavy chain regulates mammalian metabolic homeostasis through the NRF2 pathway

doi: 10.1126/sciadv.aed2478

Figure Lengend Snippet: ( A to Db ) Cross sections through the Gas muscle of Pax +/+ , Myh7 fl/+ (A to Bb) and Pax7 icre/+ , Myh7 Δ/fl (C to Db) mice at 2 and 12 months, respectively, labeled by immunofluorescence for MyHC-slow (green), troponin T1 (red), and DAPI (blue). Scale bars, 100 μm (Cb and Db). ( E to H ) SDH staining on Gas muscle sections of Pax +/+ , Myh7 fl/+ (E and G) and Pax7 icre/+ , Myh7 Δ/fl (Ea and Ga) mice and quantification of the percentage SDH activity (F and H) at 2 and 12 months of age, respectively ( n = 5). Scale bars, 100 μm (Ea and Ga). ( I to L ) Representative Western blots for troponin T1, PGC-1α, and α-tubulin (loading control) using Gas muscle protein lysates of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 2 and 6 months (I) and their densitometric quantification (J to L) ( n = 4). ( M to P ) Representative Western blots for mitochondrial complexes and α-tubulin (loading control) using protein lysates from the Gas muscle of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 6 months (M and O) and their densitometric quantification (N to P) ( n = 4 to 6). ( Q to T ) Representative Western blots for FIS1, pDRP1, DRP1, OPA1, Mitofusin 1, Mitofusin 2, and α-tubulin (loading control) using protein lysates from the Gas muscle of Pax +/+ , Myh7 fl/+ , Pax3 cre/+ , Myh7 Δ/fl (P0), and Pax7 icre/+ , Myh7 Δ/fl mice at P0 and 2 and 6 months (Q) and densitometric quantification (R to T) ( n = 4). ( U and V ) Quantification of ATP levels in the Gas muscle of Pax +/+ , Myh7 fl/+ and Pax7 icre/+ , Myh7 Δ/fl mice at 2 and 12 months of age ( n = 5). Data are presented as means ± SEM. * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001, and **** P ≤ 0.0001.

Article Snippet: The antibodies used for Western blotting were as follows: anti-mouse MyHC-IIa antibody (SC-71, Developmental Studies Hybridoma Bank) at 1:10 dilution; anti-mouse MyHC-IIb antibody (BFF3, Developmental Studies Hybridoma Bank) at 1:10; anti-mouse alpha-tubulin antibody (30021290, Cell Signaling Technology) at 1:10,000; anti-rabbit GAPDH antibody (PAB932Mu01, Cloud-Clone Corp) at 1:10,000; anti-rabbit Akt antibody (4641, Cell Signaling Technology) at 1:1000; anti-rabbit P-Akt S473 (4640, Cell Signaling Technology) at 1:1000; anti-rabbit Histone H3 antibody (Ab1741, Abcam) at 1:10,000; anti-rabbit troponin T1 antibody (NBP238855, Novus Biologicals) at 1:5000; anti-rabbit PGC-1α antibody (A12348, ABclonal; 66369, Proteintech; and 2178S, Cell Signaling Technology) at 1:2000, 1:2000, and 1:1000, respectively; anti-mouse total OXPHOS cocktail (ab110413, Abcam) at 1:1000; anti-rabbit DRP1 antibody (A21968, ABclonal) at 1:2000; anti-rabbit FIS1 antibody (A19666, ABclonal) at 1:2000; anti-rabbit mitofusin1 antibody (A9880, ABclonal) at 1:2000; anti-rabbit mitofusin2 antibody (A12771, ABclonal) at 1:2000; anti-rabbit GLUT4 (MA5-17176, Thermo Fisher Scientific) at 1:1000; anti-rabbit NRF2 antibody (A0674, ABclonal and 98020000, Proteintech) at 1:2000; anti-rabbit P-NRF2 antibody (AP1133, ABclonal) at 1:2000; anti-rabbit SOD1 antibody (A0274, ABclonal) at 1:2000; anti-rabbit Prdx1 antibody (A13524, ABclonal) at 1:2000; anti-rabbit Gpx1 antibody (A1110, ABclonal) at 1:1000; anti-rabbit catalase antibody (A11220, ABclonal) at 1:2000; anti-rabbit KEAP1 antibody (A1820, ABclonal) at 1:1000; anti-rabbit Tom20 antibody (HPA011582, Merck) at 1:2500, anti-rabbit VDAC1 antibody ( Ab154856 , Abcam) at 1:2500; anti-rabbit pDRP1 (S616) antibody (AP0849, ABclonal) at 1:2500; and anti-rabbit OPA1 antibody (A9833, ABclonal) at 1:2500.

Techniques: Labeling, Immunofluorescence, Staining, Activity Assay, Western Blot, Control

( A ) Schematic depicting the sulforaphane dosing strategy starting from 16 weeks. ( B to F ) Body weight (grams) and muscle weight (TA, Gas, Quad, and soleus) (milligrams) of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice at 6 months of age ( n = 5 to 6). ( G to Gc ) Gas muscle cross sections labeled by immunofluorescence for laminin (red) and DAPI (blue) of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice at 6 months of age and quantification of the proportion of myofibers grouped according to myofiber area (Gb) and average myofiber area (μm 2 ) (Gc) through the Gas ( n = 4). Scale bar, 100 μm (Ga). ( H to Ia ) Ex vivo contractility quantifying the absolute and maximal absolute force of TA and Gas in DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice ( n = 4). ( J and K ) Treadmill running distance and speed of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice ( n = 6). ( L to V ) Representative Western blots for P-NRF2, NRF2, KEAP1 (Gas and TA), SOD1, GPx1, Prdx1, catalase, MyHC-IIa, MyHC-IIb, PGC-1α, mitochondrial complex, carbonylated proteins (Gas), and α-tubulin (loading control) using protein lysates of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice (L, O, S, and T) and their densitometry (M, N, P to R, U, and V) ( n = 4). ( W ) Grip strength quantification of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice normalized to body weight ( n = 6). ( X to Ya ) GTT and ITT of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice and their area under the curve ( n = 5 to 6). ( Z ) Quad muscle ATP level quantification of DMSO- or sulforaphane-treated Pax +/+ , Myh7 fl/+ and Pax7 icre/+ , Myh7 Δ/fl mice ( n = 5). Data are presented as means ± SEM. * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001, and **** P ≤ 0.0001.

Journal: Science Advances

Article Title: The skeletal muscle slow myosin heavy chain regulates mammalian metabolic homeostasis through the NRF2 pathway

doi: 10.1126/sciadv.aed2478

Figure Lengend Snippet: ( A ) Schematic depicting the sulforaphane dosing strategy starting from 16 weeks. ( B to F ) Body weight (grams) and muscle weight (TA, Gas, Quad, and soleus) (milligrams) of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice at 6 months of age ( n = 5 to 6). ( G to Gc ) Gas muscle cross sections labeled by immunofluorescence for laminin (red) and DAPI (blue) of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice at 6 months of age and quantification of the proportion of myofibers grouped according to myofiber area (Gb) and average myofiber area (μm 2 ) (Gc) through the Gas ( n = 4). Scale bar, 100 μm (Ga). ( H to Ia ) Ex vivo contractility quantifying the absolute and maximal absolute force of TA and Gas in DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice ( n = 4). ( J and K ) Treadmill running distance and speed of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice ( n = 6). ( L to V ) Representative Western blots for P-NRF2, NRF2, KEAP1 (Gas and TA), SOD1, GPx1, Prdx1, catalase, MyHC-IIa, MyHC-IIb, PGC-1α, mitochondrial complex, carbonylated proteins (Gas), and α-tubulin (loading control) using protein lysates of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice (L, O, S, and T) and their densitometry (M, N, P to R, U, and V) ( n = 4). ( W ) Grip strength quantification of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice normalized to body weight ( n = 6). ( X to Ya ) GTT and ITT of DMSO- or sulforaphane-treated Pax7 icre/+ , Myh7 Δ/fl mice and their area under the curve ( n = 5 to 6). ( Z ) Quad muscle ATP level quantification of DMSO- or sulforaphane-treated Pax +/+ , Myh7 fl/+ and Pax7 icre/+ , Myh7 Δ/fl mice ( n = 5). Data are presented as means ± SEM. * P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001, and **** P ≤ 0.0001.

Article Snippet: The antibodies used for Western blotting were as follows: anti-mouse MyHC-IIa antibody (SC-71, Developmental Studies Hybridoma Bank) at 1:10 dilution; anti-mouse MyHC-IIb antibody (BFF3, Developmental Studies Hybridoma Bank) at 1:10; anti-mouse alpha-tubulin antibody (30021290, Cell Signaling Technology) at 1:10,000; anti-rabbit GAPDH antibody (PAB932Mu01, Cloud-Clone Corp) at 1:10,000; anti-rabbit Akt antibody (4641, Cell Signaling Technology) at 1:1000; anti-rabbit P-Akt S473 (4640, Cell Signaling Technology) at 1:1000; anti-rabbit Histone H3 antibody (Ab1741, Abcam) at 1:10,000; anti-rabbit troponin T1 antibody (NBP238855, Novus Biologicals) at 1:5000; anti-rabbit PGC-1α antibody (A12348, ABclonal; 66369, Proteintech; and 2178S, Cell Signaling Technology) at 1:2000, 1:2000, and 1:1000, respectively; anti-mouse total OXPHOS cocktail (ab110413, Abcam) at 1:1000; anti-rabbit DRP1 antibody (A21968, ABclonal) at 1:2000; anti-rabbit FIS1 antibody (A19666, ABclonal) at 1:2000; anti-rabbit mitofusin1 antibody (A9880, ABclonal) at 1:2000; anti-rabbit mitofusin2 antibody (A12771, ABclonal) at 1:2000; anti-rabbit GLUT4 (MA5-17176, Thermo Fisher Scientific) at 1:1000; anti-rabbit NRF2 antibody (A0674, ABclonal and 98020000, Proteintech) at 1:2000; anti-rabbit P-NRF2 antibody (AP1133, ABclonal) at 1:2000; anti-rabbit SOD1 antibody (A0274, ABclonal) at 1:2000; anti-rabbit Prdx1 antibody (A13524, ABclonal) at 1:2000; anti-rabbit Gpx1 antibody (A1110, ABclonal) at 1:1000; anti-rabbit catalase antibody (A11220, ABclonal) at 1:2000; anti-rabbit KEAP1 antibody (A1820, ABclonal) at 1:1000; anti-rabbit Tom20 antibody (HPA011582, Merck) at 1:2500, anti-rabbit VDAC1 antibody ( Ab154856 , Abcam) at 1:2500; anti-rabbit pDRP1 (S616) antibody (AP0849, ABclonal) at 1:2500; and anti-rabbit OPA1 antibody (A9833, ABclonal) at 1:2500.

Techniques: Labeling, Immunofluorescence, Ex Vivo, Western Blot, Control