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Analysis of oxidative stress markers in each group. (A) <t>SOD),</t> (B) <t>Catalase</t> <t>(CAT),</t> and (C) Malondialdehyde (MDA). Data are presented as the mean ± SEM; n=5 per group. **P<0.01, SOD, superoxide dismutase; CAT, catalase; MDA, malondialdehyde; HG, high-glucose; DP, dexmedetomidine preconditioning; H 2 O 2 , hydrogen peroxide; mgprot, mg protein.
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Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of <t>SOD-2</t> and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.
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Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of <t>SOD-2</t> and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.
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Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of <t>SOD-2</t> and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.
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Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of <t>SOD-2</t> and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.
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Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of <t>SOD-2</t> and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.
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Analysis of oxidative stress markers in each group. (A) SOD), (B) Catalase (CAT), and (C) Malondialdehyde (MDA). Data are presented as the mean ± SEM; n=5 per group. **P<0.01, SOD, superoxide dismutase; CAT, catalase; MDA, malondialdehyde; HG, high-glucose; DP, dexmedetomidine preconditioning; H 2 O 2 , hydrogen peroxide; mgprot, mg protein.

Journal: Molecular Medicine Reports

Article Title: Dexmedetomidine mitigates oxidative stress in H9C2 cardiac myoblasts under a high-glucose environment via the PI3K/AKT signaling pathway

doi: 10.3892/mmr.2025.13616

Figure Lengend Snippet: Analysis of oxidative stress markers in each group. (A) SOD), (B) Catalase (CAT), and (C) Malondialdehyde (MDA). Data are presented as the mean ± SEM; n=5 per group. **P<0.01, SOD, superoxide dismutase; CAT, catalase; MDA, malondialdehyde; HG, high-glucose; DP, dexmedetomidine preconditioning; H 2 O 2 , hydrogen peroxide; mgprot, mg protein.

Article Snippet: These measurements were carried out using ELISA kits from Nanjing Jiancheng Bioengineering Institute, including the SOD (cat. no. A001-3-2), CAT assay kit (cat. no. A007-2-1), and MDA assay kit (cat. no. A003-4-1).

Techniques:

Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of SOD-2 and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.

Journal: International Journal of Molecular Sciences

Article Title: Umbilical Cord Mesenchymal Stem Cell-Derived Extracellular Vesicles Enhance Chondrocyte Function by Reducing Oxidative Stress in Chondrocytes

doi: 10.3390/ijms26167683

Figure Lengend Snippet: Effect of UCMSC-EVs on oxidative stress of chondrocytes. Chondrocytes were treated with UCMSC-EVs at concentrations of 0 (Control group) or 10 8 –10 10 particles/mL (UCMSC-EVs group) for 7 days to assess oxidative stress. ( A ) Mitochondrial superoxide levels were evaluated by quantifying MitoSOX Red fluorescence intensity ( n = 6). ( B , C ) Protein expression levels of SOD-2 and Sirt-3 were analyzed by Western blotting following treatment with 10 10 particles/mL UCMSC-EVs. β-actin was used as the internal control. Protein expression data are normalized to the Control group (defined as 1) and presented as mean ± standard error of the mean (SEM; n = 3–5). * and ** indicate p < 0.05 and p < 0.01, respectively, compared to the chondrocytes in the Control group.

Article Snippet: The antibodies used in this study are as follows: Superoxide Dismutase 2 (SOD-2) (cat. no. 24127-1-AP, proteintech; 1:5000), Sirt-3 (cat. no. 12186-1-AP, proteintech; 1:1000), and β-actin (cat. no. A5441, Sigma).

Techniques: Control, Fluorescence, Expressing, Western Blot