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Pulmonary redox changes in female and male mice. Lung levels of (a) <t>thiobarbituric</t> acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .
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Pulmonary redox changes in female and male mice. Lung levels of (a) <t>thiobarbituric</t> acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .
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Pulmonary redox changes in female and male mice. Lung levels of (a) <t>thiobarbituric</t> acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .
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Pulmonary redox changes in female and male mice. Lung levels of (a) <t>thiobarbituric</t> acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .
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Pulmonary redox changes in female and male mice. Lung levels of (a) <t>thiobarbituric</t> acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .
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Pulmonary redox changes in female and male mice. Lung levels of (a) <t>thiobarbituric</t> acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .
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Pulmonary redox changes in female and male mice. Lung levels of (a) thiobarbituric acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .

Journal: Physiological Reports

Article Title: Sex differences in the redox response to fine particulate matter ( PM 2.5 ) air pollution protects female mice against metabolic and cardiac injury

doi: 10.14814/phy2.70536

Figure Lengend Snippet: Pulmonary redox changes in female and male mice. Lung levels of (a) thiobarbituric acid reactive substances (TBARS) and (b) reduced glutathione (GSH, i), (oxidized) glutathione disulfide (GSSG, ii), and GSH: GSSG ratios (iii) in female and male mice kept either on a regular light cycle (RLC, upper panel) or placed on a disturbed light cycle (DLC, lower panel) that inhaled air or concentrated ambient fine particulate matter (CAP) for 30 days. Data are presented as mean ± SE, n = 5 per group. A two‐way analysis of variance (ANOVA) followed by a Tukey's multiple comparisons test was used to determine statistical significance. Statistical significance between air and CAP inhaling male or female mice kept either on an RLC or DLC is indicated by * ( p < 0.05, air vs. CAP). Statistically significant differences between female and male mice inhaling air or CAP kept either on an RLC or DLC is indicated by # ( p < 0.05, air‐male vs. air‐female, CAP male v. CAP‐female). (c) Pulmonary mRNA abundance of the antioxidant enzymes superoxide dismutase ( Sod1 , 2 , 3 ), glutathione transferase ( Gst‐a , m , p ), catalase ( Cat ), and heme oxygenase 1 ( Hmox1 ) and their transcription factor nuclear factor erythroid 2–related factor 2 ( Nrf2 ) in air inhaling female and male mice that were kept on an RLC. Data are mean ± SE normalized to male‐ air‐RLC, n = 5 per group. Statistical significance between male and female mice was tested by an unpaired two‐tailed student's t ‐test and is indicated by * ( p < 0.05, male vs. female). (d) Female mice express more SOD and GST in the lungs and are protected against pulmonary lipid peroxidation and GST depletion induced by the exposure to concentrated PM 2.5 .

Article Snippet: To measure pulmonary redox changes, we used commercially available kits to detect either thiobarbituric acid reactive substances (TBARS, ZeptoMetrix, United States TBARS Assay Kit, 0801192) or reduced (GSH) and oxidized (GSSG) glutathione (Glutathione Colorimetric Detection Kit, United States, no. EIAGSHC) in the collected lung tissue.

Techniques: Two Tailed Test