captopril Search Results


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Enamine Ltd enamine z19802699 435 449 ndm
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MedChemExpress captopril
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Cell Signaling Technology Inc captopril suppression test
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Santa Cruz Biotechnology captopril
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
Captopril, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/captopril/Captopril/10__1080_slash_2162402x__2020__1836766-154-20-21
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Thermo Fisher captopril
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
Captopril, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/captopril/Captopril/pmc10655806-241-34-35
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Selleck Chemicals captopril
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
Captopril, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/captopril/Captopril/pmc06527541-48-16-17
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Aladdin Scientific Corporation captopril cap
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
Captopril Cap, supplied by Aladdin Scientific Corporation, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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European Directorate for the Quality of Medicines and HealthCare e 2s
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
E 2s, supplied by European Directorate for the Quality of Medicines and HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/captopril/Captopril+impurity+E+CRS/10__24193_slash_subbchem__2019__2__19-75-26-30
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Biosynth Carbosynth captopril
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
Captopril, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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European Directorate for the Quality of Medicines and HealthCare b 2s
Figure 4. Effect of <t>captopril</t> on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.
B 2s, supplied by European Directorate for the Quality of Medicines and HealthCare, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FUJIFILM captopril
Effects of nitrite and <t>captopril</t> supplementation on body, liver, and heart weights in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, # p < 0.05 vs. SHRSP5/Dmcr + HFC diet group. SP diet, stroke-prone diet; HFC diet, high-fat/high-cholesterol diet; WKY, Wistar Kyoto rat.
Captopril, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Figure 4. Effect of captopril on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.

Journal: OncoImmunology

Article Title: Angiotensin-converting enzyme (ACE) inhibitor prescription affects non-small-cell lung cancer (NSCLC) patients response to PD-1/PD-L1 immune checkpoint blockers

doi: 10.1080/2162402x.2020.1836766

Figure Lengend Snippet: Figure 4. Effect of captopril on macrophages. (a to c) Human monocytes (n = 3) were differentiated for 6 d into M1 or M2 macrophages. (a and b) Expression level (mean MFI of 3 different donors) of different markers after cell staining with specific antibodies to analyze M1 and M2 differentiation by flow cytometry. (a) MFI z-score of markers expression at basal level. (b) Fold expression of the different markers analyzed by flow cytometry to compare human monocytes differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) or candesartan (10 µM). (c) Human monocytes were differentiated for 6 d into M1 or M2 macrophages with or without captopril (100 µM) and substance P concentration in cell supernatants was evaluated by ELISA. Data represent the mean of 3 different donors ± s.d. *, p < .05; **, p < .01. (d and e) MC38 tumor bearing mice were daily treated or not per os with 25mg/kg captopril with or without i.p. injections of 10mg/kg anti-PD-1 mAb three times a week. (d) Macrophage occurrence in tumors and CD206 expression in TAMs (n = 4 or 5 animals per group) were analyzed by flow cytometry. (e) Tumor size was monitored (mean ± s.e.m) and mice survival was calculated (n = 7 to 9 animals per group). *, p < .05; **, p < .01; ***, p < .005.

Article Snippet: Animals were treated from day 7 after tumor-cell injection (tumor size, 30 mm2), every day per os with 25 mg/kg captopril (Santa Cruz Biotechnology) in hypromellose and every 2–3 d i.p. with 10 mg/kg inVivo mAb anti-mouse PD-1 (BioXcell BE0146).

Techniques: Expressing, Staining, Flow Cytometry, Concentration Assay, Enzyme-linked Immunosorbent Assay

Effects of nitrite and captopril supplementation on body, liver, and heart weights in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, # p < 0.05 vs. SHRSP5/Dmcr + HFC diet group. SP diet, stroke-prone diet; HFC diet, high-fat/high-cholesterol diet; WKY, Wistar Kyoto rat.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Effects of nitrite and captopril supplementation on body, liver, and heart weights in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, # p < 0.05 vs. SHRSP5/Dmcr + HFC diet group. SP diet, stroke-prone diet; HFC diet, high-fat/high-cholesterol diet; WKY, Wistar Kyoto rat.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques:

Effects of nitrite and captopril on blood pressure in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05, vs. the WKY + SP diet group, † p < 0.05, vs. the SHRSP5/Dmcr + SP diet group. SBP, systolic blood pressure; MBP, mean blood pressure; DBP, diastolic blood pressure.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Effects of nitrite and captopril on blood pressure in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05, vs. the WKY + SP diet group, † p < 0.05, vs. the SHRSP5/Dmcr + SP diet group. SBP, systolic blood pressure; MBP, mean blood pressure; DBP, diastolic blood pressure.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques:

Macroscopic appearance and histological analysis (HE staining) of liver in WKY and SHRSP5/Dmcr rats fed SP diets and nonalcoholic steatohepatitis model rats treated with or without nitrite and captopril. Values represent mean ± SE ( n = 6), * p < 0.05, vs. the WKY + SP diet group, † p < 0.05, vs. the SHRSP5/Dmcr + SP diet group.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Macroscopic appearance and histological analysis (HE staining) of liver in WKY and SHRSP5/Dmcr rats fed SP diets and nonalcoholic steatohepatitis model rats treated with or without nitrite and captopril. Values represent mean ± SE ( n = 6), * p < 0.05, vs. the WKY + SP diet group, † p < 0.05, vs. the SHRSP5/Dmcr + SP diet group.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques: Staining

Immunohistochemical analysis of p47phox-positive area in the hepatic tissues of the rat nonalcoholic steatohepatitis model treated with nitrite and captopril. Results are expressed as mean ± SE ( n = 6), Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Immunohistochemical analysis of p47phox-positive area in the hepatic tissues of the rat nonalcoholic steatohepatitis model treated with nitrite and captopril. Results are expressed as mean ± SE ( n = 6), Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques: Immunohistochemical staining

Immunohistochemical analysis of CD68-positive area in the hepatic tissues of the rat nonalcoholic steatohepatitis model and the effects of nitrite and captopril on the inflammatory response in the liver. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Immunohistochemical analysis of CD68-positive area in the hepatic tissues of the rat nonalcoholic steatohepatitis model and the effects of nitrite and captopril on the inflammatory response in the liver. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques: Immunohistochemical staining

Histological analysis of liver fibrosis (Sirius Red stain) in the rat nonalcoholic steatohepatitis model treated with nitrite and captopril. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Histological analysis of liver fibrosis (Sirius Red stain) in the rat nonalcoholic steatohepatitis model treated with nitrite and captopril. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques: Staining

Gross photograph of midventricular short-axis section and quantitative analysis of left ventricular muscle area and chamber size following treatment with nitrite and captopril. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Gross photograph of midventricular short-axis section and quantitative analysis of left ventricular muscle area and chamber size following treatment with nitrite and captopril. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques:

Effects of nitrite and captopril supplementation on the plasma levels of NOx in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group. NOx, nitrite, and nitrate.

Journal: International Journal of Molecular Sciences

Article Title: Beneficial Effects of Dietary Nitrite on a Model of Nonalcoholic Steatohepatitis Induced by High-Fat/High-Cholesterol Diets in SHRSP5/Dmcr Rats: A Preliminary Study

doi: 10.3390/ijms23062931

Figure Lengend Snippet: Effects of nitrite and captopril supplementation on the plasma levels of NOx in the rat nonalcoholic steatohepatitis model. Values represent mean ± SE ( n = 6), * p < 0.05 vs. WKY + SP diet group, † p < 0.05 vs. SHRSP5/Dmcr + SP diet group, ♯ p < 0.05 vs. SHRSP5/Dmcr + HFC diet group. NOx, nitrite, and nitrate.

Article Snippet: Sodium nitrite and the ACE inhibitor captopril were purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan).

Techniques: