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protective effect of ellagic acid against angiotensin ii-induced cardiomyocyte hypertrophy in h9c2 myocardial cells: role of calcineurin/nfat pathway
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نویسنده
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asadi firouzeh ,razmi ali ,ghazizadeh foad ,shafiei massoumeh
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منبع
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journal of medicinal plants - 2021 - دوره : 20 - شماره : 78 - صفحه:1 -13
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چکیده
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Background: ellagic acid, a major ellagitannin found in pomegranate extract, might be an attractive natural and safe bioactive compound for prevention of cardiac hypertrophy in many pathological conditions that are associated with elevated circulating angiotensin ii (ang ii). ang ii stimulates multiple signal transduction pathways involved in hypertrophy including calcineurin/nuclear factor of activated t cell (nfat). objective: the present study aimed to explore the possible antihypertrophic activity of ellagic acid against ang iiinduced cardiomyocyte hypertrophy and the role of calcineurin/ nfat signaling pathway in this action. methods: h9c2 myocardial cells were treated with different concentrations of ellagic acid one hour before exposure to ang ii. biological markers of cardiac hypertrophy including changes in cell size and protein content, and atrial natriuretic peptide (anp) protein expression were assessed using light microscopy, bradford method and western blotting, respectively. the effects of ellagic acid on the protein expression of calcineurin and nuclear localization of nfatc4 were also investigated using western blotting and immunofluorescence assay, respectively. results: the results showed that pretreatment with ellagic acid could efficiently prevent ang iiinduced hypertrophic response which was associated with changes in hypertrophyrelated biomarkers including increase in cell size and protein content, and anp overexpression. moreover, ellagic acid inhibited ang iiinduced calcineurin upregulation and nuclear localization of nfatc4. conclusion: in summary, our findings showed that ellagic acid effectively inhibited ang iiinduced cardiomyocyte hypertrophy. this is the first report demonstrating the role of calcineurin/nfat pathway inhibition in this protective effects. future in vivo studies are required to elucidate if ellagic acid could ameliorate cardiac hypertrophy and its transition to heart failure.
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کلیدواژه
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ellagic acid ,cardiomyocyte-hypertrophy ,angiotensin ii ,calcineurin ,h9c2 cells
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آدرس
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lorestan university of medical sciences, school of pharmacy, department of pharmacology and toxicology, iran, academic center for education, culture and research (acecr), institute of medicinal plants, medicinal plants research center, iran, iran university of medical sciences, school of medicine, department of pharmacology, iran, iran university of medical sciences, school of medicine, department of pharmacology, iran
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پست الکترونیکی
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shafiei.m@iums.ac.ir
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Protective effect of ellagic acid against angiotensin II-induced cardiomyocyte hypertrophy in H9c2 myocardial cells: Role of calcineurin/NFAT pathway
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Authors
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Asadi Firouzeh ,Razmi Ali ,Ghazizadeh Foad ,Shafiei Massoumeh
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Abstract
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Background: Ellagic acid, a major ellagitannin found in pomegranate extract, might be an attractive natural and safe bioactive compound for prevention of cardiac hypertrophy in many pathological conditions that are associated with elevated circulating angiotensin II (Ang II). Ang II stimulates multiple signal transduction pathways involved in hypertrophy including calcineurin/nuclear factor of activated T cell (NFAT). Objective: The present study aimed to explore the possible antihypertrophic activity of ellagic acid against Ang IIinduced cardiomyocyte hypertrophy and the role of calcineurin/ NFAT signaling pathway in this action. Methods: H9c2 myocardial cells were treated with different concentrations of ellagic acid one hour before exposure to Ang II. Biological markers of cardiac hypertrophy including changes in cell size and protein content, and atrial natriuretic peptide (ANP) protein expression were assessed using light microscopy, Bradford method and western blotting, respectively. The effects of ellagic acid on the protein expression of calcineurin and nuclear localization of NFATc4 were also investigated using western blotting and immunofluorescence assay, respectively. Results: The results showed that pretreatment with ellagic acid could efficiently prevent Ang IIinduced hypertrophic response which was associated with changes in hypertrophyrelated biomarkers including increase in cell size and protein content, and ANP overexpression. Moreover, ellagic acid inhibited Ang IIinduced calcineurin upregulation and nuclear localization of NFATc4. Conclusion: In summary, our findings showed that ellagic acid effectively inhibited Ang IIinduced cardiomyocyte hypertrophy. This is the first report demonstrating the role of calcineurin/NFAT pathway inhibition in this protective effects. Future in vivo studies are required to elucidate if ellagic acid could ameliorate cardiac hypertrophy and its transition to heart failure.
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Keywords
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Ellagic acid ,Cardiomyocyte-hypertrophy ,Angiotensin II ,Calcineurin ,H9c2 cells
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