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Ameliorative Potential of Biochanin-A against Dexamethasone Induced Hypertension through Modulation of Relative mRNA and Protein Expressions in Experimental Rats
- Authors: V. V. Sathibabu Uddandrao1, P. P. Sethumathi2, Parim Brahma Naidu3, S. Vadivukkarasi4, Mustapha Sabana Begum5, G. Saravanan6
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View Affiliations Hide AffiliationsAffiliations: 1 Centre for Biological Sciences, Department of Biochemistry, K.S. Rangasamy College of Artsand Science (Autonomous), Tiruchengode, Namakkal District, Tamilnadu, 637215, India 2 Department of Pharmacology, Nandha College of Pharmacy, Erode, Tamil Nadu, 638052, India 3 Animal Physiology and Biochemistry Laboratory, ICMR National Animal Resource Facility forBiomedical Research (ICMR-NARFBR), Hyderabad, 500078, India 4 Centre for Biological Sciences, Department of Biochemistry, K.S. Rangasamy College of Artsand Science (Autonomous), Tiruchengode, Namakkal District, Tamilnadu, 637215, India 5 Department of Biochemistry, Muthayammal College of Arts and Science, Rasipuram, Namakkal,Tamil Nadu 637408, India 6 Centre for Biological Sciences, Department of Biochemistry, K.S. Rangasamy College of Artsand Science (Autonomous), Tiruchengode, Namakkal District, Tamilnadu, 637215, India
- Source: Advancements in Cardiovascular Research and Therapeutics: Molecular and Nutraceutical Perspectives , pp 156-170
- Publication Date: October 2022
- Language: English
In this study, we made an attempt to attenuate the dexamethasone induced hypertension through Biochanin-A (BCA) in experimental rats. Hypertension was induced in male albino Wistar rats by subcutaneous administration of dexamethasone (10µg/kg body weight). The rats were orally treated with BCA (10mg/kg body weight) once daily for 45 days and Nicorandil-treated group (6mg/kg body weight) included for comparison. We evaluated the changes in mean arterial pressure, heart rate, blood pressure, vascular function, oxidative stress markers, and gene expression of histone deacetylases (HDAC)-1, HDAC-2, and HDAC-8. Administration of BCA or Nicorandil showed noteworthy improvement in vascular function in experimental rats. Moreover, aortic eNOS expression was down regulated, and NADPH oxidase subunit p47phox was up regulated in hypertensive rats. The antihypertensive effects of BCA were connected with concomitant downregulation of p47phox expression and upregulation of eNOS expression. Dexamethasone exposure led to increased mRNA expression of HDACs expression in the kidneys and these were restored after BCA administration. In conclusion, our results are, therefore, BCA reduces hypertension in experimental rats and suggests that BCA might be used against the hypertension.
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