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Updated: Jan 19, 2026

MicroRNA-based Regulation of Picornavirus Tropism
Published on: February 6, 2017
GALLIC ACID IMPROVES OXIDATIVE STRESS AND INFLAMMATION THROUGH REGULATING MICRORNAS EXPRESSIONS IN THE BLOOD OF
F Ramezani Ali Akbari1,2, M Badavi1,2,3, M Dianat1,2
1Ahvaz Jundishapur University of Medical Sciences, Ahvaz Physiology Research Center, Ahvaz, Iran.
Gallic acid (GA) treatment in diabetic rats improved cardiovascular health by restoring body weight, blood pressure, and lipid profiles. GA also reduced inflammation and oxidative stress, likely by increasing plasma miR-24 and miR-126 levels.
Area of Science:
- Cardiovascular Science
- Endocrinology
- Biochemistry
Background:
- Diabetes mellitus is linked to endothelial dysfunction and diabetic cardiomyopathy.
- Gallic acid (GA) shows potential in managing diabetes-related cardiovascular complications.
- Plasma miR-24 and miR-126 are implicated in endothelial dysfunction associated with diabetes.
Purpose of the Study:
- To investigate the therapeutic effects of Gallic acid (GA) on plasma miR-24 and miR-126 levels in a rat model of diabetes.
- To assess GA's impact on cardiovascular risk factors in diabetic rats.
Main Methods:
- Adult male Sprague-Dawley rats were allocated into control, diabetic, and diabetic groups treated with GA (25 mg/kg/day via gavage) for eight weeks.
- Key parameters measured included blood glucose, body weight, lipid profile, blood pressure, plasma miR-24 and miR-126, and oxidative/inflammatory biomarkers.
Main Results:
- Diabetic rats exhibited elevated blood glucose, lipids (TC, TG, VLDL-c, LDL-c), MDA, IL-6, TNF-α, and blood pressure, alongside reduced body weight, HDL-c, and TAC.
- Gallic acid (GA) treatment reversed these adverse effects, restoring normal levels of body weight, blood pressure, lipids, glucose, HDL-c, MDA, TAC, IL-6, TNF-α, miR-24, and miR-126 compared to diabetic rats.
Conclusions:
- Gallic acid (GA) demonstrates protective effects against diabetes-induced inflammation, oxidative stress, and hypotension.
- These beneficial actions of GA are likely mediated through the upregulation of plasma miR-24 and miR-126 levels.
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