The PDF file you selected should load here if your Web browser has a PDF reader plug-in installed (for example, a recent version of Adobe Acrobat Reader).

If you would like more information about how to print, save, and work with PDFs, Highwire Press provides a helpful Frequently Asked Questions about PDFs.

Alternatively, you can download the PDF file directly to your computer, from where it can be opened using a PDF reader. To download the PDF, click the Download link above.

Fullscreen Fullscreen Off


The present study was aimed to evaluate the cardioprotective and antihypertensive effect of ethyl acetate soluble fraction of Morus alba L. in rats.Rats were orally treated with the ethyl acetate soluble fraction of methanol extract of Morus alba leaves (EASF 25, 50, and 100 mg/kg) for three weeks. Isoproterenol (85 mg/kg, s.c.) was administered at an interval of 24 h for two days for induction of myocardial infarction. The parameters like ST segment, heart rate, mean arterial blood pressure, pressure-rate index, vascular reactivity, heart weight, cardiac markers, and antioxidant enzymes were measured. Hypertension was induced by left renal artery ligation method. The effect of EASF was evaluated on blood pressure and cumulative concentration response curve (CCRC) of CaCl2 on phenylephrine pre-ontracted isolated rat aortas. Oral administrati on of EASF signifi cantly reduced ST segment, heart rate, arterial pressure, pressure-rate index, heart weight, LDH, CK-MB, and SGOT, whereas the levels of antioxidant enzymes were increased significantly. EASF reduced the pressor response to catecholamines and also showed protection from hypertrophy and degenerative changes on myocardial muscles. The ligation of renal artery significantly increased the blood pressure and CCRC of CaCl2 shift ed to the left. EASF significantly reversed these changes. The observations propose that Morus alba may possess beneficial role in the treatment of myocardial infarction and hypertension through the regulation of antioxidant defensive mechanisms and blockade of calcium channels, respectively.

Keywords

Isoproterenol, Oxidative Stress, Left renal artery ligation
Font Size

User

Notifications
JOURNAL COVERS