Please use this identifier to cite or link to this item:
https://ir.swu.ac.th/jspui/handle/123456789/12339
Title: | Rosmarinic acid improves hypertension and skeletal muscle glucose transport in angiotensin II-treated rats |
Authors: | Prasannarong M. Saengsirisuwan V. Surapongchai J. Buniam J. Chukijrungroat N. Rattanavichit Y. |
Keywords: | angiotensin II glucose glyceraldehyde 3 phosphate dehydrogenase glycogen synthase kinase 3alpha glycogen synthase kinase 3beta Janus kinase mitogen activated protein kinase mitogen activated protein kinase 1 mitogen activated protein kinase 3 mitogen activated protein kinase p38 protein kinase B rosmarinic acid angiotensin II cinnamic acid derivative depside glucose insulin rosmarinic acid animal tissue Article body weight controlled study diastolic blood pressure drug effect enzyme activity glucose blood level glucose transport heart weight hypertension liver weight long term care male mean arterial pressure nonhuman oral glucose tolerance test rat sham procedure single drug dose skeletal muscle Sprague Dawley rat systolic blood pressure treatment duration animal blood pressure hypertension metabolism organ size signal transduction skeletal muscle Angiotensin II Animals Blood Pressure Body Weight Cinnamates Depsides Glucose Hypertension Insulin Male Muscle, Skeletal Organ Size Rats Rats, Sprague-Dawley Signal Transduction |
Issue Date: | 2019 |
Abstract: | Background: Rosmarinic acid (RA) is a natural pure compound from herbs belonging to the Lamiaceae family, such as rosemary, sage, basil, and mint. The antioxidant, angiotensin-converting enzyme inhibitory, and vasodilatory effects of RA have been revealed. Angiotensin II (ANG II) is a potent agent that generates hypertension and oxidative stress. Hypertension and skeletal muscle insulin resistance are strongly related. The aim of this study was to evaluate the effects of acute and chronic RA treatment on blood pressure and skeletal muscle glucose transport in ANG II-induced hypertensive rats. Methods: Eight-week-old male Sprague Dawley rats were separated into SHAM and ANG II-infused (250 ng/kg/min) groups. ANG II rats were treated with or without acute or chronic RA at 10, 20, or 40 mg/kg. At the end of the experiment, body weight, liver and heart weights, oral glucose tolerance, skeletal muscle glucose transport activity, and signaling proteins were evaluated. Results: Both acute and chronic RA treatment decreased systolic, diastolic, and mean arterial blood pressure. Only acute RA at 40 mg/kg resulted in a reduction of fasting plasma glucose levels and an induction of skeletal muscle glucose transport activity. These effects might involve increased ERK activity in skeletal muscle. Meanwhile, chronic RA treatment with 10, 20, and 40 mg/kg prevented ANG II-induced hyperglycemia. Conclusions: Both acute and chronic RA treatment attenuated ANG II-induced cardiometabolic abnormalities in rats. Therefore, RA would be an alternative strategy for improving skeletal muscle glucose transport and protecting against ANG II-induced hypertension and hyperglycemia. © 2019 The Author(s). |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/12339 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85068844277&doi=10.1186%2fs12906-019-2579-4&partnerID=40&md5=2fc5ced36ddc1e5c6efdca0b01009e8c |
ISSN: | 14726882 |
Appears in Collections: | Scopus 1983-2021 |
Files in This Item:
There are no files associated with this item.
Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.