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

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