Protection of Ischemic and Reperfused Rat Heart by Aqueous Extract of Urtica Dioica

Author(s):
Dareuosh ShackebaeiDareuosh Shackebaei1,*, AA  GodiniAA Godini1, M  AbolghaziM Abolghazi2, MB  MajnouniMB Majnouni2, M  HesariM Hesari1
1Medical Biology Research Center, Iran
2School of pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran
*Corresponding Author: Corresponding author: Dareuosh Shackebaei, Medical Biology Research Center, Iran Email: [email protected]

International Cardiovascular Research Journal:Vol. 4, issue 3; e62942
Published online:Sep 01, 2010
Article type:Research Article
Received:Dec 04, 2017
Accepted:Sep 01, 2010
How to Cite:Shackebaei D, Godini A, Abolghazi M, Majnouni M, Hesari M. Protection of Ischemic and Reperfused Rat Heart by Aqueous Extract of Urtica Dioica. Int Cardiovasc Res J. 2017;4(3):e62942. doi:

Abstract

tory
effects. The objective of this study was to clarify the effects of aqueous extract of Urtica dioica on isolated
ischemia- reperfused heart.
Methods: The heart of male wistar rats were isolated and perfused according to langendorff method. In the
control group (n = 13) the hearts were subjected to three steps of stabilization (30 min), normothermic global
ischemia (40 min) and reperfusion (45 min). In addition, before and after ischemia, the aqueous extract of U.D
(200 mg/ml) was added to perfusion solution in the test group (n=14). Different cardiac variables including left
ventricular pressure, heart rate and coronary flow were measured and rate pressure product was calculated.
Results: Results showed that left ventricular pressure (59.11±4.7) and rate pressure product (13680±1136) in
45th minute of reperfusion in the test group were significantly (P=0.0187 and 0.0321 respectively) greater than
the control group (39.1±6.0, 9480±1480) respectively. These findings indicated decreased cardiac damage following
ischemia in the test group, compared with that of control group.
Conclusion: Results of the present study showed that the aqueous extract of U.D, increased the tolerance of
isolated rat hearts against ischemic damage. This effect can be explained by potent antioxidant activity of the
U.D extract, suggesting its clinical use in ischemic heart disease.

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Copyright

© 2017, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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