Leicester Research Archive

Leicester Research Archive >
College of Medicine, Biological Sciences and Psychology >
Medical and Social Care Education, Department of >
Published Articles, Dept. of Medical and Social Care Education >

Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/9386

Title: Effects of Hydrogen Sulphide on the Isolated Perfused Rat Heart
Authors: Hussain, Afthab
Maddock, Helen
Al-Rajaibi, Hajar
Carson, Ray J.
Issue Date: May-2011
Publisher: Sultan Qaboos University
Citation: Sultan Qaboos University Medical Journal (SQU Med J), 2011, 11(2), pp. 236-244.
Abstract: Objectives: Hydrogen sulphide has been identified as a gas signalling molecule in the body, and has previously been shown to have vasorelaxant properties. The aim of the study was to investigate the effects of sodium hydrosulphide (NaHS), a hydrogen sulphide donor, on heart rate (HR), left ventricular developed pressure (LVDP) and coronary flow (CF) in the isolated perfused rat heart. Methods: A Langendorff isolated heart preparation was used to investigate the effect of a dose range of sodium hydrosulphide, in the presence and absence of inhibitors, on heart rate, left ventricular developed pressure and coronary flow. Results: Sodium hydrosulphide caused a significant decrease in heart rate at a concentration of 10-3 M (P <0.001). This decrease was partially inhibited by glibenclamide, a KATP channel blocker (P <0.05); L-NAME, a nitric oxide synthase inhibitor (P <0.001), and methylene blue (P <0.001), but not by H-89, a protein kinase A inhibitor. Sodium hydrosulphide significantly increased coronary flow at concentrations of 10-4 – 10-3M (P <0.05). This response was significantly increased in the presence of L-NAME (P <0.001) and methylene blue (P <0.001), whereas H-89 inhibited the increase in coronary flow due to sodium hydrosulphide (P <0.001). Sodium hydrosulphide significantly decreased LVDP at all concentrations (P <0.001). In the presence of glibenclamide and H-89, the time period of the decrease in LVDP due to sodium hydrosulphide was extended (P <0.001), whereas methylene blue and L-NAME caused a significant reduction in the response to sodium hydrosulphide (P <0.05, P <0.01 respectively). Conclusion: Sodium hydrosulphide reduced heart rate and LVDP, and increased coronary flow in the isolated perfused rat heart; however, the mechanisms of action could not be fully elucidated.
ISSN: 2075-051X (Print)
2075-0528 (Online)
Links: http://hdl.handle.net/2381/9386
Type: Article
Description: This research was originally published in SQUMJ. Hussain, A., Maddock, H., Al-Rajaibi, H., Carson, R.J. Effects of Hydrogen Sulphide on the Isolated Perfused Rat Heart. SQU Med J 2011;11(2):236-244. © by Sultan Qaboos University Medical Journal This is the original published version of the article. It is reproduced here with the publisher's permission. http://web.squ.edu.om/squmj/index.asp
Appears in Collections:Published Articles, Dept. of Medical and Social Care Education

Files in This Item:

File Description SizeFormat
Hydrogen_Sulphide.pdf1.38 MBAdobe PDFView/Open
View Statistics

Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.

 

MAINTAINER