Protective Effects of Cysteine Analogues on Acute Myocardial Ischemia: Novel Modulators of Endogenous H2S Production

Qian Wang, Xian-Li Wang, Hong-Rui Liu, Peter Rose, Yi-Zhun Zhu

Research output: Contribution to journalArticlepeer-review

100 Citations (Scopus)

Abstract

The current study was designed to evaluate the pharmacologic effects of three novel cysteine-containing compounds: S-propyl-L-cysteine (SPC), S-allyl-L-cysteine (SAC), and S-propargyl-L-cysteine (SPRC) on H2S production and antioxidant defenses in an acute myocardial infarction (MI) rat model. The enzymatic activities of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), as well as glutathione redox status and malonaldehyde (MDA) content, also were determined. All three compounds were found to preserve SOD and GPx activities and also tissue GSH levels while reducing the formation of the lipid peroxidation product MDA in ventricular tissues. With immunfluorescence assays, we observed the expression of CSE and Mn-SOD. The morphologic changes of the cardiac cells are seen with both light and electron microscopy. The corresponding pathologic alterations were characterized mainly as loss of adherence between cardiac myocytes and swollen or ruptured mitochondria at the ultrastructural level. Propargylglycine, a selective inhibitor of CSE, abolished the protective effects of each compound used in the current model. Our study provides novel evidence that SPC, SAC, and SPRC have cardioprotective effects in MI by reducing the deleterious effects of oxidative stress by modulating the endogenous levels of H2S and preserving the activities of antioxidant defensive enzymes like SOD. Antioxid. Redox Signal. 12, 1155-1165.
Original languageEnglish
Pages (from-to)1155 - 1165
Number of pages11
JournalANTIOXIDANTS AND REDOX SIGNALING
Volume12
Issue number10
DOIs
Publication statusPublished - 15 May 2010

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