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. 2020 Sep-Oct;34(5):2507-2516.
doi: 10.21873/invivo.12067.

Hydrogen Sulphide and Nitric Oxide Cooperate in Cardioprotection Against Ischemia/Reperfusion Injury in Isolated Rat Heart

Affiliations

Hydrogen Sulphide and Nitric Oxide Cooperate in Cardioprotection Against Ischemia/Reperfusion Injury in Isolated Rat Heart

Savas Ustunova et al. In Vivo. 2020 Sep-Oct.

Abstract

Background/aim: This study was designed to provide further evidence for the interactions between hydrogen sulfide (H2S) and nitric oxide (NO) in ischemia/reperfusion (I/R) injury.

Materials and methods: Rat hearts were studied with the Langendorff technique using the H2S donor sodium hydrosulfide (NaHS, 40 μM) and the cystathionine gamma-lyase (CTH or CSE) inhibitor DL-propargylglycine (PAG, 1 mM). NO synthase inhibitor L-NG-nitroarginine methyl ester (L-NAME, 30 mg/kg, 7 days) was administered before the isolation. The hearts were homogenized for biochemical and molecular analysis.

Results: NaHS reversed I/R-induced cardiac performance impairment, increased tissue nitric oxide production and decreased tissue markers for cardiac injury, while L-NAME inhibited these effects. The expression of CTH was increased with PAG, which was suppressed by L-NAME.

Conclusion: H2S and NO increase each other's production suggesting their interaction and cooperation in cardioprotection against I/R injury.

Keywords: Hydrogen sulfide; ischemia/reperfusion injury; isolated heart; nitric oxide; oxidative damage.

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Conflict of interest statement

The Authors declare that there are no conflicts of interest associated with this work.

Figures

Figure 1
Figure 1. Experimental design (↓: time points for cardiodynamic analyses).
Figure 2
Figure 2. Cardiodynamic analysis. (A) The end diastolic pressure (EDP), B) Left ventricular developed pressure (LVDP) values of all groups. *p<0.05, **p<0.01, ***p<0.001, statistical significance compared to the IR group; +p<0.05, ++p<0.01, +++p<0.001, statistical significance compared to the L-NAME group.
Figure 3
Figure 3. Cardiodynamic analysis. A) The Max dP/dt, B) Rate pressure product (RPP) values of all groups. *p<0.05, **p<0.01, ***p<0.001, statistical significance compared to the IR group; +p<0.05, ++p<0.01, +++p<0.001, statistical significance compared to the L-NAME group.
Figure 4
Figure 4. Biochemical analysis in heart tissue samples. A) CK-MB, B) LDH, C) GPx, D) H2S and E) Nitrate/nitrite levels of all groups. **p<0.01, ***p<0.001, statistical significance compared to the IR group; +p<0.05, ++p<0.01, +++p<0.001, statistical significance compared to the L-NAME group.
Figure 5
Figure 5. RT-PCR analysis in heart tissue samples. A) eNOS B) iNOS and C) Cth mRNA expressions. All expression levels were measured relative to β-actin by RT-PCR. **p<0.01, statistical significance compared to the PAG group.

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