Abstract

BackgroundHydrogen-rich saline has been reported to have antioxidant and anti-inflammatory effects and effectively protect against organ damage. Oxidative stress and inflammation contribute to the pathogenesis and/or development of pulmonary hypertension. In this study, we investigated the effects of hydrogen-rich saline on the prevention of pulmonary hypertension induced by monocrotaline in a rat model.MethodsIn male Sprague-Dawley rats, pulmonary hypertension was induced by subcutaneous administration of monocrotaline at a concentration of 6 mg/100 g body weight. Hydrogen-rich saline (5 ml/kg) or saline was administred intraperitoneally once daily for 2 or 3 weeks. Severity of pulmonary hypertension was assessed by hemodynamic index and histologic analysis. Malondialdehyde and 8-hydroxy-desoxyguanosine level, and superoxide dismutase activity were measured in the lung tissue and serum. Levels of pro-inflammatory cytokines (tumor necrosis factor-α, interleukin-6) in serum were determined with enzyme-linked immunosorbent assay.ResultsHydrogen-rich saline treatment improved hemodynamics and reversed right ventricular hypertrophy. It also decreased malondialdehyde and 8-hydroxy-desoxyguanosine levels, and increased superoxide dismutase activity in the lung tissue and serum, accompanied by a decrease in pro-inflammatory cytokines.ConclusionsThese results suggest that hydrogen-rich saline ameliorates the progression of pulmonary hypertension induced by monocrotaline in rats, which may be associated with its antioxidant and anti-inflammatory effects.

Highlights

  • Hydrogen-rich saline has been reported to have antioxidant and anti-inflammatory effects and effectively protect against organ damage

  • Compared with the control group, mean pulmonary artery pressure (mPAP), right ventricular systolic pressure (RVSP), right ventricular (RV) dP/dt max and dP/dt min in rats challenged with MCT in the MCT-treated group increased significantly (P < 0.01), indicating that rats developed severe Pulmonary hypertension (PH)

  • Hydrogen-rich saline treatment for either 2 or 3 weeks attenuated the effects of MCT, suggesting that mPAP, RVSP, RV dP/dt max and dP/dt min were decreased significantly compared with the MCT group (P < 0.05)

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Summary

Introduction

Hydrogen-rich saline has been reported to have antioxidant and anti-inflammatory effects and effectively protect against organ damage. We investigated the effects of hydrogen-rich saline on the prevention of pulmonary hypertension induced by monocrotaline in a rat model. Either idiopathic or secondary, may share some of the following pathological or functional changes, including vascular remodeling, endothelial dysfunction/increased vasoconstriction, oxidative stress and inflammation. Among these changes, the effects of oxidative stress and inflammation on PH have been investigated. It has been reported that hydrogen-rich saline has an antiinflammatory effect [13]

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