Low-Dose Sodium Nitrite Fluid Resuscitation Prevents Lethality From Crush Syndrome by Improving Nitric Oxide Consumption and Preventing Myoglobin Cytotoxicity in Kidney in A Rat Model.

Shock

*Laboratory of Drug Safety Management, Faculty of Pharmaceutical Science, Josai University, Saitama, Japan †Division of Pathophysiology, Department of Clinical Dietetics and Human Nutrition, Faculty of Pharmaceutical Science, Josai University, Saitama, Japan.

Published: July 2017

AI Article Synopsis

  • Crush syndrome (CS) is a severe condition involving muscle damage from pressure, leading to high mortality rates, even with typical fluid treatments.
  • Researchers conducted experiments on rats with CS caused by extended limb compression to test whether fluids containing sodium nitrite (NaNO2) could enhance survival.
  • The study found that administering 200 μmol/kg NaNO2 improved blood circulation and reduced inflammatory responses, resulting in better recovery and increased survival rates in the CS model.

Article Abstract

Objective: Crush syndrome (CS) is a serious medical condition characterized by muscle cell damage resulting from pressure. CS has a high mortality, even when patients receive fluid therapy. We examined whether administration of NaNO2-containing fluid can improve survival in a rat model of CS.

Design: The CS model was generated by subjecting anesthetized rats to bilateral hind limb compression with a rubber tourniquet for 5 h. Rats were then randomly divided into six groups: sham; CS with no treatment; CS with normal saline treatment; CS with normal saline + 25 mEq/L bicarbonate treatment; and CS with normal saline + 200 or 500 μmol/kg NaNO2.

Measurements And Main Results: Blood and tissue samples were collected for histological and biochemical analyses at predetermined time points before and after reperfusion. Ischemic compression of rat hind limbs reduced nitrite content in the crushed muscle, and subsequent reperfusion resulted in reactive oxygen species-induced circulatory dysfunction and systemic inflammation. Rats treated with 200 μmol/kg NaNO2 showed increased nitric oxide (NO) levels, blood circulation, and neoangiogenesis, decreased generation of reactive oxygen species, and suppression of the inflammatory response, leading to complete recovery.

Conclusions: Treatment with 200 μmol/kg NaNO2 prevents muscle damage induced by ischemia reperfusion via the protective effects of NO and suppression of systemic inflammation, thereby increasing survival rates in CS.

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Source
http://dx.doi.org/10.1097/SHK.0000000000000817DOI Listing

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