A novel, potent and selective inhibitor of the activity of inducible nitric oxide synthase [GW274150] reduces the organ injury in hemorrhagic shock

• Autorzy: McDonald M.C. , Izumi M. , Cuzzocrea S. , Thiemermann C.
• Języki publikacji: EN

Abstrakty

EN

An enhanced formation of nitric oxide (NO) by the inducible NO synfhase (iNOS) may contribute to the pathophysiology of hemorrhagic shock. This study investigates the effect of a novel, potent and selective inhibitor of iNOS activity (GW274150) on the circulatory failure and the organ injury and dysfunction associated with hemorrhagic shock in the anesthetised rat. Hemorrhage (sufficient to lower mean arterial blood pressure to 45 mmHg for 90 min) and subsequent resuscitation with shed blood resulted (within 4 h after resuscitation) in a delayed fall in blood pressure, renal and liver injury and dysfunction as well as the pancreatic injury. Pre-treatment of rats with GW274150 (5 mg/kg at 30 min prior to the onset of hemorrhage) attenuated the renal dysfunction as well as the liver and pancreatic injury caused by hemorrhage and resuscitation. Interestingly, GW274150 did not reduce the delayed fall in blood pressure associated with hemorrhagic shock. We propose that an enhanced formation of NO from iNOS contributes to the organ injury and dysfunction in hemorrhagic shock, and that highly selective inhibitors of iNOS activity, such as GW274150, may represent a novel therapeutic approach for the therapy of hemorrhagic shock.

Słowa kluczowe

EN

superoxide dismutase; hemorrhagic shock; nitric oxide; multiple organ failure; catalase; oxygen radical; superoxide anion

• Wydawca: -
• Czasopismo: Journal of Physiology and Pharmacology
• Rocznik: 2002
• Tom: 53
• Numer: 4,1
• Opis fizyczny: p.555-569,fig.

Twórcy

autor

McDonald M.C.

• The Royal London School of Medicine and Dentistry, Charterhouse Square, London EC1M6BQ, U.K.

autor

Izumi M.

autor

Cuzzocrea S.

autor

Thiemermann C.