TY - JOUR
T1 - Beneficial versus detrimental effects of nitric oxide synthase inhibitors in circulatory shock
T2 - Lessons learned from experimental and clinical studies
AU - Kilbourn, Robert G.
AU - Szabó, Csaba
AU - Traber, Daniel L.
PY - 1997
Y1 - 1997
N2 - Septic shock is a physiological derangement of the cardiovascular system characterized by pathological vasodilation. Recent studies have established a role for nitric oxide, previously known as endothelium-derived relaxing factor, in the vascular dysfunction of sepsis. This finding suggests that inhibition of nitric oxide synthase (NOS), the enzyme responsible for nitric oxide production, could be a target for therapeutic intervention. Animal studies have provided conflicting results, demonstrating both beneficial and detrimental effects. We provide here an overview of the preclinical studies of NOS inhibitors and an update of the clinical studies. The low toxicity and marked antihypotensive activity of NOS inhibitors in humans highlight some of the drawbacks of certain animal models and provide important insights into the experimental study of septic shock.
AB - Septic shock is a physiological derangement of the cardiovascular system characterized by pathological vasodilation. Recent studies have established a role for nitric oxide, previously known as endothelium-derived relaxing factor, in the vascular dysfunction of sepsis. This finding suggests that inhibition of nitric oxide synthase (NOS), the enzyme responsible for nitric oxide production, could be a target for therapeutic intervention. Animal studies have provided conflicting results, demonstrating both beneficial and detrimental effects. We provide here an overview of the preclinical studies of NOS inhibitors and an update of the clinical studies. The low toxicity and marked antihypotensive activity of NOS inhibitors in humans highlight some of the drawbacks of certain animal models and provide important insights into the experimental study of septic shock.
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U2 - 10.1097/00024382-199704000-00001
DO - 10.1097/00024382-199704000-00001
M3 - Article
C2 - 9110408
AN - SCOPUS:0031112190
SN - 1073-2322
VL - 7
SP - 235
EP - 246
JO - Shock
JF - Shock
IS - 4
ER -