The Effects of Arginine and Selective Inducible Nitric Oxide Synthase Inhibitor on Pathophysiology of Sepsis in a CLP Model
| Autor: | Nobuko Hojo, Junichi Sasaki, Satoshi Yamanouchi, Tomoyuki Endo, Ryosuke Nomura, Xiao Qi Xie, Yotaro Shinozawa, Satoshi Akaishi, Kiyotsugu Takuma, Daisuke Kudo, Michio Kobayashi |
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| Rok vydání: | 2008 |
| Předmět: |
Male
medicine.medical_specialty Arginine medicine.disease_cause Guanidines Nitric oxide Rats Sprague-Dawley Sepsis Excretion chemistry.chemical_compound Internal medicine medicine Animals Enzyme Inhibitors Nitrites Nitrates biology medicine.disease Rats Nitric oxide synthase Heme oxygenase Disease Models Animal Oxidative Stress Endocrinology Epinephrine chemistry biology.protein Drug Therapy Combination Surgery Nitric Oxide Synthase Heme Oxygenase-1 Oxidative stress medicine.drug |
| Zdroj: | Journal of Surgical Research. 146:298-303 |
| ISSN: | 0022-4804 |
| Popis: | Background Sepsis is an arginine-deficient state and is associated with overproduction of nitric oxide (NO) by inducible nitric oxide synthase (iNOS). It has been indicated that low plasma levels of arginine are related to high mortality rates in sepsis. Arginine, however, is also known to be a precursor of NO. Therefore, administration of arginine in septic patients remains controversial. We examined the effects of co-administration of arginine and aminoguanidine, a selective iNOS inhibitor, on sepsis, using rat models. Method Sepsis was induced in rats by cecal ligation and puncture (CLP). Effects of separate and combined administration of arginine and aminoguanidine were investigated by comparing plasma levels of arginine, expressions of heme oxygenase (HO)-1 and HO-2 in liver and lung, and nitrite + nitrate (NOx) excretion in urine, as well as neuroendocrine responses in urine in the early phase of sepsis. Seven-day survival rates were also examined. Results A combination of arginine and aminoguanidine recovered the plasma level of arginine at 6 h post-CLP, decreased expression of HO-1 in liver and lung at 24 h post-CLP, decreased urinary excretion of epinephrine, norepinephrine, dopamine, and 17-hydroxycorticosteroid in the first 24 h post-CLP, and increased 7-d survival. Conclusion It is demonstrated that administration of arginine together with the selective iNOS inhibitor in the early phase of sepsis restores plasma arginine, reduces oxidative stress by probably maintaining NO derived from constitutive NOS, and attenuates neuroendocrine stress responses. This co-administration may be a beneficial treatment approach against sepsis. |
| Databáze: | OpenAIRE |
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