Nitric oxide production and inducible nitric oxide synthase expression in peritoneal macrophages of cirrhotic patients

被引:36
作者
Jiménez, W
Ros, J
Morales-Ruiz, M
Navasa, M
Solé, M
Colmenero, J
Sort, P
Rivera, F
Arroyo, V
Rodés, J
机构
[1] Hosp Clin Univ, Hormonal Lab, Barcelona 08036, Spain
[2] Hosp Clin Univ, Liver Unit, Barcelona 08036, Spain
[3] Hosp Clin Univ, Dept Pathol, Barcelona 08036, Spain
[4] Univ Barcelona, Inst Invest Biomed August Pi & Sunyer, IDIBAPS, Barcelona, Spain
[5] Univ Barcelona, Inst Reina Sofia Invest Nefrol, Barcelona, Spain
关键词
D O I
10.1002/hep.510300310
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The present study assessed whether peritoneal macrophages isolated from cirrhotic patients produce nitric oxide (NO) and express NO synthase type II (NOS II) mRNA and protein. Patients with cirrhosis and ascites without peritonitis or with unresolved or resolved spontaneous bacterial peritonitis (SBP) were studied. Following paracentesis, ascites NO2- + NO3- content (NOx) was measured. Peritoneal macrophages from ascites were seeded on well plates, and NO2- in the medium was determined. NOx was higher in patients with unresolved or resolved SEP than in cirrhotic patients without peritonitis. Macrophages of patients with SEP or resolved SEP produced NO2- after 30 hours in culture, but those obtained from patients without peritonitis did not. Reverse-transcription polymerase chain reaction (RT-PCR) and immunocytochemical analysis revealed the presence of a clear signal for NOS II mRNA and protein in macrophages of SEP patients, regardless of whether or not the infection subsided. Therefore, peritoneal macrophages isolated from cirrhotic patients with unresolved or resolved SEP produce NO and express the NOS II mRNA and protein, suggesting that NOS II may contribute to the control of SEP, or to its associated pathology, in human cirrhosis.
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页码:670 / 676
页数:7
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