Effects of janus kinase/signal transducer and activator of transcription pathway on synthesis of iNOS and NO in pulmonary and vascular tissues of infectious shock rats
WANG Song-bai,PEI Shu-jun,XU Chang-fu,LI Hai.Effects of janus kinase/signal transducer and activator of transcription pathway on synthesis of iNOS and NO in pulmonary and vascular tissues of infectious shock rats[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(15):1511-1513.
WANG Song-bai,PEI Shu-jun,XU Chang-fu,LI Hai.Effects of janus kinase/signal transducer and activator of transcription pathway on synthesis of iNOS and NO in pulmonary and vascular tissues of infectious shock rats[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(15):1511-1513.DOI:
Objective To determine the effects of janus kinase/signal transducer and activator of transcription on the synthesis of inducible nitric oxide synthase (iNOS) and nitric oxide (NO) in infectious shock rats. Methods Forty-eight male Wistar rats were randomly divided into normal control
sham operation group
cecal ligation puncture (CLP) group
and inhibitor of JAK (AG490) treatment group. CLP group and AG490 group were established into the sepsis model induced by CLP
and at 2
6
24 h after CLP
the rats were sacrificed. The pulmonary
vascular tissues and serum samples of all rats were harvested to determine iNOS mRNA expression levels by reverse transcription polymerase chain reaction (RT-PCR) and NO content respectively. Meanwhile
the mean arterial pressure (MAP) and pulse were monitored. Results No notable difference was detected in all parameters between sham operation group and normal control. Compared with normal control
iNOS mRNA and NO levels in pulmonary
vascular tissues and serum at 2
6 and 24 h following CLP significantly elevated respectively
and MAP fell notably and pulse increased (P0.05 or 0.01). AG490 treatment decreased iNOS mRNA and NO levels markedly at 2 or 6 h after CLP
meanwhile MAP and pulse deteriorated by sepsis were also ameliorated (P0.05 or 0.01). Conclusion Inhibiting the activation of JAK/STAT pathway can reduce tissues and serum iNOS mRNA and NO expressions in infectious shock rats and can ameliorate the circulatory function deteriorated by sepsis.