Levels of some plasma fibrotic factors and hepatic nitric oxide synthase in experimentally induced cirrhotic rats

Fawzy, Eman; Gad, Mohammed; Abd Al-Rahman, Ehsan

doi:10.21608/besps.2006.37521

Levels of some plasma fibrotic factors and hepatic nitric oxide synthase in experimentally induced cirrhotic rats

Document Type : Original Article

Authors

¹ Department of Phyiology, Faculty of Medicine, Alexandria University

² Department of Internal Medicine , Faculty of Medicine, Alexandria University

³ Department of Medical Biochemistry , Faculty of Medicine, Alexandria University

10.21608/besps.2006.37521

Abstract

Hepatic fibrogenesis is a consequence of hepatic stellate cells that become activated
and transdifferentiated into a myofibroblastic phenotype with the ability to proliferate
and synthesize large quantities of extracellular matrix components. Aim: The aim of
the present study was to investigate plasma levels of tumor necrosis factor alpha
(TNF-α) and interleukin-6 (IL-6) as proinflammatory and profibrogenic cytokines in
cirrhotic rats and relate them with the level of plasminogen activator inhibitor-1(PAI-
1) as a marker of fibrinolytic activity. In addition, these cytokines were correlated
with hepatic nitric oxide synthase activity (NOS). Subjects and methods: The study
included 31 cirrhotic rats and 10 healthy controls. Induction of cirrhosis; Hepatic
injury and fibrosis were done in rats by intraperitoneal injection (IP) of
dimethylnitrosamine.(DMN). That were divided into 5 groups. Group I: as a control,
group II were 8 cirrhotic rats, while group III were 7 cirrhotic ones with ascites.
Group IV and V (n=8 rats) were cirrhotic rats injected with Ng nitro L-arginine
methylester (L-NAME). Group V were ascitic in addition. Plasma TNF-α, IL-6 and
PAI-1 and nitric oxide (NO) metabolites were measured. Hepatic nitrite level and
NOS activity were also estimated. Results: Plasma TNF-α was significantly increased
in all studied groups compared to control group. Plasma IL-6 was significantly
higher in cirrhotic group with ascites and L-NAME administered groups compared to
control one. Levels of plasma IL-6 were increased progressively with evolution of the
disease. There was no statistically significant difference in plasma levels of PAI-1
between cirrhotic rats and control group, whereas, it was significantly increased in
cirrhotic group with ascites upon L-NAME administration compared to control
group. NOS activity is positively correlated with hepatic nitrite level. A positive
significant correlation, also, existed between plasma TNF-α, IL-6 and NOS activity
and hepatic nitrite in cirrhotic rats. Conclusion: The present study revealed that in
cirrhotic rats; plasma levels of TNF-α and IL-6 were significantly elevated, and the
elevation was more with progression of fibrosis. Plasma PAI-1 was increased in
severe fibrotic liver with other injury. It could be suggested that the profibrogenic
cytokines TNF-α and IL-6 are implicated in fibrogenesis in cirrhotic rats and are
correlated with NOS activity which functions as an adaptive mechanism. They could
be used clinically as indicators for occurrence and progression of fibrosis.

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