Acute liver injury induced by low dose dimethylnitrosamine alters mediators of hepatic vascular flow

Toxicology Reports

Archana Kini¹  Aparna Venkatraman¹  Ashish Goel²  Eapen C.E.²  Raghupathy V.³  Balasubramanian K.A.³  Anna B. Pulimood³  Anup Ramachandran³  Kavitha R. Thangaraj³  G. Jayakumar Amirtharaj³ 

[1] Center for Stem Cell Research, Christian Medical College, Vellore 632004, India;Department of Hepatology, Division of Gastrointestinal Sciences, Christian Medical College, Vellore 632004, India;The Wellcome Trust Research Laboratory, Division of Gastrointestinal Sciences, Christian Medical College, Vellore 632004, India;

关键词: Liver injury;    Nitric oxide;    Hydrogen sulfide;    Stellate cell;    Rhodanese;    Oxidant stress;   

DOI  :  10.1016/j.toxrep.2014.09.001

来源: DOAJ

【 摘 要 】

Alterations in liver vascular tone play an important role in chronic liver disease. The hepatic stellate cell (HSC) and mediators such as nitric oxide (NO) and hydrogen sulfide (H2S) have been implicated in regulation of vascular tone and intra-hepatic pressure. Though these have been studied in chronic liver damage, changes in response to acute liver injury induced by hepatotoxins such as dimethyl nitrosamine are not well understood. Liver injury was induced in mice by a single intra-peritoneal injection of dimethylnitrosamine (DMN), following which animals were sacrificed at 24, 48 and 72 h. Changes in vascular mediators such as NO and H2S as well as stellate cell activation was then examined. It was found that a single low dose of DMN in mice is sufficient to induce activation of hepatic stellate cells within 24 h, accompanied by oxidative stress, compromised metabolism of H2S and decreased levels of the von Willebrand factor (vWF) cleaving protease; a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13), which functions in intravascular thrombosis. A suppression of hepatic NO levels is also initiated at this time point, which progresses further and is sustained up to 72 h, at which point the HSC activation is still present. Compromised levels of ADAMTS13 and H2S metabolism however, begin to recover by 48 h and are almost similar to control by 72 h. In conclusion, these data suggest that even moderate acute insults in the liver can have far reaching consequences on a number of mediators of vascular flow in the liver.

【 授权许可】

Unknown