Literature DB >> 3693862

A morphological study of the early stages of hepatic fibrosis induced by low doses of dimethylnitrosamine in the rat.

A M Jézéquel1, R Mancini, M L Rinaldesi, G Macarri, C Venturini, F Orlandi.   

Abstract

Hepatic fibrosis has been induced in rats by low doses of dimethylnitrosamine (DMN) and special attention has been paid to early morphological events. DMN (10 microliter/kg body wt., i.p.) was given 3 days a week for 3 weeks to Sprague-Dawley rats. Liver samples were taken on days 7, 14, 21, 28 and 35 and examined by light and electron microscopy. Hemorrhagic necrosis, mainly centrolobular, was evident on day 7, with disruption of the sinusoidal lining, and widening or disappearance of the spaces of Disse invaded by erythrocytes and lymphocytes. Large granular lymphocytes similar to pit cells were also present in close contact with hepatocytes. At day 14, fibrotic septa were associated with cells bearing 'transitional' features between those of lipocytes, myofibroblasts and fibroblasts. Hepatocytes showed foci of increased smooth endoplasmic reticulum, and altered sinusoidal and canalicular membranes. At day 21, all animals showed nodularity of the parenchyma, with evidence of micronodular cirrhosis associated with ascites in two animals. At day 35 (19 days after cessation of treatment) there was little residual inflammation, but well-defined micronodules were still present in all animals. This shows that, in the rat, 3-week treatment with a low dose of DMN produces micronodular cirrhosis following diffuse hemorrhagic necrosis without steatosis. The response of the animals was uniform and reproducible. Lesions of the sinusoidal wall and of membranes of liver cells associated with the inflammatory reaction appeared prominent.

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Year:  1987        PMID: 3693862     DOI: 10.1016/s0168-8278(87)80570-6

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  27 in total

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3.  Effects of octreotide on intestinal transit and bacterial translocation in conscious rats with portal hypertension and liver fibrosis.

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4.  Global gene expression profiling of dimethylnitrosamine-induced liver fibrosis: from pathological and biochemical data to microarray analysis.

Authors:  Li-Jen Su; Shih-Lan Hsu; Jyh-Shyue Yang; Huei-Hun Tseng; Shiu-Feng Huang; Chi-Ying F Huang
Journal:  Gene Expr       Date:  2006

5.  Blockade of type beta transforming growth factor signaling prevents liver fibrosis and dysfunction in the rat.

Authors:  Z Qi; N Atsuchi; A Ooshima; A Takeshita; H Ueno
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

6.  The Dimethylnitrosamine Induced Liver Fibrosis Model in the Rat.

Authors:  Kum Fai Chooi; Dinesh Babu Kuppan Rajendran; Siew Siang Gary Phang; Han Hui Alden Toh
Journal:  J Vis Exp       Date:  2016-06-17       Impact factor: 1.355

7.  Pathophysiological characteristics of dimethylnitrosamine-induced liver fibrosis in acute and chronic injury models: a possible contribution of KLF5 to fibrogenic responses.

Authors:  Fumihiro Ohara; Aisuke Nii; Yojiro Sakiyama; Megumi Tsuchiya; Shinji Ogawa
Journal:  Dig Dis Sci       Date:  2007-12-20       Impact factor: 3.199

8.  Pharmacokinetics of oltipraz in diabetic rats with liver cirrhosis.

Authors:  C Y Ahn; S K Bae; S H Bae; T Kim; Y S Jung; Y C Kim; M G Lee; W G Shin
Journal:  Br J Pharmacol       Date:  2009-03       Impact factor: 8.739

9.  Iron deposition and fat accumulation in dimethylnitrosamine-induced liver fibrosis in rat.

Authors:  Jin-Yang He; Wen-Hua Ge; Yuan Chen
Journal:  World J Gastroenterol       Date:  2007-04-14       Impact factor: 5.742

10.  An interleukin-1 receptor antagonist decreases fibrosis induced by dimethylnitrosamine in rat liver.

Authors:  R Mancini; A Benedetti; A M Jezequel
Journal:  Virchows Arch       Date:  1994       Impact factor: 4.064

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