Literature DB >> 62098

Experimental induction of hepatocellular hyalin (Mallory bodies) in mice by griseofulvin treatment. 1. Light microscopic observation.

H Denk, R Eckerstorfer, F Gschnait, K Konrad, K Wolff.   

Abstract

Griseofulvin (GF) feeding of mice resulted in protoporphyria, liver cell damage, bile duct alterations, and finally hepatoma formation. In addition, hepatocellular hyalin developed, resembling in its morphology classic Mallory bodies (MB) as seen in alcoholic and nonalcoholic liver disorders in man. Liver cells containing MB often displayed features of severe cell damage and MB were finally released into the sinusoids and degraded by macrophages. The rapid disappearance of MB following GF discontinuation and the reappearance after resumption of GF feeding suggest an intimate relationship between metabolic alterations in the hepatocytes exerted by the drug and MB formation. This assumption is further supported by the fact that MB change their tinctoreal properties in chromotrope aniline blue-stained sections after GF discontinuation, possibly relfecting degeneration. Long term GF treatment apparently primed the liver for MB formation since the cells were able to respond almost instantly with MB to a GF challenge after a 1-month GF-free period.

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Year:  1976        PMID: 62098

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  9 in total

1.  Bile acid-induced Mallory body formation in drug-primed mouse liver.

Authors:  Peter Fickert; Michael Trauner; Andrea Fuchsbichler; Conny Stumptner; Kurt Zatloukal; Helmut Denk
Journal:  Am J Pathol       Date:  2002-12       Impact factor: 4.307

2.  Mallory body filaments become insoluble after normal assembly into intermediate filaments.

Authors:  M S Pollanen; P Markiewicz; L Weyer; M C Goh; C Bergeron
Journal:  Am J Pathol       Date:  1994-11       Impact factor: 4.307

3.  Cytoarchitectural analysis of epithelial sheets formed in vitro by hepatic tumor cells possessing defined intermediate-sized filament cytoskeletal abnormalities.

Authors:  M P Ryan; E Borenfreund; P J Higgins
Journal:  Am J Pathol       Date:  1989-02       Impact factor: 4.307

4.  Mallory bodies: lesions of hepatocytes containing proteins of the keratin-myosin-epidermin group.

Authors:  S N Meloan; H Puchtler
Journal:  Histochemistry       Date:  1982

Review 5.  The role of cytoskeletal and cytocontractile elements in pathologic processes.

Authors:  E Rungger-Brändle; G Gabbiani
Journal:  Am J Pathol       Date:  1983-03       Impact factor: 4.307

6.  Formation and involution of Mallory bodies ("alcoholic hyalin") in murine and human liver revealed by immunofluorescence microscopy with antibodies to prekeratin.

Authors:  H Denk; W W Franke; R Eckerstorfer; E Schmid; D Kerjaschki
Journal:  Proc Natl Acad Sci U S A       Date:  1979-08       Impact factor: 11.205

7.  A metabolomic perspective of griseofulvin-induced liver injury in mice.

Authors:  Ke Liu; Jiong Yan; Madhav Sachar; Xinju Zhang; Ming Guan; Wen Xie; Xiaochao Ma
Journal:  Biochem Pharmacol       Date:  2015-09-05       Impact factor: 5.858

8.  Ultrastructure of alcoholic hyaline filaments in alcoholic hepatitis.

Authors:  T Okanoue; T Okuno; O Ou; J Yoshida; T Ogasawara; T Takino
Journal:  Gastroenterol Jpn       Date:  1982-10

9.  Immunohistochemical and ultrastructural analyses of cytoplasmic blood plasma inclusions of rat hepatocytes.

Authors:  Tomoaki Tochitani; Kaoru Toyosawa; Izumi Matsumoto; Mami Kouchi; Yoshiko Michimae; Takatoshi Koujitani; Hitoshi Funabashi; Takaki Seki
Journal:  J Toxicol Pathol       Date:  2012-01-07       Impact factor: 1.628

  9 in total

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