Literature DB >> 4569312

A morphometric study of the removal of phenobarbital-induced membranes from hepatocytes after cessation of threatment.

R P Bolender, E R Weibel.   

Abstract

It is well known that phenobarbital (PB) treatment produces an increase in the amount of cytoplasmic membranes of hepatocytes, with a parallel enhancement in the activity of drug-metabolizing enzymes. However, little is known about how the induced membranes are removed after the drug treatment is stopped. To consider this problem, the recovery of rat hepatocytes from PB induction (five daily injections, 100 mg/kg) was followed morphometrically. Treatment with PB produced a cellular enlargement (26%) due to increases in the volume of the cytoplasmic matrix (20%) and the volume (100%) and surface area (90%) of the smooth-surfaced endoplasmic reticulum (SER). The volume of the nuclei and the surface area of the Golgi apparatus were also increased, but no changes were detected in the volumes of the mitochondria or peroxisomes. The SER membranes induced by the PB were removed within 5 days after the end of the treatment period. During this period of membrane removal, we observed an increase in the volume (800%) and number (96%) of autophagic vacuoles without a change in dense bodies. A morphometric analysis of the content of the autophagic vacuoles showed that the endoplasmic reticulum membranes were preferentially removed, and from this we conclude that the formation of autophagic vacuoles was not a random process. Our findings show that the removal of excess cytoplasmic membranes is associated with an increase in autophagic activity and thus demonstrates the presence of a specific cellular mechanism which may be responsible for the bulk removal of PB-induced membranes.

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Year:  1973        PMID: 4569312      PMCID: PMC2108940          DOI: 10.1083/jcb.56.3.746

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  19 in total

1.  Turnover of constituents of the endoplasmic reticulum membranes of rat hepatocytes.

Authors:  T Omura; P Siekevitz; G E Palade
Journal:  J Biol Chem       Date:  1967-05-25       Impact factor: 5.157

2.  Pharmacological implications of microsomal enzyme induction.

Authors:  A H Conney
Journal:  Pharmacol Rev       Date:  1967-09       Impact factor: 25.468

3.  Studies on cellular autophagocytosis. The formation of autophagic vacuoles in the liver after glucagon administration.

Authors:  A U Arstila; B F Trump
Journal:  Am J Pathol       Date:  1968-11       Impact factor: 4.307

4.  The effect of phenobarbital on the turnover of microsomal phospholipid in male and female rats.

Authors:  J L Holtzman; J R Gillette
Journal:  J Biol Chem       Date:  1968-06-10       Impact factor: 5.157

5.  Hypertrophy of the agranular endoplasmic reticulum in hamster liver induced by phenobarbital (with a review on the functions of this organelle in liver).

Authors:  A L Jones; D W Fawcett
Journal:  J Histochem Cytochem       Date:  1966-03       Impact factor: 2.479

6.  Cell junctions in amphibian skin.

Authors:  M G Farquhar; G E Palade
Journal:  J Cell Biol       Date:  1965-07       Impact factor: 10.539

7.  The ultrastructural basis of capillary permeability studied with peroxidase as a tracer.

Authors:  M J Karnovsky
Journal:  J Cell Biol       Date:  1967-10       Impact factor: 10.539

8.  Electron microscopic examination of subcellular fractions. II. Quantitative analysis of the mitochondrial population isolated from rat liver.

Authors:  P Baudhuin; J Berthet
Journal:  J Cell Biol       Date:  1967-12       Impact factor: 10.539

9.  Enzyme-membrane relationship in phenobarbital induction of synthesis of drug-metabolizing enzyme system and proliferation of endoplasmic membranes.

Authors:  S Orrenius; J L Ericsson
Journal:  J Cell Biol       Date:  1966-02       Impact factor: 10.539

10.  A quantitative stereological description of the ultrastructure of normal rat liver parenchymal cells.

Authors:  A V Loud
Journal:  J Cell Biol       Date:  1968-04       Impact factor: 10.539

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Journal:  Proc Natl Acad Sci U S A       Date:  1984-09       Impact factor: 11.205

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Journal:  PLoS One       Date:  2010-01-06       Impact factor: 3.240

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