Literature DB >> 103773

Effect or oral administration of propylene glycol on the induction of enzymes and proteins in microsomes and cytosol of the rat liver.

T Yamamoto, Y Adachi.   

Abstract

Male Wistar rats were divided into 4 groups, receiving water, propylene glycol (PG), sodium phenobarbital (PB) and PB + PG, respectively. After oral administration of these materials for 7 days, various enzymes in hepatic microsomes and the binding capacity of Y and Z fractions in the cytosol were assayed. As compared with the water group, the aniline hydroxylase activity, the cytochrome b5 content and the amount of Z fraction increased in the PG group. As compared with the PB group, the microsomal protein increased but the activities of paranitrophenol-UDP-glucuronyltransferase (pNP-GT) and aminopyrine demethylase (AD) decreased in the PB + PG group. When the PB + PG group and the PG group were compared with the PB group and the water group respectively, there was no parallel change. Even though PG added to hepatic microsomes of untreated rats in vitro, there was no change in the difference spectrum produced by binding of cytochrome p-450 and aniline and also in the activities of AH and pNP-GT. Based on these observations, it can be concluded that PG affected the in vitro assay data of drug-metabolizing enzyme without changing the cytochrome P-450 content by its certain in vivo action rather than by its direct interaction with microsomes, and modified the effect of PB on the microsomal enzymes and the cytosol proteins. Therefore, it is not appropriate to investigate the effect of the drugs on enzymes and proteins of the liver cell by the use of PG as a solvent.

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Year:  1978        PMID: 103773     DOI: 10.1007/bf02776012

Source DB:  PubMed          Journal:  Gastroenterol Jpn        ISSN: 0435-1339


  10 in total

1.  Influence of drugs and chemical upon hepatic enzymes and proteins-I. Structure-activity relationship between various barbiturates and microsomal enzyme induction in rat liver.

Authors:  Y Adachi; T Yamamoto
Journal:  Biochem Pharmacol       Date:  1976-03-15       Impact factor: 5.858

2.  THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. II. SOLUBILIZATION, PURIFICATION, AND PROPERTIES.

Authors:  T OMURA; R SATO
Journal:  J Biol Chem       Date:  1964-07       Impact factor: 5.157

3.  THE CARBON MONOXIDE-BINDING PIGMENT OF LIVER MICROSOMES. I. EVIDENCE FOR ITS HEMOPROTEIN NATURE.

Authors:  T OMURA; R SATO
Journal:  J Biol Chem       Date:  1964-07       Impact factor: 5.157

4.  Biochemical and pharmacological changes in the rat following chronic administration of morphine nalorphine and normorphine.

Authors:  J COCHIN; J AXELROD
Journal:  J Pharmacol Exp Ther       Date:  1959-02       Impact factor: 4.030

Review 5.  Toxicology, metabolism, and biochemistry of 1,2-propanediol.

Authors:  J A Ruddick
Journal:  Toxicol Appl Pharmacol       Date:  1972-01       Impact factor: 4.219

6.  Evidence for biochemically different types of vesicles in the hepatic microsomal fraction.

Authors:  Y Imai; A Ito; R Sato
Journal:  J Biochem       Date:  1966-10       Impact factor: 3.387

7.  Propylene glycol as a drug solvent in the study of hepatic microsomal enzyme metabolism in the rat.

Authors:  M E Dean; B H Stock
Journal:  Toxicol Appl Pharmacol       Date:  1974-04       Impact factor: 4.219

8.  Propylene glycol as a drug solvent in pharmacologic studies.

Authors:  J F Zaroslinski; R K Browne; L H Possley
Journal:  Toxicol Appl Pharmacol       Date:  1971-08       Impact factor: 4.219

9.  Stimulation of hepatic microsomal aniline p-hydroxylase activity by dimethyl sulfoxide administration to rats.

Authors:  B H Stock; A R Hansen; J R Fouts
Journal:  Toxicol Appl Pharmacol       Date:  1970-05       Impact factor: 4.219

10.  Two hepatic cytoplasmic protein fractions, Y and Z, and their possible role in the hepatic uptake of bilirubin, sulfobromophthalein, and other anions.

Authors:  A J Levi; Z Gatmaitan; I M Arias
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808

  10 in total

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