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Studies on drug metabolism and liver ultrastructure after conjoint treatment with pregnenolone-16alpha-carbonitrile and dl-ethionine.

Abstract
Zoxazolamine paralysis, hexobarbital anesthesia and digitoxin convulsions were diminished in rats by 3 days of pretreatment with pregnenolone-16alpha-carbonitrile (PCN). Simultaneous injection of dl-ethionine did not block this effect of PCN. Dl-Ethionine decreased, while PCN or PCN + ethionene increased, zoxazolamine metabolism by the 9,000g supernatant fraction of the liver. Dl-ethionine neutralized the influence of PCN and phenobarbital on zoxazolamine metabolism in rats that were pretreated with PCN or phenobarbital for 1 day, and it inhibited the action of phenobarbital on hexobarbital anesthesia. PCN augmented the liver weight of animals given dl-ehtionine whereas dl-ethionine in itself did not. PCN produced SER proliferation in hepatocytes and dl-ethionine caused lipid accumulation, SER proliferation and myelin-figure formation. When administered conjointly, these compounds had an additive effect on the liver cell ultrastructure.
AuthorsB D Garg, P Kourounakis, B Tuchweber, S Szabo, K Kovacs
JournalArchives internationales de pharmacodynamie et de therapie (Arch Int Pharmacodyn Ther) Vol. 227 Issue 2 Pg. 283-93 (Jun 1977) ISSN: 0003-9780 [Print] Belgium
PMID907413 (Publication Type: Journal Article)
Chemical References
  • Pharmaceutical Preparations
  • Pregnenolone Carbonitrile
  • Zoxazolamine
  • Hexobarbital
  • Digitoxin
  • Ethionine
  • Phenobarbital
Topics
  • Animals
  • Digitoxin (pharmacology)
  • Drug Interactions
  • Ethionine (pharmacology)
  • Female
  • Hexobarbital (pharmacology)
  • In Vitro Techniques
  • Liver (drug effects, ultrastructure)
  • Microscopy, Electron
  • Paralysis (chemically induced, physiopathology)
  • Pharmaceutical Preparations (metabolism)
  • Phenobarbital (pharmacology)
  • Pregnenolone Carbonitrile (pharmacology)
  • Rats
  • Seizures (chemically induced, physiopathology)
  • Sleep (drug effects)
  • Zoxazolamine (metabolism, pharmacology)

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