Literature DB >> 4094625

Distribution of fentanyl in rats: an autoradiographic study.

E Schneider, K Brune.   

Abstract

Unexpected respiratory depression reported to have occurred up to 2 h after neurolept analgesia with fentanyl has been proposed to be a redistribution phenomenon due to a gastro-entero systemic recirculation of fentanyl sequestered in the stomach. In the study presented here, this redistribution hypothesis was tested by employing whole-body autoradiography (WBAR) in two series of time-course experiments, designated to further elucidate the distribution of intravenously administered fentanyl which was radiolabelled in different parts of the molecule respectively. However, there was no evidence of a secondary accumulation of radioactivity in the brain. The possibility that fentanyl trapped in the stomach may be reabsorbed as it passes through the small intestines was investigated by intragastric administration of the drug. Its oral bioavailability was found to be only 1.5%. Also, evidence of a strong metabolic effect was obtained by analysis employing high performance thin-layer chromatography (HPTLC). In conclusion, the results obtained from this work do not support the hypothesis that the fentanyl rebound effect is due to a secondary rise in brain levels of the parent drug and its major metabolites, an event which could be brought about by reabsorption of fentanyl sequestered in the stomach.

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Year:  1985        PMID: 4094625     DOI: 10.1007/BF00500820

Source DB:  PubMed          Journal:  Naunyn Schmiedebergs Arch Pharmacol        ISSN: 0028-1298            Impact factor:   3.000


  10 in total

1.  Pharmacokinetics of fentanyl in rabbits in view of the importance for limiting the effect.

Authors:  R Hess; A Herz; K Friedel
Journal:  J Pharmacol Exp Ther       Date:  1971-12       Impact factor: 4.030

2.  [Fentanyl pharmacokinetics and postoperative respiratory depression (author's transl)].

Authors:  K A Lehmann; J Freier; D Daub
Journal:  Anaesthesist       Date:  1982-03       Impact factor: 1.041

3.  Antibodies to fentanyl.

Authors:  G L Henderson; J Frincke; C Y Leung; M Torten; E Benjamini
Journal:  J Pharmacol Exp Ther       Date:  1975-02       Impact factor: 4.030

4.  Plasma fentanyl concentrations and the occurrence of respiratory depression in volunteers.

Authors:  H Stoeckel; J Schüttler; H Magnussen; J H Hengstmann
Journal:  Br J Anaesth       Date:  1982-10       Impact factor: 9.166

5.  Delayed respiratory depression after use of fentanyl during anaesthesia.

Authors:  A P Adams; D A Pybus
Journal:  Br Med J       Date:  1978-02-04

6.  Differences in the autoradiographic localization of labelled morphine-like analgesics in the mouse.

Authors:  L E Appelgren; L Terenius
Journal:  Acta Physiol Scand       Date:  1973-06

7.  Pharmacokinetics of fentanyl as a possible explanation for recurrence of respiratory depression.

Authors:  H Stoeckel; J H Hengstmann; J Schüttler
Journal:  Br J Anaesth       Date:  1979-08       Impact factor: 9.166

8.  Biphasic respiratory depression after fentanyldroperidol or fentanyl alone used to supplement nitrous oxide anesthesia.

Authors:  L D Becker; B A Paulson; R D Miller; J W Severinghaus; E I Eger
Journal:  Anesthesiology       Date:  1976-04       Impact factor: 7.892

9.  [Biotransformation of fentanyl. III. Effect of chronic drug exposure on the distribution, metabolism and excretion in the rat].

Authors:  K A Lehmann; L Hunger; K Brandt; D Daub
Journal:  Anaesthesist       Date:  1983-04       Impact factor: 1.041

10.  [I. Metabolism by mouse tissue homogenates in vitro (author's transl)].

Authors:  K A Lehmann; G Möseler; D Daub
Journal:  Anaesthesist       Date:  1981-09       Impact factor: 1.041

  10 in total
  1 in total

1.  Comparative physiological pharmacokinetics of fentanyl and alfentanil in rats and humans based on parametric single-tissue models.

Authors:  S Björkman; D R Wada; D R Stanski; W F Ebling
Journal:  J Pharmacokinet Biopharm       Date:  1994-10
  1 in total

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