Effect of sequence of administration on the pharmacokinetic interaction between the anticholinergic drug biperiden and [3H]Quinuclidinyl benzylate or [3H]N-Methylscopolamine in rats

Junko Ishizaki, Koichi Yokogawa, Emi Nakashima, Tatsunori Takayasu, Tohru Ohshima, Fujio Ichimura

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Abstract

In rats the pharmacokinetic interactions between the anticholinergic drug biperiden and [3H]quinuclidinyl benzylate ([3H]QNB) or [3H]N-methylscopolamine ([3H]NMS) is affected by the sequence in which the drugs are administered. Drug concentrations in various tissues were determined after intravenous administration of [3H]QNB or [3H]NMS (325 ng kg-1). Biperiden (6.4 mg kg-1) was administered either 5 min before, concomitantly with or 20 min after injection of [3H]QNB or [3H]NMS. When biperiden was administered concomitantly with or before [3H]QNB, distribution of [3H]QNB among the regions of the brain and other tissues was reduced; at 4 h the ratio of the distribution of [3H]QNB for experimental animals to that for control animals ranged from 0.15 to 0.9. When biperiden was administered after [3H]QNB, the distribution of [3H]QNB in the brain and other tissues was significantly higher than for the other two treatments (P < 0.01). However, for [3H]NMS the sequence of administration had no effect on the distribution of the drug in the brain and other tissues except for the kidney. In-vitro, in crude synaptosomal membranes, the amount of [3H]QNB at 2 h relative to the control concentration at equilibrium was 87% when biperiden was added before [3H]QNB and 56% when biperiden was added after [3H]QNB. In both instances the concentration of [3H]NMS reached equilibrium within 30 min. These findings suggest that the difference between the rate constant of association and dissociation at the possible site of action gives rise to the effect of the sequence of administration on the pharmacokinetic interaction.

Original languageEnglish
Pages (from-to)189-196
Number of pages8
JournalJournal of Pharmacy and Pharmacology
Volume50
Issue number2
Publication statusPublished - 1998 Feb

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Biperiden
N-Methylscopolamine
Cholinergic Antagonists
Pharmacokinetics
Pharmaceutical Preparations
Brain
Intravenous Administration
Kidney
Injections
Membranes

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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Effect of sequence of administration on the pharmacokinetic interaction between the anticholinergic drug biperiden and [3H]Quinuclidinyl benzylate or [3H]N-Methylscopolamine in rats. / Ishizaki, Junko; Yokogawa, Koichi; Nakashima, Emi; Takayasu, Tatsunori; Ohshima, Tohru; Ichimura, Fujio.

In: Journal of Pharmacy and Pharmacology, Vol. 50, No. 2, 02.1998, p. 189-196.

Research output: Contribution to journalArticle

Ishizaki, Junko ; Yokogawa, Koichi ; Nakashima, Emi ; Takayasu, Tatsunori ; Ohshima, Tohru ; Ichimura, Fujio. / Effect of sequence of administration on the pharmacokinetic interaction between the anticholinergic drug biperiden and [3H]Quinuclidinyl benzylate or [3H]N-Methylscopolamine in rats. In: Journal of Pharmacy and Pharmacology. 1998 ; Vol. 50, No. 2. pp. 189-196.
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abstract = "In rats the pharmacokinetic interactions between the anticholinergic drug biperiden and [3H]quinuclidinyl benzylate ([3H]QNB) or [3H]N-methylscopolamine ([3H]NMS) is affected by the sequence in which the drugs are administered. Drug concentrations in various tissues were determined after intravenous administration of [3H]QNB or [3H]NMS (325 ng kg-1). Biperiden (6.4 mg kg-1) was administered either 5 min before, concomitantly with or 20 min after injection of [3H]QNB or [3H]NMS. When biperiden was administered concomitantly with or before [3H]QNB, distribution of [3H]QNB among the regions of the brain and other tissues was reduced; at 4 h the ratio of the distribution of [3H]QNB for experimental animals to that for control animals ranged from 0.15 to 0.9. When biperiden was administered after [3H]QNB, the distribution of [3H]QNB in the brain and other tissues was significantly higher than for the other two treatments (P < 0.01). However, for [3H]NMS the sequence of administration had no effect on the distribution of the drug in the brain and other tissues except for the kidney. In-vitro, in crude synaptosomal membranes, the amount of [3H]QNB at 2 h relative to the control concentration at equilibrium was 87{\%} when biperiden was added before [3H]QNB and 56{\%} when biperiden was added after [3H]QNB. In both instances the concentration of [3H]NMS reached equilibrium within 30 min. These findings suggest that the difference between the rate constant of association and dissociation at the possible site of action gives rise to the effect of the sequence of administration on the pharmacokinetic interaction.",
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