Pharmacological responses to pentobarbital in different strains of mice

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Abstract

This study was designed to assess the strain differences in pentobarbital toxicity, narcosis, the development of tolerance and physical dependence, the half-life of pentobarbital and the activities of hepatic microsomal electron transfer chain in DBA/2J, C57BL/6J and ICR mice. The comparisons of responses to acute pentobarbital-induced narcosis with two different doses revealed that DBA was most sensitive among these strains. When continuous administration of pentobarbital by pentobarbital pellet implantation is concerned, four criteria were used to assess strain differences: determination of the duration of the loss of righting reflex during phenobarbital pellet implantation; cumulative mortality after pentobarbital pellet implantation; degree of tolerance development after 3 days of s.c. implantation of a 75-mg pentobarbital pellet by the relative decrease in the pentobarbital sleeping time; and assessment of hyperexcitability by pentylenetetrazol- and audiogenic-induced seizures after pellet removal. The order of susceptibility to continuous pentobarbital pellet implantation was found to be as follows: DBA/2J > C57BL/6J > ICR. The biochemical data also revealed that the half-life of pentobarbital in DBA/2J mice was significantly longer than that of C57BL/6J or ICR mice in both brain and serum. Further studies also showed that DBA/2J mice have lower hepatic cytochrome P-450 and cytochrome b5 levels and NADPH dehydrogenase and NADPH-cytochrome c reductase activities as compared with the other strains of mice. However, these parameters were markedly induced in DBA/2J mice after the development of tolerance to pentobarbital. It appears that the differences in genetic variation could be of importance for further studies in gaining insight of the mechanism of barbiturate tolerance and dependence.

Original languageEnglish
Pages (from-to)198-204
Number of pages7
JournalJournal of Pharmacology and Experimental Therapeutics
Volume216
Issue number1
Publication statusPublished - 01-01-1981
Externally publishedYes

Fingerprint

Pentobarbital
Pharmacology
Inbred DBA Mouse
Stupor
Inbred ICR Mouse
Inbred C57BL Mouse
Half-Life
Righting Reflex
Cytochromes b5
NADPH Dehydrogenase
NADPH-Ferrihemoprotein Reductase
Pentylenetetrazole
Liver
Phenobarbital
Cytochrome P-450 Enzyme System
Seizures
Electrons

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Pharmacology

Cite this

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title = "Pharmacological responses to pentobarbital in different strains of mice",
abstract = "This study was designed to assess the strain differences in pentobarbital toxicity, narcosis, the development of tolerance and physical dependence, the half-life of pentobarbital and the activities of hepatic microsomal electron transfer chain in DBA/2J, C57BL/6J and ICR mice. The comparisons of responses to acute pentobarbital-induced narcosis with two different doses revealed that DBA was most sensitive among these strains. When continuous administration of pentobarbital by pentobarbital pellet implantation is concerned, four criteria were used to assess strain differences: determination of the duration of the loss of righting reflex during phenobarbital pellet implantation; cumulative mortality after pentobarbital pellet implantation; degree of tolerance development after 3 days of s.c. implantation of a 75-mg pentobarbital pellet by the relative decrease in the pentobarbital sleeping time; and assessment of hyperexcitability by pentylenetetrazol- and audiogenic-induced seizures after pellet removal. The order of susceptibility to continuous pentobarbital pellet implantation was found to be as follows: DBA/2J > C57BL/6J > ICR. The biochemical data also revealed that the half-life of pentobarbital in DBA/2J mice was significantly longer than that of C57BL/6J or ICR mice in both brain and serum. Further studies also showed that DBA/2J mice have lower hepatic cytochrome P-450 and cytochrome b5 levels and NADPH dehydrogenase and NADPH-cytochrome c reductase activities as compared with the other strains of mice. However, these parameters were markedly induced in DBA/2J mice after the development of tolerance to pentobarbital. It appears that the differences in genetic variation could be of importance for further studies in gaining insight of the mechanism of barbiturate tolerance and dependence.",
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Pharmacological responses to pentobarbital in different strains of mice. / Nabeshima, Toshitaka; Ho, I. K.

In: Journal of Pharmacology and Experimental Therapeutics, Vol. 216, No. 1, 01.01.1981, p. 198-204.

Research output: Contribution to journalArticle

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