Literature DB >> 3128813

Phenobarbitone: adverse effects on reproductive performance and offspring development in the Mongolian gerbil, (Meriones unguiculatus).

J B Chapman1, M G Cutler.   

Abstract

Phenobarbitone at a concentration of 500 mg/l in drinking fluid of gerbils during pregnancy (60 mg/kg) and lactation (136 mg/kg) markedly reduced the proportion of animals bearing litters, decreased pup weights at birth and during later life and delayed development of the self-righting reflex, auditory startle reaction, eye opening and full fur coverage. It also prolonged the period of suckling. Scars of implantation were evident in uterine horns of 60% of treated and in none of control females that had failed to give birth. Treated offspring after weaning were given phenobarbitone (500 mg/l; 42-124 mg/kg) as their drinking fluid throughout life and a further group of gerbils received this concentration of the drug from the time of weaning. Seizure susceptibility was unaltered by the drug treatment, and the only evidence of behavioural change was seen in offspring gerbils at 6 weeks when the bout length of social investigation during encounters was increased. Drug-treated offspring showed no abnormality in brain weight relative to body weight. Weight gain and brain weight remained normal among the gerbils given phenobarbitone after weaning. The drug treatment reduced scent gland size in breeding males, though not in the offspring, and had no effect on weights of the testes or ovaries and uterus. no effect on weights of the testes or ovaries and uterus. Plasma concentrations of phenobarbitone in females of the postweaning group amounted on average to 4.4 mg/kg. Most of the adverse effects of this dose of phenobarbitone in the gerbil can thus be seen to be associated either with reproductive impairment or with exposure during sensitive periods of early development.

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Year:  1988        PMID: 3128813     DOI: 10.1007/bf00174691

Source DB:  PubMed          Journal:  Psychopharmacology (Berl)        ISSN: 0033-3158            Impact factor:   4.530


  43 in total

1.  Placental transfer of phenobarbitone in epileptic women, and elimination in newborns.

Authors:  J C Melchior; O Svensmark; D Trolle
Journal:  Lancet       Date:  1967-10-21       Impact factor: 79.321

2.  Letter: Anticonvulsant drugs and congenital abnormalities.

Authors:  J M Aase
Journal:  Am J Dis Child       Date:  1974-05

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Authors:  W M Fox
Journal:  Anim Behav       Date:  1965 Apr-Jul       Impact factor: 2.844

4.  Phenytoin and phenobarbitone plasma clearance during pregnancy.

Authors:  K I Mygind; M Dam; J Christiansen
Journal:  Acta Neurol Scand       Date:  1976-08       Impact factor: 3.209

5.  Autoradiographic study of phenobarbital's effect on development of the central nervous system.

Authors:  J Yanai; M Woolf; J J Feigenbaum
Journal:  Exp Neurol       Date:  1982-11       Impact factor: 5.330

6.  Growth retardation, dysmorphic facies and minor malformations following massive exposure to phenobarbitone in utero.

Authors:  M Seip
Journal:  Acta Paediatr Scand       Date:  1976-09

7.  Anticonvulsant serum levels: relationship to impairments of cognitive functioning.

Authors:  P J Thompson; M R Trimble
Journal:  J Neurol Neurosurg Psychiatry       Date:  1983-03       Impact factor: 10.154

8.  Phenobarbital: effects of long-term administration on behavior and brain of artificially reared rats.

Authors:  J Diaz; R J Schain
Journal:  Science       Date:  1978-01-06       Impact factor: 47.728

Review 9.  The pregnant epileptic: a review and recommendations.

Authors:  G D Montouris; G M Fenichel; L W McLain
Journal:  Arch Neurol       Date:  1979-10

10.  Placental transfer of anticonvulsants (phenobarbital, phenytoin, valproic acid) and the elimination from neonates.

Authors:  T Ishizaki; K Yokochi; K Chiba; T Tabuchi; T Wagatsuma
Journal:  Pediatr Pharmacol (New York)       Date:  1981
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