Administration of aspartame potentiates pentylenetetrazole-induced and fluorothyl-induced seizures in mice

Pinto, JMB; Maher, TJ

HERO ID

31527

Reference Type

Journal Article

Year

1988

Language

English

PMID

3352866

HERO ID 31527
In Press No
Year 1988
Title Administration of aspartame potentiates pentylenetetrazole-induced and fluorothyl-induced seizures in mice
Authors Pinto, JMB; Maher, TJ
Journal Neuropharmacology
Volume 27
Issue 1
Page Numbers 51-55
Abstract An association has recently been proposed between the incidence of seizures and prolonged consumption of the phenylalanine-containing artificial sweetener, aspartame. Since consumption of aspartame, unlike dietary protein, can elevate phenylalanine in brain, and thereby inhibit the synthesis and release of neurotransmitters known to protect against seizure activity, the effect of oral doses of aspartame on the sensitivity of mice to the proconvulsant agents, pentylenetetrazole and fluorothyl was studied. Doses of aspartame were used which increased phenylalanine more than tyrosine in brain, as occurs in humans after the consumption of any dose of aspartame. Pretreatment with aspartame significantly increased the percentage of animals convulsing after administration of pentylenetetrazole and significantly lowered the CD50 for this convulsant. The average time to onset of seizures induced by fluorothyl in control mice was 510 sec; pretreatment with oral doses of 1000, 1500 and 2000 mg/kg of aspartame 1 hr earlier significantly reduced the time required to elicit seizures (394, 381 and 339 sec, respectively). The seizure-promoting effect of aspartame could be demonstrated 30, 60 or 120 min after the 1000 mg/kg dose. The seizures induced by either convulsant were potentiated by equimolar amounts of phenylalanine, a major endogenous metabolite of aspartame, while the other metabolites, aspartic acid and methanol, were without effect. Administration together with aspartame of the large neutral amino acid valine, which competes with phenylalanine for entry into the brain, completely abolished the seizure-promoting effect of aspartame.(ABSTRACT TRUNCATED AT 250 WORDS)
Doi 10.1016/0028-3908(88)90200-6
Pmid 3352866
Is Certified Translation No
Dupe Override No
Comments Neuropharmacology 27: 51-55.
Is Public Yes
Language Text English
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