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-hydroxybutyrahe
Department of pediatrics (Dr. Snead), Biomedical Engineering (Dr. Bearden), and the Neuroscience Program, University of Alabama School of Medicine, Birmingham, AL.
The specific opiate antagonistsnaloxone and naltrexoneattenuated or abolished the electrical seizure activity, behavioral abnormalities, and increased striatal dopamine content produced by
-butyrolactone, the prodrug of
-hydroxybutyrate. The effects of naloxone and naltrexone were dose-dependent. These data suggest that
-hydroxybutyric acid exerts its effects by action either at the opiate receptor or on enkephalinergic systems, which may be involved in petit mal epilepsy.
Address correspondence and reprint requests to Dr. Snead, 1601 6th Avenue South, Birmingham, AL 35233
Accepted for publication October 15, 1979.
Presented in part at the thirty-first annual meeting of the American Academy of Neurology, Chicago, IL, April 1979.
This article has been cited by other articles:
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M. Trabucchi, S. Bassi, and L. Frattola Effect of Naloxone on the 'On-Off' Syndrome in Patients Receiving Long-term Levodopa Therapy Arch Neurol, February 1, 1982; 39(2): 120 - 121. [Abstract] [PDF] |
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O. Snead 3rd and L. Bearden Anticonvulsants specific for petit mal antagonize epileptogenic effect of leucine enkephalin Science, November 28, 1980; 210(4473): 1031 - 1033. [Abstract] [PDF] |
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