Protective effect of carnosine on febrile seizures in immature mice
•Carnosine attenuated FSs through increasing the latency and decreasing the duration.•The inhibitory effects of carnosine were through its conversion to histamine.•Carnosine caused a decrease of glutamate but not GABA levels. Febrile seizures (FSs) are the most common type of convulsions in childhoo...
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Published in | Neuroscience letters Vol. 588; pp. 95 - 100 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Ireland
Elsevier Ireland Ltd
19.02.2015
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Subjects | |
Online Access | Get full text |
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Summary: | •Carnosine attenuated FSs through increasing the latency and decreasing the duration.•The inhibitory effects of carnosine were through its conversion to histamine.•Carnosine caused a decrease of glutamate but not GABA levels.
Febrile seizures (FSs) are the most common type of convulsions in childhood and complex FSs represent an increased risk for development of temporal lobe epilepsy. The aim of this study was to analyze the anticonvulsant effects of carnosine, an endogenous dipeptide composed of alanine and histidine, on hyperthermia induced seizure in immature mice. Injection of carnosine significantly increased the latency and decreased the duration of FSs in a dose-dependent manner. In addition, histidine had similar effects on FSs as carnosine. The protective effect of carnosine or histidine was completely abolished by α-fluoromethylhistidine (α-FMH), a selective and irreversible histidine decarboxylase inhibitor, or in histidine decarboxylase deficient (HDC-KO) mice. Peripheral carnosine administration increased the level of carnosine, histidine and histamine in the cortex and hippocampus of mice pups, but decreased glutamate contents in the cortex and hippocampus. These results indicate that carnosine can protect against FSs in mice pups through its conversion to histamine, suggesting that it may serve as an efficient anti-FSs drug in the future. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0304-3940 1872-7972 1872-7972 |
DOI: | 10.1016/j.neulet.2014.12.061 |