Abstract
Daily administration of FMH to neonatal rats produced long-lasting inhibition of histidine decarboxylase in hypothalamus and cerebral cortex and led to depletion of histamine in both brain regions. The onset of depletion was more rapid in cerebral cortex, a region in which non-neurotransmitter pools of histamine predominate in early postnatal life, appearing as early as postnatal day 3; depletion in the hypothalamus, a region rich in histaminergic neuronal projections, appeared later. No effects were seen on body or brain growth, nor was development of other biogenic amine systems affected. FMH thus provides a selective probe for examining the role of histamine in brain development.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Aging
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Animals
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Animals, Newborn
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Carboxy-Lyases / antagonists & inhibitors*
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Catecholamines / metabolism*
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Cerebral Cortex / drug effects
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Cerebral Cortex / enzymology
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Cerebral Cortex / growth & development*
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Dopamine / metabolism
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Histamine / metabolism*
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Histidine / analogs & derivatives*
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Histidine Decarboxylase / antagonists & inhibitors*
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Hypothalamus / drug effects
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Hypothalamus / enzymology
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Hypothalamus / growth & development*
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Methylhistidines / pharmacology*
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Norepinephrine / metabolism
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Rats
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Rats, Inbred Strains
Substances
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Catecholamines
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Methylhistidines
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Histidine
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alpha-fluoromethylhistidine
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Histamine
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Carboxy-Lyases
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Histidine Decarboxylase
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Dopamine
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Norepinephrine