Catalepsy induced by α-methyl-p-tyrosine and d-amphetamine: The rÔle of catecholamine metabolism |
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Authors: | Dr A C Sayers Sheila L Handley |
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Institution: | (1) The Department of Pharmacy, The University of Aston in Birmingham, Gosta Green, Birmingham 4, England;(2) Present address: Research Institute Wander (a Sandoz research unit), Berne, Switzerland |
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Abstract: | The effect of inhibition of monoamine oxidase (MAO), catechol-O-methyltransferase (COMT) and Dopa-decarboxylase on the catalepsy induced by d-amphetamine in -methyl-p-tyrosine ( -MpT) treated rats has been investigated.Administration of an MAO inhibitor concomitant with -MpT slightly antagonized the cataleptic state, but when given 2 h later was without an appreciable effect. Only when an inhibitor was injected at an extremely high dose level 18 h prior to -MpT did catalepsy fail to develop.Following COMT inhibition the cataleptic state was enhanced. After Dopa decarboxylase inhibition the catalepsy developed as usual for the first 3 h post-amphetamine, but then declined in intensity.It is concluded that neither deaminated nor O-methylated products are responsible for the development of catalepsy. In fact, the indication is that the catalepsy may be antagonised by an O-methylated derivative. A possible explanation for the action of the Dopa decarboxylase inhibitor is discussed. |
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Keywords: | Catalepsy Catecholamine Metabolism Amphetamine -Methyl-p-tyrosine" target="_blank">gif" alt="agr" align="BASELINE" BORDER="0">-Methyl-p-tyrosine |
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