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. 1987;69(3-4):221-8.
doi: 10.1007/BF01244343.

Striatal membrane-bound and soluble catechol-O-methyl-transferase after selective neuronal lesions in the rat

Striatal membrane-bound and soluble catechol-O-methyl-transferase after selective neuronal lesions in the rat

S Kaakkola et al. J Neural Transm. 1987.

Abstract

Activities of the two forms of catechol-O-methyltransferase (COMT), viz. the soluble (S-COMT) and the membrane-bound (MB-COMT), have been studied in the rat striatum to characterize their localization in relation to the nigrostriatal dopaminergic neurons. Selective unilateral nigrostriatal dopaminergic lesions were produced by an intranigral injection of 6-hydroxydopamine (6-OHDA; 8 micrograms/site). 6-OHDA caused an extensive lesion of the dopaminergic neurons as revealed by non-detectable concentrations of dopamine in the striata of the lesioned sites. In spite of that neither S-COMT nor MB-COMT activities were altered in comparison with the intact control striata. The intrastriatal injection of kainic acid significantly increased S-COMT activity but to some extent decreased MB-COMT activity. Kainic acid did not alter the striatal concentration of dopamine. These results suggest that both S-COMT and MB-COMT reside postsynaptically the nigrostriatal dopaminergic neurons. S-COMT seems to be found mainly in striatal glial cells, whereas striatal MB-COMT might be located both in postsynaptic neuronal and extraneuronal cells.

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References

    1. Brain Res. 1972 Jun 8;41(1):245-8 - PubMed
    1. J Comp Neurol. 1978 Jul 15;180(2):301-23 - PubMed
    1. Biochem Pharmacol. 1980 Nov 15;29(22):3119-22 - PubMed
    1. J Neurochem. 1984 Mar;42(3):826-32 - PubMed
    1. Anal Biochem. 1984 Feb;137(1):69-73 - PubMed

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