Cocaine self-administration differentially alters mRNA expression of striatal peptides
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Dynorphin
Ventral striatum
Using a combination of radioactive and non-radioactive in situ hybridization, the μ opioid receptor mRNA was localized in enkephalin as well as dynorphin neurones of the rat striatum. The proportion of enkephalin neurones showing co-localized μ opioid receptor mRNA was dependent on the rostrocaudal level (17–39% in rostral/ intermediate levels vs 0.4–5% caudally) but did not differ between striatal subregions. For dynorphin neurones the reverse was true, with consistently higher levels of co-localization in the caudate-putamen (56–77%) than the nucleus accumbens (15–43%), but no differences along the rostrocaudal axis. Furthermore, the degree of enkephalin/μ co-localization was significantly lower than that of dynorphin/μ. These results suggest a finegrained topological differentiation of μ receptor modulation of striatal opioid systems.
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Dynorphin A
Ventral striatum
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Proenkephalin
Ventral striatum
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κ-opioid receptor
Mesolimbic pathway
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A subpopulation of projection neurons in the nucleus accumbens uses the neuropeptide enkephalin as a neurotransmitter. The synthesis of enkephalin in striatal neurons is regulated by dopaminergic inputs. In the present study quantitative in situ hybridization histochemistry was used to examine the effects of unilateral 6-hydroxydopamine lesions of the ascending dopaminergic fibres on levels of enkephalin mRNA in subregions of the nucleus accumbens. It was found that the levels of enkephalin mRNA were increased throughout the nucleus after the lesion. However, the increase appeared to be much higher in rostral parts of the nucleus than in caudal parts, indicating regional differences in the effects of blockade of the dopaminergic neurotransmission. Possible causative factors for these differences are discussed.
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Proenkephalin
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Endogenous opioid
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Dynorphin A
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Proenkephalin
Dynorphin A
Putamen
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