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Dopamine and cyclic AMP‐regulated phosphoprotein‐32 phosphorylation pattern in cocaine and morphine‐sensitized rats
Author(s) -
Scheggi S.,
Rauggi R.,
Gambarana C.,
Tagliamonte A.,
De Montis M. G.
Publication year - 2004
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.2004.02510.x
Subject(s) - phosphoprotein , phosphorylation , morphine , dopamine , chemistry , pharmacology , medicine , endocrinology , biochemistry
This study reports some of the modifications in dopaminergic signalling that accompany cocaine and morphine behavioural sensitization. Cocaine‐sensitized rats showed increased phosphorylation of dopamine‐ and cyclic AMP‐regulated phosphoprotein Mr 32 kDa (DARPP‐32) at threonine‐75 (Thr75) and decreased DARPP‐32 phosphorylation at Thr34, in the caudate–putamen (CPu) and nucleus accumbens (NAc) 7 days after sensitization assessment. Conversely, in morphine‐sensitized rats, no apparent modifications in DARPP‐32 phosphorylation pattern were observed. Morphine‐sensitized rats have increased binding and coupling of µ‐opioid receptors and increased dopaminergic transmission in striatal areas and, upon morphine challenge, exhibit dopamine D1 receptor‐dependent stereotypies. Thus, the DARPP‐32 phosphorylation pattern was studied in morphine‐sensitized rats at different times after morphine challenge. Morphine challenge increased levels of phospho‐Thr75 DARPP‐32 and decreased levels of phospho‐Thr34 DARPP‐32 in a time‐dependent manner in the CPu and NAc. In order to assess whether these modifications were related to modified cyclic AMP‐dependent protein kinase (PKA) activity, the phosphorylation levels of two other PKA substrates were examined, the GluR1 and NR1 subunits of α‐amino‐3‐hydroxy‐5‐methylisoxazole‐4‐propionate and NMDA receptors respectively. The phosphorylation levels of GluR1 and NR1 subunits decreased in parallel with those of phospho‐Thr‐34 DARPP‐32, supporting the hypothesis that morphine challenge elicited a decrease in PKA activity in morphine‐sensitized rats.