Recent evidence suggest that antagonism of adenosine A(2A) receptors represent an alternative therapeutic approach to Parkinson's disease (PD). Coactivation of A(2A) and the glutamate subtype 5 metabotropic receptors (mGlu(5)) synergistically stimulates DARPP-32 phosphorylation and c-fos expression in the striatum, This study therefore tested the effects of a joint blockade of these receptor's to alleviate the motor dysfunction in a rat model of PD. 6-Hydroxydopamine infusions in the striatum produced akinetic deficits in rats trained to release a lever after a stimulus in a reaction time (RT) task. At 2 weeks after the lesion, A(2A) and mGlu(5) receptors selective antagonists 8-(3-chlorostyryl)caffeine (CSC) and 2-methyl-6-(phenylethynyl)-pyridine (MPEP) were administered daily for 3 weeks either as a single or joint treatment. Injections of CSC (1.25 mg/kg) and MPEP (1.5 mg/kg) separately or in combination reduced the increase of delayed responses and RTs induced by 6-OHDA lesions, while the same treatment had no effect in controls. Furthermore, coadministration of lower doses of 0.625 mg/kg CSC and 0.375 mg/kg MPEP noneffective as a single treatment promoted a full and immediate recovery of akinesia, which was found to be more efficient than the separate blockade of these receptors. These results demonstrate that the combined inactivation of A(2A) and mGlu(5) receptor potentiate their beneficial effects supporting this pharmacological strategy as a promising anti-Parkinsonian therapy.
Simultaneous blockade of adenosine A(2A) and metabotropic glutamate mGlu(5) receptors increase their efficacy in reversing parkinsonian deficits in rats
Coccurello R;
2004
Abstract
Recent evidence suggest that antagonism of adenosine A(2A) receptors represent an alternative therapeutic approach to Parkinson's disease (PD). Coactivation of A(2A) and the glutamate subtype 5 metabotropic receptors (mGlu(5)) synergistically stimulates DARPP-32 phosphorylation and c-fos expression in the striatum, This study therefore tested the effects of a joint blockade of these receptor's to alleviate the motor dysfunction in a rat model of PD. 6-Hydroxydopamine infusions in the striatum produced akinetic deficits in rats trained to release a lever after a stimulus in a reaction time (RT) task. At 2 weeks after the lesion, A(2A) and mGlu(5) receptors selective antagonists 8-(3-chlorostyryl)caffeine (CSC) and 2-methyl-6-(phenylethynyl)-pyridine (MPEP) were administered daily for 3 weeks either as a single or joint treatment. Injections of CSC (1.25 mg/kg) and MPEP (1.5 mg/kg) separately or in combination reduced the increase of delayed responses and RTs induced by 6-OHDA lesions, while the same treatment had no effect in controls. Furthermore, coadministration of lower doses of 0.625 mg/kg CSC and 0.375 mg/kg MPEP noneffective as a single treatment promoted a full and immediate recovery of akinesia, which was found to be more efficient than the separate blockade of these receptors. These results demonstrate that the combined inactivation of A(2A) and mGlu(5) receptor potentiate their beneficial effects supporting this pharmacological strategy as a promising anti-Parkinsonian therapy.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
