Details

Autor(en) / Beteiligte

• Frouni, Imane
• Kwan, Cynthia
• Bédard, Dominique
• Belliveau, Sébastien
• Bourgeois-Cayer, Élodie
• Gaudette, Fleur
• Beaudry, Francis
• Hamadjida, Adjia
• Huot, Philippe

Titel

Effect of the selective 5-HT2A receptor antagonist EMD-281,014 on l-DOPA-induced abnormal involuntary movements in the 6-OHDA-lesioned rat

Ist Teil von

• Experimental brain research, 2019-01, Vol.237 (1), p.29-36

Ort / Verlag

Berlin/Heidelberg: Springer Berlin Heidelberg

Erscheinungsjahr

2019

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• l -3,4-Dihydroxyphenylalanine ( l -DOPA) is the most effective therapy for motor symptoms of Parkinson’s disease (PD); however, with repeated administration, as many as 94% of PD patients develop complications such as l -DOPA-induced dyskinesia. We previously demonstrated that EMD-281,014, a highly selective serotonin 2A (5-HT 2A ) receptor antagonist, reduces the severity of dyskinesia in the parkinsonian marmoset, without interfering with l -DOPA anti-parkinsonian benefit. Here, we assessed the effects of EMD-281,014 on l -DOPA-induced abnormal involuntary movements (AIMs) in the 6-hydroxydopamine (6-OHDA)-lesioned rat. We first determined the pharmacokinetic profile of EMD-281,014, to administer doses leading to clinically relevant plasma levels in the behavioural experiments. Dyskinetic 6-OHDA-lesioned rats were then administered EMD-281,014 (0.01, 0.03 and 0.1 mg/kg) or vehicle in combination with l -DOPA and AIMs severity was evaluated. We also assessed the effect of EMD-281,014 on l -DOPA anti-parkinsonian action with the cylinder test. We found that the addition of EMD-281,014 (0.01, 0.03 and 0.1 mg/kg) to l -DOPA did not reduce AIMs severity ( P  > 0.05), when compared to vehicle. EMD-281,014 did not compromise l -DOPA anti-parkinsonian action. Our results suggest that the highly selective 5-HT 2A receptor antagonist EMD-281,014 is well-tolerated by parkinsonian rats, but does not attenuate l -DOPA-induced AIMs. Our results highlight differences between rodent and primate models of PD when it comes to determining the anti-dyskinetic action of 5-HT 2A receptor antagonists.