Inhibition of Adenylyl Cyclase Type 5 Prevents l-DOPA-Induced Dyskinesia in an Animal Model of Parkinson's Disease

• DOI: 10.1523/jneurosci.0864-14.2014
• Publication Date: 2014-09-08T22:26:44Z
• Authors: Hye-Yeon Park; Young-Mi Kang; Young Kang; Tae-Shin Park; Young-Kyoung Ryu; Jung-Hwan Hwang; Yong-Hoon Kim; Bong-Hyun Chung; Ki-Hoan Nam; Mee-Ree Kim; Chul-Ho Lee; Pyung-Lim Han; Kyoung-Shim Kim
• Keywords: Mice, Knockout; 0301 basic medicine; Dyskinesia, Drug-Induced; Reverse Transcriptase Polymerase Chain Reaction; Blotting, Western; Real-Time Polymerase Chain Reaction; Immunohistochemistry; 3. Good health; Antiparkinson Agents; Levodopa; Mice, Inbred C57BL; Disease Models, Animal; Mice; 03 medical and health sciences; Parkinsonian Disorders; Adenylyl Cyclase Inhibitors; Animals; Adenylyl Cyclases

The dopamine precursorl-3,4-dihydroxyphenylalanine (l-DOPA) is widely used as a therapeutic choice for the treatment of patients with Parkinson's disease. However, the long-term use ofl-DOPA leads to the development of debilitating involuntary movements, calledl-DOPA-induced dyskinesia (LID). The cAMP/protein kinase A (PKA) signaling in the striatum is known to play a role in LID. However, from among the nine known adenylyl cyclases (ACs) present in the striatum, the AC that mediates LID remains unknown. To address this issue, we prepared an animal model with unilateral 6-hydroxydopamine lesions in the substantia nigra in wild-type and AC5-knock-out (KO) mice, and examined behavioral responses to short-term or long-term treatment withl-DOPA. Compared with the behavioral responses of wild-type mice, LID was profoundly reduced in AC5-KO mice. The behavioral protection of long-term treatment withl-DOPA in AC5-KO mice was preceded by a decrease in the phosphorylation levels of PKA substrates ERK (extracellular signal-regulated kinase) 1/2, MSK1 (mitogen- and stress-activated protein kinase 1), and histone H3, levels of which were all increased in the lesioned striatum of wild-type mice. Consistently, FosB/ΔFosB expression, which was induced by long-terml-DOPA treatment in the lesioned striatum, was also decreased in AC5-KO mice. Moreover, suppression of AC5 in the dorsal striatum with lentivirus-shRNA-AC5 was sufficient to attenuate LID, suggesting that the AC5-regulated signaling cascade in the striatum mediates LID. These results identify the AC5/cAMP system in the dorsal striatum as a therapeutic target for the treatment of LID in patients with Parkinson's disease.