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[Q. Neuroscience-34]



              Development of levodopa induced dyskinesia mouse model


                        combining with mutant α-synuclein and MPTP




         Eunji Namgung¹˙²˙³˙#, Soo jeong Kim¹˙³˙#, Min Jeong Ryu¹, Yunseon Jang¹˙²˙³, Min joung Lee¹˙²˙³, Xianshu Ju¹˙²˙³,
         Jianchen Cui¹˙²˙³, Yu Lim Lee¹˙²˙³, Jiebo Zhu¹˙²˙³, Dahyun Go¹˙²˙³, Chang Jun Seo¹˙²˙³, Woosuk Chung¹˙²˙³,

                                        Gi Ryang Kweon¹˙²˙³, Jun Young Heo¹˙²˙³˙*


         ¹Biochemistry, Chungnam National University School of Medicine, Daejeon 35015, South Korea, ²Medical Science,
         Chungnam National University School of Medicine, Daejeon 35015, South Korea, ³nfection Control Convergence

        Research Center, Chungnam National University School of Medicine, Daejeon 35015, South Korea, ⁴Anesthesiology
                    and Pain medicine, Chungnam National University Hospital, Daejeon 35015, South Korea




        Levodopa (LD)  is  the first line  therapy  for  Parkinson's  disease  (PD),  which  improves  PD  behavioral  symptoms.

        However, long terms (10 years) treatment of LD could occur dyskinetic movement over 80% of PD patients. Levodopa
        induced dyskinesia (LID) can be treated with DBS (deep brain stimulation), but there is a risk of bleeding, infection

        accompany with surgery, so the development of a medicine that alleviates LID symptom is essential. For pre-clinical
        trial, the development of animal model which recapitulates LID patient symptoms should be preceded, at present

        the predominantly used model of LID is neurotoxin induced PD animal model. To develop the recapitulate the LID
        patient  symptoms,  we  generate  the  LID  animal  model  combine  with  α-synuclein(α-syn)  and  MPTP.  Here,  we

        performed stereotaxic surgery with α-syn A53T virus in the SN region, and administrated MPTP after two weeks
        later and then treated LD twice a day for a week to induce LID. We established a new combined LID animal model

        by confirming more severe abnormal involuntary movement scale (AIMS) than only α-syn or MPTP treated model.
        This result will provide an important experimental platform that serves for clinical trial as animal models that most

        closely recapitulate patients with LID symptoms.
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