PET Imaging of Serotonin Transporters with 4-[18F]-ADAM in a Parkinsonian Rat Model

Author:

Weng Shao-Ju12,Shiue Chyng-Yann3,Huang Wen-Sheng4,Cheng Cheng-Yi3,Huang San-Yuan5,Li I-Hsun6,Tao Chih-Chieh2,Chou Ta-Kai3,Liao Mei-Hsiu7,Chang Yung-Ping8,Ma Kuo-Hsing2

Affiliation:

1. Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei, Taiwan

2. Department of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan

3. Department of Nuclear Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

4. Departments of Nuclear Medicine and Medical Research, Changhua Christian Hospital, Changhua, Taiwan

5. Department of Psychiatry, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan

6. School of Pharmacy, National Defense Medical Center, Taipei, Taiwan

7. Institute of Nuclear Energy Research, Taoyaun, Taiwan

8. Department of Pharmacy, Songshan Armed Forces General Hospital, Taipei, Taiwan

Abstract

This study was undertaken to address the effects of fetal mesencephalic tissue transplantation on the serotonin system in a rat model of Parkinson's disease (PD) while also investigating the usefulness of 4-[18F]-ADAM (a serotonin transporter imaging agent) coupled with micro-PET for imaging serotonin transporters (SERTs). A PD model was induced by unilateral injection of 6-hydroxydopamine (6-OHDA) into the right medial forebrain bundle of the nigrostriatal pathway, while cell transplantation was performed via intrastriatal injection of mesencephalic brain tissue dissected from embryonic (E14) rats. The 4-[18F]-ADAM/micro-PET scanning was performed following both 6-OHDA lesioning and transplantation. Immunohistochemistry (IHC) studies were also performed following the final PET scan, and the results were compared to show a 17–43% decrease in the specific uptake ratio (SUR) and a 23–52% decrease in serotonin transporter immunoreactivity (SERT-ir) within various brain regions on the lesioned side. The number of methamphetamine-induced rotations also decreased significantly at the 4th week postgraft. In addition, striatal SUR and the SERT-ir levels were restored to 77% and 83% 5 weeks postgraft. These results suggest that Parkinson's disease also affects the serotonergic system, while both the dopaminergic and serotonergic systems can be partially restored in a rat model of PD after E14 mesencephalic tissue transplantation. In addition, we have also determined that 4-[18F]-ADAM/micro-PET can be used to detect serotonergic neuron loss, monitor the progress of Parkinson's disease, and oversee the effectiveness of therapy.

Publisher

SAGE Publications

Subject

Transplantation,Cell Biology,Biomedical Engineering

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