## Abstract ## Purpose To evaluate the feasibility of using manganese‐based MR imaging contrast agent EVP‐ABD to detect diffuse liver disease in an established rat hepatitis model. ## Materials and Methods Hepatitis was induced by administration of CCl~4~ in corn oil vehicle to rats intraperiton
Manganese-enhanced MRI in a rat model of Parkinson's disease
✍ Scribed by Galit Pelled; Hagai Bergman; Tamir Ben-Hur; Gadi Goelman
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 989 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1053-1807
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Purpose
To measure intra‐ and inter‐hemispheric connectivity within the basal ganglia (BG) nuclei in healthy and in unilateral 6‐hydroxydopamine (6‐OHDA) Parkinson disease rat model in order to test the BG interhemispheric connectivity hypothesis.
Material and Methods
The manganese‐enhanced MRI (MEMRI) method with direct injection of manganese chloride into the entopeduncular (EP), substantia nigra (SN), and the Habenula nuclei in unilateral 6‐OHDA (N = 22) and sham‐operated (N = 16) rat groups was used. MEMRI measurements were applied before, 3, 24, and 48 hours post‐manganese injection. Signal enhancements in T1‐weighted images were compared between groups.
Results
Manganese injection into the EP nucleus resulted with bihemispheric signal enhancements in the habenular complex (Hab) at both groups with stronger enhancements in the 6‐OHDA group. It also exhibited lower sensorimotor cortex signal enhancement in the 6‐OHDA rat group. SN manganese injection caused enhanced anteroventral thalamic and habenular nuclei signals in the 6‐OHDA rat group. Manganese habenula injection revealed enhanced interpeduncular (IP) and raphe nuclei signals of the 6‐OHDA rat group.
Conclusion
Modulations in the effective intra‐ and interhemispheric BG connectivity in unilateral 6‐OHDA Parkinson's disease (PD) rat model support the BG interhemispheric connectivity hypothesis and suggest a linkage between the dopaminergic and serotonergic systems in PD, in line with clinical symptoms. J. Magn. Reson. Imaging 2007;26:863–870. © 2007 Wiley‐Liss, Inc.
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