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Neurotrophic and neuroprotective efficacy of intranasal GDNF in a rat model of Parkinson's disease.
- Source :
-
Neuroscience [Neuroscience] 2014 Aug 22; Vol. 274, pp. 11-23. Date of Electronic Publication: 2014 May 17. - Publication Year :
- 2014
-
Abstract
- Glial cell line-derived neurotrophic factor (GDNF) exerts neurotrophic and neuroprotective effects on substantia nigra (SN) dopamine neurons and has great therapeutic potential for Parkinson's disease (PD). Hindering this potential is the fact that GDNF cannot cross the blood-brain barrier. The aim of this study was to assess the effects of GDNF administered by the intranasal route in normal rats, and in the unilateral 6-hydroxydopamine (6-OHDA) model of PD. In the first study, rats received single intranasal doses of 50-μg GDNF in phosphate-buffered saline (PBS) or cationic liposomes, but no 6-OHDA. In the second study, rats were nasally administered 10, 50 or 150 μg of GDNF in PBS or cationic liposomes 1h before injection of 6-OHDA. All groups were sacrificed 3-4 weeks later. Both intranasal GDNF treatments induced a neurotrophic effect in the SN insofar as the number of tyrosine hydroxylase (TH)-positive neurons was significantly higher than in controls given intranasal PBS liposomes. Dopamine cell counts were also higher in the intact SN of 6-OHDA-lesioned rats compared to controls given PBS liposomes. Most importantly, intranasal GDNF provided significant neuroprotective efficacy indicated by greater TH immunostaining density in the lesioned versus intact SN of rats given single 50-μg doses of GDNF in PBS, or 150-μg doses of liposomal GDNF, compared to lesioned rats given PBS liposomes. Three 50-μg doses given at daily intervals (1 day before, 1h before, and 1 day after 6-OHDA) provided even greater protection than single 150-μg doses. Multiple doses at short intervals may therefore provide greater neuroprotection than single bolus doses. These results demonstrate both a neurotrophic effect of intranasal GDNF in the intact SN as well as neuroprotective efficacy in the unilateral 6-OHDA model, supporting pursuit of this approach as a potential treatment for PD.<br /> (Copyright © 2014 IBRO. Published by Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Body Weight drug effects
Cell Count
Disease Models, Animal
Dopaminergic Neurons drug effects
Dose-Response Relationship, Drug
Liposomes
Male
Oxidopamine
Parkinson Disease metabolism
Rats
Rats, Sprague-Dawley
Substantia Nigra metabolism
Tyrosine 3-Monooxygenase metabolism
Administration, Intranasal
Glial Cell Line-Derived Neurotrophic Factor administration & dosage
Neuroprotective Agents administration & dosage
Parkinson Disease drug therapy
Substantia Nigra drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7544
- Volume :
- 274
- Database :
- MEDLINE
- Journal :
- Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 24845869
- Full Text :
- https://doi.org/10.1016/j.neuroscience.2014.05.019