Abstract |
Parkinson's disease (PD) is a neurodegenerative disorder, characterized by a loss of dopamine (DA) neurons in the substantia nigra pars compacta (SNc). Caloric restriction (CR) has been shown to exert ghrelin-dependent neuroprotective effects in the 1-methyl-4-phenyl-1,2,3,6-tetrathydropyridine ( MPTP)-based animal model for PD. We here investigated whether CR is neuroprotective in the lactacystin (LAC) mouse model for PD, in which proteasome disruption leads to the destruction of the DA neurons of the SNc, and whether this effect is mediated via the ghrelin receptor. Adult male ghrelin receptor wildtype (WT) and knockout (KO) mice were maintained on an ad libitum (AL) diet or on a 30% CR regimen. After 3 weeks, LAC was injected unilaterally into the SNc, and the degree of DA neuron degeneration was evaluated 1 week later. In AL mice, LAC injection significanty reduced the number of DA neurons and striatal DA concentrations. CR protected against DA neuron degeneration following LAC injection. However, no differences were observed between ghrelin receptor WT and KO mice. These results indicate that CR can protect the nigral DA neurons from toxicity related to proteasome disruption; however, the ghrelin receptor is not involved in this effect.
|
Authors | Jessica Coppens, Eduard Bentea, Jacqueline A Bayliss, Thomas Demuyser, Laura Walrave, Giulia Albertini, Joeri Van Liefferinge, Lauren Deneyer, Najat Aourz, Ann Van Eeckhaut, Jeanelle Portelli, Zane B Andrews, Ann Massie, Dimitri De Bundel, Ilse Smolders |
Journal | International journal of molecular sciences
(Int J Mol Sci)
Vol. 18
Issue 3
(Mar 04 2017)
ISSN: 1422-0067 [Electronic] Switzerland |
PMID | 28273852
(Publication Type: Journal Article)
|
Chemical References |
- Neuroprotective Agents
- Receptors, Ghrelin
- lactacystin
- Acetylcysteine
|
Topics |
- Acetylcysteine
(administration & dosage, analogs & derivatives, pharmacology)
- Age Factors
- Animals
- Caloric Restriction
- Cell Count
- Dopaminergic Neurons
(drug effects, metabolism)
- Male
- Mice
- Mice, Knockout
- Neuroprotective Agents
- Receptors, Ghrelin
(genetics, metabolism)
- Substantia Nigra
(drug effects, metabolism, pathology)
|