Literature DB >> 16185148

Vasoactive intestinal peptide family as a therapeutic target for Parkinson's disease.

Elena Gonzalez-Rey1, Alejo Chorny, Amelia Fernandez-Martin, Nieves Varela, Mario Delgado.   

Abstract

Parkinson's disease (PD) is a common neurodegenerative disorder with no effective protective treatment, characterised by a massive degeneration of dopaminergic neurons in the substantia nigra and the subsequent loss of their projecting nerve fibres in the striatum. Because current treatments for PD are not effective, considerable research has been focused recently on a number of regulatory molecules that regulate inflammation characteristic of PD, induce neurotrophic and survival factors and reduce oxidative stress. Vasoactive intestinal peptide (VIP), a neuropeptide with a potent anti-inflammatory, antiapoptotic and neurotrophic effect, has been found to be protective in several inflammatory disorders. This review examines the putative protective effect of VIP and analogues in different models for PD. VIP emerges as a potential valuable neuroprotective agent for the treatment of pathological conditions in the CNS, such as PD, in which inflammation-induced neurodegeneration occurs.

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Year:  2005        PMID: 16185148     DOI: 10.1517/14728222.9.5.923

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  6 in total

Review 1.  VPAC receptors: structure, molecular pharmacology and interaction with accessory proteins.

Authors:  Alain Couvineau; Marc Laburthe
Journal:  Br J Pharmacol       Date:  2012-05       Impact factor: 8.739

2.  Antioxidant and anti-apoptotic activity of vasoactive intestinal peptide (VIP) against 6-hydroxy dopamine toxicity in the rat corpus striatum.

Authors:  Neşe Tunçel; Orhan Tansel Korkmaz; Neslihan Tekin; Erol Şener; Fahrettin Akyüz; Mine Inal
Journal:  J Mol Neurosci       Date:  2011-08-18       Impact factor: 3.444

3.  Vasoactive intestinal peptide enhances striatal plasticity and prevents dopaminergic cell loss in Parkinsonian rats.

Authors:  OrhanTansel Korkmaz; Hakan Ay; Emel Ulupinar; Neşe Tunçel
Journal:  J Mol Neurosci       Date:  2012-04-29       Impact factor: 3.444

4.  Vasoactive intestinal peptide (VIP) treatment of Parkinsonian rats increases thalamic gamma-aminobutyric acid (GABA) levels and alters the release of nerve growth factor (NGF) by mast cells.

Authors:  Orhan Tansel Korkmaz; Neşe Tunçel; Muzaffer Tunçel; Elif Mine Oncü; Varol Sahintürk; Mustafa Celik
Journal:  J Mol Neurosci       Date:  2009-12-02       Impact factor: 3.444

5.  The VPAC1 receptor: structure and function of a class B GPCR prototype.

Authors:  A Couvineau; E Ceraudo; Y-V Tan; P Nicole; M Laburthe
Journal:  Front Endocrinol (Lausanne)       Date:  2012-11-16       Impact factor: 5.555

6.  Receptor oligomerization in family B1 of G-protein-coupled receptors: focus on BRET investigations and the link between GPCR oligomerization and binding cooperativity.

Authors:  Sarah Norklit Roed; Anne Orgaard; Rasmus Jorgensen; Pierre De Meyts
Journal:  Front Endocrinol (Lausanne)       Date:  2012-05-07       Impact factor: 5.555

  6 in total

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