Parkinson-like phenotype in insulin-resistant PED/PEA-15 transgenic mice

• Published in: Scientific reports Vol. 6; no. 1; p. 29967
• Main Authors: Perruolo, Giuseppe, Viggiano, Davide, Fiory, Francesca, Cassese, Angela, Nigro, Cecilia, Liotti, Antonietta, Miele, Claudia, Beguinot, Francesco, Formisano, Pietro
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 18.07.2016; Nature Publishing Group
• Subjects: 631/378/2632/1323; 631/443/319/1642/2815; Animal diseases; Animal models; Animals; Behavior, Animal; Diabetes; Dopamine - metabolism; Fibers; Genotype & phenotype; Humanities and Social Sciences; Insulin Resistance; Male; Memory; Mice, Transgenic; Motor Activity; multidisciplinary; Neostriatum - metabolism; Neurophysiology; Parkinson Disease - pathology; Phenotype; Phosphoproteins - metabolism; Putamen - metabolism; Rotarod Performance Test; Science; Transgenic animals; Tyrosine 3-Monooxygenase - metabolism; Italy
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep29967

Neurological abnormalities, such as Parkinson-like disorders (PlD), are often co-morbidities of Type 2 Diabetic (T2D) patients, although the epidemiological link between these two disorders remains controversial. The PED/PEA-15 protein represents a possible candidate linking T2D and PD, because it is increased in subjects with T2D and is highly expressed in the brain. To test this hypothesis, we have analyzed the neurological and neurochemical phenotype of transgenic mice overexpressing PED/PEA-15 (tgPED). These mice develop impaired glucose tolerance and insulin resistance, accompanied by neurological features resembling PlD: feet clasping, slow and delayed locomotor movements in different behavioral tests in absence of clear cognitive deficits, ataxia or anxiety. Morphological analysis of the brains showed selective modifications of metabolic activity in the striatal region. In the same region, we have observed 26% decrease of dopamine fibers, confirmed by immunohistochemistry and Western Blot for tyrosine hydroxylase. Moreover, they also showed 48% reduction of dopamine levels in the striatum. Thus the tgPED mice may represent a genetic animal model of neurological disease linked to T2D.