Neuroprotection by hypothalamic peptide proline-rich peptide-1 in A beta 25-35 model of Alzheimer's disease

作者：Galoyan Armen A; Sarkissian John S^*; Chavushyan Vergineh A; Meliksetyan Irina B; Avagyan Zaruhi E; Poghosyan Mikhail V; Vahradyan Hasmik G; Mkrtchian Hovhannes H; Abrahamyan Davit O

来源：Alzheimer's and Dementia, 2008, 4(5): 332-344.

DOI：10.1016/j.jalz.2007.10.019

• hippocampus
• entorhinal cortex
• amyloid peptide A beta 25-35
• hypothalamic proline-rich peptide PRP-1
• histochemical study
• tetanic and posttetanic potentiation and depression
• learning in water maze

Background: This work sought to determine the effects of hypothalamic proline-rich peptide (PRP)-1 in a rat model of Alzheimer's disease.
Methods: Complex histochemical, electrophysiologic, and behavioral analyses were performed on intact or diseased Wistar rats (n = 28). Pathologic conditions were induced by bilateral intracerebroventricular injection of amyloid peptide A beta 25-35. The diseased rats received systemic administration of PRP-1 or placebo control.
Results: A beta 25-35 caused cellular neurodegeneration with marked glial reaction in the hippocampal complex and almost full destruction of the dentate fascia, which was not observed in conditions of PRP-1 administration after A beta 25-35 injection. Hippocampal neurons of intact animals responded to high-frequency (tetanic) stimulation of entorhinal cortex of ipsilateral cerebral hemisphere by tetanic and posttetanic potentiation of a different intensity and duration, which was accompanied by posttetanic depression. A beta 25-35 led to significant changes in the level and pattern of hippocampal neuronal activity, indicating the absence of both tetanic and posttetanic activity. Poststimulus activity manifestations rarely occurred and rapidly decreased after repeated trials. This indicated the focal character of lesion. Regular administration of PRP-1 for 4 weeks resulted in optimal restoration of electrophysiologic parameters. PRP-1 maintained the initial learning level achieved in a behavioral study in a Morris water maze.
Conclusions: Systemic administration of PRP-1 possesses neuroprotective effects and can prevent the neurodegeneration in hippocampus induced by A beta 25-35. This suggests that PRP-1 could be a potential therapeutic agent for specific neurodegenerative diseases.

• 出版日期2008-9