Systemic Administration of Substance P Recovers Beta Amyloid-Induced Cognitive Deficits in Rat: Involvement of Kv Potassium Channels |
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| Authors: | Patrizia Campolongo Patrizia Ratano Maria Teresa Ciotti Fulvio Florenzano Stefania Lucia Nori Roberta Marolda Maura Palmery Anna Maria Rinaldi Cristina Zona Roberta Possenti Pietro Calissano Cinzia Severini |
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| Affiliation: | 1. Department of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.; 2. Institute of Cell Biology and Neurobiology, CNR, Rome, Italy.; 3. European Brain Research Institute, Rome, Italy.; 4. Department of Medicine and Surgery, University of Salerno Medicine Campus, Baronissi (SA), Italy.; 5. Department of Neuroscience, University of Rome “Tor Vergata”, Rome, Italy.; 6. IRCCS Fondazione Santa Lucia, Rome, Italy.; University of the Witwatersrand, South Africa, |
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| Abstract: | Reduced levels of Substance P (SP), an endogenous neuropeptide endowed with neuroprotective and anti-apoptotic properties, have been found in brain and spinal fluid of Alzheimer''s disease (AD) patients. Potassium (K+) channel dysfunction is implicated in AD development and the amyloid-β (Aβ)-induced up-regulation of voltage-gated potassium channel subunits could be considered a significant step in Aβ brain toxicity. The aim of this study was to evaluate whether SP could reduce, in vivo, Aβ-induced overexpression of Kv subunits. Rats were intracerebroventricularly infused with amyloid-β 25–35 (Aβ25–35, 20 µg) peptide. SP (50 µg/Kg, i.p.) was daily administered, for 7 days starting from the day of the surgery. Here we demonstrate that the Aβ infused rats showed impairment in cognitive performances in the Morris water maze task 4 weeks after Aβ25–35 infusion and that this impairing effect was prevented by SP administration.Kv1.4, Kv2.1 and Kv4.2 subunit levels were quantified in hippocampus and in cerebral cortex by Western blot analysis and immunofluorescence. Interestingly, SP reduced Kv1.4 levels overexpressed by Aβ, both in hippocampus and cerebral cortex.Our findings provide in vivo evidence for a neuroprotective activity of systemic administration of SP in a rat model of AD and suggest a possible mechanism underlying this effect. |
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