Nitric oxide synthase and Long Term Potentiation (LTP) participate in the Ghr induced hippocampal-dependent memory facilitation

VALERIA P. CARLINI; MARIELA F. PEREZ; ESTELA SALDE; HELGI B. SCHIÖTH; OSCAR A RAMIREZ; RUBIALES DE BARIOGLIO, SUSANA ELIZABETH

PHYSIOLOGY AND BEHAVIOR

PERGAMON-ELSEVIER SCIENCE LTD

Año: 2010 vol. 101 p. 117 - 123

0031-9384

Although the hypothalamus has been long considered the main ghrelin (Ghr) target organ mediating orexigenic effects, recently it has been shown that in-vivo Ghr hippocampus administration improves learning and memory in the inhibitory avoidance paradigm. However, the possible mechanisms underlying this memory facilitation effect have not been clarified. Given that the biochemical memory cascade into the hippocampus involves nitric oxide (NO) synthesis via NO synthase (NOS) activation, we investigated 1) if Ghr administration modulated NOS activity in the hippocampus; and 2) if hippocampal NOS inhibition influenced Ghr-induced memory facilitation, using a behavioral paradigm, biochemical determinations and an electrophysiological model. Our results showed that intra-hippocampal Ghr administration increased the NOS activity in a dose dependent manner, and reduced the threshold for LTP generation in dentate gyrus of rat hippocampus. Moreover, pre-administration of NG-nitro-L-arginine ( -NOArg) in the hippocampus partially prevented the Ghr- induced memory improvement, abolished the increase in NOS activity, and prevented the decreased threshold to generate LTP induced by Ghr. These findings suggest that activation of the NOS/NO pathway in hippocampus participates in the effects of Ghr on memory consolidation and is related with plastic properties of the hippocampal tree-synaptic loop.