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Volume 8, Issue 6

J Neurol Neurosci

ISSN: 2171-6625 Neuro, an open access journal

Neuroscience 2017

October 16-17, 2017

OCTOBER 16-17, 2017 OSAKA, JAPAN

17

TH

Global Neuroscience Conference

Interaction between 5-HT4 and CB1 function in the pre-limbic cortex on memory consolidation

deficit in inhibitory avoidance task

Nargol Ahmadi-Mahmoodabadi

1

, Mohammad Nasehi

1

, Masoumeh Emamghoreishi

1

and Mohammad-Reza Zarrindast

1,3

1

Institute for Cognitive Science Studies, Iran

2

Shiraz University of Medical Sciences, Iran

3

Tehran University of Medical Sciences, Iran

T

his study performed to investigate the influence of bilateral post-training intra-pre limbic (PL) microinjections of

serotonergic 5-HT4 receptor agents (RS67333, as a 5-HT4 receptor agonist and RS23597-190, as a 5-HT4 receptor

antagonist) upon amnesia induced by a cannabinoid CB1 receptor agonist, Arachidonylcyclopropylamide (ACPA) in rats.

The step-through Inhibitory Avoidance (IA) and open filed apparatuses were used to examine the memory consolidation

and locomotion behaviors, respectively. Bilateral guide-cannulae were implanted to allow intra-PL microinjections of the

drugs. Also, post-training administration of the drugs was performed with the volume of 0.6 μl/rat (0.3 μl/side). Based on our

findings, post-training bilateral intra-PL microinjection of ACPA (0.1 and 0.5 µg/rat) decreased, whereas RS67333 (0.5 μg/rat)

increased IA memory consolidation. Meanwhile, post-training bilateral intra-PL administration of RS23597-190 (0.005, 0.01,

0.1 and 0.5 μg/rat) did not alter memory consolidation. Moreover, intra-PL micro-infusion of RS67333 (0.005 μg/rat) plus the

lower (0.001 µg/rat) or the higher (0.1 µg/rat) dose of ACPA potentiated or restored the memory consolidation impairment

induced by ACPA, respectively. While, post-training administration of RS23597-190 (0.5 μg/rat) plus the higher dose of ACPA

(0.1 μg/rat) potentiated the ACPA response. However none of the above interventions affect locomotors activity. In conclusion,

our results suggest that the PL 5-HT4

dr.ahmadi2012@gmail.com

J Neurol Neurosci 2017, 8:6

DOI: 10.21767/2171-6625-C1-006