Spermidine-induced improvement of memory involves a cross-talk between protein kinases C and A

被引:34
作者
Guerra, Gustavo P. [1 ]
Mello, Carlos F. [2 ]
Bochi, Guilherme V. [2 ]
Pazini, Andreia M. [2 ]
Rosa, Michelle M. [1 ]
Ferreira, Juliano [1 ]
Rubin, Maribel A. [1 ]
机构
[1] Univ Fed Santa Maria, Grad Program Biol Sci Toxicol Biochem, Ctr Exact & Nat Sci, BR-97105900 Santa Maria, RS, Brazil
[2] Univ Fed Santa Maria, Grad Program Pharmacol, Ctr Hlth Sci, BR-97105900 Santa Maria, RS, Brazil
关键词
CREB; GF109203X; hippocampus; inhibitory avoidance; polyamine; ELEMENT-BINDING PROTEIN; INHIBITORY AVOIDANCE PERFORMANCE; LONG-TERM-MEMORY; STIMULATED ADENYLYL CYCLASES; PHORBOL ESTER TREATMENT; SPATIAL-LEARNING TASKS; NMDA RECEPTOR BLOCKADE; ONE-TRIAL AVOIDANCE; NULL MUTANT MICE; RAT-BRAIN;
D O I
10.1111/j.1471-4159.2012.07778.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
J. Neurochem. (2012) 122, 363373. Abstract Spermidine (SPD) is an endogenous aliphatic amine with polycationic structure that modulates NMDA receptor activity and improves memory. Recent evidence suggests that cAMP-dependent protein kinase (PKA) and cAMP response element-binding protein (CREB) play a role in SPD-induced improvement of memory. In the current study, we determined whether the calcium-dependent protein kinase (PKC) signaling pathway is involved in SPD-induced facilitation of memory of inhibitory avoidance task in adult rats. The post-training administration of the PKC inhibitor, 3-[1-(dimethylaminopropyl)indol-3-yl]-4-(indol-3-yl)maleimide hydrochloride [GF 109203X, 2.5 ?mol, intrahippocampal (ih)] with SPD (0.2 nmol, ih) prevented memory improvement induced by SPD. Intrahippocampal administration of SPD (0.2 nmol) facilitated PKC phosphorylation in the hippocampus, 30 min after administration. GF 109203X prevented not only the stimulatory effect of SPD on PKC but also PKA and CREB phosphorylation. These results suggest that memory enhancement induced by the ih administration of SPD involves the cross-talk between PKC and PKA/CREB, with sequential activation of PKC and PKA/CREB pathways, in rats.
引用
收藏
页码:363 / 373
页数:11
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