Preferential increase in the hippocampal synaptic vesicle protein 2A (SV2A) by pentylenetetrazole kindling

被引:36
|
作者
Ohno, Yukihiro [1 ]
Ishihara, Shizuka [1 ]
Terada, Ryo [1 ]
Kikuta, Miki [1 ]
Sofue, Nobumasa [1 ]
Kawai, Yoshiko [1 ]
Serikawa, Tadao [2 ]
Sasa, Masashi [3 ]
机构
[1] Osaka Univ Pharmaceut Sci, Pharmacol Lab, Osaka 5691094, Japan
[2] Kyoto Univ, Grad Sch Med, Inst Lab Anim, Sakyo Ku, Kyoto 6068501, Japan
[3] Nagisa Clin, Osaka 5731183, Japan
关键词
SV2A; SNARE; Kindling; Pentylenetetrazole; Epileptogenesis; Hippocampus; 7S SNARE COMPLEXES; NEUROPEPTIDE-Y; ASYMMETRIC ACCUMULATION; MEMBRANE-FUSION; FOS EXPRESSION; MICE; LEVETIRACETAM; RELEASE;
D O I
10.1016/j.bbrc.2009.09.035
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
The present study evaluated the expressional levels of synaptic vesicle protein 2A (SV2A) and other secretary machinery proteins (i.e., soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complexes, Munc18-1, N-ethylmaleimide-sensitive factor (NSF) and soluble N-ethylmaleimide-sensitive factor attachment protein (SNAP)) in a pentylenetetrazole (PTZ) kindling model. Repeated administration of sub-convulsive PTZ (40 mg/kg, i.p.) progressively increased seizure susceptibility in mice and consistently induced clonic seizures in most animals tested at 15 days after the treatment. Western blot analysis revealed that, among the secretary machinery proteins examined, hippocampal SV2A was selectively elevated by PTZ kindling. PTZ kindling-induced SV2A expression appeared region-specific and the SV2A levels in the cerebral cortex or cerebellum were unaltered. In addition, SV2A expression by PTZ kindling was prominent in the hilar region of the dentate gyrus (DG) where GABAergic interneurons are located, but not in other hippocampal regions (e.g., the stratum lucidum of the CA3 and synaptic layers surrounding CA1 or CA3 pyramidal neurons). These findings suggest that RTZ kindling preferentially elevates SV2A expression in the hippocampus probably as a compensatory mechanism to activate the inhibitory neurotransmission. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:415 / 420
页数:6
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