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Carbonic anhydrase activation enhances object recognition memory in mice through phosphorylation of the extracellular signal-regulated kinase in the cortex and the hippocampus

机译:碳酸酐酶活化通过皮质中细胞外信号调节激酶和海马的细胞外信号调节激酶磷酸化增强了小鼠的物体识别记忆

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摘要

Rats injected with by D-phenylalanine, a carbonic anhydrase (CA) activator, enhanced spatial learning, whereas rats given acetazolamide, a CA inhibitor, exhibited impairments of fear memory consolidation. However, the related mechanisms are unclear. We investigated if CAs are involved in a non-spatial recognition memory task assessed using the object recognition test (ORT). Systemic administration of acetazolamide to male CD1 mice caused amnesia in the ORT and reduced CA activity in brain homogenates, while treatment with D-phenylalanine enhanced memory and increased CA activity. We provided also the first evidence that D-phenylalanine administration rapidly activated extracellular signal regulated kinase (ERK) pathways, a critical step for memory formation, in the cortex and the hippo campus, two brain areas involved in memory processing. Effects elicited by D-phenylalanine were completely blunted by co-administration of acetazolamide, but not of 1-N-(4-sulfamoylphenyl-ethyl)2,4,6-trimethylpyridinium perchlorate ((C18).) a CA inhibitor that, differently from acetazolamide, does not cross the blood brain barrier. Our results strongly suggest that brain but not peripheral CAs activation potentiates memory as a result of ERK pathway enhanced activation. (C) 2017 Elsevier Ltd. All rights reserved.
机译:通过D-苯丙氨酸注射大鼠,碳酸酐酶(CA)活化剂,增强的空间学习,而对乙酰唑胺,Ca抑制剂的大鼠表现出恐惧记忆合并的损伤。但是,相关机制尚不清楚。我们调查了如果CAS参与使用对象识别测试(ORT)评估的非空间识别存储器任务。将乙酰唑胺对雄性CD1小鼠施用的全身施用导致ORT中的胃癌和脑匀浆中的CA活性降低,同时用D-苯丙氨酸增强的内存处理并增加Ca活性。我们还提供了D-苯丙氨酸给药迅速激活细胞外信号调节激酶(ERK)途径的第一种证据,对内存和河马校区中的记忆形成的关键步骤,参与内存处理的两个脑区。通过共唑胺完全钝化D-苯丙氨酸的效果,但不含1-N-(4-磺酰苯基 - 乙基)2,4,6-三甲基吡啶(高氯酸((C18))的Ca抑制剂来自乙酰唑胺,不会穿过血脑屏障。我们的结果强烈表明,由于ERK途径增强了激活,脑而不是外围CAS激活增强记忆。 (c)2017 Elsevier Ltd.保留所有权利。

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