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IIA 组分泌型磷脂酶 A2 加重轴突切断诱导的神经退行性变

Deterioration of axotomy-induced neurodegeneration by group IIA secretory phospholipase A2.

作者信息

Yagami T, Ueda K, Asakura K, Hori Y

机构信息

Discovery Research Laboratories, Shionogi and Co., Ltd., 12-4 Sagisu 5-Chome, Fukushima-ku, 553-0002, Osaka, Japan.

出版信息

Brain Res. 2001 Nov 2;917(2):230-4. doi: 10.1016/s0006-8993(01)02994-8.

Abstract

Phospholipase A2 (PLA2) is proposed to play a role in the repair of the ruptured membrane after axotomy. In neonatal rats, we examined the effect of Group IIA secretory PLA2 (sPLA2-IIA) on axotomy-induced cell death of motoneurons. sPLA2-IIA significantly induced death of axotomized motoneurons. Indoxam, a specific inhibitor for sPLA2-IIA, protected motoneurons from the sPLA2-IIA-induced deterioration. The present study indicated that sPLA2-IIA possessed neurotoxic effect rather than neuroprotective effect against facial nerve.

摘要

磷脂酶A2(PLA2)被认为在轴突切断后破裂膜的修复中起作用。在新生大鼠中,我们研究了IIA组分泌型磷脂酶A2(sPLA2-IIA)对轴突切断诱导的运动神经元细胞死亡的影响。sPLA2-IIA显著诱导轴突切断的运动神经元死亡。吲哚昔康是sPLA2-IIA的特异性抑制剂,可保护运动神经元免受sPLA2-IIA诱导的恶化。本研究表明,sPLA2-IIA对面神经具有神经毒性作用而非神经保护作用。

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