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高眼压诱导短暂性缺血后 PACAP 对大鼠视网膜神经节细胞死亡的抑制作用。

Suppression of rat retinal ganglion cell death by PACAP following transient ischemia induced by high intraocular pressure.

机构信息

Department of Anatomy, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8555, Japan.

出版信息

J Mol Neurosci. 2011 Jan;43(1):30-4. doi: 10.1007/s12031-010-9410-5. Epub 2010 Jun 29.

Abstract

Glaucoma is a neurodegenerative disease in which increasing intraocular pressure leads to the progressive loss of retinal ganglion cells (RGCs) and blindness. Here, we report a neuroprotective effect of pituitary adenylate cyclase-activating polypeptide (PACAP) against RGC loss induced by high intraocular pressure in the rat. Vehicle or PACAP (1 fM to 1,000 pM) solution was injected into the vitreous body once after induction of a high intraocular pressure (110 mmHg). Seven days later, the number of viable RGCs was reduced to 45% of that in the intact control. However, PACAP treatment significantly reduced this RGC death in a bimodal manner, with peaks at 10 fM and 10-100 pM. The cAMP antagonist Rp-cAMP significantly blocked the neuroprotective effect of PACAP at both high and low doses, whereas the MAP kinase inhibitor PD-98059 only prevented the effect of the low dose of PACAP. These findings suggest that PACAP has bimodal effects in the neuroprotection of RGCs against ischemia and that these effects are mediated via different signaling pathways.

摘要

青光眼是一种神经退行性疾病,其中眼内压升高导致视网膜神经节细胞(RGCs)的进行性丧失和失明。在这里,我们报告了垂体腺苷酸环化酶激活肽(PACAP)对大鼠高眼压诱导的 RGC 丧失的神经保护作用。在诱导高眼压(110mmHg)后,将载体或 PACAP(1fM 至 1000pM)溶液一次注入玻璃体。7 天后,存活的 RGC 数量减少到正常对照组的 45%。然而,PACAP 处理以双峰方式显著降低了这种 RGC 死亡,峰值分别为 10fM 和 10-100pM。cAMP 拮抗剂 Rp-cAMP 显著阻断了高剂量和低剂量 PACAP 的神经保护作用,而 MAP 激酶抑制剂 PD-98059 仅阻止了低剂量 PACAP 的作用。这些发现表明,PACAP 在 RGC 对缺血的神经保护中具有双峰作用,并且这些作用是通过不同的信号通路介导的。

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