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大鼠急性眼压升高可阻断视网膜神经节细胞中脑源性神经营养因子的逆行轴突运输。

Retrograde axonal transport of BDNF in retinal ganglion cells is blocked by acute IOP elevation in rats.

作者信息

Quigley H A, McKinnon S J, Zack D J, Pease M E, Kerrigan-Baumrind L A, Kerrigan D F, Mitchell R S

机构信息

Glaucoma Research Laboratory, Wilmer Ophthalmological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3460-6.

Abstract

PURPOSE

To determine whether acute experimental glaucoma in rats obstructs retrograde transport of brain-derived neurotrophic factor (BDNF) to retinal ganglion cells (RGCs).

METHODS

Forty rats had unilateral injection of either (125)I-BDNF (20 animals) or a mixture of (125)I-BDNF and 100-fold excess nonradiolabeled BDNF (20 animals). In each group of 20 animals, eyes contralateral to injection had either normal intraocular pressure (IOP; 10 animals) or IOP elevated to 25 mm Hg below the systolic blood pressure of the eye (10 animals). In each group of 20 rats, ipsilateral eyes had IOP set at systolic blood pressure (4 eyes), had optic nerve transection (10 eyes), or had normal IOP (6 eyes). Six hours after injection, animals were killed and tissues were fixed, embedded, and sectioned for autoradiography. Grain counts were performed over retina and optic nerve using automated image analysis.

RESULTS

IOP elevation to 25 mm Hg below systolic blood pressure (perfusion pressure [PP] 25) decreased median retinal nerve fiber layer (NFL) grains by 38% compared with controls (P: < 0.001). Competition by cold BDNF reduced NFL grains by 28% (P: = 0.013). Considering only the radioactivity representing specific retrograde transport of BDNF, IOP elevation to PP25 reduced transport by 74%, whereas elevation to PP0 (equaling systolic blood pressure) reduced specific transport by 83%.

CONCLUSIONS

BDNF is transported retrogradely from the superior colliculus in adult rats, and this transport is substantially inhibited by acute IOP elevation. Deprivation of BDNF among RGCs may contribute to neuron loss in glaucoma.

摘要

目的

确定大鼠急性实验性青光眼是否会阻碍脑源性神经营养因子(BDNF)向视网膜神经节细胞(RGCs)的逆行运输。

方法

40只大鼠单侧注射(125)I-BDNF(20只动物)或(125)I-BDNF与100倍过量非放射性标记BDNF的混合物(20只动物)。在每组20只动物中,注射对侧眼的眼压要么正常(眼压[IOP];10只动物),要么眼压升高至低于眼收缩压25 mmHg(10只动物)。在每组20只大鼠中,同侧眼的眼压设定为收缩压(4只眼),进行视神经横断(10只眼),或眼压正常(6只眼)。注射后6小时,处死动物,固定、包埋组织并切片进行放射自显影。使用自动图像分析对视网膜和视神经进行颗粒计数。

结果

与对照组相比,眼压升高至低于收缩压25 mmHg(灌注压[PP]25)使视网膜神经纤维层(NFL)颗粒中位数减少38%(P:<0.001)。冷BDNF的竞争使NFL颗粒减少28%(P:=0.013)。仅考虑代表BDNF特异性逆行运输的放射性,眼压升高至PP25使运输减少74%,而升高至PP0(等于收缩压)使特异性运输减少83%。

结论

BDNF在成年大鼠中从视上丘逆行运输,这种运输受到急性眼压升高的显著抑制。RGCs中BDNF的缺乏可能导致青光眼患者的神经元丢失。

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