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银杏叶对大鼠视神经钳夹模型中视网膜神经节细胞存活的影响。

The effect of ginkgo biloba on the rat retinal ganglion cell survival in the optic nerve crush model.

机构信息

Beijing Institute of Ophthalmology, Beijing TongRen Eye Hospital, Capital Medical University, Beijing, China.

出版信息

Acta Ophthalmol. 2010 Aug;88(5):553-7. doi: 10.1111/j.1755-3768.2008.01486.x. Epub 2009 Aug 14.

Abstract

PURPOSE

To investigate the effect of ginkgo biloba on the retinal ganglion cell survival in a rat optic nerve crush model.

METHODS

Twenty-four Sprague-Dawley rats were divided randomly into a study group of 12 animals receiving intraperitoneal injections of ginkgo biloba and a control group of 12 animals receiving intraperitoneal saline injections. All injections were performed 1 hr before the optic nerve crush and daily afterwards. For each animal, the right optic nerve was crushed closely behind the globe for 60 seconds using a microclip with 40 g power. The left optic nerve was kept intact. At 23 days after the optic nerve crush, the retinal ganglion cells were labelled retrogradely by injecting 3% fluorogold into both sides of the superior colliculus of the brain. At 4 weeks after the optic nerve crush, the animals were killed. Photographs taken from retinal flat mounts were assessed for the number and density of the retinal ganglion cells.

RESULTS

The survival rate, defined as the ratio of the retinal ganglion cell density in the right eye with the optic nerve crush divided by the retinal ganglion cell density in left eye without an optic nerve trauma, was significantly (p=0.035) higher in the study group with ginkgo biloba than in the control group (60.0+/-6.0% versus 53.5+/-8.0%).

CONCLUSION

The results suggest that intraperitoneal injections of a ginkgo biloba extract given prior to and daily after an experimental and standardized optic nerve crush in rats were associated with a higher survival rate of retinal ganglion cells.

摘要

目的

研究银杏叶提取物对大鼠视神经钳夹伤模型中视网膜神经节细胞存活的影响。

方法

24 只 Sprague-Dawley 大鼠随机分为实验组(12 只动物,腹腔内注射银杏叶提取物)和对照组(12 只动物,腹腔内注射生理盐水)。所有注射均在视神经钳夹伤前 1 小时进行,随后每天进行一次。对于每只动物,使用 40g 力量的微夹将右侧视神经在眼球后紧密钳夹 60 秒。左侧视神经保持完整。视神经钳夹伤后 23 天,通过向大脑上丘两侧注射 3%荧光金逆行标记视网膜神经节细胞。视神经钳夹伤后 4 周,处死动物。从视网膜平铺片上拍摄的照片评估视网膜神经节细胞的数量和密度。

结果

存活率定义为右侧视神经钳夹伤眼的视网膜神经节细胞密度与未受伤眼的左侧视网膜神经节细胞密度之比,实验组(银杏叶提取物)显著高于对照组(60.0+/-6.0%比 53.5+/-8.0%,p=0.035)。

结论

结果表明,在大鼠视神经钳夹伤实验前和每日给予腹腔内注射银杏叶提取物与视神经钳夹伤后大鼠视网膜神经节细胞更高的存活率相关。

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