在大鼠视网膜中评估两种神经保护剂--膳食藏红花和光生物调节的作用时间过程。

American journal of neurodegenerative disease Pub Date : 2013-09-18 eCollection Date: 2013-01-01
Fabiana Di Marco, Stefania Romeo, Charith Nandasena, Sivaraman Purushothuman, Charean Adams, Silvia Bisti, Jonathan Stone
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引用次数: 0

摘要

背景:膳食藏红花和光生物调节(低强度红外线辐射,PBM)正在成为治疗神经退行性疾病(如视网膜营养不良症)的有效保护剂。在动物模型中,每天服用一定剂量的藏红花和 PBM 可保护视网膜和大脑免受毒素或光线引起的压力。本研究使用光损伤模型研究了每天服用一定剂量的藏红花和 PBM 在诱导斯普拉格道利(Srague Dawley)大鼠感光器变性方面的神经保护作用:在昏暗的周期性(12 小时 5 勒克斯,12 小时黑暗)光照下饲养大鼠,用藏红花或 PBM 治疗 2-10 天,然后将其暴露在强光(1,000 勒克斯,24 小时)下。视网膜存活 1 周后,使用免疫组化方法评估感光细胞的死亡情况(使用 TUNEL 反应)、存活的感光细胞损伤情况(核外层厚度)以及应激相关蛋白 GFAP 的表达情况。用藏红花或 PBM 对视网膜进行预处理可减少光感受器的死亡,保留存活的光感受器数量,并减少 Müller 细胞中 GFAP 的上调。使用藏红花的日剂量(1 毫克/千克)时,保护作用可在 2 天后检测到,然后延长至 10 天。使用 PBM 的日剂量(5 焦耳/厘米(2),波长 670 纳米)时,保护作用可在 5 天后检测到,然后延长至 7-10 天:这些结果为探索藏红花和 PBM 提供保护的机制和持久性提供了时间参数。
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The time course of action of two neuroprotectants, dietary saffron and photobiomodulation, assessed in the rat retina.

Background: Dietary saffron and photobiomodulation (low-level infrared radiation, PBM) are emerging as therapeutically promising protectants for neurodegenerative conditions, such as the retinal dystrophies. In animal models, saffron and PBM, given in limited daily doses, protect retina and brain from toxin- or light-induced stress. This study addresses the rate at which saffron and PBM, given in daily doses, induce neuroprotection, using a light damage model of photoreceptor degeneration in Sprague Dawley (SD) rats.

Results: Rats were raised in dim cyclic (12 h 5 lux, 12 h dark) illumination, treated with saffron or PBM for 2-10 d, and then exposed to bright damaging light (1,000 lux for 24 h). After 1 week survival, the retina was assessed for photoreceptor death (using the TUNEL reaction), for surviving photoreceptor damage (thickness of the outer nuclear layer) and for the expression of a stress-related protein GFAP, using immunohistochemistry. Preconditioning the retina with saffron or PBM reduced photoreceptor death, preserved the population of surviving photoreceptors and reduced the upregulation of GFAP in Müller cells. At the daily dose of saffron used (1 mg/kg), protection was detectable at 2 d, increasing to 10 d. At the daily dose of PBM used (5 J/cm(2) at 670 nm) protection was detectable at 5 d, increasing to 7-10 d.

Conclusions: The results provide time parameters for exploration of the mechanisms and durability of the protection provided by saffron and PBM.

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