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(-)Δ9-四氢大麻酚在青光眼大鼠模型中的神经保护和降低眼压作用

Neuroprotective and intraocular pressure-lowering effects of (-)Delta9-tetrahydrocannabinol in a rat model of glaucoma.

作者信息

Crandall James, Matragoon Suraporn, Khalifa Yousuf M, Borlongan Caesar, Tsai Nai-Tse, Caldwell Ruth B, Liou Gregory I

机构信息

Department of Ophthalmology, Medical College of Georgia, Augusta, GA 30912, USA.

出版信息

Ophthalmic Res. 2007;39(2):69-75. doi: 10.1159/000099240. Epub 2007 Feb 2.

Abstract

In glaucoma, retinal ganglion cell (RGC) death is induced by many risk factors, including ocular hypertension. It has been proposed that glutamate-mediated oxidative stress may also contribute to this RGC death. Cannabinoids are known to possess therapeutic properties including ocular hypotension and antioxidation. In this study, we test the hypothesis that (-)Delta(9)-tetrahydrocannabinol (THC) lowers intraocular pressure (IOP) and prevents RGC death in a rat model of glaucoma. Arat model of experimental glaucoma with chronic, moderately elevated IOP was produced unilaterally by cauterization of episcleral vessels. Rats received weekly injections of THC at a level of 5 mg/kg or vehicle for 20 weeks. IOP of both eyes was measured weekly on anesthetized animals immediately before THC treatment. RGCs were labeled in a retrograde fashion and counted in whole-mounted retinas. IOP was elevated in all operated eyes 1 day after the operation and remained elevated in the vehicle-treated rats throughout 20 weeks. In THC-treated rats, IOP elevation in operated eyes was diminished 2 weeks after operation and remained reduced. IOP in the contralateral control eyes was not affected by THC. In the operated eyes of vehicle-treated animals, there was a loss of approximately 50 and 40% of the RGCs in the peripheral and central retina, respectively. The RGC loss in the operated eyes of the THC-treated animals was reduced to 10-20%. These results demonstrate that THC is a neuroprotectant that preserves RGCs in an experimental model of glaucoma, possibly through a reduction in IOP.

摘要

在青光眼患者中,视网膜神经节细胞(RGC)死亡是由包括高眼压在内的多种危险因素诱发的。有人提出,谷氨酸介导的氧化应激也可能导致这种RGC死亡。已知大麻素具有治疗特性,包括降低眼压和抗氧化作用。在本研究中,我们检验了(-)Δ⁹-四氢大麻酚(THC)可降低青光眼大鼠模型眼压并预防RGC死亡这一假设。通过烧灼巩膜血管单侧建立慢性、中度眼压升高的实验性青光眼大鼠模型。大鼠每周接受5mg/kg的THC或赋形剂注射,持续20周。在每次THC治疗前,每周对麻醉动物的双眼眼压进行测量。RGC采用逆行标记法标记,并在视网膜铺片中计数。术后1天,所有手术眼的眼压均升高,在接受赋形剂治疗的大鼠中,眼压在20周内一直保持升高。在接受THC治疗的大鼠中,手术眼的眼压升高在术后2周有所减轻,并持续降低。对侧对照眼的眼压不受THC影响。在接受赋形剂治疗动物的手术眼中,周边视网膜和中央视网膜的RGC分别损失了约50%和40%。在接受THC治疗动物的手术眼中,RGC损失减少到10%-20%。这些结果表明,THC是一种神经保护剂,在青光眼实验模型中可能通过降低眼压来保护RGC。

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