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牛磺酸对vigabatrin、高强度光照和散瞳诱导的色素沉着大鼠视网膜毒性的影响。

The effects of taurine on vigabatrin, high light intensity and mydriasis induced retinal toxicity in the pigmented rat.

作者信息

Rasmussen Allan D, Truchot Nathalie, Pickersgill Nigel, Thale Zia Irene, Rosolen Serge G, Botteron Catherine

机构信息

H. Lundbeck A/S, Ottiliavej 9, DK-2500 Valby, Denmark.

WIL Research Europe-Lyon, Department of General Toxicology, 329 Impasse du Domaine Rozier, Les Oncins, 69210 Saint-Germain-Nuelles, France.

出版信息

Exp Toxicol Pathol. 2015 Jan;67(1):13-20. doi: 10.1016/j.etp.2014.09.004. Epub 2014 Oct 16.

Abstract

The overall purpose of this study was to establish a model that may be used for examining the effect of Vigabatrin-induced retinal toxicity in pigmented rats, and subsequently examine the possible effects of taurine on the retinal toxicity. In the first part of the study, pigmented Long Evans rats were subjected to combinations of induced mydriasis, low/high light intensities (40/2000 lx) and oral administration of near-MTD (Maximum Tolerated Dose) doses (200 mg/kg/day) of Vigabatrin for up to 6 weeks. The combination of mydriasis and high light intensity applied to Long Evans rats resulted in retinal damage that was increased by the administration of Vigabatrin. In the second part of the study Long Evans rats were subjected to combinations of induced mydriasis and high/low light intensity (40/2000 lx) while being orally administered low (30 mg/kg/day) or high (200 mg/kg/day) doses of Vigabatrin for up to 6 weeks. In addition, selected groups of animals were administered taurine via the drinking water (20 mg/ml), resulting in systemic taurine concentrations of approximately threefold the endogenous concentration. The combined results of the studies demonstrate that retinal damage can be induced in pigmented animals when combining mydriasis and high light intensity. Retinal damage was functionally evaluated by electroretinography (ERG), then confirmed by histopathology. While depending on mydriasis and high light intensity, administration of Vigabatrin increased the retinal toxicity and resulted in the formation of rosette-like structures in the retina in a dose-related manner. Administration of taurine did not alleviate the Vigabatrin-induced retinal toxicity, as demonstrated either functionally by ERG or morphologically, although systemic concentrations of 3-fold the endogenous levels were reached, and it was thus not possible to demonstrate a protective effect of taurine in these pigmented animals.

摘要

本研究的总体目的是建立一个模型,该模型可用于检测氨己烯酸诱导的有色大鼠视网膜毒性作用,随后检测牛磺酸对视网膜毒性的可能影响。在研究的第一部分,对有色朗-埃文斯大鼠进行散瞳、低/高光强度(40/2000勒克斯)组合处理,并口服接近最大耐受剂量(MTD)(200毫克/千克/天)的氨己烯酸,持续6周。对朗-埃文斯大鼠应用散瞳和高光强度的组合会导致视网膜损伤,而氨己烯酸的给药会加剧这种损伤。在研究的第二部分,朗-埃文斯大鼠在口服低剂量(30毫克/千克/天)或高剂量(200毫克/千克/天)氨己烯酸的同时,进行散瞳和高/低光强度(40/2000勒克斯)组合处理,持续6周。此外,选定的动物组通过饮用水给予牛磺酸(20毫克/毫升),使全身牛磺酸浓度达到内源性浓度的约三倍。研究的综合结果表明,散瞳和高光强度相结合时可在有色动物中诱导视网膜损伤。通过视网膜电图(ERG)对视网膜损伤进行功能评估,然后通过组织病理学进行确认。虽然取决于散瞳和高光强度,但氨己烯酸的给药会增加视网膜毒性,并以剂量相关的方式导致视网膜中形成玫瑰花结样结构。尽管全身浓度达到内源性水平的三倍,但牛磺酸的给药并未减轻氨己烯酸诱导的视网膜毒性,无论是通过ERG功能检测还是形态学检测均未显示出保护作用,因此无法在这些有色动物中证明牛磺酸的保护作用。

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