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盐酸卡替洛尔可抑制活性氧的产生,并挽救培养的晶状体上皮细胞经紫外线照射后的细胞死亡。

Carteolol hydrochloride suppresses the generation of reactive oxygen species and rescues cell death after ultraviolet irradiation of cultured lens epithelial cells.

作者信息

Kaji Yuichi, Kiuchi Takahiro, Oshika Tetsuro

机构信息

Department of Ophthalmology, University of Tsukuba Institute of Clinical Medicine, Tennoudai 1-1-1, Tsukuba, Ibaraki 305-8575, Japan.

出版信息

Open Ophthalmol J. 2010 Oct 12;4:60-5. doi: 10.2174/1874364101004010060.

DOI:10.2174/1874364101004010060
PMID:21283534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3031156/
Abstract

INTRODUCTION

Anti-oxidant activities of adrenergic β-blockers are proposed in various organs. The aim of the present study was to investigate the effect of carteolol hydrochloride, an adrenergic β-blocker, on the production of reactive oxygen species (ROS) and the viable cell number after ultraviolet irradiation of cultured lens epithelial cells (LECs).

MATERIALS AND METHODOLOGY

Cultured LECs were exposed to 0, 10(-5), 10(-4), and 10(-3) M carteolol hydrochloride for 30 min followed by ultraviolet B (UVB) irradiation at intensity of 100, 200, or 400 mJ/cm(2). The amount of ROS in the LECs was measured using dichlorodihydrofluorescein at 30 min after exposure to UVB. In addition, the number of living LECs was counted at 15 h after exposure to UVB.

RESULTS

Exposure to 10(-3) M carteolol hydrochloride significantly decreased the amount of ROS after exposure to UVB at intensities of 100, 200, and 400 mJ/cm(2). In addition, 10(-3) M carteolol hydrochloride significantly increased the viable cell number after exposure to UVB at 400 mJ/cm(2). However, 10(-4) and 10(-5)M carteolol hydrochloride had no significant effect on ROS or the viable cell number in LECs.

DISCUSSIONS

Carteolol hydrochloride protects LECs against UVB irradiation by inhibiting the intracellular production of ROS.

摘要

引言

肾上腺素能β受体阻滞剂在多个器官中具有抗氧化活性。本研究旨在探讨肾上腺素能β受体阻滞剂盐酸卡替洛尔对培养的晶状体上皮细胞(LECs)紫外线照射后活性氧(ROS)生成及活细胞数量的影响。

材料与方法

将培养的LECs分别用0、10⁻⁵、10⁻⁴和10⁻³ M盐酸卡替洛尔处理30分钟,随后分别以100、200或400 mJ/cm²的强度进行紫外线B(UVB)照射。在UVB照射后30分钟,使用二氯二氢荧光素测定LECs中的ROS含量。此外,在UVB照射后15小时,对活的LECs进行计数。

结果

暴露于10⁻³ M盐酸卡替洛尔后,在100、200和400 mJ/cm²强度的UVB照射下,ROS含量显著降低。此外,在400 mJ/cm²的UVB照射后,10⁻³ M盐酸卡替洛尔显著增加了活细胞数量。然而,10⁻⁴和10⁻⁵ M盐酸卡替洛尔对LECs中的ROS或活细胞数量没有显著影响。

讨论

盐酸卡替洛尔通过抑制细胞内ROS的产生来保护LECs免受UVB照射。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/6524ad2edf90/TOOPHTJ-4-60_F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/6c6c01607bf9/TOOPHTJ-4-60_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/454519190f4a/TOOPHTJ-4-60_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/6524ad2edf90/TOOPHTJ-4-60_F3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/6c6c01607bf9/TOOPHTJ-4-60_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/454519190f4a/TOOPHTJ-4-60_F2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3c5/3031156/6524ad2edf90/TOOPHTJ-4-60_F3.jpg

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