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西维美林通过上调干眼模型小鼠眼表面黏蛋白发挥抗炎作用。

Cevimeline-induced anti-inflammatory effect through upregulations of mucins in the ocular surface of a dry eye mouse model.

机构信息

T2B infrastructure Center for Ocular Disease, Inje University Busan Paik Hospital, Busan 47392, Republic of Korea.

Department of Ophthalmology, Inje University College of Medicine, Inje University Busan Paik Hospital, Busan 47392, Republic of Korea.

出版信息

Biomed Pharmacother. 2021 Jul;139:111571. doi: 10.1016/j.biopha.2021.111571. Epub 2021 Apr 13.

Abstract

This study aimed to investigate the effects of various concentrations of cevimelines (CVMs) and compare them with commercial drugs in a murine model of dry eye. The experimental mouse model used male and female NOD.B10.H2 mice over 12 weeks of age. Desiccation stress was performed at 30-40% ambient humidity, and subcutaneous injection of 0.5 mg/0.2 mL scopolamine hydrobromide was performed four times a day for 10 days. The efficacy of various concentrations of CVMs (seven experimental groups) was first evaluated, and then 2% CVM was compared with commercial drugs, such as cyclosporine A (CsA), diquafosol (DQS), and rebamipide (REB) (seven experimental groups). The clinical changes, including tear production, corneal irregularity, and fluorescein staining, were measured after the instillation of various concentrations of CVMs and commercial drugs for 0, 3, 5, 7, and 10 days. Histological changes, such as corneal detachment, conjunctival goblet cell and mucin density staining, were assessed by staining the cornea or conjunctiva with hematoxylin-eosin, periodic acid-Schiff, and alcian blue. The expression of inflammatory markers and mucin factors was detected by immunohistochemistry and immunofluorescence in the lacrimal gland, cornea, and conjunctiva. Tear production was significantly increased in the 2% CVM group and was similar to that in the DQS and REB groups (P < 0.05). The corneal smoothness and fluorescein staining score were significantly improved in the 2% CVM group and were similar to those in the REB group (P < 0.05). Corneal epithelial cells were significantly decreased in the 2% CVM group, with similar observations made in the DQS and REB groups (P < 0.05). The conjunctival goblet cells and mucin density recovered in the 2% CVM group were similar to those in the CsA and REB groups (P < 0.05). The 2% CVM group showed suppressed expression of inflammatory factors in the lacrimal gland and was comparable to that seen in the CsA and REB groups. The expression of mucin factors was upregulated in the cornea and conjunctiva of the 2% CVM group and was similar to that of the CsA and REB groups. In conclusion, administration of CVM resulted in recovery or clinical and histological improvement of the murine dry eye model, and all the observed parameters were comparable to those with commercial drugs.

摘要

本研究旨在探讨不同浓度的盐酸依匹斯汀(CVMs)对干燥性眼病模型的影响,并与商业药物进行比较。实验采用 12 周以上的雄性和雌性 NOD.B10.H2 小鼠作为实验鼠模型。在 30-40%环境湿度下进行干燥应激,每天皮下注射 0.5mg/0.2mL 氢溴酸东莨菪碱 4 次,持续 10 天。首先评估了七种实验浓度的 CVMs 的疗效,然后将 2% CVM 与商业药物如环孢素 A(CsA)、地夸磷索(DQS)和瑞巴派特(REB)进行比较(七个实验组)。在滴注不同浓度的 CVMs 和商业药物后的第 0、3、5、7 和 10 天,测量了泪液产生、角膜不规则和荧光素染色等临床变化。通过对角膜或结膜进行苏木精-伊红、过碘酸-希夫和阿利新蓝染色,评估了角膜脱离、结膜杯状细胞和粘蛋白密度染色等组织学变化。通过免疫组化和免疫荧光检测泪腺、角膜和结膜中炎症标志物和粘蛋白因子的表达。结果显示,2% CVM 组的泪液产生明显增加,与 DQS 和 REB 组相似(P<0.05)。2% CVM 组的角膜平整度和荧光素染色评分明显改善,与 REB 组相似(P<0.05)。2% CVM 组角膜上皮细胞明显减少,与 DQS 和 REB 组观察结果相似(P<0.05)。2% CVM 组的结膜杯状细胞和粘蛋白密度恢复,与 CsA 和 REB 组相似(P<0.05)。2% CVM 组泪腺中炎症因子的表达受到抑制,与 CsA 和 REB 组相似。2% CVM 组角膜和结膜中粘蛋白因子的表达上调,与 CsA 和 REB 组相似。综上所述,CVM 的给药可使干燥性眼病模型恢复或临床和组织学改善,所有观察到的参数与商业药物相当。

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