消药散对抑郁症相关性干眼病小鼠模型的安全性及疗效研究。

Pub Date : 2022-12-01 Epub Date: 2022-10-31 DOI:10.1080/01478885.2022.2136818
Jie Li, Ke Yan, Zhaolin Liu, Xiang Lin, Yu Huang, Jian Shi, Dongdong Li, Xiaolei Yao, Zuguo Liu, Qinghua Peng
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引用次数: 1

摘要

本研究旨在观察消药散(XYS)对小鼠刺激性抑郁障碍(DD)相关干眼病(DED)的安全性和疗效。设正常对照(NC)组、Vehicle组和盐酸舍曲林(SH)、XYS低剂量(XYS- ld)、中剂量(XYS- md)、高剂量(XYS- hd)药物治疗组。采用高效液相色谱法(HPLC)评价XYS的药品质量。苏木精&伊红(H&E)染色评价XYS对肾脏和肝脏的毒性。采用血清酶联免疫吸附试验(ELISA)和体重评价小鼠抑郁状态。泪液产生、角膜敏感性、俄勒冈绿染料(OGD)染色和角膜共聚焦显微镜用于评估眼表变化。H&E染色观察角膜和泪腺病理变化。高效液相色谱法结果表明,XYS符合中药质量标准。药物治疗组肝、肾均未见药物毒性反应。SH和XYS组与Vehicle组相比,dd相关血清学指标均有改善。与Vehicle和SH相比,XYS组小鼠体重增加。XYS组小鼠泪液分泌增加,角膜敏感性降低,角膜OGD染色评分降低,形态学改善,角膜和泪腺炎症细胞浸润减少。综上所述,XYS对dd相关的DED小鼠无药物毒性,改善血清学指标,改善眼表病理改变。XYS是安全的,可能对dd相关的DED有治疗作用。
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A study on the safety and therapeutic effect of Xiaoyaosan on depressive disorder related dry eye disease in a murine animal model.

This study was done to observe the safety and effect of Xiaoyaosan (XYS) on the stimulated depressive disorder (DD) related dry eye disease (DED) in mice. Normal control (NC) group, Vehicle group, and drug treatment groups, including Sertraline Hydrochloride (SH), XYS low-dose (XYS-LD), medium-dose (XYS-MD), and high-dose (XYS-HD), were established. The drug quality of XYS was assessed by high-performance liquid chromatography (HPLC). XYS toxicity in kidney and liver was assessed with Hematoxylin & Eosin (H&E) staining. Serum enzyme-linked immunosorbent assay (ELISA) and body weights were used to evaluate the depression status of mice. Tear production, corneal sensitivity, Oregon Green Dye (OGD) staining, and corneal confocal microscopy were used to assess ocular surface changes. H&E staining was also used to assess pathological cornea and lacrimal gland changes. HPLC results showed that XYS complied with Chinese drug quality standards. The drug treatment groups observed no drug toxicity reactions in the liver and kidney. SH and XYS groups improved DD-related serological indices as compared with Vehicle. Body weight was enhanced in mice with XYS groups compared to Vehicle and SH. Mice with XYS treatments showed increased tear production and corneal sensitivity, decreased corneal OGD staining scores, improved morphology, and decreased inflammatory cell infiltration in the cornea and lacrimal gland. In conclusion, XYS had no drug toxicity, improved serological indices, and ocular surface pathological changes in DD-related DED mice. XYS is safe and may have a therapeutic effect on DD-related DED.

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