a Department of Ophthalmology, The Fourth Affiliated Hospital of China Medical University , Shenyang , China.
b Queens Hospital Center, Mt. Sinai, Icahn School of Medicine , Jamaica , NY , USA.
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):2900-2908. doi: 10.1080/21691401.2019.1640230.
The aim of the present study was to investigate the effect of Lycopus lucidus Turcz (LT) on diabetic retinopathy (DR) and its underlying mechanisms. SD rats and human retinal microvascular endothelial cells (HRECs) were applied for establishment DR model. HE and TUNEL staining were used to evaluate the pathological changes and apoptosis of retinal ganglion cells. Additionally, retinal vessels were detected by immunofluorescence staining with CD31 and VEGF. The function of BRB was observed using Evans blue. Moreover, the oxidative stress, inflammation and angiogenesis associated factors were measured respectively. The expression of p38-MAPK/NF-κB signalling proteins were detected by Western blot. The results demonstrated that pathological changes and retinal optic disc cells apoptosis in retinas of diabetic rats, both of which were reduced in the LT-treated group. And LT treatment attenuated the levels of oxidative stress, inflammation and angiogenesis factors. Importantly, the expression levels of p-p38, p-ERK, p-JNK and NF-κB were decreased. After treatment with TNF-α combined with LT, the levels of inflammatory factors were decreased but higher than the negative control. Taken together, the results suggested that LT treatment is of therapeutic benefit by ameliorating oxidative stress, inflammation and angiogenesis of DR via p38-MAPK/NF-κB signaling pathway.
本研究旨在探讨石菖蒲(LT)对糖尿病视网膜病变(DR)的作用及其机制。SD 大鼠和人视网膜微血管内皮细胞(HRECs)用于建立 DR 模型。HE 和 TUNEL 染色用于评估视网膜神经节细胞的病理变化和细胞凋亡。此外,通过免疫荧光染色用 CD31 和 VEGF 检测视网膜血管。用 Evans 蓝观察 BRB 的功能。此外,还分别测量了与氧化应激、炎症和血管生成相关的因素。通过 Western blot 检测 p38-MAPK/NF-κB 信号蛋白的表达。结果表明,糖尿病大鼠视网膜的病理变化和视网膜神经节细胞凋亡减少,LT 治疗组减轻。LT 治疗可降低氧化应激、炎症和血管生成因子的水平。重要的是,p-p38、p-ERK、p-JNK 和 NF-κB 的表达水平降低。用 TNF-α 联合 LT 处理后,炎症因子水平降低,但高于阴性对照。总之,结果表明,LT 治疗通过 p38-MAPK/NF-κB 信号通路改善 DR 的氧化应激、炎症和血管生成,具有治疗益处。