虎杖茎提取物(PSE)通过抑制炎症和细胞凋亡改善干眼病。

Bongkyun Park, Kyuhyung Jo, Tae Gu Lee, Ik Soo Lee, Jin Sook Kim, Chan-Sik Kim
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引用次数: 5

摘要

目的:研究虎杖茎提取物(PSE)对眶外泪腺切除大鼠模型和高渗应激刺激的人结膜细胞(HCCs)的影响。方法:7周龄雄性Wistar大鼠分为6组。只有对照组(NOR, n=5)未行手术治疗。术后3 d,将眶外泪腺切除大鼠随机分为5组:(1)载药治疗的干眼大鼠(DED, n=5);(2) PSE (10 mg/kg)处理DED大鼠(PSE-10, n=5);(3) PSE (100 mg/kg)处理DED大鼠(PSE-100, n=5);(4) PSE (250 mg/kg)处理DED大鼠(PSE-250, n=5)。此外,HCC细胞系用高渗介质(528 mOsm)和PSE (1-100 μg/ml)共同处理。结果:PSE治疗通过抑制严重的角膜不规则和损伤,恢复泪液体积和杯状细胞密度。PSE通过抑制肿瘤坏死因子-α (TNF-α)、白细胞介素-6 (IL-6)、白细胞介素-1β (IL-1β)和干扰素-γ (IFN-γ) mRNA表达水平以及bcl -2相关X蛋白(Bax)的表达和caspase-3的激活,显著减轻高渗应激诱导的炎症和细胞死亡。结论:PSE对干眼病的抑制作用提示了PES对炎症性疾病的营养干预潜力,且无不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polygonum cuspidatum stem extract (PSE) ameliorates dry eye disease by inhibiting inflammation and apoptosis.

Polygonum cuspidatum stem extract (PSE) ameliorates dry eye disease by inhibiting inflammation and apoptosis.

Polygonum cuspidatum stem extract (PSE) ameliorates dry eye disease by inhibiting inflammation and apoptosis.

Polygonum cuspidatum stem extract (PSE) ameliorates dry eye disease by inhibiting inflammation and apoptosis.

Purpose: Here, we aimed to determine the effect of Polygonum cuspidatum stem extract (PSE) on exorbital lacrimal gland-excised rat models and hyperosmotic stress-stimulated human conjunctival cells (HCCs).

Methods: Seven week old male Wistar rats were divided into six groups. Only the rats in the control group (NOR, n=5) did not undergo surgery. Three days after the surgery, the exorbital lacrimal gland-excised rats were randomly allocated to five groups: (1) vehicle-treated dry-eyed rats (DED, n=5); (2) PSE (10 mg/kg) treated DED rats (PSE-10, n=5); (3) PSE (100 mg/kg) treated DED rats (PSE-100, n=5); and (4) PSE (250 mg/kg) treated DED rats (PSE-250, n=5). In addition, the HCC line was co-treated with hyperosmolar media (528 mOsm) and PSE (1-100 μg/ml).

Results: PSE treatment restored the tear volume and goblet cell density by inhibiting severe corneal irregularities and damage. The treatment with PSE significantly attenuated the hyperosmolar stress-induced inflammation and cell death through the suppression of mRNA expression levels of Tumor necrosis factor-α (TNF-α), Interleukin-6 (IL-6), Interleukin-1β (IL-1β), and Interferon-γ (IFN-γ), and the expression of Bcl-2-associated X protein (Bax) as well as the activation of caspase-3 in vitro.

Conclusion: The inhibitory effects of PSE treatment on dry eye disease indicate the potential of nutritional intervention by PES against inflammatory diseases without adverse effects.

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