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Quercetin alleviates hyperthyroidism-induced liver damage via Nrf2 Signaling pathway.
Biofactors ( IF 5.0 ) Pub Date : 2020-02-20 , DOI: 10.1002/biof.1626
Pengxin Zhao 1 , Zhigang Hu 1 , Weiyuan Ma 1 , Leilei Zang 1 , Zhisheng Tian 1 , Qian Hou 1
Affiliation  

Quercetin is a plant flavonoid and has antioxidative properties. In this study, we evaluated the therapeutic effect of quercetin on thyroid dysfunction in L‐thyroxin (LT4)‐induced hyperthyroidism rats. LT4 was used to prepare the experimental hyperthyroidism model via the intraperitoneal injection. Quercetin was injected at a series doses (5, 50, and 100 mg/kg) to LT4‐induced hypothyroidism rats once a day for 14 days. The body weight and food intake were measured once a week. The levels of thyroid hormones, liver function, oxidative stress markers, and antioxidant markers were measured using commercial enzyme‐linked immunosorbent assay kits. Hematoxylin–eosin staining was used to observe the thyroid tissue histological changes. The levels of nuclear and total nuclear factor erythroid 2‐related factor 2 (Nrf2) were determined by western blot. The liver oxidative stress markers in LT4‐induced hyperthyroidism Nrf2 knockout rats were determined to evaluate the role of Nrf2 on quercetin induced protective effects. LT4 administration increased the levels of serum triiodothyronine and thyroxine, activity of oxidative stress markers with a parallel decrease in antioxidant markers and Nrf2. However, the simultaneous administration of quercetin, reversed all these effects indicating its potential in the regulation of hyperthyroidism. Furthermore, the loss function of Nrf2 diminished these effects resulting from the quercetin application, indicating the inhibitory effects caused by the quercetin may be involved in Nrf2 signaling pathway. These results indicate that quercetin could be used to protect against experimental hyperthyroidism‐induced liver damage via Nrf2 signaling pathway.

中文翻译:

槲皮素通过 Nrf2 信号通路减轻甲亢引起的肝损伤。

槲皮素是一种植物黄酮类化合物,具有抗氧化特性。在这项研究中,我们评估了槲皮素对 L-甲状腺素 (LT4) 诱导的甲状腺功能亢进大鼠甲状腺功能障碍的治疗效果。LT4用于腹腔注射制备实验性甲亢模型。槲皮素以一系列剂量(5、50 和 100 mg/kg)注射到 LT4 诱导的甲状腺功能减退大鼠,每天一次,持续 14 天。每周测量一次体重和食物摄入量。使用商业酶联免疫吸附测定试剂盒测量甲状腺激素、肝功能、氧化应激标志物和抗氧化标志物的水平。苏木精-伊红染色用于观察甲状腺组织的组织学变化。通过蛋白质印迹确定核和总核因子红细胞 2 相关因子 2 (Nrf2) 的水平。测定 LT4 诱导的甲状腺功能亢进 Nrf2 敲除大鼠的肝脏氧化应激标志物,以评估 Nrf2 对槲皮素诱导的保护作用的作用。LT4 给药增加了血清三碘甲状腺原氨酸和甲状腺素的水平,氧化应激标志物的活性与抗氧化标志物和 Nrf2 的平行降低。然而,同时服用槲皮素可以逆转所有这些影响,表明其在调节甲状腺功能亢进方面的潜力。此外,Nrf2 的丧失功能减弱了槲皮素应用产生的这些影响,表明槲皮素引起的抑制作用可能与 Nrf2 信号通路有关。这些结果表明槲皮素可用于通过 Nrf2 信号通路防止实验性甲状腺功能亢进引起的肝损伤。
更新日期:2020-02-20
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