当归苷通过调节 KAT6A/Nrf2 信号通路减少破骨细胞中 ROS 的产生,从而改善卵巢切除大鼠的骨质疏松症。

IF 5.3 3区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE Chinese Medicine Pub Date : 2024-07-02 DOI:10.1186/s13020-024-00961-7
Xiao-Feng Liu, Yi-Tao Liao, Jia-Hao Shao, Dan-Dan He, Zhi-Hong Fan, Ye-Nan Xu, Chao Li, Xian Zhang
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引用次数: 0

摘要

背景:欧当归中的当归苷可以通过阻止破骨细胞的形成来预防骨质疏松症:当归中的当归苷可通过阻止破骨细胞的形成来预防骨质疏松症,但其确切机制仍不清楚:方法:我们使用卵巢切除的骨质疏松症模型大鼠和 RAW264.7 细胞评估了当归苷对破骨细胞氧化应激水平的影响。使用 H&E 染色法和显微 CT 观察股骨骨质的变化。通过 DHE 荧光标记研究了 ROS 的含量。使用 Western 印迹、免疫组化、耐酒石酸磷酸酶染色和实时定量 PCR 检测了破骨细胞相关基因和蛋白质的表达。此外,还使用 MTT 试验、双荧光素试验、染色质免疫沉淀、免疫沉淀和 KAT6A siRNA 转染等方法评估了当归苷对破骨细胞发育的影响:结果:接受当归苷治疗的大鼠的骨矿物质密度更高,破骨细胞更少。当归苷能阻止 RAW264.7 细胞在 RANKL 刺激下体外分化为破骨细胞。实验显示,当归苷处理后,ROS水平降低,细胞内KAT6A、HO-1和Nrf2显著上调。破骨细胞特有基因(如 MMP9 和 NFATc1)的表达也被下调。最后,KAT6A siRNA转染增加了细胞内ROS水平,同时降低了破骨细胞中KAT6A、Nrf2和HO-1蛋白的表达。然而,在没有转染 KAT6A siRNA 的情况下,当归苷在破骨细胞中极大地抵消了这种效应:结论:当归苷增加了 KAT6A 的表达。结论:当归素能增加 KAT6A 的表达,而 KAT6A 表达的增加有助于激活 Nrf2/HO-1 抗氧化应激系统,降低破骨细胞中的 ROS 水平,从而抑制氧化应激水平和破骨细胞的形成。
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Angelicin improves osteoporosis in ovariectomized rats by reducing ROS production in osteoclasts through regulation of the KAT6A/Nrf2 signalling pathway.

Background: Angelicin, which is found in Psoralea, can help prevent osteoporosis by stopping osteoclast formation, although the precise mechanism remains unclear.

Methods: We evaluated the effect of angelicin on the oxidative stress level of osteoclasts using ovariectomized osteoporosis model rats and RAW264.7 cells. Changes in the bone mass of the femur were investigated using H&E staining and micro-CT. ROS content was investigated by DHE fluorescence labelling. Osteoclast-related genes and proteins were examined for expression using Western blotting, immunohistochemistry, tartrate-resistant acid phosphatase staining, and real-time quantitative PCR. The influence of angelicin on osteoclast development was also evaluated using the MTT assay, double luciferin assay, chromatin immunoprecipitation, immunoprecipitation and KAT6A siRNA transfection.

Results: Rats treated with angelicin had considerably higher bone mineral density and fewer osteoclasts. Angelicin prevented RAW264.7 cells from differentiating into osteoclasts in vitro when stimulated by RANKL. Experiments revealed reduced ROS levels and significantly upregulated intracellular KAT6A, HO-1, and Nrf2 following angelicin treatment. The expression of genes unique to osteoclasts, such as MMP9 and NFATc1, was also downregulated. Finally, KAT6A siRNA transfection increased intracellular ROS levels while decreasing KAT6A, Nrf2, and HO-1 protein expression in osteoclasts. However, in the absence of KAT6A siRNA transfection, angelicin greatly counteracted this effect in osteoclasts.

Conclusions: Angelicin increased the expression of KAT6A. This enhanced KAT6A expression helps to activate the Nrf2/HO-1 antioxidant stress system and decrease ROS levels in osteoclasts, thus inhibiting oxidative stress levels and osteoclast formation.

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来源期刊
Chinese Medicine
Chinese Medicine INTEGRATIVE & COMPLEMENTARY MEDICINE-PHARMACOLOGY & PHARMACY
CiteScore
7.90
自引率
4.10%
发文量
133
审稿时长
31 weeks
期刊介绍: Chinese Medicine is an open access, online journal publishing evidence-based, scientifically justified, and ethical research into all aspects of Chinese medicine. Areas of interest include recent advances in herbal medicine, clinical nutrition, clinical diagnosis, acupuncture, pharmaceutics, biomedical sciences, epidemiology, education, informatics, sociology, and psychology that are relevant and significant to Chinese medicine. Examples of research approaches include biomedical experimentation, high-throughput technology, clinical trials, systematic reviews, meta-analysis, sampled surveys, simulation, data curation, statistics, omics, translational medicine, and integrative methodologies. Chinese Medicine is a credible channel to communicate unbiased scientific data, information, and knowledge in Chinese medicine among researchers, clinicians, academics, and students in Chinese medicine and other scientific disciplines of medicine.
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