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柴胡皂苷 A 通过 SIRT1/Nrf2 通路抑制铁死亡缓解金黄色葡萄球菌诱导的乳腺炎。

Saikosaponin A alleviates Staphylococcus aureus-induced mastitis in mice by inhibiting ferroptosis via SIRT1/Nrf2 pathway.

机构信息

Department of Breast Surgery, China-Japan Union Hospital of Jilin University, Changchun, China.

Department of Anesthesiology, China-Japan Union Hospital of Jilin University, Changchun, China.

出版信息

J Cell Mol Med. 2023 Nov;27(22):3443-3450. doi: 10.1111/jcmm.17914. Epub 2023 Aug 29.

Abstract

Mastitis is a common and serious bacterial infection of the mammary gland. Saikosaponin A (SSA) is a triterpenoid saponin isolated from Bupleurum falcatum that has the ability to treat various diseases. However, little is known about the role of SSA in achieving mastitis remission. Here, we found that SSA alleviated Staphylococcus aureus (S. aureus)-induced mastitis by attenuating inflammation and maintaining blood-milk barrier integrity. Furthermore, S. aureus activated nuclear factor kappa B (NF-κB) pathway by upregulated p-p65 and p-IκB. S. aureus also induced ferroptosis in mammary gland in mice, mainly characterized by excessive iron accumulation, mitochondrial morphological changes and impaired antioxidant production. However, S. aureus-induced NF-κB activation and ferroptosis were prevented by SSA. Moreover, SAA could upregulate the expression of SIRT1, Nrf2, HO-1 and GPX4. And the inhibitory effects of SAA on inflammation and ferroptosis were reversed by SIRT1 inhibitor EX-527. In conclusion, SAA protected S. aureus-induced mastitis through suppressing inflammation and ferroptosis by activating SIRT1/Nrf2 pathway.

摘要

乳腺炎是一种常见且严重的乳腺细菌感染。柴胡皂苷 A(SSA)是从柴胡中分离出的一种三萜皂苷,具有治疗各种疾病的能力。然而,人们对 SSA 在实现乳腺炎缓解方面的作用知之甚少。在这里,我们发现 SSA 通过减轻炎症和维持血乳屏障完整性来缓解金黄色葡萄球菌(S. aureus)诱导的乳腺炎。此外,S. aureus 通过上调 p-p65 和 p-IκB 激活核因子 kappa B(NF-κB)通路。金黄色葡萄球菌还在小鼠的乳腺中诱导铁死亡,主要表现为铁积累过多、线粒体形态改变和抗氧化产物受损。然而,SSA 可预防 S. aureus 诱导的 NF-κB 激活和铁死亡。此外,SAA 可以上调 SIRT1、Nrf2、HO-1 和 GPX4 的表达。并且 SIRT1 抑制剂 EX-527 逆转了 SAA 对炎症和铁死亡的抑制作用。总之,SSA 通过激活 SIRT1/Nrf2 通路抑制炎症和铁死亡来保护 S. aureus 诱导的乳腺炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e50/10660613/791bbf170c2e/JCMM-27-3443-g001.jpg

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