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芍药苷通过一种氧化还原相关机制诱导淋巴细胞凋亡。

Paeoniflorin induces apoptosis of lymphocytes through a redox-linked mechanism.

作者信息

Tsuboi Hideo, Hossain Khaled, Akhand Anwarul A, Takeda Kozue, Du Jun, Rifa'i Muhaimin, Dai Yan, Hayakawa Akemi, Suzuki Haruhiko, Nakashima Izumi

机构信息

Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.

出版信息

J Cell Biochem. 2004 Sep 1;93(1):162-72. doi: 10.1002/jcb.20134.

Abstract

Paeoniflorin (PF), isolated from paeony root, has been used as a herbal medicine for more than 1,200 years in China, Korea, and Japan for its anti-allergic, anti-inflammatory, and immunoregulatory effects. In this study, we found that PF induces apoptosis in both murine T-lineage cells and human T-cell leukemia Jurkat cells. This apoptosis was mediated through the reduction of mitochondrial membrane potential, activation of caspase, and fragmentation of DNA. Interestingly, PF induced generation of reactive oxygen species (ROS) and a reducing agent, dithiothreitol (DTT), and a ROS scavenger, N-acetyl cysteine (NAC), successfully attenuated the PF-induced apoptosis. Additionally, PF induced the phosphorylation of three mitogen-activated protein (MAP) family kinases, extracellular signal-regulated kinase, c-Jun amino-terminal kinase (JNK), and p38 MAP kinase. Curcumin, an anti-oxidant and JNK inhibitor, inhibited PF-induced apoptosis, suggesting the possible involvement of curcumin-sensitive JNK or other redox-sensitive elements in PF-induced apoptosis. These results partially explain the action mechanism of PF-containing paeony root as a herbal medicine.

摘要

芍药苷(PF)从芍药根中分离得到,在中国、韩国和日本作为草药使用已有1200多年历史,因其具有抗过敏、抗炎和免疫调节作用。在本研究中,我们发现PF可诱导小鼠T系细胞和人T细胞白血病Jurkat细胞凋亡。这种凋亡是通过线粒体膜电位降低、半胱天冬酶激活和DNA片段化介导的。有趣的是,PF可诱导活性氧(ROS)生成,而还原剂二硫苏糖醇(DTT)和ROS清除剂N-乙酰半胱氨酸(NAC)可成功减弱PF诱导的凋亡。此外,PF可诱导三种丝裂原活化蛋白(MAP)家族激酶,即细胞外信号调节激酶、c-Jun氨基末端激酶(JNK)和p38 MAP激酶的磷酸化。抗氧化剂和JNK抑制剂姜黄素可抑制PF诱导的凋亡,提示姜黄素敏感的JNK或其他氧化还原敏感元件可能参与PF诱导的凋亡。这些结果部分解释了含PF的芍药根作为草药的作用机制。

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