Zhang Yongli, Cui Yuqiang, Zhu Jiayong, Li Hongzhi, Mao Jianwen, Jin Xiaobao, Wang Xiangsheng, Du Yifan, Lu Jiazheng
Department of Biology, School of Basic Courses, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Afr J Tradit Complement Altern Med. 2012 Dec 31;10(2):258-69. doi: 10.4314/ajtcam.v10i2.10. eCollection 2013.
Juglans mandshurica Maxim is a traditional herbal medicines in China, and its anti-tumor bioactivities are of research interest. Bioassay-guided fractionation method was employed to isolate anti-tumor compounds from the stem barks of the Juglans mandshurica Maxim. The anti-tumor effect and biological activities of the extracted compound JMM6 were studied in BEL-7402 cells by MTT, Cell cycle analysis, Hoechst 33342 staining, Annexin V-FITC/PI assay and Detection of mitochondrial membrane potential (ΔΨm). After treatment with the JMM6, the growth of BEL-7402 cells was inhibited and cells displayed typical morphological apoptotic characteristics. Further investigations revealed that treatment with JMM6 mainly caused G2/M cell cycle arrest and induced apoptosis in BEL-7402 cells. To evaluate the alteration of mitochondria in JMM6 induced apoptosis. The data showed that JMM6 decreased significantly the ΔΨm, causing the depolarization of the mitochondrial membrane. Our results show that the JMM6 will have a potential advantage of anti-tumor, less harmful to normal cells. This paper not only summarized the JMM6 pick-up technology from Juglans mandshurica Maxim and biological characteristic, but also may provide further evidence to exploit the potential medicine compounds from the stem-barks of the Chinese Juglans mandshurica Maxim.
胡桃楸是中国传统的草药,其抗肿瘤生物活性具有研究价值。采用生物活性追踪分离法从胡桃楸茎皮中分离抗肿瘤化合物。通过MTT法、细胞周期分析、Hoechst 33342染色、Annexin V-FITC/PI检测和线粒体膜电位(ΔΨm)检测,研究提取的化合物JMM6对BEL-7402细胞的抗肿瘤作用和生物学活性。用JMM6处理后,BEL-7402细胞的生长受到抑制,细胞呈现典型的形态学凋亡特征。进一步研究表明,JMM6处理主要导致BEL-7402细胞G2/M期细胞周期阻滞并诱导凋亡。为了评估JMM6诱导凋亡过程中线粒体的变化。数据显示,JMM6显著降低了ΔΨm,导致线粒体膜去极化。我们的结果表明,JMM6具有潜在的抗肿瘤优势,对正常细胞危害较小。本文不仅总结了从胡桃楸中提取JMM6的技术及其生物学特性,还可能为开发胡桃楸茎皮中的潜在药用化合物提供进一步的证据。