Planta Med 2007; 73(15): 1548-1553
DOI: 10.1055/s-2007-993739
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Secoaggregatalactone-A from Lindera aggregata Induces Apoptosis in Human Hepatoma Hep G2 Cells

Chien-Tsong Lin1 , Fang-Hua Chu2 , Shang-Tzen Chang2 , Pin-Ju Chueh3 , Yu-Chang Su1 , King-Tsuen Wu1 , Sheng-Yang Wang1
  • 1Department of Forestry, National Chung-Hsing University, Taichung, Taiwan
  • 2School of Forestry and Resource Conservation, National Taiwan University, Taipei, Taiwan
  • 3Institute of Biomedical Science, National Chung-Hsing University, Taichung, Taiwan
Further Information

Publication History

Received: May 26, 2007 Revised: October 5, 2007

Accepted: October 15, 2007

Publication Date:
12 November 2007 (online)

Abstract

A new secobutanolide, secoaggregatalactone A (1) was isolated from the leaves of Lindera aggregata. Results obtained from the cytotoxicity assay revealed that secoaggregatalactone A exhibited a noticeable cytotoxicity (EC50 = 6.61 μg/mL; 22.1 μM) against the human hepatoma cell line (Hep G2 cell line). According to morphological observations, flow cytometric analysis, and DNA fragmentation analysis, it was proven that the cytotoxicity of secoaggregatalactone A on human cells was due to apoptosis. Moreover, based on the results from the protein expression assay and confocal laser scanning microscope observations, it is assumed that secoaggregatalactone A induced apoptosis through the mitochondria pathway by way of cleavage of Bit to release cytochrome C and activate caspases-9 and -3, and then degradation of PARP.

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Dr. Sheng-Yang Wang

Department of Forestry

National Chung-Hsing University

250 Kuo-Kuang Road

Taichung 402

Taiwan

R.O.C.

Phone: +886-4-2284-0345 ext. 138

Fax: +886-4-2287-3628.

Email: taiwanfir@dragon.nchu.edu.tw

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