Sarcophytolide:: a new neuroprotective compound from the soft coral Sarcophyton glaucum

被引:46
作者
Badria, FA
Guirguis, AN
Perovic, S
Steffen, R
Müller, WEG
Schröder, HC
机构
[1] Johannes Gutenberg Univ Mainz, Inst Physiol Chem, Abt Angew Mol Biol, D-55099 Mainz, Germany
[2] Mansoura Univ, Fac Pharm, Dept Pharmacognosy, Mansoura 35516, Egypt
[3] Mansoura Univ, Fac Sci, Dept Zool, Mansoura 35516, Egypt
关键词
Sarcophyton glaucum; sarcophytolide; neuroprotective activity; glutamate; cell death; calcium;
D O I
10.1016/S0300-483X(98)00124-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bioactivity-guided fractionation of an alcohol extract of the soft coral Sarcophyton glaucum collected from the intertidal areas and the fringing coral reefs near Hurghada, Red Sea, Egypt resulted in the isolation of a new lactone cembrane diterpene, sarcophytolide. The structure of this compound was deduced from its spectroscopic data and by comparison of the spectral data with those of known closely related cembrane-type compounds. In antimicrobial assays, the isolated compound exhibited a good activity towards Staphylococcus aureus, Pseudomonas aeruginosa, and Saccharomyces cerevisiae. Sarcophytolide was found to display a strong cytoprotective effect against glutamate-induced neurotoxicity in primary cortical cells from rat embryos. Preincubation of the neurons with 1 or 10 mu g/ml of sarcophytolide resulted in a significant increase of the percentage of viable cells from 33 +/- 4% (treatment of the cells with glutamate only) to 44 +/- 4 and 92 +/- 6%, respectively. Administration of sarcophytolide during the post-incubation period following glutamate treatment did not prevent neuronal cell death. Pretreatment of the cells with sarcophytolide for 30 min significantly suppressed the glutamate-caused increase in the intracellular Ca2+ level ([Ca2+](i)). Evidence is presented that the neuroprotective effect of sarcophytolide against glutamate may be partially due to an increased expression of the proto-oncogene bcl-2. The coral secondary metabolite, sarcophytolide, might be of interest as a potential drug for treatment of neurodegenerative disorders. (C) 1998 Elsevier Science ireland Ltd. All rights reserved.
引用
收藏
页码:133 / 143
页数:11
相关论文
共 38 条
[11]   NEW CEMBRANE-TYPE DITERPENOIDS FROM THE OKINAWAN SOFT CORAL SINULARIA SP [J].
IGUCHI, K ;
SHIMURA, H ;
YAMADA, Y .
JOURNAL OF NATURAL PRODUCTS, 1992, 55 (12) :1779-1782
[12]   PROGRAMMED CELL-DEATH AND BCL-2 PROTECTION IN VERY-LOW OXYGEN [J].
JACOBSON, MD ;
RAFF, MC .
NATURE, 1995, 374 (6525) :814-816
[13]  
Karuso P., 1987, BIOORGANIC MARINE CH, P31, DOI DOI 10.1007/978-3-642-72726-9_2
[14]  
Kaul P. N., 1978, DRUGS FOOD SEA MYTH
[16]   GLUTAMATE TRIGGERS INTERNUCLEOSOMAL DNA CLEAVAGE IN NEURONAL CELLS [J].
KURE, S ;
TOMINAGA, T ;
YOSHIMOTO, T ;
TADA, K ;
NARISAWA, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (01) :39-45
[17]  
LI RS, 1992, STEROIDS, V57, P3
[18]   GP120 OF HIV-1 INDUCES APOPTOSIS IN RAT CORTICAL CELL-CULTURES - PREVENTION BY MEMANTINE [J].
MULLER, WEG ;
SCHRODER, HC ;
USHIJIMA, H ;
DAPPER, J ;
BORMANN, J .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1992, 226 (03) :209-214
[19]   CYTOPROTECTIVE EFFECT OF NMDA RECEPTOR ANTAGONISTS ON PRION PROTEIN (PRION(SC))-INDUCED TOXICITY IN RAT CORTICAL CELL-CULTURES [J].
MULLER, WEG ;
USHIJIMA, H ;
SCHRODER, HC ;
FORREST, JMS ;
SCHATTON, WFH ;
RYTIK, PG ;
HEFFNERLAUC, M .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1993, 246 (03) :261-267
[20]   POTENTIATION OF THE CYTOSTATIC EFFECT OF BLEOMYCIN ON L5178Y MOUSE LYMPHOMA-CELLS BY PEPLEOMYCIN [J].
MULLER, WEG ;
GEISERT, M ;
ZAHN, RK ;
MAIDHOF, A ;
BACHMANN, M ;
UMEZAWA, H .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1983, 19 (05) :665-670