Flavonoids of Inula britannica protect cultured cortical cells from necrotic cell death induced by glutamate

被引:101
作者
Kim, SR
Park, MJ
Lee, MK
Sung, SH
Park, EJ
Kim, J
Kim, SY
Oh, TH
Markelonis, GJ
Kim, YC
机构
[1] Seoul Natl Univ, Coll Pharm, Kwanak Gu, Seoul 151742, South Korea
[2] Kyung Hee Univ, Grad Sch E W Med Sci, Seoul, South Korea
[3] Univ Maryland, Sch Med, Dept Anat & Neurobiol, Baltimore, MD 21201 USA
关键词
flavonoids; Inula britannica; oxidative stress; primary cultures of rat cortical cells; glutamate; glutathione; antioxidative enzymes; free radicals;
D O I
10.1016/S0891-5849(02)00751-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We previously reported 12 antioxidative flavonoids isolated from the n-BuOH extract of Inula britannica (Asteraceae). This prompted us to investigate further whether these flavonoids also showed antioxidative activity upon live cells grown in a culture system. Among the 12 flavonoids tested, only patuletin, nepetin, and axillarin protected primary cultures of rat cortical cells from oxidative stress induced by glutamate. These flavonoids exerted significant neuroprotective activity when they were administered either before or after the glutamate insult. Treatment with these flavonoids maintained the activities of such antioxidant enzymes as catalase. glutathione-peroxidase, and glutathione reductase. all of which play important roles in the antioxidative defense mechanism. Moreover, these three flavonoids also attenuated significant drops in glutathione induced by glutamate which is a routine concomitant of oxidative stress by inhibiting glutathione diminution. Accordingly. these flavonoids did not stimulate the synthesis of glutathione. With regard to structure-activity relationships, our results indicated that the 6-methoxyl group in the A ring and the 3', 4'-hydroxyl groups in the B ring are crucial for the protection against the oxidative stress: glycosylation greatly reduced their protective activities. Collectively, these results indicated that patuletin. nepetin. and axillarin strongly protect primary cultured neurons against glutamate-induced oxidative stress. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:596 / 604
页数:9
相关论文
共 36 条
[1]  
BEERS RF, 1952, J BIOL CHEM, V195, P133
[2]   HYDROGEN-PEROXIDE MEDIATES AMYLOID-BETA PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, JB ;
LESLEY, R ;
SCHUBERT, D .
CELL, 1994, 77 (06) :817-827
[3]   OXIDATIVE STRESS IN A CLONAL CELL-LINE OF NEURONAL ORIGIN - EFFECTS OF ANTIOXIDANT ENZYME MODULATION [J].
BUCKMAN, TD ;
SUTPHIN, MS ;
MITROVIC, B .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (06) :2046-2058
[4]  
CARLBERG I, 1975, J BIOL CHEM, V250, P5475
[5]   GLUTAMATE NEUROTOXICITY IN CORTICAL CELL-CULTURE IS CALCIUM DEPENDENT [J].
CHOI, DW .
NEUROSCIENCE LETTERS, 1985, 58 (03) :293-297
[6]  
CHOI DW, 1987, J NEUROSCI, V7, P369
[7]   OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[9]  
Desagher S, 1996, J NEUROSCI, V16, P2553
[10]  
FLOHE L, 1984, METHOD ENZYMOL, V105, P114