科研之友
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摘要
Background & Aims: Germander was withdrawn from the market after ifs use for weight control caused an epidemic of hepatitis, Its toxicity was shown to be caused by diterpenoids and their cytochrome P4503A-mediated metabolic activation into electrophilic metabolites that deplete cellular thiols, The aim of the present study was to determine the mechanisms of cell death, Me?hods: isolated rat hepatocytes were incubated for 2 hours with germander diterpenoids (100 mu g/mL). Results: Diterpenoids decreased cell glutathione, increased cytosolic [Ca2+], activated Ca2+-dependent tissue transglutaminase forming a cross-linked protein scaffold, and caused internucleosomal DNA fragmentation and the ultrastructural features of apoptosis. Cell death was prevented by decreasing metabolic activation (with troleandomycin), preventing depletion of glutathione (with cystine), blocking activation of Ca2+-modulated enzymes (With calmidazolium), or inhibiting internucleosomal DNA fragmentation (with aurintricarboxylic acid), Apoptosis was increased acid diterpenoids caused overexpression of p53 and interleukin 1 beta-converting enzyme in rats treated with dexamethasone (cytochrome P4503A inducer), Apoptosis was also increased by a diet deficient in sulfur amino, acids, Conclusions: The germander furano diterpenoids cause apoptosis within 2 hours in isolated rat hepatocytes. Electrophilic metabolites may stimulate apoptosis by decreasing thiols, increasing [Ca2+], and activating Ca2+-dependent transglutaminase and endonucleases.
- 出版日期1997-10
