Natriuretic peptides inhibit apoptosis and prolong the survival of serum-deprived PC12 cells

被引:56
作者
Fiscus, RR [1 ]
Tu, AWK
Chew, SBC
机构
[1] Chinese Univ Hong Kong, Fac Med, Epithelial Cell Biol Res Ctr, Dept Physiol, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Ctr Gerontol, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Ctr Geriatr, Shatin, Hong Kong, Peoples R China
关键词
apoptosis; atrial natriuretic peptide; brain natriuretic peptide; cell survival; cGMP; DNA fragmentation; neural cell; neuroprotection;
D O I
10.1097/00001756-200102120-00003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) were investigated to determine effects on apoptotic DNA fragmentation and survival in serum-deprived PC 12 cells. Both peptides caused prolonged cGMP (but not cAMP) elevations lasting for greater than or equal to 6 h. The cGMP elevations were 10-, 50- and 68-fold for ANP and 26-, 100- and 148-fold for BNP at 1, 10 and 100 nM, respectively. BNP caused dose-dependent increases in cell survival rates during 3 days of serum deprivation. BNP (1 nM) increased 24 h survival rate from 36% to 67%. ANP(1 nM), BNP (1 nM) and 8-bromo-cGMP (0.1 mM) inhibited by 74.8%, 46.7% and 8.8%, respectively, the apoptotic DNA fragmentation in serum-deprived PC12 cells, measured by our recently developed quantitative technique using capillary electrophoresis with laser-induced fluorescence detector (CE-LIF). The data suggest prolonged cGMP elevations caused by ANP or BNP inhibit apoptotic DNA fragmentation and prolong the survival of serum-deprived PC12 cells. Neuro-Report 12:185-189 (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:185 / 189
页数:5
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