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Terfenadine induces thyrnocyte apoptosis via mitochondrial pathway
被引:15
|作者:
Enomoto, R
Komai, T
Yoshida, Y
Sugahara, C
Kawaguchi, E
Okazaki, K
Kinoshita, H
Komatsu, H
Konishi, Y
Lee, E
[1
]
机构:
[1] Kobe Gakuin Univ, Fac Pharmaceut Sci, Dept Pharmacol, Kobe, Hyogo 6512180, Japan
[2] Kobe Gakuin Univ, High Technol Res Ctr, Kobe, Hyogo 6512180, Japan
[3] Natl Res Council Canada, Biotechnol Res Inst, Montreal, PQ H4P 2R2, Canada
关键词:
terfenadine;
apoptosis;
thymocyte;
mitochondria;
fexofenadine;
voltage-dependent K+ channel;
D O I:
10.1016/j.ejphar.2004.05.048
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The treatment of rat thymocytes with 10 muM terfenadine resulted in a significant increase in DNA fragmentation. The DNA fragmentation induced by terfenadine was dependent on its concentration and incubation time. In terfenadine-treated cells, the translocation of phosphatidylserine from the inside of plasma membrane to the outside, an early event of the apoptotic process, and chromatin condensation, the morphological characterization of apoptotic cell death, were observed. Terfenadine stimulated caspase-8, -9 and -3-like activities in an incubation time-dependent manner in thymocytes. The active forms of caspase-3 and -9 were detected in the extract from terfenadine-treated cells by immunoblotting analysis using specific antibodies to caspases, but active caspase-8 was not found in this fraction. Decrease in mitochondrial membrane potential and the release of cytochrome c from mitochondria to cytosol were observed in terfenadine-treated thymocytes. These results suggest that terfenadine induces apoptosis in rat thymocytes via mitochondrial pathway. (C) 2004 Elsevier B.V. All rights reserved.
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页码:11 / 21
页数:11
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