Toxicity of quinacrine can be reduced by Co-administration of p-glycoprotein inhibitor in sporadic Creutzfeldt-Jakob disease

被引:16
作者
Satoh, K
Shirabe, S
Eguchi, K
Yamauchi, A
Kataoka, Y
Niwa, M
Nishida, N
Katamine, S
机构
[1] Nagasaki Univ, Dept Internal Med 1, Grad Sch Biomed Sci, Nagasaki 8528501, Japan
[2] Fukuoka Univ, Fac Pharmaceut Sci, Dept Pharmaceut Care & Hlth Sci, Jonan Ku, Fukuoka 8128582, Japan
[3] Nagasaki Univ, Grad Sch Biomed Sci, Dept Pharmacol, Nagasaki, Japan
[4] Nagasaki Univ, Grad Sch Biomed Sci, Dept Mol Microbiol & Immunol, Nagasaki 8528501, Japan
关键词
quinacrine; sporadic Creutzfeldt-Jakob disease; p-glycoprotein inhibitor;
D O I
10.1007/s10571-004-6926-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
1. Recent publication has suggested that quinacrine may be a candidate for treatment of Creutzfeldt-Jakob disease (CJD). But serious toxicity of quinacrine to liver and hematological system has been reported. 2. We disclosed the permeability of quinacrine can be enhanced by presence of p-glycoprotein inhibitor at blood-brain barrier in vitro. Therefore, we tried the protocol of combination of quinacrine and p-glycoprotein inhibitor, verapamil for patients with CJD. 3. When compared clinical effects by quinacrine and the combination therapy, improvement of clinical findings was observed at the same level without any adverse effects. Low-dose quinacrine with verapamil can be used as safe treatment of CJD.
引用
收藏
页码:873 / 875
页数:3
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