Angiotensin converting enzyme inhibitors suppress production of tumor necrosis factor-alpha in vitro and in vivo

被引:81
作者
Fukuzawa, M [1 ]
Satoh, J [1 ]
Sagara, M [1 ]
Muto, G [1 ]
Muto, Y [1 ]
Nishimura, S [1 ]
Miyaguchi, S [1 ]
Qiang, XL [1 ]
Sakata, Y [1 ]
Nakazawa, T [1 ]
Ikehata, F [1 ]
Ohta, S [1 ]
Toyota, T [1 ]
机构
[1] TOHOKU UNIV,SCH MED,DEPT INTERNAL MED 3,AOBA KU,SENDAI,MIYAGI 98077,JAPAN
来源
IMMUNOPHARMACOLOGY | 1997年 / 36卷 / 01期
关键词
ACE inhibitor; captopril; delapril; cilazapril; tumor necrosis factor-alpha;
D O I
10.1016/S0162-3109(96)00160-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It has been reported that angiotensin converting enzyme (ACE) inhibitors have beneficial effects on insulin resistance and congestive heart failure, in which elevations of serum tumor necrosis factor-alpha (TNF-alpha) level have been indicated. Therefore, in this study, we examined effect of ACE inhibitors on TNF-alpha production both in vitro and in vivo by using human blood mononuclear cells and mice, respectively. LPS (20 mu g/ml)-induced in vitro TNF-alpha production, measured by bioassay and enzyme-linked immunosorbent assay, was significantly inhibited with captopril, delapril and cilazapril in a concentration of 10(-3) mol/l. A single, oral administration of captopril, delapril and cilazapril at more than 10-fold doses of common clinical use in man significantly inhibited LPS (2 mg/kg)-induced serum TNF-alpha activity in Balb/c mice. These results indicate that ACE inhibitors such as captopril, delapril and cilazapril have an inhibitory effect on TNF-alpha production not only in vitro as previously reported, but also in vivo, although relatively high concentrations and large doses were required in this study.
引用
收藏
页码:49 / 55
页数:7
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