Modulation of tumor necrosis factor-α production with anti-hypertensive drugs

被引:34
作者
Fukuzawa, M
Satoh, J
Ohta, S
Takahashi, K
Miyaguchi, S
Qiang, XL
Sakata, Y
Nakazawa, T
Takizawa, Y
Toyota, T
机构
[1] Tohoku Univ, Sch Med, Dept Internal Med 3, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohokukosai Hosp, Dept Internal Med, Aoba Ku, Sendai, Miyagi 9800803, Japan
来源
IMMUNOPHARMACOLOGY | 2000年 / 48卷 / 01期
关键词
TNF-alpha; Ca channel blocker; alpha(1)-blocker; beta(1)-blocker; insulin resistance;
D O I
10.1016/S0162-3109(00)00179-X
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 is well known that some anti-hypertensive drugs affect insulin sensitivity and that turner necrosis factor-alpha (TNF-alpha) is a mediator of obesity-associated insulin resistance. In this study, rye have investigated the effect of anti-hypertensive drugs, calcium (Ca) channel blockers (amlodipine, manidipine and nicardipine), an alpha(1)-blocker (doxazosin), a beta(1)-blocker (metoprolol), and a thiazide diuretic (hydrochlorothiazide), on lipopolysaccharide (LPS)-induced TNF-alpha, production. TNF-alpha production, measured with a bioassay and an immunoassay, was evaluated both in vivo and in vitro, by utilizing mice and a human peripheral blued mononuclear cell culture, respectively, Nicardipine, or amlodipine, manidipine and doxazosin significantly inhibited TNF-alpha production in mice at doses more than one or ten times higher than those used clinically, respectively. On the other hand, metoprolol increased TNF-alpha production at doses of more than 10 times those used clinically, whereas hydrochlorothiazide did not alter production of the cytokine, The in vivo effects of these drugs were not necessary parallel to the in vitro effects. Because high doses of these drugs in mice correspond to clinical doses and effects in human, these actions may he related to beneficial and/or harmful effects of these drugs on TNF-alpha mediated diseases, including insulin resistance. (C) 2000 Elsevier Science B.V, All rights reserved.
引用
收藏
页码:65 / 74
页数:10
相关论文
共 42 条
[1]   THE LINK BETWEEN INSULIN-RESISTANCE AND HYPERTENSION - EFFECTS OF ANTIHYPERTENSIVE AND ANTIHYPERLIPIDAEMIC DRUGS ON INSULIN SENSITIVITY [J].
BABA, T ;
NEUGEBAUER, S .
DRUGS, 1994, 47 (03) :383-404
[2]  
BORG KO, 1975, ACTA PHARMACOL TOX, V36, P104
[3]  
BOYD RA, 1987, J PHARMACOL EXP THER, V243, P118
[4]  
BURGES RA, 1987, J CARDIOVASC PHARM, V9, P110, DOI 10.1097/00005344-198701000-00018
[5]  
CHAUDHRI G, 1989, J IMMUNOL, V143, P1290
[6]  
CHICHESTER CO, 1987, J CARDIOVASC PHARM, V10, pS21
[7]   PROSTACYCLIN ANALOGS SUPPRESS THE SYNTHESIS OF TUMOR-NECROSIS-FACTOR-ALPHA IN LPS-STIMULATED HUMAN PERIPHERAL-BLOOD MONONUCLEAR-CELLS [J].
EISENHUT, T ;
SINHA, B ;
GROTTRUPWOLFERS, E ;
SEMMLER, J ;
SIESS, W ;
ENDRES, S .
IMMUNOPHARMACOLOGY, 1993, 26 (03) :259-264
[8]   MODULATION OF LIPOPOLYSACCHARIDE-INDUCED TUMOR-NECROSIS-FACTOR-ALPHA PRODUCTION BY SELECTIVE ALPHA-ADRENERGIC AND BETA-ADRENERGIC DRUGS IN MICE [J].
ELENKOV, IJ ;
HASKO, G ;
KOVACS, KJ ;
VIZI, ES .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 61 (02) :123-131
[9]  
FEINSTEIN R, 1993, J BIOL CHEM, V268, P26055
[10]   Inhibition of tumor necrosis factor-α with anti-diabetic agents [J].
Fukuzawa, M ;
Satoh, J ;
Qiang, X ;
Miyaguchi, S ;
Sakata, Y ;
Nakazawa, T ;
Ikehata, F ;
Ohta, S ;
Toyota, T .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1999, 43 (03) :147-154