ACE inhibitors and all receptor antagonists in the treatment and prevention of bone marrow transplant nephropathy

被引:50
作者
Moulder, JE
Fish, BL
Cohen, EP
机构
[1] Med Coll Wisconsin, Dept Radiat Oncol, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
关键词
angiotensin II receptors; ACE inhibitors; captopril; kidney; radiation injuries; bone marrow transplant;
D O I
10.2174/1381612033455422
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Radiation nephropathy has emerged as a major complication of bone marrow transplantation (BMT) when total body irradiation (TBI) is used as part of the regimen. Classically, radiation nephropathy has been assumed to be inevitable, progressive, and untreatable. However, in the early 1990's, it was demonstrated that experimental radiation nephropathy could be treated with a thiol-containing ACE inhibitor, captopril. Further studies showed that enalapril (a non-thiol ACE inhibitor) was also effective in the treatment of experimental radiation nephropathy, as was an All receptor antagonist. Studies also showed that ACE inhibitors and All receptor antagonists were effective in the prophylaxis of radiation nephropathy. Interestingly, other types of antiltypertensive drugs were ineffective in prophylaxis, but brief use of a high-salt diet in the immediate post-irradiation period decreased renal injury. A placebo-controlled trial of captopril to prevent BMT nephropathy in adults is now underway. Since excess activity of the renin-angiotensin system (RAS) causes hypertension, and hypertension is a major feature of radiation nephropathy; an explanation for the efficacy of RAS antagonism in the prophylaxis of radiation nephropathy would be that radiation leads to RAS activation. However, current studies favor an alternative explanation, namely that the normal activity of the RAS is deleterious in the presence of radiation injury. On-going studies suggest that efficacy of RAS antagonists may involve interactions with a radiation-induced decrease in renal nitric oxide activity or with radiation-induced tubular cell proliferation. We hypothesize that while prevention (prophylaxis) of radiation nephropathy with ACE inhibitors, All receptor antagonists, or a high-salt diet work by suppression of the RAS, the efficacy of ACE inhibitors and All receptor antagonists in treatment of established radiation nephropathy depends on blood pressure control.
引用
收藏
页码:737 / 749
页数:13
相关论文
共 113 条
[61]   A new cause of renal thrombotic microangiopathy: Yttrium 90-DOTATOC internal radiotherapy [J].
Moll, S ;
Nickeleit, V ;
Mueller-Brand, J ;
Brunner, FP ;
Maecke, HR ;
Mihatsch, MJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (04) :847-851
[62]   Prevention of radiation-induced nephropathy and fibrosis in a model of bone marrow transplant by an angiotensin II receptor blocker [J].
Molteni, A ;
Moulder, JE ;
Cohen, EP ;
Fish, BL ;
Taylor, JM ;
Veno, PA ;
Wolfe, LF ;
Ward, WF .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2001, 226 (11) :1016-1023
[63]  
Moltenti A, 2000, INT J RADIAT BIOL, V76, P523, DOI 10.1080/095530000138538
[64]   ENDOGENOUS NITRIC-OXIDE - PHYSIOLOGY, PATHOLOGY AND CLINICAL RELEVANCE [J].
MONCADA, S ;
HIGGS, EA .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1991, 21 (04) :361-374
[65]   Angiotensin-converting enzyme inhibitors, angiotensin II receptor antagonists and calcium channel blocking agents: A review of potential benefits and possible adverse reactions [J].
Moser, M .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 29 (07) :1414-1421
[66]  
Moulder J E, 1997, Radiat Oncol Investig, V5, P50, DOI 10.1002/(SICI)1520-6823(1997)5:2<50::AID-ROI2>3.0.CO
[67]  
2-I
[68]   Noncontinuous use of angiotensin converting enzyme inhibitors in the treatment of experimental bone marrow transplant nephropathy [J].
Moulder, JE ;
Fish, BL ;
Cohen, EP .
BONE MARROW TRANSPLANTATION, 1997, 19 (07) :729-735
[69]   TREATMENT OF RADIATION NEPHROPATHY WITH ACE-INHIBITORS [J].
MOULDER, JE ;
FISH, BL ;
COHEN, EP .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1993, 27 (01) :93-99
[70]  
MOULDER JE, 1987, TRANSPLANTATION, V43, P589