Relationship of asymmetric dimethylarginine to haemodialysis hypotension

被引:22
作者
Bergamini, S
Vandelli, L
Bellei, E
Rota, C
Manfredini, P
Tomasi, A
Albertazzi, A
Iannone, A [1 ]
机构
[1] Univ Modena & Reggio Emilia, Dept Biomed Sci, Modena, Italy
[2] Univ Modena & Reggio Emilia, Div Nephrol Dialysis & Renal Transplantat, Modena, Italy
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2004年 / 11卷 / 03期
关键词
asymmetric dimethylarginine; haemodialysis hypotension; nitric oxide; end stage renal disease; cytokine;
D O I
10.1016/j.niox.2004.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hypotension is one of the major complications in patients undergoing haemodialysis (HD), that is well evident in patients defined as "hypotension-prone." The mechanisms underlying the hypotensive episodes are not known. We carried out a clinical study on hypotension-prone HD patients to test the existence of a dysregulation in the nitric oxide (NO) generating pathway. Since asymmetric dimethylarginine (ADMA) is an endogenous compound which regulates NO synthesis, we measured its variation in plasma of stable-HD and hypotension-prone patients before, during, and at the end of HD. Before HD, the hypotension-prone patients have higher ADMA levels than stable-HD patients. The HD procedure significantly removes ADMA from plasma of stable-HD patients, while in the hypotension-prone ADMA levels are unchanged at the end of the HD. Moreover, in the hypotension-prone patients, during the hypotensive episode, a dramatic drop of ADMA levels is observed, followed by a rapid increase at the end of the HD. The symmetric dimethylarginine (SDMA), which has no effect on NO synthesis, is also high in plasma of both groups of HD patients compared to normal subjects, and in both groups its levels at the end of HD are significantly reduced. The hypotension-prone patients have basal TNF-alpha levels lower than the stable-HD groups, that significantly increase during the hypotensive episode. On the basis of these findings, we suggest that the hypotensive syndrome could be related to a dysregulation between ADMA metabolism and clearance due both to cytokines release and to an extremely fast ADMA clearance during HD, leading to an increase in NO blood levels. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:273 / 278
页数:6
相关论文
共 23 条
[11]   An enzyme hydrolyzing methylated inhibitors of nitric oxide synthase is present in circulating human red blood cells [J].
Kang, ES ;
Cates, TB ;
Harper, DN ;
Chang, TM ;
Myers, LK ;
Acchiardo, SR ;
Kimoto, M .
FREE RADICAL RESEARCH, 2001, 35 (06) :693-707
[12]   Hemodialysis hypotension: Interaction of inhibitors, iNOS, and the interdialytic period [J].
Kang, ES ;
Tevlin, MT ;
Wang, YB ;
Chiang, TM ;
Cardenas, R ;
Myers, LK ;
Acchiardo, SR .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 1999, 317 (01) :9-21
[13]   DETECTION OF N(G), N(G)-DIMETHYLARGININE DIMETHYLAMINOHYDROLASE IN THE NITRIC OXIDE-GENERATING SYSTEMS OF RATS USING MONOCLONAL-ANTIBODY [J].
KIMOTO, M ;
TSUJI, H ;
OGAWA, T ;
SASAOKA, K .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (02) :657-662
[14]  
Kozlov AV, 1996, METHOD ENZYMOL, V268, P229
[15]   EFFECTS OF AN ENDOGENOUS INHIBITOR OF NITRIC-OXIDE SYNTHESIS ON POSTCAPILLARY VENULES [J].
KUROSE, I ;
WOLF, R ;
GRISHAM, MB ;
GRANGER, DN .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (06) :H2224-H2231
[16]  
MACALLISTER R, 1994, J AM SOC NEPHROL, V5, P1057
[17]   Endogenous nitric oxide synthase inhibitor - A novel marker of atherosclerosis [J].
Miyazaki, H ;
Matsuoka, H ;
Cooke, JP ;
Usui, M ;
Ueda, S ;
Okuda, S ;
Imaizumi, T .
CIRCULATION, 1999, 99 (09) :1141-1146
[18]  
OGAWA T, 1989, J BIOL CHEM, V264, P10205
[19]  
ONHNISHI ST, 1998, NITRIC OXIDE PROTOCO, V100, P129
[20]   Hemodynamic changes during hemodialysis: Role of nitric oxide and endothelin [J].
Raj, DSC ;
Vincent, B ;
Simpson, K ;
Sato, E ;
Tones, KL ;
Welbourne, TC ;
Levi, M ;
Shah, V ;
Blandon, P ;
Zager, P ;
Robbins, RA .
KIDNEY INTERNATIONAL, 2002, 61 (02) :697-704