The liver is an important organ in the metabolism of asymmetrical dimethylarginine (ADMA)

被引:153
作者
Nijveldt, RJ
Teerlink, T
Siroen, MPC
Van Lambalgen, AA
Rauwerda, JA
Van Leuuwen, PAM
机构
[1] Vrije Univ Amsterdam, Ctr Med, Inst Cardiovasc Res, Dept Surg, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Ctr Med, Inst Cardiovasc Res, Dept Clin Chem, NL-1007 MB Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Ctr Med, Inst Cardiovasc Res, Dept Physiol, NL-1007 MB Amsterdam, Netherlands
关键词
asymmetrical dimethylarginine; symmetrical dimethylarginine; liver; kidney;
D O I
10.1054/clnu.2002.0612
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background and Aims: Asymmetrical dimethylarginine (ADMA) is an endogenous inhibitor of nitric oxide (NO) synthase enzymes, whereas symmetrical dimethylarginine (SDMA) competes with arginine transport. Although both dimethylarginines may be important regulators of the arginine-NO pathway, their metabolism is largely unknown. Both dimethylarginines are removed from the body by urinary excretion. However, ADMA is also subject to enzymatic degradation by the enzyme dimethylarginine dimethylaminohydrolase (DDAH), which is highly expressed in the liver. To elucidate the role of the liver in the metabolism of ADMA, we aimed to investigate dimethylarginine handling of the liver in detail. Methods: Ten male Wistar rats were used for this study Blood flow was measured using radiolabeled microspheres according to the reference sample method. Concentrations of dimethylarginines were measured by HPLC. The combination of arteriovenous concentration difference and organ blood flow allowed calculation of net organ fluxes and fractional extraction rates. Results: Both the liver (0.89 +/- 011) and the kidney (0.68 +/- 0.06) showed a high net uptake (nmol/100 g body weight (BW)/min) of ADMA, whereas a significant net uptake of SDMA was only observed in the kidney (0.34 +/- 0.04). For the liver, fractional extraction rates were 29.5% +/- 3.0 for ADMA and 0.0% +/- 3.7 for SDMA. Fractional extraction rates of ADMA and SDMA for the kidney were 36.0% +/- 2.7 and 31.6% +/- 3.8, respectively. Conclusions: The liver plays an important role in the metabolism of ADMA by taking up large amounts of ADMA from the systemic circulation. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:17 / 22
页数:6
相关论文
共 41 条
[31]   Total nitric oxide production is low in patients with chronic renal disease [J].
Schmidt, RJ ;
Baylis, C .
KIDNEY INTERNATIONAL, 2000, 58 (03) :1261-1266
[32]   Reduced urinary excretion of nitric oxide metabolites and increased plasma levels of asymmetric dimethylarginine in men with essential hypertension [J].
Surdacki, A ;
Nowicki, M ;
Sandmann, J ;
Tsikas, D ;
Boeger, RH ;
Bode-Boeger, SM ;
Kruszelnicka-Kwiatkowska, O ;
Kokot, F ;
Dubiel, JS ;
Froelich, JC .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1999, 33 (04) :652-658
[33]   Determination of arginine, asymmetric dimethylarginine, and symmetric dimethylarginine in human plasma and other biological samples by high-performance liquid chromatography [J].
Teerlink, T ;
Nijveldt, RJ ;
de Jong, S ;
van Leeuwen, PAM .
ANALYTICAL BIOCHEMISTRY, 2002, 303 (02) :131-137
[34]   Colocalization of demethylating enzymes and NOS and functional effects of methylarginines in rat kidney [J].
Tojo, A ;
Welch, WJ ;
Bremer, V ;
Kimoto, M ;
Kimura, K ;
Omata, M ;
Ogawa, T ;
Vallance, P ;
Wilcox, CS .
KIDNEY INTERNATIONAL, 1997, 52 (06) :1593-1601
[35]   Increased endogenous nitric oxide synthase inhibitor in patients with congestive heart failure [J].
Usui, M ;
Matsuoka, H ;
Miyazaki, H ;
Ueda, S ;
Okuda, S ;
Imaizumi, T .
LIFE SCIENCES, 1998, 62 (26) :2425-2430
[36]   ENDOGENOUS DIMETHYLARGININE AS AN INHIBITOR OF NITRIC-OXIDE SYNTHESIS [J].
VALLANCE, P ;
LEONE, A ;
CALVER, A ;
COLLIER, J ;
MONCADA, S .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1992, 20 :S60-S62
[37]  
VALLANCE P, 1992, LANCET, V339, P572
[38]   Dimethylarginines in chronic renal failure [J].
Wahbi, N ;
Dalton, RN ;
Turner, C ;
Denton, M ;
Abbs, I ;
Swaminathan, R .
JOURNAL OF CLINICAL PATHOLOGY, 2001, 54 (06) :470-473
[39]   Arginine metabolism: nitric oxide and beyond [J].
Wu, GY ;
Morris, SM .
BIOCHEMICAL JOURNAL, 1998, 336 :1-17
[40]   INCREASE OF AN ENDOGENOUS INHIBITOR OF NITRIC-OXIDE SYNTHESIS IN SERUM OF HIGH CHOLESTEROL-FED RABBITS [J].
YU, XJ ;
LI, YJ ;
XIONG, Y .
LIFE SCIENCES, 1994, 54 (12) :753-758