Literature DB >> 9219162

Prevention of radiocontrast-induced nephropathy by adenosine antagonists in rats with chronic nitric oxide deficiency.

C M Erley1, N Heyne, K Burgert, J Langanke, T Risler, H Osswald.   

Abstract

To evaluate therapeutic options for the prevention of radiocontrast media (RCM)-induced nephropathy, a model was developed in which rats received NG-nitro-L-arginine methyl ester (L-NAME) for 10 wk in order to inhibit nitric oxide (NO) synthetase. This study tests the hypothesis that infusion of an adenosine antagonist before RCM application may avoid the vasoconstrictive response in NO-depleted rats. Rats received L-NAME for 10 wk orally (50 mg/L drinking water) to achieve NO depletion. Renal function was determined by [3H]inulin clearance for analysis of the GFR and by flowmetry for assessing renal blood flow (RBF). After a control clearance period (baseline clearance period), the renal response to RCM application (sodium diatrizoate, 2 ml/kg body wt) was measured two times every 30 min starting 30 min after RCM application (clearance periods 1 and 2). L-NAME rats and control rats received two adenosine antagonists. The nonselective adenosine antagonist theophylline was given as an initial bolus of 50 mumol/kg body wt within 10 min, followed by continuous infusion of 100 mumol/kg body wt per h, and the specific adenosine A1-receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX) was given as a bolus of 100 micrograms/kg body wt before RCM application. Results were compared with vehicle infusion. In the control group, no significant change of GFR or RBF could be detected after application of RCM with or without prior infusion of DPCPX or theophylline. In L-NAME rats, RBF decreased significantly after RCM application (baseline, 5.6 +/- 0.2 ml/min; first clearance period, 4.6 +/- 0.3 ml/min [P < 0.05]; second clearance period, 4.3 +/- 0.3 [P < 0.01]). GFR was also reduced in L-NAME rats without previous infusion of theophylline or DPCPX (baseline, 0.95 +/- 0.1 ml/min; first clearance period, 0.83 +/- 0.1 ml/min; second clearance period, 0.69 +/- 0.1 ml/min [P = 0.058]). Prior treatment with either theophylline or DPCPX resulted in complete protection against a decline of RBF and GFR induced by RCM in L-NAME rats. Rats with chronic NO blockade showed a significant increase of the renal vasoconstrictive effect of contrast media. Application of L-NAME in rats seems to constitute a suitable animal model to study the pathophysiology of radiocontrast media-induced nephropathy. In this animal model, administration of adenosine antagonists prevented the decline of GFR and RBF.

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Year:  1997        PMID: 9219162     DOI: 10.1681/ASN.V871125

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  12 in total

Review 1.  Adenosine receptors and the kidney.

Authors:  Volker Vallon; Hartmut Osswald
Journal:  Handb Exp Pharmacol       Date:  2009

2.  Disposition of the acyclic nucleoside phosphonate (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl)adenine.

Authors:  M K Bijsterbosch; L J Smeijsters; T J van Berkel
Journal:  Antimicrob Agents Chemother       Date:  1998-05       Impact factor: 5.191

Review 3.  Methylxanthines and the kidney.

Authors:  Hartmut Osswald; Jürgen Schnermann
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Review 4.  [Iodinated contrast agent-induced nephropathy].

Authors:  C Erley
Journal:  Radiologe       Date:  2007-09       Impact factor: 0.635

5.  Comparison of renal damage by iodinated contrast or gadolinium in an acute renal failure rat model based on serum creatinine levels and apoptosis degree.

Authors:  Hyo-Sung Kwak; Young-Hwan Lee; Young-Min Han; Gong-Yong Jin; Won Kim; Gyung-Ho Chung
Journal:  J Korean Med Sci       Date:  2005-10       Impact factor: 2.153

6.  Effectiveness of aminophylline prophylaxis of renal impairment after coronary angiography in patients with chronic renal insufficiency.

Authors:  A Rohani
Journal:  Indian J Nephrol       Date:  2010-04

7.  Iohexol plasma clearance, a simple and reliable method to measure renal function in conscious mice.

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Journal:  Pflugers Arch       Date:  2016-06-17       Impact factor: 3.657

Review 8.  Why is diabetes mellitus a risk factor for contrast-induced nephropathy?

Authors:  Samuel N Heyman; Christian Rosenberger; Seymour Rosen; Mogher Khamaisi
Journal:  Biomed Res Int       Date:  2013-11-21       Impact factor: 3.411

9.  Oxidative stress caused by activation of NADPH oxidase 4 promotes contrast-induced acute kidney injury.

Authors:  Bo Young Jeong; Hoi Young Lee; Chang Gyo Park; Jaeku Kang; Seong-Lan Yu; Du-Ri Choi; Seung-Yun Han; Moon Hyang Park; Sungkwon Cho; Soo Young Lee; Won-Min Hwang; Sung-Ro Yun; Hye-Myung Ryu; Eun-Joo Oh; Sun-Hee Park; Yong-Lim Kim; Se-Hee Yoon
Journal:  PLoS One       Date:  2018-01-12       Impact factor: 3.240

Review 10.  Radiographic contrast-media-induced acute kidney injury: pathophysiology and prophylactic strategies.

Authors:  Umar Sadat
Journal:  ISRN Radiol       Date:  2013-09-16
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