Literature DB >> 12163343

Renal targeting of captopril selectively enhances the intrarenal over the systemic effects of ACE inhibition in rats.

R Folgert G Haverdings1, Marijke Haas, Gerjan Navis, Anne-Miek Van Loenen-Weemaes, Dirk K F Meijer, Dick De Zeeuw, Frits Moolenaar.   

Abstract

1 In previous studies on the renal targeting of the ACE inhibitor captopril, we demonstrated that a 6 fold increased concentration of this drug could be obtained in the kidney after conjugation to the low-molecular-weight protein lysozyme. In this study, we investigated in unrestrained rats whether systemic administration of captopril-lysozyme also results in an enhanced effect on renal parameters, relative to the systemic effects. 2 Renal effects: intravenous infusion of captopril-lysozyme for 6 h resulted in a more pronounced increment of renal blood flow (31+/-2% vs 17+/-4% at 0.5 mg kg(-1) 6h(-1), P<0.01) and an approximately 5 fold enhanced natriuresis (167+/-17% vs 36+/-7% at 1 mg kg(-1) 6 h(-1), P<0.001) in comparison with equimolar amounts of captopril as a free drug. In correspondence with these findings, renal ACE inhibition was potentiated approximately 5 fold (-50+/-4% vs -22+/-3% at 1 mg kg(-1) 6 h(-1), P<0.001). 3 Systemic effects: conjugated captopril did not affect blood pressure in dosages up to 5 mg kg(-1) 6 h(-1). This effect coincided with a less pronounced inhibition of the pressor response to intravenously administered angiotensin I (-12+/-3% vs -66+/-5% at 1 mg kg(-1) 6 h(-1), P<0.001), and a markedly attenuated plasma ACE inhibition (-19+/-2% vs -37+/-3% at 1 mg kg(-1) 6 h(-1), P<0.001) compared to an equivalent dose of free captopril. 4 An experiment of continued intravenous administration of captopril-lysozyme for 7 days in nephrotic syndrome demonstrated that the conjugate is also active in renal disease: the antiproteinuric response was substantially augmented (-67+/-5% vs -15+/-7% at 4 mg kg(-1) 24 h(-1), P<0.001) compared to the free drug, in the absence of blood pressure reduction. 5 These data demonstrate that intravenous administration of a captopril-lysozyme conjugate leads to more selective renal ACE inhibition and enhanced renal effects as well as less systemic effects compared to captopril itself.

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Year:  2002        PMID: 12163343      PMCID: PMC1573442          DOI: 10.1038/sj.bjp.0704814

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  51 in total

1.  Sodium depletion enhances the antiproteinuric effect of ACE inhibition in established experimental nephrosis.

Authors:  R T Gansevoort; F H Wapstra; J J Weening; P E de Jong; D de Zeeuw
Journal:  Nephron       Date:  1992       Impact factor: 2.847

Review 2.  Structural and functional features of protein handling in the kidney proximal tubule.

Authors:  E I Christensen; S Nielsen
Journal:  Semin Nephrol       Date:  1991-07       Impact factor: 5.299

Review 3.  Circulatory and extracirculatory effects of angiotensin-converting enzyme inhibition.

Authors:  M A Weber; J M Neutel; D H Smith
Journal:  Am Heart J       Date:  1992-05       Impact factor: 4.749

4.  Effect of intrarenal renin inhibition on renal hemodynamics and excretory function.

Authors:  K M Verburg; J R Kadam; G A Young; S H Rosenberg; H D Kleinert
Journal:  Am J Physiol       Date:  1990-07

5.  Combined intrarenal blockade of the renin-angiotensin system in the conscious dog.

Authors:  H M Siragy; N L Howell; M J Peach; R M Carey
Journal:  Am J Physiol       Date:  1990-03

6.  Control of renal function by intrarenal angiotensin II in the dog.

Authors:  N R Levens
Journal:  J Cardiovasc Pharmacol       Date:  1990       Impact factor: 3.105

7.  Therapeutic benefit of captopril in salt-loaded stroke-prone spontaneously hypertensive rats is independent of hypotensive effect.

Authors:  C T Stier; P Chander; W H Gutstein; S Levine; H D Itskovitz
Journal:  Am J Hypertens       Date:  1991-08       Impact factor: 2.689

8.  Comparison of systemic and intrarenal converting enzyme inhibition by MK-422 on renal hemodynamics in conscious dogs.

Authors:  B G Zimmerman; C J Finis
Journal:  J Cardiovasc Pharmacol       Date:  1985 Jul-Aug       Impact factor: 3.105

9.  Analysis of influence of extra- and intrarenally formed angiotensin II on renal blood flow.

Authors:  M E Rassier; T Li; B G Zimmerman
Journal:  J Cardiovasc Pharmacol       Date:  1986       Impact factor: 3.105

10.  Intrarenal converting enzyme inhibition in rabbit.

Authors:  T Li; B G Zimmerman
Journal:  J Cardiovasc Pharmacol       Date:  1987       Impact factor: 3.105

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  2 in total

1.  Low molecular weight hydroxyethyl chitosan-prednisolone conjugate for renal targeting therapy: synthesis, characterization and in vivo studies.

Authors:  Xia-kai He; Zhi-xiang Yuan; Xiao-juan Wu; Chao-qun Xu; Wan-yu Li
Journal:  Theranostics       Date:  2012-11-06       Impact factor: 11.556

Review 2.  Kidney-targeted drug delivery systems.

Authors:  Peng Zhou; Xun Sun; Zhirong Zhang
Journal:  Acta Pharm Sin B       Date:  2014-01-23       Impact factor: 11.413

  2 in total

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