Skip to main content

Advertisement

Log in

Evaluation of adrenomedullin levels in renal parenchyma subjected to extracorporeal shockwave lithotripsy

  • Original Paper
  • Published:
Urological Research Aims and scope Submit manuscript

Abstract

Despite its safety and efficacy, the traumatic effects of high-energy shock waves (HESW) on renal morphology and function during long-term follow-up have yet to be elucidated. Although the main target of shock waves is the stone located in the kidney, the surrounding tissue and other organs are also subjected to trauma during this procedure. In contrast to renal blood flow evaluation after shock wave treatment, ischemic development, causing varying degrees of damage at the tissue level, has not been well evaluated. . The renoprotective peptide adrenomedullin (AM) is a potent vasorelaxing, natriuretic and cell growth modulating peptide, which is thought to act as an autocrine/paracrine regulator in renal glomeruli and tubules. In this experimental study, renal parenchymal AM levels were assessed in an attempt to evaluate the effect of HESW on the tissue levels of this peptide, which may be responsible for the regulation of ischemia induced by extracorporeal shock wave lithotripsy(ESWL), in a rabbit model. Thirty white New Zealand rabbits, each weighing 3–5 kg were used. The animals were divided into three main groups, and varying numbers of shock waves (1,000, 1,500, 2,000) were applied under fluoroscopic localization to the same kidney of all animals. Ketamine HCl anesthesia was administered (15–20 mg/kg) and all of the procedures were performed with a Multimed 2000 lithotriptor. Untreated contralateral kidneys were evaluated as controls. Following HESW application, the treated and untreated kidneys of each animal were removed through bilateral flank incisions under ketamine HCl anesthesia after 24 h and 7 days, respectively. Tissue AM levels were assessed with immunohistochemistry. During the early follow-up period (24 h), both treated and untreated kidneys showed a moderate to high degree of AM positivity. The number of tubules stained with AM increased as the number of shock waves increased and the expression of this protein became evident, possibly due to a higher degree of tissue damage. Additionally, a limited degree of AM positivity was noted in the contralateral kidneys although this was not as evident as the positivity seen in the treated kidneys. Assessment of tissue AM levels during late follow-up (7 days) in both kidneys demonstrated a moderate or limited degree of positivity in the treated kidneys. Limited or no positivity could be demonstrated in the contralateral kidneys at this time.Taking the certain traumatic effects of HESW, which causes transient ischemia during ESWL, into account, we conclude that the application of HESW results in a transient decrease in renal perfusion, causing ischemic injury in treated as well as in contralateral (untreated) kidneys. This ischemic event lasts for a short time and seemed to be dose- and time-dependent. Increased tissue levels of AM appear to be a potential defence against ESWL induced ischemia.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.

Similar content being viewed by others

References

  1. Akbay C, Sayın C, Sarıca K, Soygür T, Sabuncuoğlu B (1998) Effect of verapamil on rabbit renal tissue after shock wave lithotripsy: an ultrastructural approach. Electron Microsc 4: 493

    CAS  Google Scholar 

  2. Baltacı S, Özer G, Soygür T, Yaman Ö, Sarıca K, Müftüoğlu YZ, Göğüş O (1996) Effects of extracorporeal shock wave lithotripsy (ESWL) on urinary epidermal growth (EGF) levels. J Endourol 10: 519

    PubMed  Google Scholar 

  3. Bauer V, Bauer F(1996) Reactive oxygen species as mediators of tissue protection and injury. Gen Physiol Biophys 18: 7

    Google Scholar 

  4. Bedük Y, Erden İ, Sarıca K, Aytaç S, Karalezli G, Göğüş O (1994) Evaluation of renal morphology and function by CFDS immediately after ESWL. J Endourol 7: 457

    Google Scholar 

  5. Bomanji J, Boddy S, Britton KE, Nimmon CC, Whitfield HN (1987) Radionuclide evaluation pre-and post extracorporeal shock wave lithotripsy for renal calculi. J Nucl Med 28: 1284

    Google Scholar 

  6. Frick J, Sarıca K, Köhle R, Kunit, G (1991) Long-term follow-up after extracorporeal shock wave lithotripsy in children. Eur Urol 19: 225

    CAS  PubMed  Google Scholar 

  7. Hirata Y, Hayakawa H, Suzuki Y, Suzuki E, Ikenouchi H, Kohmoto O, Kimura K, Kitamura K, Eto T, Kangawa K, Matsuo H, Omata M (1995) Mechanisms of adrenomedullin-induced vasodilatation in the rat kidney. Hypertension 25: 790

    CAS  PubMed  Google Scholar 

  8. Jougasaki M, Wei CM, Aarhus LL, Heublein DM, Sandberg SM, Burnett JC (1995) Renal localization and actions of adrenomedullin: a natriuretic peptide. Am J Physiol 268: F675

    Google Scholar 

  9. Karalezli G, Göğüş O, Bedük Y, Köküuslu C, Sarıca K, Köksal O (1993) Histopathologic effects of ESWL on rabbit kidney. Urol Res 21: 67

    CAS  PubMed  Google Scholar 

  10. Kaude JV, Williams CM, Miliner MR, Scott KN, Finlayson B (1985) Renal morphology and function immediately after ESWL. Am J Roentgenol 145: 305

    CAS  Google Scholar 

  11. Kitamura K, Kangawa K, Kawamoto M, Ichiki Y, Nakamura S, Matsuo H, Eto T (1995) Adrenomedullin: a novel hypotensive peptide isolated from human pheochromacytoma. Biochem Biophys Res Commun 192: 553

    Article  Google Scholar 

  12. Krysiewicz S (1992) Complications of renal extracorporeal shock wave lithotripsy reviewed. Urol Radiol 13: 139

    CAS  PubMed  Google Scholar 

  13. Küpeli B, Sarıca K, Koşar A, Alçığır G, Budak M, Özdiler E (1995) Histopathologic effects of high energy shock waves on rat ovary. In: Tiselius HG (ed) Renal stones: aspects on their formation, removal and prevention. Proceedings of the 6th European Symposium on Urolithiasis. Stockholm, Sweden, p 242

  14. Mashiach E, Sela S, Winaver J, Shasha SM, Kristal B (1998) Renal ischemia-reperfusion injury: contribution of nitric oxide and renal blood flow. Nephron 80: 458

    Article  CAS  PubMed  Google Scholar 

  15. Mukoyama M, Sugavara A, Nagae T, Mori K, Murabe H, Itoh H, Tanaka I, Nakao K (2001) Role of adrenomedullin and its receptor system in renal pathophysiology. Peptides 22: 1925

    Article  CAS  PubMed  Google Scholar 

  16. Nagata D, Hirata Y, Suzuki E, Kakoki M, Hayaakawa H, Goto A, Ishimitsu T, Minamino N, Ono Y, Kangawa K, Matsuo H, Omata M (1999) Hypoxia induced adrenomedullin production in the kidney. Kidney Int 55: 1259

    Article  CAS  PubMed  Google Scholar 

  17. Sarıca K, Koşar A, Yaman O, Bedük Y, Durak I, Gögüş O, Kavukcu M (1996) Evaluation of ischemia after ESWL: detection of free oxygen radical scavenger enzymes in renal parenchyma subjected to high-energy shock waves. Urol Int 57 :221

    PubMed  Google Scholar 

  18. Sarıca K, Soygür T, Yaman Ö., Özer G, Sayın N, Akbay C, Küpeli S, Yaman LS (1996) Stone recurrence after shock wave lithotripsy: evaluation of possible enhanced crystal deposition in traumatized tissue in rabbit model. J Endourol 10: 513

    PubMed  Google Scholar 

  19. Sarıca K, Süzer O, Yaman O, Küpeli B, Baltaci S, Bilaloglu E, Tasman S (1996) Leucine aminopeptidase enzymuria: quantification of renal tubular damage following extracorporeal shock wave lithotripsy. Int Urol Nephrol 28: 621

    PubMed  Google Scholar 

  20. Sarıca K, Özer G, Soygür T, Yaman Ö, Özer E, Ustün H, Yaman LS, Gogus O (1997) Preservation of shock wave-induced renal histologic changes by dermatan sulphate. Urology 49: 145

    Article  PubMed  Google Scholar 

  21. Sarıca K, Türkölmez K, Koşar A, Alçığır G, Özdiler E, Göğüş O (1998) Evaluation of basal membrane antibody (immunoglobulin G) formation after high energy shock wave application in rats. J Endourol 12: 505

    PubMed  Google Scholar 

  22. Sarıca K, Bakır K, Yağcı F, Topçu O, Akbay C, Sayın N, Korkmaz C (1999) Limitation of possible enhanced crystal deposition by Verapamil in renal parenchyma after shock wave application in rabbit model. J Endourol 13: 343

    PubMed  Google Scholar 

  23. Strohmaier WL, Lahme S, Weidenbach PM, Bichler KH (1999) Reduction of high-energy shock-wave-induced renal tubular injury by selenium. Urol Res 27: 382

    PubMed  Google Scholar 

  24. Thamilselvan S, Byer KJ, Hackett RL, Khan SR (2000) Free radical scavengers, catalase and superoxide dismutase provide protection from oxalate-associated injury to LLC-PK1 and MDCK cells. J Urol 64: 224

    Google Scholar 

  25. Willis LR, Evan AP, Connors BA, Blomgren P, Fineberg NS, Lingeman JE (1999) Relationship between kidney size, renal injury, and renal impairment induced by shock wave lithotripsy. J Am Soc Nephrol 10: 1753

    CAS  PubMed  Google Scholar 

  26. Yaman Ö, Sarıca K, Özer G, Soygür T, Kutsal O, Yaman LS, Göğüş O (1996) Protective effect of Verepamil on renal histology following shock wave application in rabbit model. J Endourol.10: 329

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Kemal Sarica or İbrahim Sari.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sarica, K., Sari, İ., Balat, A. et al. Evaluation of adrenomedullin levels in renal parenchyma subjected to extracorporeal shockwave lithotripsy. Urol Res 31, 267–271 (2003). https://doi.org/10.1007/s00240-003-0323-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00240-003-0323-4

Keywords

Navigation