Renal haemodynamic, microcirculatory, metabolic and histopathological responses to peritonitis-induced septic shock in pigs
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19108740
PubMed Central
PMC2646329
DOI
10.1186/cc7164
PII: cc7164
Knihovny.cz E-resources
- MeSH
- Hemodynamics physiology MeSH
- Laser-Doppler Flowmetry MeSH
- Kidney diagnostic imaging metabolism pathology MeSH
- Microcirculation physiology MeSH
- Peritonitis complications MeSH
- Swine MeSH
- Shock, Septic physiopathology MeSH
- Ultrasonography MeSH
- Research Design MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
INTRODUCTION: Our understanding of septic acute kidney injury (AKI) remains incomplete. A fundamental step is the use of animal models designed to meet the criteria of human sepsis. Therefore, we dynamically assessed renal haemodynamic, microvascular and metabolic responses to, and ultrastructural sequelae of, sepsis in a porcine model of faecal peritonitis-induced progressive hyperdynamic sepsis. METHODS: In eight anaesthetised and mechanically ventilated pigs, faecal peritonitis was induced by inoculating autologous faeces. Six sham-operated animals served as time-matched controls. Noradrenaline was administered to maintain mean arterial pressure (MAP) greater than or equal to 65 mmHg. Before and at 12, 18 and 22 hours of peritonitis systemic haemodynamics, total renal (ultrasound Doppler) and cortex microvascular (laser Doppler) blood flow, oxygen transport and renal venous pressure, acid base balance and lactate/pyruvate ratios were measured. Postmortem histological analysis of kidney tissue was performed. RESULTS: All septic pigs developed hyperdynamic shock with AKI as evidenced by a 30% increase in plasma creatinine levels. Kidney blood flow remained well-preserved and renal vascular resistance did not change either. Renal perfusion pressure significantly decreased in the AKI group as a result of gradually increased renal venous pressure. In parallel with a significant decrease in renal cortex microvascular perfusion, progressive renal venous acidosis and an increase in lactate/pyruvate ratio developed, while renal oxygen consumption remained unchanged. Renal histology revealed only subtle changes without signs of acute tubular necrosis. CONCLUSION: The results of this experimental study argue against the concept of renal vasoconstriction and tubular necrosis as physiological and morphological substrates of early septic AKI. Renal venous congestion might be a hidden and clinically unrecognised contributor to the development of kidney dysfunction.
See more in PubMed
Schrier RW, Wang W. Acute renal failure and sepsis. N Engl J Med. 2004;351:159–169. PubMed
Wan L, Bagshaw SM, Langenberg C, Saotome T, May C, Bellomo R. Pathophysiology of septic acute kidney injury: what do we really know? Crit Care Med. 2008;36(4 Suppl):198–203. PubMed
Langenberg C, Bellomo R, May CN, Wan L, Moritoki E, Morgera S. Renal blood flow in sepsis. Crit Care. 2005;9:363–374. PubMed PMC
Molitoris BA. Renal blood flow in sepsis: a complex issue. Crit Care. 2005;9:327–328. PubMed PMC
Langenberg C, Wan L, Egi M, May CN, Bellomo R. Renal blood flow in experimental septic acute renal failure. Kidney Int. 2006;69:1996–2002. PubMed
Langenberg C, Bellomo R, May CN, Egi M, Wan L, Morgera S. Renal vascular resistance in sepsis. Nephron Physiol. 2006;104:1–11. PubMed
Langenberg C, Wan L, Bagshaw SM, Egi M, May CN, Bellomo R. Urinary biochemistry in experimental septic acute renal failure. Nephrol Dial Transplant. 2006;21:3389–3397. PubMed
Langenberg C, Wan L, Egi M, May CN, Bellomo R. Renal blood flow and function during recovery from experimental septic acute kidney injury. Intensive Care Med. 2007;33:1614–1618. PubMed
Rector F, Goyal S, Rosenberg IK, Lucas CE. Sepsis: a mechanism for vasodilatation in the kidney. Ann Surg. 1973;178:222–226. PubMed PMC
Matejovic M, Radermacher P, Joannidis M. Acute kidney injury in sepsis: is renal blood flow more than just an innocent bystander? Intensive Care Med. 2007;33:1498–1500. PubMed
Matejovic M, Krouzecky A, Martinkova V, Rokyta R, Jr, Radej J, Kralova H, Treska V, Radermacher P, Novak I. Effects of tempol, a free radical scavenger, on long-term hyperdynamic porcine bacteremia. Crit Care Med. 2005;33:1057–1063. PubMed
Matejovic M, Krouzecky A, Martinkova V, Rokyta R, Jr, Radej J, Kralova H, Treska V, Radermacher P, Novak I. Effects of combining inducible nitric oxide synthase inhibitor and radical scavenger during porcine bacteremia. Shock. 2007;27:61–68. PubMed
Heyman SN, Lieberthal W, Rogiers P, Bonventre JV. Animal models of acute tubular necrosis. Curr Opin Crit Care. 2002;8:526–534. PubMed
Bellomo R, Ronco C, Kellum JA, Mehta RL, Palevsky P. Acute Dialysis Quality Initiative workgroup Acute renal failure – definition, outcome measures, animal models, fluid therapy and information technology needs: the Second International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI) Group. Crit Care. 2004;8:204–212. PubMed PMC
Lieberthal W, Nigam SK. Acute renal failure. II. Experimental models of acute renal failure: imperfect but indispensable. Am J Physiol Renal Physiol. 2000;278:1–12. PubMed
Goldfarb RD, Glock D, Kumar A, McCarthy RJ, Mei J, Guynn T, Matushek M, Trenholme G, Parrillo JE. A porcine model of peritonitis and bacteremia simulates human septic shock. Shock. 1996;6:442–451. PubMed
Matejovic M, Radermacher P, Thongboonkerd V. From hemodynamics to proteomics: Unrevealing the komplexity of acute kidney injury in sepsis. In: Vincent JL, editor. Yearbook of Intensive care and emergency medicine. Berlin Heidelberg: Springer-Verlag; 2008. pp. 568–578.
Tiwari MM, Brock RW, Megyesi JK, Kaushal GP, Mayeux PR. Disruption of peritubular blood flow in lipopolysaccharide-induced renal failure: role f nitric oxide and caspase. Am J Physiol Renal Physiol. 2005;289:1324–1332. PubMed
Wu L, Tiwari MM, Messer KJ, Holthoff JH, Gokden N, Brock RW, Mayeux PR. Peritubular capillary dysfunction and renal tubular epithelial cell stress following lipopolysaccharide administration in mice. Am J Physiol Renal Physiol. 2007;292:261–268. PubMed
Wu L, Gokden N, Mayeux PR. Evidence for the role of reactive nitrogen species in polymicrobial sepsis-induced renal peritubular capillary dysfunction and tubular injury. J Am Soc Nephrol. 2007;18:1807–1815. PubMed
Miller CG, Thiemermann C. Intrarenal haemodynamics and renal dysfunction in endotoxaemia: effects of nitric oxide synthase inhibition. Br J Pharmacol. 1997;121:1824–1830. PubMed PMC
Cohen RI, Hassell AM, Marzouk K, Marini C, Liu SF, Scharf SM. Renal effects of nitric oxide in endotoxemia. Am J Respir Crit Care Med. 2001;164:1890–1895. PubMed
Gullichsen E, Nelimarkka O, Halkola L, Niinikoski J. Renal oxygenation in endotoxin shock in dogs. Crit Care Med. 1989;17:547–550. PubMed
Di Giantomasso D, Morimatsu H, May CN, Bellomo R. Intrarenal blood flow distribution in hyperdynamic septic shock: effect of norepinephrine. Crit Care Med. 2003;31:2509–2513. PubMed
Weber A, Schwieger IM, Poinsot O, Klohn M, Gaumann DM, Morel DR. Sequential changes in renal oxygen consumption and sodium transport during hyperdynamic sepsis in sheep. Am J Physiol. 1992;262:965–971. PubMed
Heemskerk AE, Husman E, van Lambalgen AA, Bos GC van den, Hennekes M, Thijs LG, Tangelder GJ. Renal function and oxygen consumption during bacteraemia and endotoxaemia in rats. Nephrol Dial Transplant. 1997;12:1586–1594. PubMed
Johanes T, Mik EG, Nohé B, Raat NJ, Unertl KE, Ince C. Influence of fluid resuscitation on renal microvascular PO2 in a normotensive rat model of endotoxemia. Crit Care. 2006;10:88. PubMed PMC
Porta F, Takala J, Weikert C, Bracht H, Kolarova A, Lauterburg BH, Borotto E, Jakob SM. Effects of prolonged endotoxemia on liver, skeletal muscle and kidney mitochondrial function. Crit Care. 2006;10:118. PubMed PMC
O'Connor PM. Renal oxygen delivery: matching delivery to metabolic demand. Clin Exp Pharmacol Physiol. 2006;33:961–967. PubMed
Johannes T, Mik EG, Ince C. Nonresuscitated endotoxemia induces microcirculatory hypoxic areas in the renal cortex in the rat. Shock. 2009;31:97–103. PubMed
Langenberg C, Bagshaw SM, May CN, Bellomo R. The histopathology of septic acute kidney injury: a systematic review. Crit Care. 2008;12:38. PubMed PMC
Renal mitochondria response to sepsis: a sequential biopsy evaluation of experimental porcine model
Searching for mechanisms that matter in early septic acute kidney injury: an experimental study