Skip to main content
Erschienen in: Inflammation 5/2013

01.10.2013

Continuous Renal Replacement Therapy (CRRT) Attenuates Myocardial Inflammation and Mitochondrial Injury Induced by Venovenous Extracorporeal Membrane Oxygenation (VV ECMO) in a Healthy Piglet Model

verfasst von: Juanhong Shen, Wenkui Yu, Qiyi Chen, Jialiang Shi, Yimin Hu, Juanjuan Zhang, Tao Gao, Fengchan Xi, Changsheng He, Jianfeng Gong, Ning Li, Jieshou Li

Erschienen in: Inflammation | Ausgabe 5/2013

Einloggen, um Zugang zu erhalten

Abstract

In this study, we investigated the myocardial inflammation and mitochondrial function during venovenous extracorporeal membrane oxygenation (VV ECMO) and further evaluated the effects of continuous renal replacement therapy (CRRT) on them. Eighteen piglets were assigned to the control group, ECMO group, and ECMO+CRRT group. Myocardial inflammation was assessed by the activity of myeloperoxidase (MPO), myocardial concentrations, and mRNA expression of TNF-α, IL-1β, and IL-6; mitochondrial function was assessed by activities of mitochondrial complexes I–V. VV ECMO elicited a general activation of serum and myocardial inflammation and significantly decreased the activities of mitochondrial complexes I and IV. After being combined with CRRT, serum and myocardial concentrations of IL-1β and IL-6, myocardial mRNA expression of IL-6, and the activity of MPO were decreased significantly; the activities of mitochondrial complexes were increased. We conclude that myocardial inflammation was activated during ECMO therapy, inducing mitochondrial injury; moreover, CRRT reduced myocardial inflammation and partially ameliorated mitochondrial function.
Literatur
1.
Zurück zum Zitat MacLaren, G., A. Combes, and R.H. Bartlett. 2012. Contemporary extracorporeal membrane oxygenation for adult respiratory failure: life support in the new era. Intensive Care Medicine 38: 210–220.PubMedCrossRef MacLaren, G., A. Combes, and R.H. Bartlett. 2012. Contemporary extracorporeal membrane oxygenation for adult respiratory failure: life support in the new era. Intensive Care Medicine 38: 210–220.PubMedCrossRef
2.
Zurück zum Zitat Tiruvoipati, R., J. Botha, and G. Peek. 2012. Effectiveness of extracorporeal membrane oxygenation when conventional ventilation fails: valuable option or vague remedy? Journal of Critical Care 27: 192–198.PubMedCrossRef Tiruvoipati, R., J. Botha, and G. Peek. 2012. Effectiveness of extracorporeal membrane oxygenation when conventional ventilation fails: valuable option or vague remedy? Journal of Critical Care 27: 192–198.PubMedCrossRef
3.
Zurück zum Zitat Peek, G.J., M. Mugford, R. Tiruvoipati, A. Wilson, E. Allen, M.M. Thalanany, et al. 2009. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial. The Lancet 374: 1351–1363.CrossRef Peek, G.J., M. Mugford, R. Tiruvoipati, A. Wilson, E. Allen, M.M. Thalanany, et al. 2009. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial. The Lancet 374: 1351–1363.CrossRef
4.
Zurück zum Zitat Noah, M.A., G.J. Peek, S.J. Finney, M.J. Griffiths, D.A. Harrison, R. Grieve, et al. 2011. Referral to an extracorporeal membrane oxygenation center and mortality among patients with severe 2009 influenza A(H1N1). JAMA: The Journal of the American Medical Association 306: 1659–1668.CrossRef Noah, M.A., G.J. Peek, S.J. Finney, M.J. Griffiths, D.A. Harrison, R. Grieve, et al. 2011. Referral to an extracorporeal membrane oxygenation center and mortality among patients with severe 2009 influenza A(H1N1). JAMA: The Journal of the American Medical Association 306: 1659–1668.CrossRef
5.
Zurück zum Zitat Schmid, C., A. Philipp, M. Hilker, L. Rupprecht, M. Arlt, A. Keyser, et al. 2012. Venovenous extracorporeal membrane oxygenation for acute lung failure in adults. The Journal of Heart and Lung Transplantation 31: 9–15.PubMedCrossRef Schmid, C., A. Philipp, M. Hilker, L. Rupprecht, M. Arlt, A. Keyser, et al. 2012. Venovenous extracorporeal membrane oxygenation for acute lung failure in adults. The Journal of Heart and Lung Transplantation 31: 9–15.PubMedCrossRef
6.
Zurück zum Zitat Brogan, T.V., R.R. Thiagarajan, P.T. Rycus, R.H. Bartlett, and S.L. Bratton. 2009. Extracorporeal membrane oxygenation in adults with severe respiratory failure: a multi-center database. Intensive Care Medicine 35: 2105–2114.PubMedCrossRef Brogan, T.V., R.R. Thiagarajan, P.T. Rycus, R.H. Bartlett, and S.L. Bratton. 2009. Extracorporeal membrane oxygenation in adults with severe respiratory failure: a multi-center database. Intensive Care Medicine 35: 2105–2114.PubMedCrossRef
7.
Zurück zum Zitat Nehra, D., A.M. Goldstein, D.P. Doody, D.P. Ryan, Y. Chang, and P.T. Masiakos. 2009. Extracorporeal membrane oxygenation for nonneonatal acute respiratory failure: the Massachusetts General Hospital experience from 1990 to 2008. Archives of Surgery 144: 427–432.PubMedCrossRef Nehra, D., A.M. Goldstein, D.P. Doody, D.P. Ryan, Y. Chang, and P.T. Masiakos. 2009. Extracorporeal membrane oxygenation for nonneonatal acute respiratory failure: the Massachusetts General Hospital experience from 1990 to 2008. Archives of Surgery 144: 427–432.PubMedCrossRef
8.
Zurück zum Zitat Steinhorn, R.H., B. Isham-Schopf, C. Smith, and T.P. Green. 1989. Hemolysis during long-term extracorporeal membrane oxygenation. The Journal of Pediatrics 115: 625–630.PubMedCrossRef Steinhorn, R.H., B. Isham-Schopf, C. Smith, and T.P. Green. 1989. Hemolysis during long-term extracorporeal membrane oxygenation. The Journal of Pediatrics 115: 625–630.PubMedCrossRef
9.
Zurück zum Zitat Kurundkar, A.R., C.R. Killingsworth, R.B. McIlwain, J.G. Timpa, Y.E. Hartman, D. He, et al. 2010. Extracorporeal membrane oxygenation causes loss of intestinal epithelial barrier in the newborn piglet. Pediatric Research 68: 128–133.PubMedCrossRef Kurundkar, A.R., C.R. Killingsworth, R.B. McIlwain, J.G. Timpa, Y.E. Hartman, D. He, et al. 2010. Extracorporeal membrane oxygenation causes loss of intestinal epithelial barrier in the newborn piglet. Pediatric Research 68: 128–133.PubMedCrossRef
10.
Zurück zum Zitat Adrian, K., K. Mellgren, M. Skogby, L.G. Friberg, G. Mellgren, and H. Wadenvik. 1998. Cytokine release during long-term extracorporeal circulation in an experimental model. Artificial Organs 22: 859–863.PubMedCrossRef Adrian, K., K. Mellgren, M. Skogby, L.G. Friberg, G. Mellgren, and H. Wadenvik. 1998. Cytokine release during long-term extracorporeal circulation in an experimental model. Artificial Organs 22: 859–863.PubMedCrossRef
11.
Zurück zum Zitat Fortenberry, J.D., V. Bhardwaj, P. Niemer, J.D. Cornish, J.A. Wright, and L. Bland. 1996. Neutrophil and cytokine activation with neonatal extracorporeal membrane oxygenation. The Journal of Pediatrics 128: 670–678.PubMedCrossRef Fortenberry, J.D., V. Bhardwaj, P. Niemer, J.D. Cornish, J.A. Wright, and L. Bland. 1996. Neutrophil and cytokine activation with neonatal extracorporeal membrane oxygenation. The Journal of Pediatrics 128: 670–678.PubMedCrossRef
12.
Zurück zum Zitat McILwain, B., T. Joseph, A.R. Kurundkar, D.W. Holt, D.R. Kelly, and Y. Hartman. 2010. Plasma concentrations of inflammatory cytokines rise rapidly during ECMO-related SIRS due to the release of pre-formed stores in the intestine. Laboratory Investigation 1: 128–139.CrossRef McILwain, B., T. Joseph, A.R. Kurundkar, D.W. Holt, D.R. Kelly, and Y. Hartman. 2010. Plasma concentrations of inflammatory cytokines rise rapidly during ECMO-related SIRS due to the release of pre-formed stores in the intestine. Laboratory Investigation 1: 128–139.CrossRef
13.
Zurück zum Zitat Zanotti-Cavazzoni, S.L., and S.M. Hollenberg. 2009. Cardiac dysfunction in severe sepsis and septic shock. Current Opinion in Critical Care 15: 392–397.PubMedCrossRef Zanotti-Cavazzoni, S.L., and S.M. Hollenberg. 2009. Cardiac dysfunction in severe sepsis and septic shock. Current Opinion in Critical Care 15: 392–397.PubMedCrossRef
14.
Zurück zum Zitat Ventura-Clapier, R., A. Garnier, and V. Veksler. 2004. Energy metabolism in heart failure. The Journal of Physiology 555: 1–13.PubMedCrossRef Ventura-Clapier, R., A. Garnier, and V. Veksler. 2004. Energy metabolism in heart failure. The Journal of Physiology 555: 1–13.PubMedCrossRef
15.
Zurück zum Zitat Matsuda, K., H. Hirasawa, S. Oda, H. Shiga, and K. Nakanishi. 2001. Current topics on cytokine removal technologies. Therapeutic Apheresis 5: 306–314.PubMedCrossRef Matsuda, K., H. Hirasawa, S. Oda, H. Shiga, and K. Nakanishi. 2001. Current topics on cytokine removal technologies. Therapeutic Apheresis 5: 306–314.PubMedCrossRef
16.
Zurück zum Zitat Schetz M. 1999. Non-renal indications for continuous renal replacement therapy. Kidney International. Supplement 72:S88–94. Schetz M. 1999. Non-renal indications for continuous renal replacement therapy. Kidney International. Supplement 72:S88–94.
17.
Zurück zum Zitat De Vriese, A.S., R.C. Vanholder, M. Pascual, N.H. Lameire, and F.A. Colardyn. 1999. Can inflammatory cytokines be removed efficiently by continuous renal replacement therapies? Intensive Care Medicine 25: 903–910.PubMedCrossRef De Vriese, A.S., R.C. Vanholder, M. Pascual, N.H. Lameire, and F.A. Colardyn. 1999. Can inflammatory cytokines be removed efficiently by continuous renal replacement therapies? Intensive Care Medicine 25: 903–910.PubMedCrossRef
18.
Zurück zum Zitat Skogby, M., K. Adrian, L.G. Friberg, G. Mellgren, and K. Mellgren. 2000. Influence of hemofiltration on plasma cytokine levels and platelet activation during extra corporeal membrane oxygenation. Scandinavian Cardiovascular Journal 34: 315–320.PubMedCrossRef Skogby, M., K. Adrian, L.G. Friberg, G. Mellgren, and K. Mellgren. 2000. Influence of hemofiltration on plasma cytokine levels and platelet activation during extra corporeal membrane oxygenation. Scandinavian Cardiovascular Journal 34: 315–320.PubMedCrossRef
19.
Zurück zum Zitat Mu, T.S., E.G. Palmer, S.G. Batts, S.L. Lentz-Kapua, J.H. Uyehara-Lock, and C.F. Uyehara. 2012. Continuous renal replacement therapy to reduce inflammation in a piglet hemorrhage–reperfusion extracorporeal membrane oxygenation model. Pediatric Research 72: 249–255.PubMedCrossRef Mu, T.S., E.G. Palmer, S.G. Batts, S.L. Lentz-Kapua, J.H. Uyehara-Lock, and C.F. Uyehara. 2012. Continuous renal replacement therapy to reduce inflammation in a piglet hemorrhage–reperfusion extracorporeal membrane oxygenation model. Pediatric Research 72: 249–255.PubMedCrossRef
20.
Zurück zum Zitat Naran, N., M. Sagy, and K.R. Bock. 2010. Continuous renal replacement therapy results in respiratory and hemodynamic beneficial effects in pediatric patients with severe systemic inflammatory response syndrome and multiorgan system dysfunction. Pediatric Critical Care Medicine 11: 737–740.PubMedCrossRef Naran, N., M. Sagy, and K.R. Bock. 2010. Continuous renal replacement therapy results in respiratory and hemodynamic beneficial effects in pediatric patients with severe systemic inflammatory response syndrome and multiorgan system dysfunction. Pediatric Critical Care Medicine 11: 737–740.PubMedCrossRef
21.
Zurück zum Zitat Ishihara, S., J.A. Ward, O. Tasaki, B.J. Pruitt, and D.W. Mozingo. 2009. Cardiac contractility during hemofiltration in an awake model of hyperdynamic endotoxemia. The Journal of Trauma 67: 1055–1061.PubMedCrossRef Ishihara, S., J.A. Ward, O. Tasaki, B.J. Pruitt, and D.W. Mozingo. 2009. Cardiac contractility during hemofiltration in an awake model of hyperdynamic endotoxemia. The Journal of Trauma 67: 1055–1061.PubMedCrossRef
22.
Zurück zum Zitat Li, C.M., J.H. Chen, P. Zhang, Q. He, J. Yuan, R.J. Chen, et al. 2007. Continuous veno-venous haemofiltration attenuates myocardial mitochondrial respiratory chain complexes activity in porcine septic shock. Anaesthesia and Intensive Care 35: 911–919.PubMed Li, C.M., J.H. Chen, P. Zhang, Q. He, J. Yuan, R.J. Chen, et al. 2007. Continuous veno-venous haemofiltration attenuates myocardial mitochondrial respiratory chain complexes activity in porcine septic shock. Anaesthesia and Intensive Care 35: 911–919.PubMed
23.
Zurück zum Zitat Bradford, M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72: 248–254.PubMedCrossRef Bradford, M.M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry 72: 248–254.PubMedCrossRef
24.
Zurück zum Zitat Poderoso, J.J., M.C. Carreras, C. Lisdero, N. Riobo, F. Schopfer, and A. Boveris. 1996. Nitric oxide inhibits electron transfer and increases superoxide radical production in rat heart mitochondria and submitochondrial particles. Archives of Biochemistry and Biophysics 328: 85–92.PubMedCrossRef Poderoso, J.J., M.C. Carreras, C. Lisdero, N. Riobo, F. Schopfer, and A. Boveris. 1996. Nitric oxide inhibits electron transfer and increases superoxide radical production in rat heart mitochondria and submitochondrial particles. Archives of Biochemistry and Biophysics 328: 85–92.PubMedCrossRef
25.
Zurück zum Zitat Sudheesh, N.P., T.A. Ajith, and K.K. Janardhanan. 2009. Ganoderma lucidum (Fr.) P. Karst enhances activities of heart mitochondrial enzymes and respiratory chain complexes in the aged rat. Biogerontology 10: 627–636.PubMedCrossRef Sudheesh, N.P., T.A. Ajith, and K.K. Janardhanan. 2009. Ganoderma lucidum (Fr.) P. Karst enhances activities of heart mitochondrial enzymes and respiratory chain complexes in the aged rat. Biogerontology 10: 627–636.PubMedCrossRef
26.
Zurück zum Zitat Bedard, P.M., B. Zweiman, and P.C. Atkins. 1983. Quantitation by myeloperoxidase assay of neutrophil accumulation at the site of in vivo allergic reactions. Journal of Clinical Immunology 3: 84–89.PubMedCrossRef Bedard, P.M., B. Zweiman, and P.C. Atkins. 1983. Quantitation by myeloperoxidase assay of neutrophil accumulation at the site of in vivo allergic reactions. Journal of Clinical Immunology 3: 84–89.PubMedCrossRef
27.
Zurück zum Zitat Wan, S., J.M. DeSmet, L. Barvais, M. Goldstein, J.L. Vincent, and J.L. LeClerc. 1996. Myocardium is a major source of proinflammatory cytokines in patients undergoing cardiopulmonary bypass. The Journal of Thoracic and Cardiovascular Surgery 112: 806–811.PubMedCrossRef Wan, S., J.M. DeSmet, L. Barvais, M. Goldstein, J.L. Vincent, and J.L. LeClerc. 1996. Myocardium is a major source of proinflammatory cytokines in patients undergoing cardiopulmonary bypass. The Journal of Thoracic and Cardiovascular Surgery 112: 806–811.PubMedCrossRef
28.
Zurück zum Zitat Galley, H.F. 2011. Oxidative stress and mitochondrial dysfunction in sepsis. British Journal of Anaesthesia 107: 57–64.PubMedCrossRef Galley, H.F. 2011. Oxidative stress and mitochondrial dysfunction in sepsis. British Journal of Anaesthesia 107: 57–64.PubMedCrossRef
29.
Zurück zum Zitat Rudiger, A., and M. Singer. 2007. Mechanisms of sepsis-induced cardiac dysfunction. Critical Care Medicine 35: 1599–1608.PubMedCrossRef Rudiger, A., and M. Singer. 2007. Mechanisms of sepsis-induced cardiac dysfunction. Critical Care Medicine 35: 1599–1608.PubMedCrossRef
30.
Zurück zum Zitat Zimmerman, G.A., A.H. Morris, and M. Cengiz. 1982. Cardiovascular alterations in the adult respiratory distress syndrome. The American Journal of Medicine 73: 25–34.PubMedCrossRef Zimmerman, G.A., A.H. Morris, and M. Cengiz. 1982. Cardiovascular alterations in the adult respiratory distress syndrome. The American Journal of Medicine 73: 25–34.PubMedCrossRef
31.
Zurück zum Zitat Bajwa, E.K., P.D. Boyce, J.L. Januzzi, M.N. Gong, B.T. Thompson, and D.C. Christiani. 2007. Biomarker evidence of myocardial cell injury is associated with mortality in acute respiratory distress syndrome. Critical Care Medicine 35: 2484–2490.PubMedCrossRef Bajwa, E.K., P.D. Boyce, J.L. Januzzi, M.N. Gong, B.T. Thompson, and D.C. Christiani. 2007. Biomarker evidence of myocardial cell injury is associated with mortality in acute respiratory distress syndrome. Critical Care Medicine 35: 2484–2490.PubMedCrossRef
32.
Zurück zum Zitat Askenazi, D.J., D.T. Selewski, M.L. Paden, D.S. Cooper, B.C. Bridges, M. Zappitelli, et al. 2012. Renal replacement therapy in critically ill patients receiving extracorporeal membrane oxygenation. Clinical Journal of the American Society of Nephrology 7: 1328–1336.PubMedCrossRef Askenazi, D.J., D.T. Selewski, M.L. Paden, D.S. Cooper, B.C. Bridges, M. Zappitelli, et al. 2012. Renal replacement therapy in critically ill patients receiving extracorporeal membrane oxygenation. Clinical Journal of the American Society of Nephrology 7: 1328–1336.PubMedCrossRef
33.
Zurück zum Zitat Smith, A.H., D.C. Hardison, C.R. Worden, G.M. Fleming, and M.B. Taylor. 2009. Acute renal failure during extracorporeal support in the pediatric cardiac patient. ASAIO Journal 55: 412–416.PubMedCrossRef Smith, A.H., D.C. Hardison, C.R. Worden, G.M. Fleming, and M.B. Taylor. 2009. Acute renal failure during extracorporeal support in the pediatric cardiac patient. ASAIO Journal 55: 412–416.PubMedCrossRef
34.
Zurück zum Zitat Hirasawa, H. 2010. Indications for blood purification in critical care. Contributions to Nephrology 166: 21–30.PubMedCrossRef Hirasawa, H. 2010. Indications for blood purification in critical care. Contributions to Nephrology 166: 21–30.PubMedCrossRef
35.
Zurück zum Zitat Honore, P.M., O. Joannes-Boyau, W. Boer, and V. Collin. 2009. High-volume hemofiltration in sepsis and SIRS: current concepts and future prospects. Blood Purification 28: 1–11.PubMedCrossRef Honore, P.M., O. Joannes-Boyau, W. Boer, and V. Collin. 2009. High-volume hemofiltration in sepsis and SIRS: current concepts and future prospects. Blood Purification 28: 1–11.PubMedCrossRef
Metadaten
Titel
Continuous Renal Replacement Therapy (CRRT) Attenuates Myocardial Inflammation and Mitochondrial Injury Induced by Venovenous Extracorporeal Membrane Oxygenation (VV ECMO) in a Healthy Piglet Model
verfasst von
Juanhong Shen
Wenkui Yu
Qiyi Chen
Jialiang Shi
Yimin Hu
Juanjuan Zhang
Tao Gao
Fengchan Xi
Changsheng He
Jianfeng Gong
Ning Li
Jieshou Li
Publikationsdatum
01.10.2013
Verlag
Springer US
Erschienen in
Inflammation / Ausgabe 5/2013
Print ISSN: 0360-3997
Elektronische ISSN: 1573-2576
DOI
https://doi.org/10.1007/s10753-013-9654-7

Weitere Artikel der Ausgabe 5/2013

Inflammation 5/2013 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Notfall-TEP der Hüfte ist auch bei 90-Jährigen machbar

26.04.2024 Hüft-TEP Nachrichten

Ob bei einer Notfalloperation nach Schenkelhalsfraktur eine Hemiarthroplastik oder eine totale Endoprothese (TEP) eingebaut wird, sollte nicht allein vom Alter der Patientinnen und Patienten abhängen. Auch über 90-Jährige können von der TEP profitieren.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Bei schweren Reaktionen auf Insektenstiche empfiehlt sich eine spezifische Immuntherapie

Insektenstiche sind bei Erwachsenen die häufigsten Auslöser einer Anaphylaxie. Einen wirksamen Schutz vor schweren anaphylaktischen Reaktionen bietet die allergenspezifische Immuntherapie. Jedoch kommt sie noch viel zu selten zum Einsatz.

Therapiestart mit Blutdrucksenkern erhöht Frakturrisiko

25.04.2024 Hypertonie Nachrichten

Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.