Lactate: The Fallacy of Oversimplification
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
PubMed
38137413
PubMed Central
PMC10741081
DOI
10.3390/biomedicines11123192
PII: biomedicines11123192
Knihovny.cz E-zdroje
- Klíčová slova
- hyperlactatemia, hypoxia, lactate, lactate metabolism, lactic acidosis, sepsis, septic shock, shock,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Almost a quarter of a millennium after the discovery of an acidic substance in sour milk by Swedish chemist Carl Wilhelm Scheele and more than 100 years after the demonstration of a tight connection between this lactic acid and tissue hypoxia in shock, we are still surrounded by false beliefs and misunderstandings regarding this fascinating molecule. Common perceptions of lactate, the conjugate base of lactic acid, as a plain waste product of anaerobic metabolism and a marker of cellular distress could not be further from the truth. Lactate is formed and utilized continuously by our cells, even under fully aerobic conditions, in large quantities, and although marked hyperlactatemia is always a red flag in our patients, not all these conditions are life-threatening and vice versa-not all critically ill patients have hyperlactatemia. Lactate also does not promote acidosis by itself; it is not toxic, nor is it a metabolic renegade. On the contrary, it has many beneficial properties, and an interpretation of hyperlactatemia might be trickier than we tend to think. The aim of this article is to debunk some of the deeply rooted myths regarding this fascinating molecule.
Zobrazit více v PubMed
Seligmann H., Halkin H., Rauchfleisch S., Kaufmann N., Tal R., Motro M., Vered Z., Ezra D. Thiamine deficiency in patients with congestive heart failure receiving long-term furosemide therapy: A pilot study. Am. J. Med. 1991;91:151–155. doi: 10.1016/0002-9343(91)90007-K. PubMed DOI
Cohen R.D., Woods H.F. Lactic acidosis revisited. Diabetes. 1983;32:181–191. doi: 10.2337/diab.32.2.181. PubMed DOI
Rishu A.H., Khan R., Al-Dorzi H.M., Tamim H.M., Al-Qahtani S., Al-Ghamdi G., Arabi Y.M. Even mild hyperlactatemia is associated with increased mortality in critically ill patients. Crit. Care. 2013;17:R197. doi: 10.1186/cc12891. PubMed DOI PMC
Evans L., Rhodes A., Alhazzani W., Antonelli M., Coopersmith C.M., French C., Machado F.R., Mcintyre L., Ostermann M., Prescott H.C., et al. Surviving sepsis campaign: International guidelines for management of sepsis and septic shock 2021. Crit. Care Med. 2021;49:e1063–e1143. doi: 10.1097/CCM.0000000000005337. PubMed DOI
Weil M.H., Afifi A.A. Experimental and clinical studies on lactate and pyruvate as indicators of the severity of acute circulatory failure (shock) Circulation. 1970;41:989–1001. doi: 10.1161/01.CIR.41.6.989. PubMed DOI
Boekstegers P., Weidenhöfer S., Kapsner T., Werdan K. Skeletal muscle partial pressure of oxygen in patients with sepsis. Crit. Care Med. 1994;22:640–650. doi: 10.1097/00003246-199404000-00021. PubMed DOI
Sair M., Etherington P.J., Peter Winlove C., Evans T.W. Tissue oxygenation and perfusion in patients with systemic sepsis. Crit. Care Med. 2001;29:1343–1349. doi: 10.1097/00003246-200107000-00008. PubMed DOI
Levy B., Gibot S., Franck P., Cravoisy A., Bollaert P.-E. Relation between muscle Na+K+ ATPase activity and raised lactate concentrations in septic shock: A prospective study. Lancet. 2005;365:871–875. doi: 10.1016/S0140-6736(05)71045-X. PubMed DOI
Opdam H., Bellomo R. Oxygen Consumption and Lactate Release by the Lung after Cardiopulmonary Bypass and during Septic Shock. [(accessed on 20 February 2023)];Crit. Care Resusc. 1999 Available online: https://pubmed.ncbi.nlm.nih.gov/16599894/ PubMed
Kellum J.A., Kramer D.J., Lee K., Mankad S., Bellomo R., Pinsky M.R. Release of lactate by the lung in acute lung injury. Chest. 1997;111:1301–1305. doi: 10.1378/chest.111.5.1301. PubMed DOI
De Backer D., Creteur J., Silva E., Vincent J.L. The hepatosplanchnic area is not a common source of lactate in patients with severe sepsis. Crit. Care Med. 2001;29:256–261. doi: 10.1097/00003246-200102000-00005. PubMed DOI
Spronk P.E., Zandstra D.F., Ince C. Bench-to-bedside review: Sepsis is a disease of the microcirculation. Crit. Care. 2004;8:462–468. doi: 10.1186/cc2894. PubMed DOI PMC
Singer M. Critical illness and flat batteries. Crit. Care. 2017;21:309. doi: 10.1186/s13054-017-1913-9. PubMed DOI PMC
Singer M. Mitochondrial function in sepsis: Acute phase versus multiple organ failure. Crit. Care Med. 2007;35:S441–S448. doi: 10.1097/01.CCM.0000278049.48333.78. PubMed DOI
Van Wyngene L., Vandewalle J., Libert C. Reprogramming of basic metabolic pathways in microbial sepsis: Therapeutic targets at last? EMBO Mol. Med. 2018;10:e8712. doi: 10.15252/emmm.201708712. PubMed DOI PMC
Nuzzo E., Berg K.M., Andersen L.W., Balkema J., Montissol S., Cocchi M.N., Liu X., Donnino M.W. Pyruvate dehydrogenase activity is decreased in the peripheral blood mononuclear cells of patients with sepsis. A prospective observational trial. Ann. Am. Thorac. Soc. 2015;12:1662–1666. doi: 10.1513/AnnalsATS.201505-267BC. PubMed DOI PMC
Alamdari N., Constantin-Teodosiu D., Murton A.J., Gardiner S.M., Bennett T., Layfield R., Greenhaff P.L. Temporal changes in the involvement of pyruvate dehydrogenase complex in muscle lactate accumulation during lipopolysaccharide infusion in rats. J. Physiol. 2008;586:1767–1775. doi: 10.1113/jphysiol.2007.149625. PubMed DOI PMC
Stacpoole P.W., Nagaraja N.V., Hutson A.D. Efficacy of dichloroacetate as a lactate-lowering drug. J. Clin. Pharmacol. 2003;43:683–691. doi: 10.1177/0091270003254637. PubMed DOI
Totaro R.J., Raper R.F. Epinephrine-induced lactic acidosis following cardiopulmonary bypass. Crit. Care Med. 1997;25:1693–1699. doi: 10.1097/00003246-199710000-00019. PubMed DOI
Xue J., Mannem S., Al Jandeel A., Ruvo A., Levi D. Epinephrine causes severe lactic acidosis in a patient with shellfish-induced anaphylaxis. Chest. 2020;157:A7. doi: 10.1016/j.chest.2020.05.008. DOI
Sauer C.M., Gómez J., Botella M.R., Ziehr D.R., Oldham W.M., Gavidia G., Rodríguez A., Elbers P., Girbes A., Bodi M., et al. Understanding critically ill sepsis patients with normal serum lactate levels: Results from U.S. and European ICU cohorts. Sci. Rep. 2021;11:20076. doi: 10.1038/s41598-021-99581-6. PubMed DOI PMC
Manoj Kumar R.M., Narayanan N.K., Raghunath K.J., Rajagopalan S. Composite pheochromocytoma presenting as severe lactic acidosis and back pain: A case report. Indian J. Nephrol. 2019;29:353–356. doi: 10.4103/ijn.IJN_67_18. PubMed DOI PMC
Rodrigo G.J., Rodrigo C. Elevated plasma lactate level associated with high dose inhaled albuterol therapy in acute severe asthma. Emerg. Med. J. 2005;22:404–408. doi: 10.1136/emj.2003.012039. PubMed DOI PMC
de Ridder S., Kuijpers P., Crijns H. Lactate: Panicking doctor or panicking patient? BMJ Case Rep. 2010;2010:2319. doi: 10.1136/bcr.10.2009.2319. PubMed DOI PMC
Blohm E., Lai J., Neavyn M. Drug-induced hyperlactatemia. Clin. Toxicol. 2017;55:869–878. doi: 10.1080/15563650.2017.1317348. PubMed DOI
Contenti J., Occelli C., Corraze H., Lemoël F., Levraut J. Long-term β-blocker therapy decreases blood lactate concentration in severely septic patients. Crit. Care Med. 2015;43:2616–2622. doi: 10.1097/CCM.0000000000001308. PubMed DOI
Emmett M., Szerlip H., Sterns R.H., Forman J.P. Causes of Lactic Acidosis. UpToDate. 2023. [(accessed on 5 May 2023)]. Available online: https://www.uptodate.com/contents/causes-of-lactic-acidosis.
Kraut J.A., Madias N.E. Lactic acidosis. N. Engl. J. Med. 2014;371:2309–2319. doi: 10.1056/NEJMra1309483. PubMed DOI
Gattinoni L., Vasques F., Camporota L., Meessen J., Romitti F., Pasticci I., Duscio E., Vassalli F., Forni L.G., Payen D., et al. Understanding lactatemia in human sepsis. Potential impact for early management. Am. J. Respir. Crit. Care Med. 2019;200:582–589. doi: 10.1164/rccm.201812-2342OC. PubMed DOI
Qian Q. Reply to Robergs et al. Physiology. 2018;33:13. doi: 10.1152/physiol.00034.2017. PubMed DOI
Burnell J.M., Scribner B.H., Uyeno B.T., Villamil M.F. The effect in humans of extracellular pH change on the relationship between serum potassium concentration and intracellular potassium. J. Clin. Investig. 1956;35:935–939. doi: 10.1172/JCI103352. PubMed DOI PMC
Fulop M. Serum potassium in lactic acidosis and ketoacidosis. N. Engl. J. Med. 1979;300:1087–1089. doi: 10.1056/NEJM197905103001905. PubMed DOI
Aronson P.S., Giebisch G. Effects of pH on potassium: New explanations for old observations: New explanations for old observations. J. Am. Soc. Nephrol. 2011;22:1981–1989. doi: 10.1681/ASN.2011040414. PubMed DOI PMC
Bellomo R. Bench-to-bedside review: Lactate and the kidney. Crit. Care. 2002;6:322–326. doi: 10.1186/cc1518. PubMed DOI PMC
Gu W.-J., Zhang Z., Bakker J. Early lactate clearance-guided therapy in patients with sepsis: A meta-analysis with trial sequential analysis of randomized controlled trials. Intensive Care Med. 2015;41:1862–1863. doi: 10.1007/s00134-015-3955-2. PubMed DOI
Vincent J.L., Quintairos e Silva A., Couto L., Taccone F.S. The value of blood lactate kinetics in critically ill patients: A systematic review. Crit. Care. 2016;20:1–14. doi: 10.1186/s13054-016-1403-5. PubMed DOI PMC
Middleton P., Kelly A.-M., Brown J., Robertson M. Agreement between arterial and central venous values for pH, bicarbonate, base excess, and lactate. Emerg. Med. J. 2006;23:622–624. doi: 10.1136/emj.2006.035915. PubMed DOI PMC
Jones A.E., Leonard M.M., Hernandez-Nino J., Kline J.A. Determination of the effect of in vitro time, temperature, and tourniquet use on whole blood venous point-of-care lactate concentrations. Acad. Emerg. Med. 2007;14:587–591. doi: 10.1197/j.aem.2007.03.1351. PubMed DOI
Sagar A.S., Jimenez C.A., Mckelvy B.J. Lactate gap as a tool in identifying ethylene glycol poisoning. BMJ Case Rep. 2018;2018:bcr-2018. doi: 10.1136/bcr-2018-224243. PubMed DOI PMC
Matejovic M., Radermacher P., Fontaine E. Lactate in shock: A high-octane fuel for the heart? Intensive Care Med. 2007;33:406–408. doi: 10.1007/s00134-006-0524-8. PubMed DOI
Beadle R.M., Frenneaux M. Modification of myocardial substrate utilisation: A new therapeutic paradigm in cardiovascular disease. Heart. 2010;96:824–830. doi: 10.1136/hrt.2009.190256. PubMed DOI
van Hall G. Lactate kinetics in human tissues at rest and during exercise: Tissue lactate kinetics. Acta Physiol. 2010;199:499–508. doi: 10.1111/j.1748-1716.2010.02122.x. PubMed DOI
Nalos M., Leverve X., Huang S., Weisbrodt L., Parkin R., Seppelt I., Ting I., Mclean A.S. Half-molar sodium lactate infusion improves cardiac performance in acute heart failure: A pilot randomised controlled clinical trial. Crit. Care. 2014;18:R48. doi: 10.1186/cc13793. PubMed DOI PMC
Brooks G.A. The science and translation of lactate shuttle theory. Cell Metab. 2018;27:757–785. doi: 10.1016/j.cmet.2018.03.008. PubMed DOI
Li X., Yang Y., Zhang B., Lin X., Fu X., An Y., Zou Y., Wang J.-X., Wang Z., Yu T. Lactate metabolism in human health and disease. Signal Transduct. Target. Ther. 2022;7:305. doi: 10.1038/s41392-022-01151-3. PubMed DOI PMC
Zhang D., Tang Z., Huang H., Zhou G., Cui C., Weng Y., Liu W., Kim S., Lee S., Perez-Neut M., et al. Metabolic regulation of gene expression by histone lactylation. Nature. 2019;574:575–580. doi: 10.1038/s41586-019-1678-1. PubMed DOI PMC
Boysen S.R., Dorval P. Effects of rapid intravenous 100% L-isomer lactated Ringer’s administration on plasma lactate concentrations in healthy dogs: In vivo effects of lactated Ringer’s in healthy dogs. J. Vet. Emerg. Crit. Care. 2014;24:571–577. doi: 10.1111/vec.12213. PubMed DOI
Connor H., Woods H.F. Ciba Foundation Symposium 87—Metabolic Acidosis. Wiley; Hoboken, NJ, USA: 1982. Quantitative aspects of L(+)-lactate metabolism in human beings; pp. 214–234. PubMed DOI
Caldarini M.I., Pons S., D’Agostino D., Depaula J.A., Greco G., Negri G., Ascione A., Bustos D. Abnormal fecal flora in a patient with short bowel syndrome: Anin vitro study on effect of pH ond-lactic acid production. Dig. Dis. Sci. 1996;41:1649–1652. doi: 10.1007/BF02087915. PubMed DOI
Bongaerts G., Tolboom J., Naber T., Bakkeren J., Severijnen R., Willems H. D-lactic acidemia and aciduria in pediatric and adult patients with short bowel syndrome. Clin. Chem. 1995;41:107–110. doi: 10.1093/clinchem/41.1.107. PubMed DOI
Uribarri J., Oh M.S., Carroll H.J. D-lactic acidosis: A review of clinical presentation, biochemical features, and pathophysiologic mechanisms. Medicine. Medicine. 1998;77:73–82. doi: 10.1097/00005792-199803000-00001. PubMed DOI
Tsao Y.-T., Tsai W.-C., Yang S.-P. A life-threatening double gap metabolic acidosis. Am. J. Emerg. Med. 2008;26:385.e5–385.e6. doi: 10.1016/j.ajem.2007.07.026. PubMed DOI
Lu J., Zello G.A., Randell E., Adeli K., Krahn J., Meng Q.H. Closing the anion gap: Contribution of d-lactate to diabetic ketoacidosis. Clin. Chim. Acta. 2011;412:286–291. doi: 10.1016/j.cca.2010.10.020. PubMed DOI
Renal mitochondria response to sepsis: a sequential biopsy evaluation of experimental porcine model