N-acetylcysteine decreases lactate signal intensities in liver tissue and improves liver function in septic shock patients, as shown by magnetic resonance spectroscopy: extended case report
© Vargas Hein et al., licensee BioMed Central Ltd. 2004
Received: 19 November 2003
Accepted: 17 December 2003
Published: 22 January 2004
N-acetylcysteine (NAC) has been shown to improve splanchnic blood flow in experimental studies. This report evaluates the effects of NAC on liver perfusion and lactate signal intensities in the liver tissue of septic shock patients using proton magnetic resonance imaging and spectroscopy. Furthermore, the monoethylglycinexylidide (MEGX) test was used to investigate hepatic function.
Five septic shock patients received 150 mg/kg body weight NAC as an intravenous bolus injection over 15 min. Lidocaine was injected both prior to and following NAC administration in order to determine MEGX formation. Measurements (hemodynamics, oxygen transport-related variables, blood samples for lactate, liver-related markers) were performed 1 hour before and 1 hour after NAC injection. In addition to the proton magnetic resonance imaging patients received two proton magnetic resonance spectra, one prior to and one 30 min subsequent to the onset of the NAC infusion at a 1.5 Tesla clinical scanner, for measurement of liver perfusion and liver lactate signal intensity.
Following NAC infusion, the lactate signal intensity in the liver tissue showed a median decrease of 89% (11–99%), there was a median increase in liver perfusion of 41% (-14 to 559%), and the MEGX serum concentration increased three times (1.52–5.91).
A decrease in the lactate signal intensity in the liver tissue and an increase in the MEGX serum concentration and in liver perfusion might indicate improved liver function as a result of NAC administration. Patients with compromised hepatosplanchnic function, such as patients with septic shock due to peritonitis, may therefore benefit from NAC therapy.
In septic shock, the vasoconstriction in splanchnic vessels is disproportionally greater than in other vascular beds and may persist despite the presence of normal systemic hemodynamic measurements . Takala and Ruokonen found, in spite of normal global cardiopulmonary physiology, that inadequate perfusion and oxygenation of the splanchnic region increases the risk of Multiple Organ Dysfunction Syndrome . The gut is described as the 'motor' of Multiple Organ Dysfunction Syndrome .
N-acetylcysteine (NAC), a precursor of glutathione synthesis, can exert important antioxidant cytoprotective effects and anti-inflammatory effects [4–8]. When endotoxic shock occurred, there was a significant increase in the absolute mesenteric blood flow but not in the fractional blood flow (i.e. hepatic flow index/cardiac index) following NAC administration [4, 9]. In patients, NAC has been shown to increase the cardiac index and oxygen delivery in fulminant hepatic failure and in septic shock [4, 6, 10]. Devlin and colleagues showed in a recent study that the indocyanine green elimination in patients with hepatic dysfunction increased after NAC administration . It is not clear, however, whether the increase in elimination rate is related to an increased hepatosplanchnic perfusion or to a better hepatic function .
The aim of this report was therefore to investigate whether the administration of NAC improves liver function and liver blood flow in septic shock patients. Owing to the fact that splanchnic dysoxia is usually presumed in sepsis , we focused on the measurement of lactate in the liver tissue accumulating following cell dysfunction . Furthermore, the monoethylglycinexylidide (MEGX) test was used to investigate hepatic function.
Materials and methods
All patients were included after written informed consent of legislative and ethical committee approval. For continuous cardiovascular monitoring a fiber optic, pulmonary artery flotation catheter (Baxter Swan-Ganz® Intelicath™ continuous cardiac output thermodilution catheter 139H – 7.5 French; Baxter/Edwards Critical-Care, Irvine, California, USA) and a radial artery catheter were inserted. After adequate fluid resuscitation, norepinephrine was titrated to maintain the mean arterial pressure between 70 and 90 mmHg. All patients were mechanically ventilated and received a continuous infusion of the analgesic sedatives fentanyl and flunitrazepam. The mechanical ventilation was pressure controlled (Servo 900 C; Siemens, Solna, Sweden), and ventilator settings were not altered during the study period. All patients were normoventilated (arterial carbon dioxide tension = 35–45 Torr). None of the patients had a change in body temperature > 0.5°C during the study period, as documented by continuous monitoring of a catheter thermistor.
Blood was collected and hemodynamic measurements were performed 1 hour before and 1 hour after NAC injection. Patients received 150 mg/kg body weight NAC as an intravenous bolus injection over 15 min. Each hemodynamic measurement included the heart rate and cardiovascular pressures with reference to the midaxillary line. The hemodynamic measurements were immediately followed by the withdrawal of mixed venous and radial artery blood samples. Part of each sample was immediately analyzed for arterial and mixed venous oxygen and carbon dioxide tensions (ABL 300; Radiometer, Copenhagen, Denmark), along with arterial and mixed venous hemoglobin content and oxygen saturation (Hemoximeter OSM-3; Radiometer).
An intravenous bolus of 1 mg/kg body weight lidocaine was injected 1 hour before and 1 hour after NAC administration. Blood samples to determine the MEGX test were taken before and 15 min after lidocaine injection. The serum concentration of the lidocaine metabolite MEGX was determined by means of a fluorescence polarization immunoassay (Abbott GmbH, Wiesbaden, Germany). MEGX concentration values measured before lidocaine administration were subtracted from concentrations measured after 15 min, and the results were reported as serum MEGX concentrations (ng/ml). Blood samples were centrifuged at 4650 × g for 10 min, and serum was stored at -80°C until analysis.
The measurements of bilirubin, aspartate aminotransferase, alanine aminotransferase and serum lactate were analyzed as part of the clinical routine (Clinical Chemistry Department).
Proton magnetic resonance spectroscopy (1H-MRS) measurements for measurement of lactate liver intensities were acquired at a 1.5 Tesla clinical scanner (Magnetom Vision; Siemens) with a stimulated echo acquisition mode sequence. A fast imaging procedure was performed prior to spectroscopy using a technique involving a gradient echo sequence, fast low angle shot (FLASH 2D), while the breath was held for several seconds. In these images a volume of interest of 64 ml resolution was positioned in the liver parenchyma of the right lobe. A localized shimming procedure was performed. The number of acquisitions was 256. We used echo times of 135 ms and 270 ms, respectively, to differentiate between the fatty acid signal and the lactate signal at 1.35 ppm. This was necessary as both signals consist of almost identical resonance frequencies but have different phase angles at varied echo times. Evaluation of the spectra was performed by means of the LC Model program  and data are expressed in arbitrary units that correspond to micromoles per liter. The liver perfusion measurement was performed with the gadolinium-enhanced proton magnetic resonance (MR) imaging method [16, 17].
Patient data: basic patient characteristics, scores, hemodynamic-related parameters, and laboratory parameters
APACHE II (points)
MOD score (points)
The most important results of this report were threefold. There was a median decrease of 89% in lactate signal intensities in liver tissues, although the plasma lactate did not change markedly. Second, there was an increase in liver perfusion after NAC application and, finally, there was an improvement in liver function measured by the MEGX plasma concentration.
Liver function test and MEGX formation
All patients had MEGX concentrations lower than 50 ng/ml prior to administration of NAC (i.e. hepatic dysfunction was manifest) [21, 22], without remarkable elevation in conventional routine parameters such as aspartate aminotransferase, alanine aminotransferase, bilirubin or serum lactate. After the treatment with NAC the 15 min MEGX concentration showed an increase up to 4.6-fold. The rate of hepatic uptake of lidocaine and MEGX elimination depends primarily on the hepatic blood flow, while MEGX is formed by P-450 in hepatic microsomes [4, 22–24]. Cytochrome P-450 is predominantly localized in zone 3 of the hepatic lobule. In a nonseptical setting, MEGX formation increased due to an improved blood flow [23, 25]. NAC may enhance zone 3 perfusion by increasing sinusoidal blood flow, since zone 3 misdistribution may exist in septic shock patients [21, 22, 26].
Liver lactate and MR spectroscopy
All patients showed a decrease in the lactate signal intensities in their liver tissue. In an animal study, Salzman and colleagues showed a significant transmesenteric lactate concentration (lactate between arterial and mesenteric venous blood) increase after a 90 min ileal hypoxic period . An in vitro study has shown that cell dysfunction leads to the inhibition of pyruvate dehydrogenase within minutes, thus leading to a pyruvate and lactate accumulation in the cell . Accordingly, the decrease in liver lactate signal intensities identified in the present report could be due to a decreased splanchnic lactate production as a result of a NAC-induced increase in regional perfusion with improvement in microcirculation. The improvement in liver perfusion in four patients could be directly associated with the decrease in liver lactate signal intensities. This assumption is supported by the fact that MEGX formation increased after NAC application as a sign of an improved hepatic oxidative metabolism. The beneficial effects of NAC on tissue perfusion have already been shown in animal and clinical studies [10, 26]. Blood lactate levels did not change. In order to cause a significant increase in blood, the rate of lactate production must exceed skeletal muscle, renal and hepatic uptake . Since we did not measure hepatic lactate uptake or release to plasma it is difficult to say what should be expected.
We chose 1H-MRS to determine biochemical changes in hepatic tissue. To the best of our knowledge, no studies have been published concerning 1H-MRS determination of lactate signal intensities in liver tissue in vivo. Only one previous paper exists, which describes in vivo1H-MRS of the liver, assigning the peaks of carnitin, taurine, glutamate and glutamin . Studies have been carried out on human bile and cerebral samples and on animals referring to lactate signal intensities in liver tissue [30–32]. 1H-MRS is often used to determine lactate in other tissues (e.g. cerebral tissue) . The technical advantage of 1H-MRS is its increased sensitivity; with an equal quantity of nuclei, it is approximately 15 times more sensitive than 31P-MR spectroscopy.
Furthermore, the effects of respiratory motions complicate liver studies. We decided against respiration synchronization, as this would have required three times as much measuring time. We used the stimulated echo acquisition mode in conjunction with water suppression techniques . Spectral evaluation and quantification of metabolite concentrations was based on a fully automated program . The spectra, however, have to be regarded critically. The resonance sequences can only be identified with an optimal signal/noise ratio. Therefore, the quantity of acquisitions is important. Acquisitions, similar to respiration synchronization, lead to a time problem. At a later stage, the signal/noise ratio depends on the coil. We used the body coil; however, a local surface coil would have optimized the signal/noise ratio.
Liver blood flow and MR imaging
In order to measure the liver perfusion, we selected gadolinium-enhanced MR imaging as a noninvasive assessment [16, 17]. To the best of our knowledge, liver blood flow measurements have not been performed to date in humans, but portal venous flow, azygos venous blood flow and focal liver lesion blood flow measurements have been carried out in previous studies [35–37]. Our measurements were taken in the manual expiration hold at the respirator. Otherwise noise, which can worsen the signal/noise ratio, and the respiratory motions would lead to an inconsistent slice position and reproduction. The MR imaging in our study showed a median improvement of 41% in liver perfusion in our patients associated with a decrease in lactate signal intensities in liver tissue, and an increase in four patients in the cardiac index. The increase in cardiac index after NAC administration has already been shown in clinical studies [6, 10]. These results suggest that NAC may have a beneficial effect on regional perfusion, which has already been shown in clinical and experimental studies [4, 9]. The decrease in pulmonary vascular and systemic vascular resistance has been illustrated in some studies on endotoxemia in animals [9, 38].
The vasodilating effects of NAC may be caused by a direct relaxing action on vascular smooth muscle or by modulation of nitric oxide, which activates guanylate cyclase, leading to an increase in cyclic guanosine monophosphate accumulation and smooth muscle relaxation [4, 39]. This vasodilating property could have been the cause of the decrease in the PaO2/FiO2 ratio seen in three of the five patients and of the increase in the norepinephrine dose seen in two of the five patients after NAC application, with a consecutive improvement in the PaO2/FiO2 ratio several hours after the intervention.
This report has shown, for the first time, that NAC decreases liver lactate signal intensities and increases perfusion measured by MR imaging and spectroscopy. The MEGX formation improved in all patients, probably due to a NAC-induced improvement in regional perfusion.
N-acetylcysteine decreases liver lactate signal intensities in magnetic resonance spectroscopy
N-acetylcysteine increases liver perfusion measured by magnetic resonance imaging
N-acetylcysteine improves MEGX formation
proton magnetic resonance spectroscopy
proton magnetic resonance
partial arterial oxygen tension/inspirator oxygen fraction
- Edouard AR, Degremont AC, Duranteau J: Hetereogenous regional vascular responses to simulated transient hypovolemia in men.Intensive Care Med 1994, 20:414–420.View ArticleGoogle Scholar
- Takala J, Ruokonen E: Regional blood flow and oxygen transport in septic shock.Crit Care Med 1993, 21:1296–1303.View ArticleGoogle Scholar
- Deitch E: The role of intestinal barrier failure and bacterial translocation in the development of systemic infection and multiple organ failure.Arch Surg 1990, 125:403–408.View ArticleGoogle Scholar
- Rank N, Michel C, Haertel C, Lenhart A, Welte M, Meier-Hellmann A, Spies C: N-acetylcysteine increases liver blood flow and improves liver function in septic shock patients: results of a prospective, randomized, double-blind study.Crit Care Med 2000, 28:3799–3807.View ArticleGoogle Scholar
- Aruoma OI, Halliwell B, Hoey BM, Butler B: The antioxidant action ofN-acetylcysteine; its reaction with hydrogen peroxide, hydroxyl radical, superoxide, and hypochlorous acid.J Free Radic Biol Med 1989, 6:593–597.View ArticleGoogle Scholar
- Harrison PM, Wendon JA, Gimson AES, Graeme JMA, Williams R: Improvement by acetylcysteine of haemodynamics and oxygen transport in fulminant hepatic failure.N Engl J Med 1991, 324:1852–1857.View ArticleGoogle Scholar
- Fox ES, Brower JS, Bellezo JM, Leingang KA: N-acetylcysteine and α-tocopherol reverse the inflammatory response in activated rat Kupffer cells.J Immunol 1997, 158:5418–5423.Google Scholar
- Miller EJ, Cohen AB, Matthay MA: Increased interleukin-8 concentrations in the pulmonary edema fluid of patients with acute respiratory distress syndrom from sepsis.Crit Care Med 1996, 24:1448–1454.View ArticleGoogle Scholar
- Zhang H, Spapen H, Nguyen DN, Rogiers P, Bakker J, Vincent JL: Effects ofN-acetyl-L-cysteine on regional blood flow during endotoxic shock.Eur Surg Res 1995, 27:292–300.View ArticleGoogle Scholar
- Spies C, Reinhart K, Witt I, Meier-Hellmann A, Hannemann L, Donald L, Bredle PD, Schaffartzik W: Influence ofN-acetylcysteine on indirect indicators of tissue oxygenation in septic shock patients: results from a prospective, randomized, double-blind study.Crit Care Med 1994, 22:1738–1746.View ArticleGoogle Scholar
- Devlin J, Ellis AE, McPeake J, Heaton N, Wendon JA, Williams R: N-acetylcysteine improves indocyanine green extraction and oxygen transport during hepatic dysfunction.Crit Care Med 1997, 26:236–242.View ArticleGoogle Scholar
- Ott P: Effects ofN-acetylcysteine on hepatic blood flow and function [letter].Crit Care Med 1998, 26:415.View ArticleGoogle Scholar
- De Backer D, Creteur J, Noordally O, Small N, Bulbis B, Vincent JL: Does hepato-splanchnic VO 2 /DO 2 dependency exist in critically ill septic patients?Am J Respir Crit Care Med 1998, 157:1219–1225.View ArticleGoogle Scholar
- Kilpatrick-Smith L, Erecinska M: Cellular effects of endotoxin in vitro: I. Effect of endotoxin on mitochondrial substrate metabolism and intracellular calcium.Circ Shock 1983, 11:85–99.Google Scholar
- Provencher SW: Estimation of metabolite concentrations from localized in vivo NMR.Magn Reson Med 1993, 30:672–679.View ArticleGoogle Scholar
- Brix G, Schreiber W, Hoffmann U, Guckel F, Hawighorst H, Knopp MV: Methodological approaches to quantitative evaluation of microcirculation in tissues with dynamic magnetic resonance tomography.Radiologe 1997, 37:470–480.View ArticleGoogle Scholar
- Zapletal C, Mehrabi A, Scharf J, Hess T, Kraus T, Herfarth C, Klar E: Experimental evaluation of dynamic MRI for quantifying liver perfusion.Langenbecks Arch Chir 1998, Suppl I:581–584.Google Scholar
- American College of Chest Physicans/Society of Critical Care Medicine Consensus Conference: Definitions for sepsis and organ failure and guidelines for the use of innovative therapies in sepsis.Crit Care Med 1992, 20:864–874.View ArticleGoogle Scholar
- Knaus WA, Wagner DP, Draper EA, Zimmermann JE: APACHE II: a severity disease classification.Crit Care Med 1992, 13:818–828.View ArticleGoogle Scholar
- Goris RJA, Boekhorst TPA, Nuytnick JKS: Multiple organ failure.Arch Surg 1985, 120:1109–1115.View ArticleGoogle Scholar
- Igonin AA, Armstrong VW, Shipkova M, Kukes VG, Oellerich M: The monoethylglycinexylidine (MEGX) test as a marker of hepatic dysfunction in septic patients with pneumonia.Clin Chem Lab Med 2000, 38:1125–1128.View ArticleGoogle Scholar
- Oellerich M, Raude E, Burdelski M, Schulz M, Schmidt FW, Ringe B, Lamesch P, Pichlmayr P, Raith H, Scheruhn M, Wrenger M, Wittekind CH: Monoethylglycinxylidide formation kinetics. A novel approach to assessment of liver function.J Chem Clin Biochem 1987, 25:845–853.Google Scholar
- Goldfarb B, Debaene B, Ang ET, Roulot D, Jolis P, Lebrec D: Hepatic blood flow in humans during isoflurane-N 2 O and halothane-N 2 O anesthesia.Anesth Analg 1990, 71:349–353.View ArticleGoogle Scholar
- Imakoa S, Enomoto K, Oda Y, Asada A, Fujimori M, Shimada T, Fujita H, Guenderich FP, Funae Y: Lidocaine metabolism by human cytochrome P-450s purified from hepatic microsomes: comparison of those with rat hepatic cytochrome P-450s.J Pharmacol Exp Ther 1990, 255:1385–1391.Google Scholar
- Oda Y, Kariya N, Nakamoto T, Nishi S, Asada A, Fujimori M: The monoethylglycinexylidide test is more useful for evaluating liver function than indocyanine green test: case of a patient with remarkably decreased indocyanine green half-life.Ther Drug Monit 1995, 17:207–210.View ArticleGoogle Scholar
- Koeppel TA, Thies JC, Lehmann T, Gebhar MM: Improvement of hepatic microhemodynamics byN-acetylcysteine after warm ischemia.Eur Surg Res 1996, 28:270–277.View ArticleGoogle Scholar
- Salzman AL, Wang H, Wollert PS, Vandermeer JT, Compton CC, Denenberg AG, Fink MP: Endotoxin-induced ileal mucosal hyperpermeability in pigs: role of tissue acidosis.Am J Physiol 1994, 266:G633-G646.Google Scholar
- Kruse JA, Carlson RW: Lactate metabolism.Crit Care Clin 1987, 3:725–746.Google Scholar
- Bárány M, Langer BG, Glieck RP, Venkatasubramanian NP, Wilbur AC, Spigos DG: In vivo 1-H spectroscopy in humans at 1.5 T.Radiology 1988, 167:839–844.View ArticleGoogle Scholar
- Nishijima T, Nishina M, Fujiwara K: Measurement of lactate levels in serum and bile using proton magnetic resonance in patients with hepatobiliary disease: its utility in detection of malignancies.Jpn J Clin Oncol 1997, 27:13–17.View ArticleGoogle Scholar
- Lockett CJ, Busza AL, Proctor TA, Churchill TA, Williams SR, Fuller BJ: Proton nuclear magnetic resonance spectroscopy of lactate production in isolated rat liver during cold preservation.Cryobiology 1996, 33:271–275.View ArticleGoogle Scholar
- Chung Y, Jue T: 1H NMR observation of redox potential in liver.Biochemistry 1992, 31:11159–11165.View ArticleGoogle Scholar
- Frahm J, Hanefeld F: Localized proton magnetic resonance spectroscopy of cerebral metabolites.Neuropediatrics 1996, 27:64–69.View ArticleGoogle Scholar
- Frahm J, Merboldt KD, Hanicke W: Localised proton spectroscopy using stimulated echos.J Magn Reson 1987, 72:502–508.Google Scholar
- Kuo PC, King L, Alfrey JE, Jeffry RB, Garcia G, Dafoe CD: Magnetic resonance imaging and hepatic haemodynamics: correlation with metabolic function in liver transplantation candidates.Surgery 1995, 117:373–379.View ArticleGoogle Scholar
- Lomas DJ, Hayball MP, Jones DP, Sims C, Allison ME, Alexander GJ: Non-invasive measurements of azygos venous blood flow using magnetic resonance.J Hepatol 1995, 22:399–403.View ArticleGoogle Scholar
- Taupitz M, Speidel A, Hamm B, Deimling M, Reichel M, Bock A, Wolf KJ: T2-weighted breath-hold MR-imaging of the liver at 1.5 T: results with a three-dimensional steady-state free procession sequence in 87 patients.Radiology 1995, 194:439–446.View ArticleGoogle Scholar
- Bernard GR, Lucht WD, Niedermeyer ME, Snapper JR, Ogletree ML, Brigham KL: Effect ofN-acetylcysteine on the pulmonary response to endotoxin in the awake sheep and upon in vitro granulocyte function.J Clin Invest 1984, 73:1772–1784.View ArticleGoogle Scholar
- Waldmann SA, Murad F: Biochemical mechanisms underlying vascular smoth muscle relaxation: the guanylate cyclase-cyclic GMP system.J Cardiovasc Pharmakol 1988, 12:115–118.View ArticleGoogle Scholar
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