Abstract
Quantitative evaluation of organ damage can be achieved by non-invasive, direct or indirect methods. Direct methods include echography, tomography, scintigraphy and magnetic resonance. The accuracy of these imaging techniques has been demonstrated in human medicine. Most of them have not been validated in animals, however, and their use is limited by cost. Indirect methods are based on determination of the total release of intracellular markers (mainly enzymes) into body fluids. Quantification of organ damage depends on extracellular disposition of the marker. Thus, in the kidney, the marker is directly and totally leaked into the urine and is voided at each micturition. The amount of marker eliminated in this way allows easy quantification of organ damage occurring during the period preceding the micturition.
Muscle markers with molecular weights exceeding 50 kDa reach the blood via the lymph. This results in (a) partial inactivation, (b) delay between cell damage and increased plasma concentration and (c) accumulation in the plasma as long as delivery into the plasma exceeds clearance. In such cases, quantitative evaluation requires pharmacokinetic tools and calculation of the area under the curve (concentration vs time) and of the plasma clearance. Comparison of the intensity and chronology of markers located in different cell compartments may contribute to the understanding of pathophysiological events.
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Aktas M, Vinclair P, Lefebvre HP et al. (1995a) In vivo quantification of muscle damage in dogs after intramuscular administration of drugs. Br Vet J 151:189–196
Aktas M, Lefebvre HP, Toutain PL et al. (1995b) Disposition of creatine kinase activity in dog plasma following intravenous and intramuscular injection of skeletal muscle homogenates. J Vet Pharmacol Ther 18:1–6
Beneke R, Neuerburg J, Bohndorf K (1991) Muscle cross-section measurement by magnetic resonance imaging. Eur J Appl Physiol 63:424–429
Bhattacharya S, Lahiri A (1991) Clinical role of indium-111 antimyosin imaging. Eur J Nucl Med 18:889–895
Blebea J, Kerr JC, Franco CD et al. (1988) Technetium 99m pyrophosphate quantitation of skeletal muscle ischemia and reperfusion injury. J Vase Surg 8:117–124
Braun JP, Aktas M, Lefebvre H et al. (1993) Clinical enzymology for the assessment of organ damage: interspecific differences. Comp Haematol Int 3:27–32
Bret L, Hasim M, Lefebvre H et al. (1993) Kidney tubule enzymes and extracellular DNA in urine as markers for nephrotoxicity in the guinea pigs. Enzyme Protein 47:27–36
Carlson CJ, Meister W, Emilson B et al. (1982) Clearance of serum creatine kinase activity. Cardiovasc Res 16:66–70
Houpert P, Serthelon JP, Lefebvre HP et al. (1995) In vivo non invasive quantification of muscle damage following a single intramuscular injection of phenylbutazone in sheep. Vet Hum Toxicol 37:105–110
Kawaguchi K, Sone T, Tsuboi H et al. (1991) Quantitative estimation of infarct size by simultaneous dual radionuclide single photon emission computed tomography: comparison with peak serum creatine kinase activity. Am Heart J 121:1353–1360
Lefebvre HP, Jaeg JP, Rico AG et al. (1992) Variations of plasma creatine kinase in rabbits following repetitive blood sampling. Effects of pretreatment with acepromazine, carazolol and dantrolene. Eur J Clin Chem Clin Biochem 30:425–428
Lefebvre HP, Toutain PL, Bret L et al. (1993a) Compared kinetics of plasma creatine kinase activity in rabbits after intravenous injection of different preparations of skeletal muscle. Vet Res 24:468–476
Lefebvre HP, Serthelon JP, Ferré JP et al. (1993b) Un cas d'intolér-ance locale après administration intramusculaire d'une formulation retard chez une vache: biologie clinique et échographie. Rev Med Vet 144:229–233
Lefebvre HP, Toutain PL, Serthelon JP et al. (1994) Pharmacokinetic variables and bioavailability from muscle of creatine kinase in cattle. Am J Vet Res 55:487–493
Lehto M, Alanen A (1987) Healing of a muscle trauma. Correlation of sonographical and histological findings in an experimental study in rats. J Ultrasound Med 6:425–429
Morguet AJ, Munz DL, Klein HH et al. (1992) Myocardial distribution of indium-111-antimyosin Fab and technetium-99m-sestamibi in experimental nontransmural infarction. J Nucl Med 33:223–228
Pohost GM, Henzlova MJ, Okada R et al. (1992) Radionuclide methods to assess cardiac perfusion, function, viability, and necrosis. In: Fozzard HA (ed) The Heart and cardiovascular process, 2nd ed. Raven Press, New York, pp 669–691
Reimers CD, Fleckenstein JL, Witt TN et al. (1993) Muscular ultrasound in idiopathic inflammatory myopathies of adults. J Neurol Sci 116:82–92
Sagar KB, Pelc LR, Rhyne TL et al. (1991) Estimation of myocardial infarct size with ultrasonic tissue characterization. Circulation 83:1419–1428
Van Holsbeeck M, Introcaso JH (1992) Musculoskeletal ultrasonography. Radiol Clin North Am 30:907–925
Van Kreel BK, van der Veen FH, Willems GM et al. (1993) Circulatory models in assessment of cardiac enzyme release in dogs. Am J Physiol 264:H747-H754
Volfinger L, Lassourd V, Michaux JM et al. (1994) Kinetic evaluation of muscle damage during exercise by calculation of amount of creatine kinase released. Am J Physiol 266:R434-R441
Yip TC, Houle S, Tittley JG et al. (1992) Quantification of skeletal muscle necrosis in the lower extremities using99Tcm pyrophosphate with single photon emission computed tomography. Nucl Med Commun 13:47–52
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Originally presented at ECCP 95.
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Lefebvre, H.P., Braun, J.P., Laroute, V. et al. Non-invasive quantification of organ damage. Comparative Haematology International 5, 120–124 (1995). https://doi.org/10.1007/BF00638930
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DOI: https://doi.org/10.1007/BF00638930