Abstract
Early changes in lysosomal enzymes must occur if their role is significant in irreversible myocardial injury. Therefore, we ligated the anterior descending coronary artery in 14 dogs and after 60 min excised epicardial and endocardial samples from the ischemic and adjacent normal heart. The collateral flow measured with radioactive microspheres in the endocardial samples averaged 19% of control. The muscle was disrupted and fractionated by ultracentrifugation into nuclear pellet (NP), heavy lysosomal pellet (HL), light lysosomal pellet (LL), microsomal pellet (M) and supernate (S). Electron microscopy demonstrated changes characteristic of sichemia in whole tissues and sedimented fractions. Acid phosphatase reaction product was present in residual bodies in the HL fraction and membrane-bound vesicles in the LL fraction and in the intact tissue. Significant decreases in the specific activity of N-acetyl-beta-glucosaminidase and beta-glucuronidase occurred in the endocardial LL fraction, while significant increases in both were found in the ts fraction (P less than 0.05). Losses of acid phosphatase occurred in both LL and S fractions. Moreover, decreases of total N-acetyl-beta-glucosaminidase in the HL fraction and of total beta-glucuronidase and acid phosphatase in the LL fraction were positively correlated (P less than 0.01) with the degree of ischemia measured with radioactive microspheres. Only insignificant enzymatic changes were found when the collateral flow was greater than 40%, and the differences were less significant in epicardial samples where the flow averaged 29%. The early loss of enzymes from the lysosomal fractions in severe ischemia suggests a role for lysosomal hydrolases in the necrosis that follows coronary occlusion.
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- Arcangeli P., Del Soldato P., Digiesi V., Melani F. Changes in the activities of lysosomal enzymes in striated muscle following ischemia. Life Sci II. 1973 Jan 8;12(1):13–23. doi: 10.1016/0024-3205(73)90175-6. [DOI] [PubMed] [Google Scholar]
- Baccino F. M., Rita G. A., Zuretti M. F. Studies on the structure-bound sedimentabolity of some rat liver lysosome hydrolases. Biochem J. 1971 Apr;122(3):363–371. doi: 10.1042/bj1220363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baggiolini M., Hirsch J. G., De Duve C. Resolution of granules from rabbit heterophil leukocytes into distinct populations by zonal sedimentation. J Cell Biol. 1969 Feb;40(2):529–541. doi: 10.1083/jcb.40.2.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Becker L. C., Fortuin N. J., Pitt B. Effect of ischemia and antianginal drugs on the distribution of radioactive microspheres in the canine left ventricle. Circ Res. 1971 Feb;28(2):263–269. doi: 10.1161/01.res.28.2.263. [DOI] [PubMed] [Google Scholar]
- Brunk U. T., Ericsson J. L. Cytochemical evidence for the leakage of acid phosphatase through ultrastructurally intact lysosomal membranes. Histochem J. 1972 Nov;4(6):479–491. doi: 10.1007/BF01011128. [DOI] [PubMed] [Google Scholar]
- Brunk U. T., Ericsson J. L. The demonstration of acid phosphatase in vitro cultured tissue cells. Studies on the significance of fixation, tonicity and permeability. Histochem J. 1972 Jul;4(4):349–363. doi: 10.1007/BF01005009. [DOI] [PubMed] [Google Scholar]
- Canonico P. G., Bird J. W. Lysosomes in skeletal muscle tissue. Zonal centrifugation evidence for multiple cellular sources. J Cell Biol. 1970 May;45(2):321–333. doi: 10.1083/jcb.45.2.321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DE DUVE C., BEAUFAY H. Tissue fractionation studies. 10. Influence of ischaemia on the state of some bound enzymes in rat liver. Biochem J. 1959 Dec;73:610–616. doi: 10.1042/bj0730610. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Domenech R. J., Hoffman J. I., Noble M. I., Saunders K. B., Henson J. R., Subijanto S. Total and regional coronary blood flow measured by radioactive microspheres in conscious and anesthetized dogs. Circ Res. 1969 Nov;25(5):581–596. doi: 10.1161/01.res.25.5.581. [DOI] [PubMed] [Google Scholar]
- GIANETTO R., DE DUVE C. Tissue fractionation studies. 4. Comparative study of the binding of acid phosphatase, beta-glucuronidase and cathepsin by rat-liver particles. Biochem J. 1955 Mar;59(3):433–438. doi: 10.1042/bj0590433. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoffstein S., Gennaro D. E., Weissmann G., Hirsch J., Streuli F., Fox A. C. Cytochemical localization of lysosomal enzyme activity in normal and ischemic dog myocardium. Am J Pathol. 1975 May;79(2):193–206. [PMC free article] [PubMed] [Google Scholar]
- Jennings R. B., Ganote C. E. Structural changes in myocardium during acute ischemia. Circ Res. 1974 Sep;35 (Suppl 3):156–172. [PubMed] [Google Scholar]
- Jennings R. B., Sommers H. M., Herdson P. B., Kaltenbach J. P. Ischemic injury of myocardium. Ann N Y Acad Sci. 1969 Jan 31;156(1):61–78. doi: 10.1111/j.1749-6632.1969.tb16718.x. [DOI] [PubMed] [Google Scholar]
- Kjekshus J. K., Maroko P. R., Sobel B. E. Distribution of myocardial injury and its relation to epicardial ST-segment changes after coronary artery occlusion in the dog. Cardiovasc Res. 1972 Sep;6(5):490–499. doi: 10.1093/cvr/6.5.490. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Oliveira M. M., Weglicki W. B., Nason A., Nair P. P. Distribution of alpha-tocopherol in beef heart mitochondria. Biochim Biophys Acta. 1969 May;180(1):98–113. doi: 10.1016/0005-2728(69)90197-2. [DOI] [PubMed] [Google Scholar]
- Ravens K. G., Gudbjarnason S. Changes in the activities of lysosomal enzymes in infarcted canine heart muscle. Circ Res. 1969 Jun;24(6):851–856. doi: 10.1161/01.res.24.6.851. [DOI] [PubMed] [Google Scholar]
- Ricciutti M. A. Lysosomes and myocardial cellular injury. Am J Cardiol. 1972 Oct;30(5):498–502. doi: 10.1016/0002-9149(72)90040-9. [DOI] [PubMed] [Google Scholar]
- Ricciutti M. A. Myocardial lysosome stability in the early stages of acute ischemic injury. Am J Cardiol. 1972 Oct;30(5):492–497. doi: 10.1016/0002-9149(72)90039-2. [DOI] [PubMed] [Google Scholar]
- SOMMERS H. M., JENNINGS R. B. EXPERIMENTAL ACUTE MYOCARDIAL INFARCTION; HISTOLOGIC AND HISTOCHEMICAL STUDIES OF EARLY MYOCARDIAL INFARCTS INDUCED BY TEMPORARY OR PERMANENT OCCLUSION OF A CORONARY ARTERY. Lab Invest. 1964 Dec;13:1491–1503. [PubMed] [Google Scholar]
- Spath J. A., Jr, Lane D. L., Lefer A. M. Protective action of methylprednisolone on the myocardium during experimental myocardial ischemia in the cat. Circ Res. 1974 Jul;35(1):44–51. doi: 10.1161/01.res.35.1.44. [DOI] [PubMed] [Google Scholar]
- WOOLLEN J. W., HEYWORTH R., WALKER P. G. Studies on glucosaminidase. 3. Testicular N-acetyl-beta-glucosaminidase and N-acetyl-beta-galactosaminidase. Biochem J. 1961 Jan;78:111–116. doi: 10.1042/bj0780111. [DOI] [PMC free article] [PubMed] [Google Scholar]


