Long-chain N-acylethanolamines inhibit lipid peroxidation in rat liver mitochondria under acute hypoxic hypoxia

Chemistry and Physics of Lipids

Volumn 97, Issue 1, 1998, Pages 49-54

  Gulaya, Nadya M ^a   Kuzmenko, Alexander I ^a   Margitich, Victor M ^a   Govseeva, Nonna M ^a   Melnichuk, Sergij D ^a   Goridko, Tetyana M ^a   Zhukov, Alexander D ^a  

^a PALLADIN INSTITUTE OF BIOCHEMISTRY   (Ukraine)

Author keywords

Chemiluminescence; Free radicals; Hypoxia; Lipid peroxidation; N acylethanolamines

Indexed keywords

ETHANOLAMINE DERIVATIVE; FREE RADICAL; PALMIDROL; SCAVENGER; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHEMOLUMINESCENCE; HYPOXIA; LIPID PEROXIDATION; LIVER MITOCHONDRION; MALE; MITOCHONDRIAL RESPIRATION; NONHUMAN; PRIORITY JOURNAL; RAT;

ANIMALS; ANOXIA; ANTIOXIDANTS; CHEMILUMINESCENT MEASUREMENTS; ETHANOLAMINES; FREE RADICALS; IRON; KINETICS; LIPID PEROXIDATION; MALE; MITOCHONDRIA, LIVER; PALMITIC ACIDS; RATS; RATS, WISTAR;

EID: 0031766266     PISSN: 00093084     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-3084(98)00093-0     Document Type: Article

References (25)

1. Ambrosini, A., Bertoli, E., Mariani, P., Tanfani, F., Wozniak, M., Zolese, G., 1993. N-Acylethanolamines as membrane topological stress compromising agents. Biochim. Biophys. Acta 1148, 351-355.
2. Braughler, J.M., Duncan, L.A., Chase, R.L., 1986. The involvement of iron in lipid peroxidation. Importance of ferric to ferrous ratio in initiation. J. Biol. Chem. 261, 10282-10289.
3. Devane, W.A., Hanus, L., Breuer, A., Pertwee, R.G., Stevenson, L.A., Griffin, G., Gibson, D., Mandelbaum, A., Etinger, A., Meshoulam, R., 1992. Isolation and structure of a brain constituent that binds to the cannabinoid receptor. Science 258, 1946-1949.
4. Emerit, J., Chaudiere, J., 1989. Free radicals and lipid peroxidation in cell biology. In: Miquel, J., Quintanilha, A.T., Weber, H. (Eds.), Handbook of Free Radicals and Antioxidants in Biomedicine. CRC Press, Boca Raton, FL, pp. 177-185.
5. Epps, D.E., Cardin, A.D., 1987. The interaction of N-oleylethanolamine with phospholipid bilayers. Biochim. Biophys. Acta 903, 533-541.
6. Epps, D.E., Schmid, P.C., Natarajan, V., Schmid, H.H.O., 1979. N-Acylethanolamine accumulation in infarcted myocardium. Biochem. Biophys. Res. Commun. 90, 628-633.
7. Epps, D.E., Natarajan, V., Schmid, P.C., Schmid, H.H.O., 1980. Accumulation of N-acylethanolamine glycerophospholipids in infarcted myocardium. Biochim. Biophys. Acta 618, 420-430.
8. Epps, D.E., Mandel, F., Schwartz, A., 1982a. The alteration of rabbit skeletal sarcoplasmic reticulum function by N-acylethanolamine, a lipid associated with myocardial infarction. Cell Calcium 3, 531-543.
9. 2+ release from mitochondria by N-acylethanolamines, a class of lipids synthesized in ischemic heart tissue. J. Biol. Chem. 257, 1383-1391.
10. Felder, C., Briley, E.M., Axelrod, J., Simpson, J.T., Mackie, K., Devane, W.A., 1993. Anandamide, an endogenous cannabimimetic eicosanoid, binds to the cloned human cannabinoid receptor and stimulates receptor-mediated signal transduction. Proc. Natl. Acad. Sci. USA 90, 7656-7660.
11. Gulaya, N.M., Melnik, A.A., Balkov, D.I., Volkov, G.L., Vysotskiy, M.V., Vaskovsky, V.E., 1993a. The effect of long-chain N-acylethanolamines on some membrane-asso ciated functions of neuroblastoma C1300 N18 cells. Biochim. Biophys. Acta 1152, 280-288.
12. Gulaya, N.M., Smirnov, I.M., Shmalko, Y.P., Melnik, A.A., Melnik, S.N., 1993b. Effect of N-palmitoyl- and N-stearoylethanolamines on lipid peroxidation in mouse tissues in metastatic Lewis carcinoma. Ukrainian Biochem. J. 65, 96-101 (in Russian, abstract in English).
13. Hansen, H.S., Lauritzen, L., Strand, A.M., Moesgaard, B., Frandsen, A., 1995. Glutamate stimulates the formation of N-acylphosphatidylethanolamine and N-acylethanolamine in cortical neurons in culture. Biochim. Biophys. Acta 1258, 303-308.
14. Hansen, H.S., Lauritzen, L., Moesgaard, B., Strand, A.M., Hansen, H.H., 1998. Formation of N-acyl-phosphatidylethanolamines and N-acylethanolamines. Proposed role in neurotixicity. Biochem. Pharmacol. 55, 719-725.
15. Kuzmenko, A.I., Morozova, R.P., Nikolenko, I.A., Korniets, G.V., Kholodova, Y.D., 1997. Effects of vitamin D3 and ecdysterone on free-radical lipid peroxidation. Biochemistry (Moscow) 62, 609-612.
16. Lowry, O.H., Rosebrough, N.J., Farr, A.L., Randall, R.J., 1951. Protein measurement with the folin phenol reagent. J. Biol. Chem. 193, 265-275.
17. Melnichuk, S.O., Kuzmenko, A.I., Margitich, V.M., Goseeva, N.N., Goridko, T.N., Gulaya, N.M., 1998. Effect of carbonic acid on proceeding of free radical processes under artificial hypobiosis in rats. Ukrainian Biochem. J. 70, 87-94 (in Russian, abstract in English).
18. Parinandi, N.L., Schmid, H.H.O., 1988. Effects of long-chain N-acylethanolamines on lipid peroxidation in cardiac mitochondria. FEBS Lett. 237, 49-52.
19. Poli, G., Albano, E., Dianzani, M.U., 1987. The role of lipid peroxidation in liver damage. Chem. Phys. Lipids 45, 117-142.
20. Schmid, H.H.O., Schmid, P.C., Natarajan, V., 1990. N-acylated glycerophospholipids and their derivitives. Prog. Lipid Res. 29, 1-43.
21. Schmid, P.C., Krebsbach, R.J., Perry, S.R., Dettmer, T.M., Maasson, J.L., Schmid, H.H.O., 1995. Occurrence and postmortem generation of anandamide and other long-chain N-acylethanolamines in mammalian brain. FEBS Lett. 375, 117-120; Corrigendum 1996 385, 125-126.
22. Schmid, P.C., Krebsbach, R.J., Perry, S.R., Dettmer, T.M., Maasson, J.L., Schmid, H.H.O., 1995. Occurrence and postmortem generation of anandamide and other long- chain N-acylethanolamines in mammalian brain. FEBS Lett. 375, 117-120; Corrigendum 1996 385, 125-126.
23. Schmid, H.H.O., Schmid, P.C., Natarajan, V., 1996. The N-acylation-phosphodiesterase pathway and cell signalling. Chem. Phys. Lipids 80, 133-142.
24. Skaper, S.D., Buriani, A., Daltoso, R., Petrelli, L., Romanello, S., Facci, L., Leon, A., 1996. The ALIAmide palmitoylethanolamide and cannabinoids, but not anandamide, are protective in a delayed postglutamate paradigm of excitotoxic death in cerebellar granule neurons. Proc. Natl. Acad. Sci. USA 93, 3984-3989.
25. Sottocasa, G., 1976. The isolation of mitochondria and their membranes. In: Maddy, A.H. (Ed.), Biochemical Analysis of Membranes. Chapman and Hall, London, pp. 54-74.