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Nonesterified fatty acids and lipid peroxidation

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Abstract

Oxygen free radicals damage cells through peroxidation of membrane lipids. Gastrointestinal mucosal membranes were found to be resistant to in vitro lipid peroxidation as judged by malonaldehyde and conjugated diene production and arachidonic acid depletion. The factor responsible for this in this membrane was isolated and chemically characterised as the nonesterified fatty acids (NEFA), specifically monounsaturated fatty acid, oleic acid. Authentic fatty acids when tested in vitro using liver microsomes showed similar inhibition. The possible mechanism by which NEFA inhibit peroxidation is through iron chelation and iron-fatty acid complex is incapable of inducing peroxidation. Free radicals generated independent of iron was found to induce peroxidaton of mucosal membranes. Gastrointestinal mucosal membranes were found to contain unusually large amount of NEFA. Circulating albumin is known to contain NEFA which was found to inhibit iron induced peroxidation whereas fatty acid free albumin did not have any effect. Addition of individual fatty acids to this albumin restored its inhibitory capacity among which monounsaturated fatty acids were more effective. These studies have shown that iron induced lipid peroxidation damage is prevented by the presence of nonesterified fatty acids.

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References

  1. Clark IA: Tissue damage caused by free oxygen radicals. Pathology 18: 181–186, 1986

    Google Scholar 

  2. Comporti M: Lipid peroxidation and cellular damage in toxic liver injury. Lab Invest 53: 599–623, 1985

    Google Scholar 

  3. Halliwell B: Oxidants and human diseases: some new concepts. FASEB J 1: 358–364, 1987

    Google Scholar 

  4. Cross CE, Halliwell B, Burish EJ et al.: Oxygen radicals and human diseases. Ann Int Med 107: 526–545, 1987

    Google Scholar 

  5. Parks DA: Oxygen free radicals: Mediators of gastrointestinal pathophysiology. Gut 30: 293–298, 1989

    Google Scholar 

  6. Komingsberger JJM, Marx JJM, Vanhuttum J: Free radicals in gastroenterology: A review. Scand J Gastroenterol (Suppl. 154) 23: 30–40, 1988

    Google Scholar 

  7. Balasubramanian KA, Manohar M, Mathan VI: An unidentified inhibitor of lipid peroxidation in intestinal mucosa. Biochim Biophys Acta 962: 51–58, 1988

    Google Scholar 

  8. Diplock AT, Balasubramanian KA, Manohar M, Mathan VI, Ashton DS: Purification and chemical characterization of the inhibitor of lipid peroxidation from intestinal mucosa. Biochim Biophys Acta 962: 42–50, 1988

    Google Scholar 

  9. Balasubramanian KA, Nalini S, Cheseman KH, Slater TF: Nonesterified fatty acids inhibit iron dependent lipid peroxidation. Biochim Biophys Acta 1003: 232–237, 1989

    Google Scholar 

  10. Simpson RJ, Moore R, Peters TJ: Significance of nonesterified fatty acids in iron uptake by intestinal brush border membrane vesicles. Biochim Biophys Acta 941: 39–47, 1988

    Google Scholar 

  11. Simpson RJ, Peters TJ: Iron-binding lipids of rabbit duodenal brush-border membrane. Biochim Biophys Acta 898: 181–186, 1987

    Google Scholar 

  12. Frei B, Stocker R, Ames BN: Antioxidant defense and lipid peroxidation in human blood plasma. Proc Natl Acad Sci USA 85: 9748–9752, 1987

    Google Scholar 

  13. Halliwell B: Albumin as an important extracellular antioxidant. Biochim Pharmacol 37: 569–571, 1988

    Google Scholar 

  14. Nutteridge JMC: Antioxidant properties of the proteins ceruloplasmin, albumin and transferrin. A study of their activity in serum and synovial fluid from patients with rheumatoid arthritis. Biochim Biophys Acta 869: 119–127, 1986

    Google Scholar 

  15. Nalini S, Balasubramanian KA: Albumin bound nonesterified fatty acids inhibit in vitro peroxidation. Ind J Biochem Biophys 26: 357–360, 1989

    Google Scholar 

  16. Steinberg D, Parthasarathy S, Carew TE, Khoo JC, Witztum JL: Beyond cholesterol: Modifications of low density lipoprotein that increases its atherogenicity. N Engl J Med 320: 915–924, 1989

    Google Scholar 

  17. Caren TE, Schwenke DC, Steinberg D: Antiatherogenic effect of probucol correlated to its hypocholesterilemic effect. Proc Natl Acad Sci USA 84: 7725–7729, 1987

    Google Scholar 

  18. Kita T, Nagano Y, Yokoda M, et al.: Probucol prevents the progression of atherosclerosis in Watanabe heritable hyperlipidemic rabbit. Proc Natl Acad Sci USA 84: 5528–5931, 1987

    Google Scholar 

  19. Grindy SM: Comparison of monounsaturated fatty acids and carbohydrates for lowering plasma cholesterol. N Engl J Med 314: 745–748, 1986

    Google Scholar 

  20. Mansink RP, Katar MB: Effect of diet enriched with monounsaturated or polyunsaturated fatty acids on levels of low density and high density lipoprotein cholesterol in healthy women and man. N Engl J Med 321: 436–441, 1989

    Google Scholar 

  21. Parthasarathy S, Khoo JC, Miller F, Burnett J, Witztum JL, Steinberg D: Low density lipoprotein rich in oleic acid is protected against oxidative modification: Implications for dietary prevention of atherosclerosis. Proc Natl Acad Sci USA 87: 3894–3898, 1990

    Google Scholar 

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Balasubramanian, K.A., Nalini, S. & Manohar, M. Nonesterified fatty acids and lipid peroxidation. Mol Cell Biochem 111, 131–135 (1992). https://doi.org/10.1007/BF00229584

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