Interaction of glyoxal and methylglyoxal with biogenic amines.
- 1 April 1975
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 72 (4) , 1610-1611
- https://doi.org/10.1073/pnas.72.4.1610
Abstract
Glyoxal and methylglyoxal interact with biogenic amines and form biologically active free radicals. Electron spin resonance absorption of the radical at room temperature is characterized by a signal at g equals 2.004 with peak-to-peak width of 29 G. An optical absorption at 400 nm with molar absorptivity of 23,000 accompanies the formation of the radical. The dry powdered preparation of the same reaction, which is considered to be the seconardy product, gives an electron spin resonance signal much narrower and 1/200 in intensity compared with the one in solution. Similarly the 400 nm absorption intensity is 1/8 that of the primary product. Possible biological significance of the primary and the secondary product, in relation to muscular dystrophy and photophosphorylation, is discussed.Keywords
This publication has 7 references indexed in Scilit:
- Electronic biology and its relation to cancerLife Sciences, 1974
- NUTRITIONAL MUSCULAR DYSTROPHY AND HUMAN MYOCARDIAL INFARCTIONThe Lancet, 1973
- Modification of Parkinsonism — Chronic Treatment with L-DopaNew England Journal of Medicine, 1969
- Autoxidation of polyunsaturated esters in water: chemical structure and biological activity of the productsJournal of Lipid Research, 1967
- Aromatic Amino Acids and Modification of ParkinsonismNew England Journal of Medicine, 1967
- [ON THE EFFECT OF HYDROXYOCTENAL ON EHRLICH ASCITES TUMOR CELLS].1964