| Radical honey Trends in Pharmacological Sciences, Volume 22, Issue 9, 1 September 2001, Pages 449 David Cutler Full Text | PDF (22 kb) |
| Are carotenoids a red herring in sexual display? Trends in Ecology & Evolution, Volume 19, Issue 7, 1 July 2004, Pages 353-354 Richard C Hartley and Malcolm W Kennedy Full Text | PDF (59 kb) |
| Cancer prevention – the potential for diet to modulate molecular signalling Trends in Molecular Medicine, Volume 9, Issue 1, 1 January 2003, Pages 11-18 Margaret M Manson Abstract As our understanding of the development of cancer and the complex signalling mechanisms involved improves, we are beginning to appreciate the enormous potential for intervention strategies that prevent or slow down the disease process. Although much research is currently aimed at developing drugs to target key molecules in tumour cells that are responsible for their proliferation and survival, dietary constituents also have potential as anti-cancer agents. Our goal should be not only to identify carcinogenic changes as early as possible and to intervene effectively long before life-threatening tumours develop, but also to understand how a balanced, healthy diet can contribute to reduced incidence, as epidemiology so tantalizingly suggests. Abstract | Full Text | PDF (895 kb) |
Copyright © 1996 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 70, Issue 5, 2203-2211, 1 May 1996
doi:10.1016/S0006-3495(96)79786-2
Research Article
S. Przestalski, J. Hladyszowski, J. Kuczera, B. Rózycka-Roszak, Z. Trela, H. Chojnacki, S. Witek and E. Fisicaro
Department of Physics and Biophysics, Agricultural University of Wrocław, Poland.
The effect of two series of amphiphilic quaternary ammonium salts on some properties of phospholipid membranes was studied. The compounds of one series, N-benzyl-N,N-dimethyl-N-alkyl ammonium bromides, exert a destructive effect on membranes and are treated as reference compounds. The compounds of the other series, N-(3,5-di-t-butyl-4-hydroxy)benzyl-N,N-dimethyl-N-alkyl ammonium bromides, are derivatives of the former ones, exhibit antioxidant properties, and do only relatively slight damage to the membranes. The aim of the work was to explain the difference in molecular interaction with membranes between the two kinds of hydrophobic compounds. Thermodynamic methods, a new mixing technique, and monolayer and quantum calculation methods were used. It has been shown that the antioxidant molecules are less hydrophobic than those of the reference compounds and disturb the membrane organization to a lesser extent. On the basis of monolayer data, we suggest that the studied antioxidant behaves like a substitutional impurity, whereas the reference behaves like an interstitial one.