Erythrocyte membrane protein damage by phenoxyacetic herbicides and their metabolites

Pesticide Biochemistry and Physiology

Volumn 82, Issue 1, 2005, Pages 59-65

  Duchnowicz, Piotr ^a   Szczepaniak, Piotr ^a   Koter, Maria ^a  

^a UNIVERSITY OF LODZ   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 16244385957     PISSN: 00483575     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pestbp.2004.12.004     Document Type: Article

References (23)

1. C. McGourty Agent Orange study blasted Nature 340 1989 179 183
2. J. Stellman, S. Stellman, R. Christian, T. Weber, and C. Tomacallo The extent and patterns of usage of agent orange and other herbicides in vietnam Nature 422 2003 681 687
3. L. Różañski, Przemiany pestycydów w organizmach żywych i środowisku [Pesticide transformation in living organisms and environmental], AGRA-ENVIRO LAB, Poznañ (1998) 299-301
4. S.C. Kim, R.F. Keizer, W. Ambrose, and G.R. Breese Effects of 2,4,5-trichlorophenoxyacetic acid and quinolinic acid on 5-hydroxy-3- indoleacetic acid transport by the rabbit choroid plexus: pharmacology and electron microscopic chemistry Toxicol. Appl. Pharmacol. 3 1987 436 444
5. K. Ozaki, J. Mahler, J. Haseman, C. Moomaw, M. Nicolette, and A. Nyska Unique renal tubule changes induced in rats and mice by the peroxisime proliferators 2,4-dichlorophenoxyacetic acid and WY-14643 Toxic. Pathol. 29 2001 440 450
6. J.M. Safi Association between chronic exposure to pesticides and record cases of human malignancy in Gaza Governorates (1990-1999) Sci. Total Environ. 284 2002 75 84
7. J.C. Skou, and M. Essman The Na,K-ATPase J. Bioenerg. Biomembr. 24 1992 249 261
8. P. Duchnowicz, M. Koter, and W. Duda Damage of erythrocyte by phenoxyacetic herbicides and their metabolites Pest. Biochem. Physiol. 74 2002 1 7
9. O.H. Lowry, N.J. Rosenboarg, A.L. Farer, and R.J. Randall Protein measurement with the Folin Phenol reagent J. Biol. Chem. 193 1951 265 275
10. 2+-ATPase by membrane disturbing agents Biochem. Mol. Biol. Int. 34 1994 521 529
11. P.P. Veldhoven van, and G.P. Mannaerts Inorganic and organic phosphate measurements in the nanomolar range Anal. Biochem. 161 1987 45 48
12. G. Ellman Tissue sulfhydryl groups Arch. Biochem. Biophys. 82 1959 70 77
13. S. Incerpi, P. Baldini, and P. Luly Cholesterol modulation in vitro of plasma membrane-bound enzymes in human erythrocytes Cell. Mol. Biol. 29 1983 285 289
14. F. Giraud, M. Claret, and R. Garay Interaction of cholesterol with the Na pump in red blood cells Nature 264 1976 646 648
15. 2+)-ATPase from cardiac muscle Biochem. Biophys. Acta 773 1984 231 236
16. K. Tsuda, I. Nishio, and Y. Masuyama Triphosphatase in the regulation of membrane fluidity of erythrocyte in spontaneously hypertensive rats Am. J. Hypertens. 10 1997 1411 1414
17. +)-ATPase activity: head group specificity and fatty acid fluidity Biochim. Biophys. Acta 282 1972 277 292
18. P.L. Else, and B.J. Wu What role for membranes in determining the higher sodium pump molecular activity of mammals compared to ectotherms? J. Comp. Physiol. B 169 1999 296 302
19. M. Suwalsky, M. Benites, F. Villena, F. Aguilar, and C.P. Sotomayor Interaction of 2,4dichlorophenoxyacetic acid (2,4-D) with cell and model membranes Biochim. Biophys. Acta 1285 1996 267 276
20. S. Han, K. Ichikawa, and H. Utsumi Quantitative analysis for the enhancement of hydroxyl radical generation by phenols during ozonation of water Water Res. 11 1998 3261 3266
21. +-pump ATPase by iron-generated free radicals. Protection by 6,7-dimethyl-2,4-DI-1-1pyrrolidinyl- 7H-pyrrolo[2,3-d]pyrimidine sulfate (U-89842D), a potent, novel, antioxidant/free radical scavenger Biochem. Pharmacol. 51 1996 471 476
22. + ATPase of human skin fibroblasts Ecotoxicol. Environ. Saf. 1 1991 38 46
23. N.M. Gevondyan, V.S. Gevondyan, E.E. Gavrilyeva, and N.N. Modyanov Analysis of free sulfhydryl groups and disulfide bonds in Na,K-ATPase FEBS Lett. 255 1989 265 268