Lipid peroxidation associated with anemia in rats experimentally infected with Trypanosoma evansi

Veterinary Parasitology

Volumn 165, Issue 1-2, 2009, Pages 41-46

  Wolkmer, Patrícia ^a   da Silva, Aleksandro Schafer ^a   Traesel, Carolina Kist ^a   Paim, Francine Chimelo ^a   Cargnelutti, Juliana Felipetto ^a   Pagnoncelli, Marciélen ^a   Picada, Mauren Emanuelli ^a   Monteiro, Sílvia Gonzalez ^a   Lopes, Sonia Terezinha dos Anjos ^a  

^a FEDERAL UNIVERSITY OF SANTA MARIA   (Brazil)

Author keywords

Anemia; Peroxidation; Rats; T. evansi; TBARS

Indexed keywords

HEMOGLOBIN; MALONALDEHYDE;

ANEMIA; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; ERYTHROCYTE COUNT; ERYTHROCYTE MEMBRANE; HEMATOCRIT; HEMOGLOBIN DETERMINATION; IN VITRO STUDY; LIPID PEROXIDATION; MALE; NONHUMAN; OXIDATIVE STRESS; PATHOGENESIS; RAT; SURRA; TRYPANOSOMA EVANSI;

ANEMIA; ANIMALS; ERYTHROCYTE COUNT; ERYTHROCYTE MEMBRANE; ERYTHROCYTES; HEMOGLOBINS; LIPID PEROXIDATION; MALE; RANDOM ALLOCATION; RATS; TIME FACTORS; TRYPANOSOMA; TRYPANOSOMIASIS;

ANIMALIA; RATTUS; RATTUS NORVEGICUS; TRYPANOSOMA EVANSI;

EID: 70349482028     PISSN: 03044017     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.vetpar.2009.06.032     Document Type: Article

References (35)

1. Aguirre F., Martin I., Grinspon D., Ruiz M., Hager A., De T., Paoli J., Ihlo J., Farach H.A., and Poole C.P. Oxidative damage, plasma antioxidant capacity and glycemic control in elderly NIDDM patients. Free Radic. Biol. Med. 24 (1998) 580-585
2. Al-Mohammed H.I. Parasitological and immunological response of experimental infection with Trypanosoma evansi in rats. J. Egypt Soc. Parasitol. 36 (2006) 363-371
3. Aquino L.P.C.T., Machado R.Z., Alessi A.C., Marques L.C., Castro M.B., and Malheiros E.B. Clinical, parasitological and immunological aspects of experimental infection with Trypanosoma evansi in dogs. Mem. Inst. Oswaldo Cruz 94 (1999) 255-260
4. Assoku R.K.G. Immunological studies of the mechanism of anaemia in experimental Trypanosoma evansi infection in rats. Int. J. Parasitol. 5 (1975) 137-145
5. Audu P.A., Esievo K.A., Mohamed G., and Ajanusi O.J. Studies of infectivity and pathogenicity of an isolate of Trypanosoma evansi in Yankasa sheep. Vet. Parasitol. 86 (1999) 185-190
6. Chaudhuri S., Varshney J.P., and Patra R.C. Erythrocytic antioxidant defense, lipid peroxides level and blood iron, zinc and copper concentrations in dogs naturally infected with Babesia gibsoni. Res. Vet. Sci. 85 (2008) 120-124
7. Cohen G., and Hochstein P. Generation of hydrogen peroxide in erythrocytes by hemolytic agents. Biochemistry 3 (1964) 895-900
8. Colpo C.B., Monteiro S.G., Stainki D.R., Colpo E.T.B., and Henriques G.B. Infecção natural por Trypanosoma evansi em cães. Cienc. Rural. 35 (2005) 717-719
9. Da Silva, A.S., Wolkmer, P., Gressler, T.L., Otto, M.A., Bess, F., Tavares, S.K.C., Zanette, R.A., Monteiro, S.M., in press. Patogenicidade de um isolado de Trypanosoma evansi em ratos inoculados com o parasite em sangue in natura e criopreservado. Cienc. Rural.
10. Duthie G.G., Arthur J.R., Brewer P., Kikuchi Y., and Nicol F. Increased peroxidation of erythrocytes of stress-susceptible pigs. An improved diagnostic test for porcine stress syndrome. Am. J. Vet. Res. 50 (1989) 84-87
11. Esterbauer H. Cytotoxicity and genotoxicity of lipid-oxidation products. Am. J. Clin. Nutr. 57 (1993) 779-785
12. Grosskinsky C.M., Ezekowitz R.A.B., Berton G., Gordon S., and Askonsas B.A. Mactrophage activation in murine African trypanosomiasis. Infect. Immun. 39 (1983) 1080-1086
13. Halliwell B., and Chirico S. Lipid peroxidation: its mechanism, measurement, and significance. Am. J. Clin. Nutr. 57 Suppl. (1993) 715S-725S
14. Harvey J.W. The erythrocyte: physiology, metabolism and biochemical disorders. In: Kaneko J.J., Harvey J.W., and Bruss M.L. (Eds). Clinical Biochemistry of Domestic Animals. 5th ed. (1997), Academic Press, London 157-203
15. Herrera H.M., Alessi A.C., Marques L.C., Santana A.E., Aquino L.P.C.T., Menezes R.F., Moraes M.A.V., and Machado R.Z. Experimental Trypanosoma evansi infection in South American coati (Nasua nasua): hematological, in blood biochemical and histopathological changes. Acta Trop. 81 (2002) 203-210
16. Igbokwe I.O., Esievo K.A., Saror D.I., and Obagaiye O.K. Increased susceptibility of erythrocytes to in vitro peroxidation in acute Trypanosoma brucei infection of mice. Vet. Parasitol. 55 (1994) 279-286
17. Igbokwe I.O., Umar I.A., Omage J.J., Ibrahim N.D., Kadima K.B., Obagaiye O.K., Saror D.I., and Esievo K.A. Effect of acute Trypanosoma vivax infection on cattle erythrocyte glutathione and susceptibility to in vitro peroxidation. Vet. Parasitol. 63 (1996) 215-224
18. Janero D.R. Malondialdehyde and thiobarbituric acid reactivity as diagnostic indices of lipid peroxidation and peroxidative tissue injury. Free Radic. Biol. Med. 9 (1990) 515-540
19. Jatkar P.R., and Purohit M.S. Pathogenesis of anaemia in T. evansi infection. I. Haematology. Indian Vet. J. 48 (1971) 239-244
20. Joshi P.P., Shegokar V.R., Powar R.M., Herder S., Katti R., Salkar H.R., Dani V.S., Bhargava A., Jannin J., and Truc P. Human trypanosomiasis caused by Trypanosoma evansi in India: the first case report. Am. J. Trop. Med. Hyg. 73 (2005) 491-549
21. Lun Z.R., and Desser S.S. Is the broad range of hosts and geographical distribution of Trypanosoma evansi attributable to the loss of maxicircle kinetoplast DNA?. Parasitol. Today 11 (1995) 131-133
22. May J.M., Qu Z.C., and Mendiratta S. Protection and recycling of alfa-tocopherol in human erythrocytes by intracellular ascorbic acid. Arch. Biochem. Biophys. 349 (1998) 281-289
23. Menezes V.T., Queiroz A.O., Gomes M.A., Marques M.A., and Jansen A.M. Trypanosoma evansi in inbred and Swiss-Webster mice: distinct aspects of pathogenesis. Parasitol. Res. 94 (2004) 193-200
24. Morita T., Saeki H., Imai S., and Ishii T. Erythrocyte oxidation inartificial Babesia gibsoni infection. Vet. Parasitol. 63 (1996) 1-7
25. Murray H.W. Cellular resistance to protozoan infection. Ann. Rev. Med. 37 (1986) 61-69
26. Ogbadoyi E.O., Ukoha A.I., and Kyewalabe E.K. Anemia in experimental African trypanosomiasis. J. Protozoo. Res. 9 (1999) 55-63
27. Omer O.H., Mousa H.M., and Al-Wabel N. Study on the antioxidant status of rats experimentally infected with Trypanosoma evansi. Vet. Parasitol. 145 (2007) 142-145
28. Queiroz A.O., Cabello P.H., and Jansen A.M. Biological and biochemical characterization of isolates of Trypanosoma evansi from Pantanal of Matogrosso - Brazil. Vet. Parasitol. 92 (2000) 107-118
29. Saleh M.A. Erythrocytic oxidative damage in crossbred cattle naturally infected with Babesia bigemina. Res. Vet. Sci. 86 (2009) 43-48
30. Schalm O.W., Jain N.C., and Carrol E.J. Veterinary Hematology. 3rd ed. (1975) 807 pp.
31. Shehu S.A., Ibrahim N.D.G., Esievo K.A.N., and Mohammed G. Neuraminidase (Sialidase) activity and its role in development of anaemia in Trypanosoma evansi infection. J. Appl. Sci. 6 (2006) 2779-2783
32. Schuster J.P., Mehlhorn H., and Raether W. Ultrastructural changes on various Trypanosoma spp. after a 30-year storage period in liquid nitrogen. Parasitol. Res. 82 (1996) 720-726
33. Taiwo V.O., Olaniyi M.O., and Ogunsanmi A.O. Comparative plasma biochemical changes and susceptibility of erythrocytes to in vitro peroxidation during experimental Trypanosome congolense and T. brucei infections in sheep. J. Isreal Vet. Med. Assoc. 58 (2003) 435-443
34. Wolkmer P., SilvaI A.S., Cargnelutti J.F., Costa M.M., Traesel C.K.T., Lopes S.T.A., and Monteiro S.G.M. Resposta eritropoética de ratos em diferentes graus de parasitemia por Trypanosoma evansi. Cienc. Rural. 37 (2007) 1682-1687
35. Yoshioka T., Kawada K., Shimada T., and Mori M. Lipid peroxidation in maternal and cord blood and protective mechanism against activated-oxygen toxicity in the blood. Am. J. Obstet. Gynecol. 135 (1979) 372-376