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Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis

Year 2015, Volume: 10 Issue: 1, 0 - , 09.04.2015
https://doi.org/10.17094/avbd.44294

Abstract

This study was aimed at evaluating the effects of Leishmania infection and AMB (amphotericin-B) treatment on hematological, biochemical and oxidative stress parameters in three Staffordshire Bull Terrier dogs with visceral leishmaniasis (VL). These dogs were presented with weight loss, weakness, and cutaneous lesions. Canine kala-azar detect kit was positive in dogs with VL. AMB was administered to cases with VL at a dose of 0.6 to 1.5 mg/kg/week for four months. Leishmania agents caused the liver injury in cases 1 and 2 due to increase in ALT level, decrease in erythrocyte, hemoglobin, and hematocrit level and increase in MDA, and decrease in GSH-Px in case 3 and did not affect the kidney functions due to normal urea and creatinine level in the dogs with VL. A gradual response to the administration of AMB was observed. At the end of treatment course, cases with VL were cured clinically. It was concluded that 4-month of AMB administration may be effective to treat VL due to no clinical recurrence for six months follow-up.

References

  • Abranches P., Silva-Pereira MC., Conceição-Silva FM., Santos-Gomes GM., Janz JG., 1991. Canine leishmaniasis: pathological and ecological factors influencing transmission of infection. Journal of Parasitology, 77, 557-561.
  • Aktas MS., Ozkanlar S., Karakoc A., Akcay F., Ozkanlar Y., 2011. Efficacy of vitamin E + selenium and Vitamin A + D + E combinations on oxidative stress induced by long-term transportation in Holstein dairy cows. Livestock Science, 141, 76-79.
  • Amusategui I., Sainz A., Rodriguez F., Tesouro MA., 2003. Distribution and relationships between clinical and biopathological parameters in canine leishmaniasis. European Journal of Epidemiology, 18, 147-156.
  • Bagchi M., Mukherjee S., Basu MK., 1993. Lipid peroxidation in hepatic microsomal membranes isolated from mice in health and in experimental leishmaniasis. Indian Journal of Biochemistry & Biophysics, 30, 277-281.
  • Baneth G., Shaw SE., 2002. Chemotherapy of canine leishmaniosis. Veterinary Parasitology, 106, 315-324.
  • Bildik A., Kargin F., Seyrek K., Pasa S., Ozensoy S., 2004. Oxidative stress and non-enzymatic antioxidative status in dogs with visceral Leishmaniasis. Research in Veterinary Science, 77, 63-66.
  • Biswas T., Pal JK., Naskar K., Ghosh DK., Ghosal J., 1995. Lipid peroxidation of erythrocytes during anemia of the hamsters infected with Leishmania donovani. Molecular and Cellular Biochemistry, 146, 99-105.
  • -
  • Croft SL., Coombs GH., 2003. Leishmaniasis-current chemotherapy and recent advances in the search for novel drugs. Trends in Parasitology, 19, 502-508.
  • Freeman K., 2010. Update on the diagnosis and management of Leishmania spp infections in dogs in the United States. Topic in Companion Animal Medicine, 25, 149-154.
  • Freitas JC., Nunes-Pinheiro DCS., Neto BEL., Santos GJLS., Amaral de Abreu CR., Braga RR., Campos RM., Fernandes de Oliveira L., 2012. Clinical and laboratory alterations in dogs naturally infected by Leishmania chagasi. Revista da Sociedade Brasileira de Medicina Tropical, 45, 24-29.
  • Halliwell B., 1991. Reactive oxygen species in living systems: source, biochemistry, and role in human disease. The American Journal of Medicine, 91, 14-22.
  • Heidarpour M., Soltani S., Mohri M., Khoshnegah J., 2012. Canine visceral leishmaniasis: relationships between oxidative stress, liver and kidney variables, trace elements, and clinical status. Parasitology Research, 111, 1491-1496.
  • Jain SK., 1989. Hyperglicemia can cause membrane lipid peroxidation and osmotic fragility in human red blood cells. The Journal of Biological Chemistry, 264, 21340-21345.
  • Lamothe J., 2001. Activity of amphotericin B in lipid emulsion in the initial treatment of canine leishmaniasis. Journal of Small Animal Practice, 42, 170-175.
  • Neupane DP., Majhi S., Chandra L., Rijal S., Baral N., 2008. Erythrocyte glutathione status in human visceral leishmaniasis. Indian Journal of Clinical Biochemistry, 23, 95-97.
  • Oliveira FJ., Cecchini R., 2000. Oxidative stress of liver in hamsters infected with Leishmania (L.) chagasi. Journal of Parasitology, 86, 1067-1072.
  • Petersen CA., 2009. Leishmaniasis, an emerging disease found in companion animals in the United States. Topics in Companion Animal Medicine, 24, 182-188.
  • Pleban PA., Munyani A., Beachum J., 1982. Determination of selenium concentration and glutathione peroxidase activity in plasma and erythrocytes. Clinical Chemistry, 28, 311-316.
  • Rathore A., Jain A., Gulbake A., Shilpi S., Khare P., Jain A., Jain SK., 2011. Mannosylated liposomes bearing amphotericin B for effective management of visceral leishmaniasis. Journal of Liposome Research, 21, 333-340.
  • Reis AB., Martins-Filho OA., Teixeira-Carvalho A., Carvalho MG., Mayrink W., França-Silva JC., Giunchetti RC., Genaro O., Correa-Oliveira R., 2006. Parasite density and impaired biochemical/hematological status are associated with severe clinical aspects of canine visceral leishmaniasis. Research in Veterinary Science, 81, 68-75.
  • Sen G., Mukhopadhyay R., Ghosal J., Biswas T., 2001. Oxidative damage of erythrocytes: a possible mechanism for premature hemolysis in experimental visceral leishmaniasis in hamsters. Annals of Hematology, 80, 32-37.
  • Toz SO., Culha G., Zeyrek FY., Ertabaklar H., Alkan MZ., Vardarlı AT., Gunduz C., Ozbel Y., 2013. A real-time ITS1-PCR based method in the diagnosis and species identification of leishmania parasite from human and dog clinical samples in Turkey. PLoS Neglected Tropical Diseases, 7, e2205.
  • Wasan KM., Wasan EL., Gershkovich P., Zhu X., Tidwell RR., Werbovetz KA., Clement JG., Thornton SJ., 2009. Highly effective oral amphotericin B formulation against murine visceral leishmaniasis. The Journal of Infectious Diseases, 200, 357-360.

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Year 2015, Volume: 10 Issue: 1, 0 - , 09.04.2015
https://doi.org/10.17094/avbd.44294

Abstract

 Bu   çalışmada   visseral   Leishmaniasis’li   (VL)   üç   Staffordshire   Bull   Terrier   köpekte   Leishmania   enfeksiyonu   ve   AMB  (amfoterisin-­‐B)   tedavisinin   hematolojik,   biyokimyasal   ve   oksidatif   stres   parametreleri   üzerine   etkilerini   değerlendirmek  amaçlandı.   Bu   köpekler   kilo   kaybı,   halsizlik   ve   deri   lezyonları   ile   kliniğe   getirildi.   Kanin   kala-­‐azar   test   kiti   VL’li   köpeklerde  pozitifti.  Visseral  Leishmaniasis’li  olgulara  AMB  0.6-­‐1.5  mg/kg/hafta  dozunda  4  ay  süre  ile  uygulandı.  Leishmania  etkenleri  olgu  1  ve  2’de  ALT  düzeyinde  artışa  bağlı  olarak  karaciğer  hasarına,  olgu  3’te  eritrosit,  hemoglobin  ve  hematokrit  düzeyde  azalmaya  ve  MDA’da  artışa  ve  GSH-­‐Px’de  azalmaya  neden  oldu  fakat  VL’li  köpeklerde  normal  üre  ve  kreatinin  düzeyine  bağlı  olarak   böbrek   fonksiyonlarını   etkilemedi.   AMB   tedavisine   kademeli   yanıt   gözlendi.   Tedavi   seyrinin   sonunda   VL’li   olgular  klinik   olarak   iyileşti.   Sonuç   olarak   6   ay   süre   ile   takipte   klinik   nüks   olmamasına   bağlı   olarak   visseral   Leishmaniasis’i   tedavi  etmek  için  4  ay  süreli  AMB  uygulamasının  etkili  olabileceği  kanısına  varıldı.  

References

  • Abranches P., Silva-Pereira MC., Conceição-Silva FM., Santos-Gomes GM., Janz JG., 1991. Canine leishmaniasis: pathological and ecological factors influencing transmission of infection. Journal of Parasitology, 77, 557-561.
  • Aktas MS., Ozkanlar S., Karakoc A., Akcay F., Ozkanlar Y., 2011. Efficacy of vitamin E + selenium and Vitamin A + D + E combinations on oxidative stress induced by long-term transportation in Holstein dairy cows. Livestock Science, 141, 76-79.
  • Amusategui I., Sainz A., Rodriguez F., Tesouro MA., 2003. Distribution and relationships between clinical and biopathological parameters in canine leishmaniasis. European Journal of Epidemiology, 18, 147-156.
  • Bagchi M., Mukherjee S., Basu MK., 1993. Lipid peroxidation in hepatic microsomal membranes isolated from mice in health and in experimental leishmaniasis. Indian Journal of Biochemistry & Biophysics, 30, 277-281.
  • Baneth G., Shaw SE., 2002. Chemotherapy of canine leishmaniosis. Veterinary Parasitology, 106, 315-324.
  • Bildik A., Kargin F., Seyrek K., Pasa S., Ozensoy S., 2004. Oxidative stress and non-enzymatic antioxidative status in dogs with visceral Leishmaniasis. Research in Veterinary Science, 77, 63-66.
  • Biswas T., Pal JK., Naskar K., Ghosh DK., Ghosal J., 1995. Lipid peroxidation of erythrocytes during anemia of the hamsters infected with Leishmania donovani. Molecular and Cellular Biochemistry, 146, 99-105.
  • -
  • Croft SL., Coombs GH., 2003. Leishmaniasis-current chemotherapy and recent advances in the search for novel drugs. Trends in Parasitology, 19, 502-508.
  • Freeman K., 2010. Update on the diagnosis and management of Leishmania spp infections in dogs in the United States. Topic in Companion Animal Medicine, 25, 149-154.
  • Freitas JC., Nunes-Pinheiro DCS., Neto BEL., Santos GJLS., Amaral de Abreu CR., Braga RR., Campos RM., Fernandes de Oliveira L., 2012. Clinical and laboratory alterations in dogs naturally infected by Leishmania chagasi. Revista da Sociedade Brasileira de Medicina Tropical, 45, 24-29.
  • Halliwell B., 1991. Reactive oxygen species in living systems: source, biochemistry, and role in human disease. The American Journal of Medicine, 91, 14-22.
  • Heidarpour M., Soltani S., Mohri M., Khoshnegah J., 2012. Canine visceral leishmaniasis: relationships between oxidative stress, liver and kidney variables, trace elements, and clinical status. Parasitology Research, 111, 1491-1496.
  • Jain SK., 1989. Hyperglicemia can cause membrane lipid peroxidation and osmotic fragility in human red blood cells. The Journal of Biological Chemistry, 264, 21340-21345.
  • Lamothe J., 2001. Activity of amphotericin B in lipid emulsion in the initial treatment of canine leishmaniasis. Journal of Small Animal Practice, 42, 170-175.
  • Neupane DP., Majhi S., Chandra L., Rijal S., Baral N., 2008. Erythrocyte glutathione status in human visceral leishmaniasis. Indian Journal of Clinical Biochemistry, 23, 95-97.
  • Oliveira FJ., Cecchini R., 2000. Oxidative stress of liver in hamsters infected with Leishmania (L.) chagasi. Journal of Parasitology, 86, 1067-1072.
  • Petersen CA., 2009. Leishmaniasis, an emerging disease found in companion animals in the United States. Topics in Companion Animal Medicine, 24, 182-188.
  • Pleban PA., Munyani A., Beachum J., 1982. Determination of selenium concentration and glutathione peroxidase activity in plasma and erythrocytes. Clinical Chemistry, 28, 311-316.
  • Rathore A., Jain A., Gulbake A., Shilpi S., Khare P., Jain A., Jain SK., 2011. Mannosylated liposomes bearing amphotericin B for effective management of visceral leishmaniasis. Journal of Liposome Research, 21, 333-340.
  • Reis AB., Martins-Filho OA., Teixeira-Carvalho A., Carvalho MG., Mayrink W., França-Silva JC., Giunchetti RC., Genaro O., Correa-Oliveira R., 2006. Parasite density and impaired biochemical/hematological status are associated with severe clinical aspects of canine visceral leishmaniasis. Research in Veterinary Science, 81, 68-75.
  • Sen G., Mukhopadhyay R., Ghosal J., Biswas T., 2001. Oxidative damage of erythrocytes: a possible mechanism for premature hemolysis in experimental visceral leishmaniasis in hamsters. Annals of Hematology, 80, 32-37.
  • Toz SO., Culha G., Zeyrek FY., Ertabaklar H., Alkan MZ., Vardarlı AT., Gunduz C., Ozbel Y., 2013. A real-time ITS1-PCR based method in the diagnosis and species identification of leishmania parasite from human and dog clinical samples in Turkey. PLoS Neglected Tropical Diseases, 7, e2205.
  • Wasan KM., Wasan EL., Gershkovich P., Zhu X., Tidwell RR., Werbovetz KA., Clement JG., Thornton SJ., 2009. Highly effective oral amphotericin B formulation against murine visceral leishmaniasis. The Journal of Infectious Diseases, 200, 357-360.
There are 24 citations in total.

Details

Primary Language English
Journal Section Olgu Sunumu
Authors

Basak Hanedan

Mehmet Borku

Yunusemre Ozkanlar This is me

Ali Haydardedeoglu

Serkal Gazyagcı This is me

Ahmet Aydın

Seckin Ozkanlar This is me

Publication Date April 9, 2015
Published in Issue Year 2015 Volume: 10 Issue: 1

Cite

APA Hanedan, B., Borku, M., Ozkanlar, Y., Haydardedeoglu, A., et al. (2015). Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis. Atatürk Üniversitesi Veteriner Bilimleri Dergisi, 10(1). https://doi.org/10.17094/avbd.44294
AMA Hanedan B, Borku M, Ozkanlar Y, Haydardedeoglu A, Gazyagcı S, Aydın A, Ozkanlar S. Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis. Atatürk Üniversitesi Veteriner Bilimleri Dergisi. April 2015;10(1). doi:10.17094/avbd.44294
Chicago Hanedan, Basak, Mehmet Borku, Yunusemre Ozkanlar, Ali Haydardedeoglu, Serkal Gazyagcı, Ahmet Aydın, and Seckin Ozkanlar. “Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in Three Staffordshire Bull Terrier Dogs With Visceral Leishmaniasis”. Atatürk Üniversitesi Veteriner Bilimleri Dergisi 10, no. 1 (April 2015). https://doi.org/10.17094/avbd.44294.
EndNote Hanedan B, Borku M, Ozkanlar Y, Haydardedeoglu A, Gazyagcı S, Aydın A, Ozkanlar S (April 1, 2015) Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis. Atatürk Üniversitesi Veteriner Bilimleri Dergisi 10 1
IEEE B. Hanedan, M. Borku, Y. Ozkanlar, A. Haydardedeoglu, S. Gazyagcı, A. Aydın, and S. Ozkanlar, “Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis”, Atatürk Üniversitesi Veteriner Bilimleri Dergisi, vol. 10, no. 1, 2015, doi: 10.17094/avbd.44294.
ISNAD Hanedan, Basak et al. “Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in Three Staffordshire Bull Terrier Dogs With Visceral Leishmaniasis”. Atatürk Üniversitesi Veteriner Bilimleri Dergisi 10/1 (April 2015). https://doi.org/10.17094/avbd.44294.
JAMA Hanedan B, Borku M, Ozkanlar Y, Haydardedeoglu A, Gazyagcı S, Aydın A, Ozkanlar S. Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis. Atatürk Üniversitesi Veteriner Bilimleri Dergisi. 2015;10. doi:10.17094/avbd.44294.
MLA Hanedan, Basak et al. “Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in Three Staffordshire Bull Terrier Dogs With Visceral Leishmaniasis”. Atatürk Üniversitesi Veteriner Bilimleri Dergisi, vol. 10, no. 1, 2015, doi:10.17094/avbd.44294.
Vancouver Hanedan B, Borku M, Ozkanlar Y, Haydardedeoglu A, Gazyagcı S, Aydın A, Ozkanlar S. Efficacy of Amphotericin-B, Clinicopathologic Variables and Oxidative Stress Markers in three Staffordshire Bull Terrier Dogs with Visceral Leishmaniasis. Atatürk Üniversitesi Veteriner Bilimleri Dergisi. 2015;10(1).