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Effect of Immunosuppressive Therapy on Proteinogram in Rats
BACKGROUND: It has been observed that the use of immunosuppressive drugs in patients after transplantation of vascularized organs may be associated with changes in the concentration of certain fractions of plasma proteins. The concentration of these proteins was correlated with an increased risk of...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913827/ https://www.ncbi.nlm.nih.gov/pubmed/27288069 http://dx.doi.org/10.12659/MSM.895856 |
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author | Kędzierska, Karolina Sindrewicz, Krzysztof Sporniak-Tutak, Katarzyna Bober, Joanna Stańczyk-Dunaj, Małgorzata Dołęgowska, Barbara Kaliszczak, Robert Sieńko, Jerzy Kabat-Koperska, Joanna Gołembiewska, Edyta Ciechanowski, Kazimierz |
author_facet | Kędzierska, Karolina Sindrewicz, Krzysztof Sporniak-Tutak, Katarzyna Bober, Joanna Stańczyk-Dunaj, Małgorzata Dołęgowska, Barbara Kaliszczak, Robert Sieńko, Jerzy Kabat-Koperska, Joanna Gołembiewska, Edyta Ciechanowski, Kazimierz |
author_sort | Kędzierska, Karolina |
collection | PubMed |
description | BACKGROUND: It has been observed that the use of immunosuppressive drugs in patients after transplantation of vascularized organs may be associated with changes in the concentration of certain fractions of plasma proteins. The concentration of these proteins was correlated with an increased risk of occurrence of stage 3 chronic kidney disease (CKD). This article examines the effect of the most commonly used immunosuppressive drugs on the concentration of plasma proteins in Wistar rats. MATERIAL/METHODS: The study involved 36 rats grouped according to the immunosuppressive regimen used (tacrolimus, mycophenolate mofetil, cyclosporine A, rapamycin, and prednisone). The rats in all study groups were treated with a 3-drug protocol for 6 months. The treatment dose was adjusted based on available data in the literature. No drugs were administered to the control group. The rats were sacrificed and blood samples collected to determine the concentration of plasma proteins using electrophoresis technique. RESULTS: Statistically significant differences were observed between protein concentrations within the studied groups. The differences related to the proteins with masses of 195 kDa, 170 kDa, 103 kDa, and 58 kDa. CONCLUSIONS: (1) Immunosuppressive drugs caused changes in the proteinogram of plasma proteins. (2) The strongest effect on rat plasma proteins was exerted by a regimen based on rapamycin. Intermediate, weak, and weakest effects were observed in regimens based on cyclosporine A, tacrolimus, and mycophenolate mofetil, respectively. |
format | Online Article Text |
id | pubmed-4913827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49138272016-06-28 Effect of Immunosuppressive Therapy on Proteinogram in Rats Kędzierska, Karolina Sindrewicz, Krzysztof Sporniak-Tutak, Katarzyna Bober, Joanna Stańczyk-Dunaj, Małgorzata Dołęgowska, Barbara Kaliszczak, Robert Sieńko, Jerzy Kabat-Koperska, Joanna Gołembiewska, Edyta Ciechanowski, Kazimierz Med Sci Monit Animal Study BACKGROUND: It has been observed that the use of immunosuppressive drugs in patients after transplantation of vascularized organs may be associated with changes in the concentration of certain fractions of plasma proteins. The concentration of these proteins was correlated with an increased risk of occurrence of stage 3 chronic kidney disease (CKD). This article examines the effect of the most commonly used immunosuppressive drugs on the concentration of plasma proteins in Wistar rats. MATERIAL/METHODS: The study involved 36 rats grouped according to the immunosuppressive regimen used (tacrolimus, mycophenolate mofetil, cyclosporine A, rapamycin, and prednisone). The rats in all study groups were treated with a 3-drug protocol for 6 months. The treatment dose was adjusted based on available data in the literature. No drugs were administered to the control group. The rats were sacrificed and blood samples collected to determine the concentration of plasma proteins using electrophoresis technique. RESULTS: Statistically significant differences were observed between protein concentrations within the studied groups. The differences related to the proteins with masses of 195 kDa, 170 kDa, 103 kDa, and 58 kDa. CONCLUSIONS: (1) Immunosuppressive drugs caused changes in the proteinogram of plasma proteins. (2) The strongest effect on rat plasma proteins was exerted by a regimen based on rapamycin. Intermediate, weak, and weakest effects were observed in regimens based on cyclosporine A, tacrolimus, and mycophenolate mofetil, respectively. International Scientific Literature, Inc. 2016-06-11 /pmc/articles/PMC4913827/ /pubmed/27288069 http://dx.doi.org/10.12659/MSM.895856 Text en © Med Sci Monit, 2016 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) |
spellingShingle | Animal Study Kędzierska, Karolina Sindrewicz, Krzysztof Sporniak-Tutak, Katarzyna Bober, Joanna Stańczyk-Dunaj, Małgorzata Dołęgowska, Barbara Kaliszczak, Robert Sieńko, Jerzy Kabat-Koperska, Joanna Gołembiewska, Edyta Ciechanowski, Kazimierz Effect of Immunosuppressive Therapy on Proteinogram in Rats |
title | Effect of Immunosuppressive Therapy on Proteinogram in Rats |
title_full | Effect of Immunosuppressive Therapy on Proteinogram in Rats |
title_fullStr | Effect of Immunosuppressive Therapy on Proteinogram in Rats |
title_full_unstemmed | Effect of Immunosuppressive Therapy on Proteinogram in Rats |
title_short | Effect of Immunosuppressive Therapy on Proteinogram in Rats |
title_sort | effect of immunosuppressive therapy on proteinogram in rats |
topic | Animal Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4913827/ https://www.ncbi.nlm.nih.gov/pubmed/27288069 http://dx.doi.org/10.12659/MSM.895856 |
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