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Gene therapy by electroporation for the treatment of chronic renal failure in companion animals
BACKGROUND: Growth hormone-releasing hormone (GHRH) plasmid-based therapy for the treatment of chronic renal failure and its complications was examined. Companion dogs (13.1 ± 0.8 years, 29.4 ± 5.01 kg) and cats (13.2 ± 0.9 years, 8.5 ± 0.37 kg) received a single 0.4 mg or 0.1 mg species-specific pl...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2663557/ https://www.ncbi.nlm.nih.gov/pubmed/19149896 http://dx.doi.org/10.1186/1472-6750-9-4 |
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author | Brown, Patricia A Bodles-Brakhop, Angela M Pope, Melissa A Draghia-Akli, Ruxandra |
author_facet | Brown, Patricia A Bodles-Brakhop, Angela M Pope, Melissa A Draghia-Akli, Ruxandra |
author_sort | Brown, Patricia A |
collection | PubMed |
description | BACKGROUND: Growth hormone-releasing hormone (GHRH) plasmid-based therapy for the treatment of chronic renal failure and its complications was examined. Companion dogs (13.1 ± 0.8 years, 29.4 ± 5.01 kg) and cats (13.2 ± 0.9 years, 8.5 ± 0.37 kg) received a single 0.4 mg or 0.1 mg species-specific plasmid injection, respectively, intramuscularly followed by electroporation, and analyzed up to 75 days post-treatment; controls underwent electroporation without plasmid administration. RESULTS: Plasmid-treated animals showed an increase in body weight (dogs 22.5% and cats 3.2%) compared to control animals, and displayed improved quality of life parameters including significant increases in appetite, activity, mentation and exercise tolerance levels. Insulin-like growth factor I (IGF-I, the downstream effector of GHRH) levels were increased in the plasmid treated animals. Hematological parameters were also significantly improved. Protein metabolism changes were observed suggesting a shift from a catabolic to an anabolic state in the treated animals. Blood urea nitrogen and creatinine did not show any significant changes suggesting maintenance of kidney function whereas the control animal's renal function deteriorated. Treated animals survived longer than control animals with 70% of dogs and 80% of cats surviving until study day 75. Only 17% and 40% of the control dogs and cats, respectively, survived to day 75. CONCLUSION: Improved quality of life, survival and general well-being indicate that further investigation is warranted, and show the potential of a plasmid-based therapy by electroporation in preventing and managing complications of renal insufficiency. |
format | Text |
id | pubmed-2663557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26635572009-04-01 Gene therapy by electroporation for the treatment of chronic renal failure in companion animals Brown, Patricia A Bodles-Brakhop, Angela M Pope, Melissa A Draghia-Akli, Ruxandra BMC Biotechnol Research Article BACKGROUND: Growth hormone-releasing hormone (GHRH) plasmid-based therapy for the treatment of chronic renal failure and its complications was examined. Companion dogs (13.1 ± 0.8 years, 29.4 ± 5.01 kg) and cats (13.2 ± 0.9 years, 8.5 ± 0.37 kg) received a single 0.4 mg or 0.1 mg species-specific plasmid injection, respectively, intramuscularly followed by electroporation, and analyzed up to 75 days post-treatment; controls underwent electroporation without plasmid administration. RESULTS: Plasmid-treated animals showed an increase in body weight (dogs 22.5% and cats 3.2%) compared to control animals, and displayed improved quality of life parameters including significant increases in appetite, activity, mentation and exercise tolerance levels. Insulin-like growth factor I (IGF-I, the downstream effector of GHRH) levels were increased in the plasmid treated animals. Hematological parameters were also significantly improved. Protein metabolism changes were observed suggesting a shift from a catabolic to an anabolic state in the treated animals. Blood urea nitrogen and creatinine did not show any significant changes suggesting maintenance of kidney function whereas the control animal's renal function deteriorated. Treated animals survived longer than control animals with 70% of dogs and 80% of cats surviving until study day 75. Only 17% and 40% of the control dogs and cats, respectively, survived to day 75. CONCLUSION: Improved quality of life, survival and general well-being indicate that further investigation is warranted, and show the potential of a plasmid-based therapy by electroporation in preventing and managing complications of renal insufficiency. BioMed Central 2009-01-16 /pmc/articles/PMC2663557/ /pubmed/19149896 http://dx.doi.org/10.1186/1472-6750-9-4 Text en Copyright © 2009 Brown et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Brown, Patricia A Bodles-Brakhop, Angela M Pope, Melissa A Draghia-Akli, Ruxandra Gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
title | Gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
title_full | Gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
title_fullStr | Gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
title_full_unstemmed | Gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
title_short | Gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
title_sort | gene therapy by electroporation for the treatment of chronic renal failure in companion animals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2663557/ https://www.ncbi.nlm.nih.gov/pubmed/19149896 http://dx.doi.org/10.1186/1472-6750-9-4 |
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