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Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats

Recombinant human granulocyte-macrophage colony stimulating factor (hGM-CSF) is a glycoprotein and hematopoietic growth factors that regulates the proliferation of myeloid precursor cells and activates mature granulocytes and macrophages. In a previous study, we reported that hGM-CSF could be produc...

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Autores principales: Ji, Jung Eun, Lee, Jung Min, Choi, Jong Min, Choi, Young Hwa, Kim, Eun Kyung, Chu, So Jung, Kim, Seok Kyun, Ahn, Kyong Hoon, Lee, Dong Hoon, Kim, Ha Hyung, Han, Kyuboem, Kim, Dae Kyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006265/
https://www.ncbi.nlm.nih.gov/pubmed/32038810
http://dx.doi.org/10.5487/TR.2008.24.4.315
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author Ji, Jung Eun
Lee, Jung Min
Choi, Jong Min
Choi, Young Hwa
Kim, Eun Kyung
Chu, So Jung
Kim, Seok Kyun
Ahn, Kyong Hoon
Lee, Dong Hoon
Kim, Ha Hyung
Han, Kyuboem
Kim, Dae Kyong
author_facet Ji, Jung Eun
Lee, Jung Min
Choi, Jong Min
Choi, Young Hwa
Kim, Eun Kyung
Chu, So Jung
Kim, Seok Kyun
Ahn, Kyong Hoon
Lee, Dong Hoon
Kim, Ha Hyung
Han, Kyuboem
Kim, Dae Kyong
author_sort Ji, Jung Eun
collection PubMed
description Recombinant human granulocyte-macrophage colony stimulating factor (hGM-CSF) is a glycoprotein and hematopoietic growth factors that regulates the proliferation of myeloid precursor cells and activates mature granulocytes and macrophages. In a previous study, we reported that hGM-CSF could be produced in transgenic rice cell suspension culture, termed rhGM-CSF. In the present study, we examined the repeated dose toxicity of rhGM-CSF in SD rats. The repeated dose toxicity study was performed at each dose of 50 and 200 µg/kg subcutaneous administration of rhGM-CSF everyday for 28-days period. The results did not show any changes in food and water intake. There were also no significant changes in both body and organ weights between the control and the tested groups. The hematological and blood biochemical parameters were statistically not different in all groups. These results suggest that rhGM-CSF may show no repeated dose toxicity in SD rats under the conditions.
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spelling pubmed-70062652020-02-07 Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats Ji, Jung Eun Lee, Jung Min Choi, Jong Min Choi, Young Hwa Kim, Eun Kyung Chu, So Jung Kim, Seok Kyun Ahn, Kyong Hoon Lee, Dong Hoon Kim, Ha Hyung Han, Kyuboem Kim, Dae Kyong Toxicol Res Article Recombinant human granulocyte-macrophage colony stimulating factor (hGM-CSF) is a glycoprotein and hematopoietic growth factors that regulates the proliferation of myeloid precursor cells and activates mature granulocytes and macrophages. In a previous study, we reported that hGM-CSF could be produced in transgenic rice cell suspension culture, termed rhGM-CSF. In the present study, we examined the repeated dose toxicity of rhGM-CSF in SD rats. The repeated dose toxicity study was performed at each dose of 50 and 200 µg/kg subcutaneous administration of rhGM-CSF everyday for 28-days period. The results did not show any changes in food and water intake. There were also no significant changes in both body and organ weights between the control and the tested groups. The hematological and blood biochemical parameters were statistically not different in all groups. These results suggest that rhGM-CSF may show no repeated dose toxicity in SD rats under the conditions. Springer Singapore 2008-12-01 2008-12 /pmc/articles/PMC7006265/ /pubmed/32038810 http://dx.doi.org/10.5487/TR.2008.24.4.315 Text en © Korean Society of Toxicology 2008 This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ji, Jung Eun
Lee, Jung Min
Choi, Jong Min
Choi, Young Hwa
Kim, Eun Kyung
Chu, So Jung
Kim, Seok Kyun
Ahn, Kyong Hoon
Lee, Dong Hoon
Kim, Ha Hyung
Han, Kyuboem
Kim, Dae Kyong
Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats
title Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats
title_full Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats
title_fullStr Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats
title_full_unstemmed Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats
title_short Subcutaneous Four-Week Repeated Dose Toxicity Studies of Rice Cell-Derived Recombinant Human Granulocyte-Macrophage Colony Stimulating Factor in Rats
title_sort subcutaneous four-week repeated dose toxicity studies of rice cell-derived recombinant human granulocyte-macrophage colony stimulating factor in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006265/
https://www.ncbi.nlm.nih.gov/pubmed/32038810
http://dx.doi.org/10.5487/TR.2008.24.4.315
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