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Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content
BACKGROUND: The TSH stimulation test to confirm canine hypothyroidism is commonly performed using a recombinant human TSH (rhTSH), as up to date, canine TSH is not yet commercially available. Limiting factors for the use of rhTSH are its high costs and occasional difficulties in product availability...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717043/ https://www.ncbi.nlm.nih.gov/pubmed/23870652 http://dx.doi.org/10.1186/1746-6148-9-141 |
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author | Schaefer, Sandra Hassa, Paul O Sieber-Ruckstuhl, Nadja S Piechotta, Marion Reusch, Claudia E Roschitzki, Bernd Boretti, Felicitas S |
author_facet | Schaefer, Sandra Hassa, Paul O Sieber-Ruckstuhl, Nadja S Piechotta, Marion Reusch, Claudia E Roschitzki, Bernd Boretti, Felicitas S |
author_sort | Schaefer, Sandra |
collection | PubMed |
description | BACKGROUND: The TSH stimulation test to confirm canine hypothyroidism is commonly performed using a recombinant human TSH (rhTSH), as up to date, canine TSH is not yet commercially available. Limiting factors for the use of rhTSH are its high costs and occasional difficulties in product availability. Less expensive bovine TSH preparations (bTSH) purified from bovine pituitary glands are readily commercially available. The aim of this study was to evaluate two different bTSH products as alternative to rhTSH using mass spectrometry. RESULTS: More than 50 proteins, including other pituitary hormones, bovine albumin, hemoglobin, and tissue proteins were identified in the bTSH preparations. In contrast, rhTSH proved to be a highly pure product. Significantly higher endotoxin levels could be detected in all bTSH products compared to the rhTSH. CONCLUSIONS: Both bTSH products are crude mixtures and therefore not an acceptable alternative to rhTSH. Their use should be discouraged to prevent unintended side effects. |
format | Online Article Text |
id | pubmed-3717043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37170432013-07-21 Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content Schaefer, Sandra Hassa, Paul O Sieber-Ruckstuhl, Nadja S Piechotta, Marion Reusch, Claudia E Roschitzki, Bernd Boretti, Felicitas S BMC Vet Res Research Article BACKGROUND: The TSH stimulation test to confirm canine hypothyroidism is commonly performed using a recombinant human TSH (rhTSH), as up to date, canine TSH is not yet commercially available. Limiting factors for the use of rhTSH are its high costs and occasional difficulties in product availability. Less expensive bovine TSH preparations (bTSH) purified from bovine pituitary glands are readily commercially available. The aim of this study was to evaluate two different bTSH products as alternative to rhTSH using mass spectrometry. RESULTS: More than 50 proteins, including other pituitary hormones, bovine albumin, hemoglobin, and tissue proteins were identified in the bTSH preparations. In contrast, rhTSH proved to be a highly pure product. Significantly higher endotoxin levels could be detected in all bTSH products compared to the rhTSH. CONCLUSIONS: Both bTSH products are crude mixtures and therefore not an acceptable alternative to rhTSH. Their use should be discouraged to prevent unintended side effects. BioMed Central 2013-07-16 /pmc/articles/PMC3717043/ /pubmed/23870652 http://dx.doi.org/10.1186/1746-6148-9-141 Text en Copyright © 2013 Schaefer 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 Schaefer, Sandra Hassa, Paul O Sieber-Ruckstuhl, Nadja S Piechotta, Marion Reusch, Claudia E Roschitzki, Bernd Boretti, Felicitas S Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
title | Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
title_full | Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
title_fullStr | Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
title_full_unstemmed | Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
title_short | Characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
title_sort | characterization of recombinant human and bovine thyroid-stimulating hormone preparations by mass spectrometry and determination of their endotoxin content |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717043/ https://www.ncbi.nlm.nih.gov/pubmed/23870652 http://dx.doi.org/10.1186/1746-6148-9-141 |
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