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Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels
Recent findings showed the presence of a reciprocal relationship between thyroid hormones and ghrelin, although the exact mechanism is not known. Design: Our study is addressed to evaluate the effect of acute exogenous rhTSH administration on serum ghrelin levels in athyreotic patients on replacemen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356021/ https://www.ncbi.nlm.nih.gov/pubmed/22654834 http://dx.doi.org/10.3389/fendo.2011.00094 |
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author | Ciuoli, Cristina Brusco, Lucia Theodoropoulou, Alexandra Castagna, Maria Grazia Neri, Ornella Pasqui, Letizia Pacini, Furio |
author_facet | Ciuoli, Cristina Brusco, Lucia Theodoropoulou, Alexandra Castagna, Maria Grazia Neri, Ornella Pasqui, Letizia Pacini, Furio |
author_sort | Ciuoli, Cristina |
collection | PubMed |
description | Recent findings showed the presence of a reciprocal relationship between thyroid hormones and ghrelin, although the exact mechanism is not known. Design: Our study is addressed to evaluate the effect of acute exogenous rhTSH administration on serum ghrelin levels in athyreotic patients on replacement l-thyroxine therapy. The study group included 50 patients (16 males and 34 females) submitted to total thyroidectomy and 131-iodine remnant ablation for differentiated thyroid cancer on l-thyroxine therapy. Mean age was 47.5 ± 16.5 years and mean BMI was 25.6 ± 5.01 kg/m(2). rhTSH was administrated at the dosage of 0.9 mg i.m. once daily for two consecutive days. Blood samples were taken between 08.00 and 09.00 after a overnight fasting for measurement of TSH, FT3, FT4, and ghrelin before the first administration of rhTSH and for measurement of TSH and ghrelin 24, 48, 72, and 96 h after the first administration of rhTSH. Results: Mean ± SD values of basal TSH were 0.54 ± 0.77 μU/ml without significant difference between females and males. As expected, after rhTSH administration TSH concentrations increased at 24 and 48 h with peak TSH values ranging from 20.20 to 313 μU/ml (mean ± SD 98.4 ± 66.7 μU/ml). Mean ± SD values of basal ghrelin were 1085 ± 373 pg/ml without significant difference between males and females. After rhTSH administration ghrelin concentrations decreased significantly (p < 0.01) at 24 h (mean ± SD 934 ± 314 pg/ml p < 0.01) and returned to pre-treatment levels at 96 h. Conclusion: Our study demonstrates that acute exogenous TSH administration has a suppressive effect on ghrelin secretion independent from changes in thyroid status. |
format | Online Article Text |
id | pubmed-3356021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33560212012-05-31 Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels Ciuoli, Cristina Brusco, Lucia Theodoropoulou, Alexandra Castagna, Maria Grazia Neri, Ornella Pasqui, Letizia Pacini, Furio Front Endocrinol (Lausanne) Endocrinology Recent findings showed the presence of a reciprocal relationship between thyroid hormones and ghrelin, although the exact mechanism is not known. Design: Our study is addressed to evaluate the effect of acute exogenous rhTSH administration on serum ghrelin levels in athyreotic patients on replacement l-thyroxine therapy. The study group included 50 patients (16 males and 34 females) submitted to total thyroidectomy and 131-iodine remnant ablation for differentiated thyroid cancer on l-thyroxine therapy. Mean age was 47.5 ± 16.5 years and mean BMI was 25.6 ± 5.01 kg/m(2). rhTSH was administrated at the dosage of 0.9 mg i.m. once daily for two consecutive days. Blood samples were taken between 08.00 and 09.00 after a overnight fasting for measurement of TSH, FT3, FT4, and ghrelin before the first administration of rhTSH and for measurement of TSH and ghrelin 24, 48, 72, and 96 h after the first administration of rhTSH. Results: Mean ± SD values of basal TSH were 0.54 ± 0.77 μU/ml without significant difference between females and males. As expected, after rhTSH administration TSH concentrations increased at 24 and 48 h with peak TSH values ranging from 20.20 to 313 μU/ml (mean ± SD 98.4 ± 66.7 μU/ml). Mean ± SD values of basal ghrelin were 1085 ± 373 pg/ml without significant difference between males and females. After rhTSH administration ghrelin concentrations decreased significantly (p < 0.01) at 24 h (mean ± SD 934 ± 314 pg/ml p < 0.01) and returned to pre-treatment levels at 96 h. Conclusion: Our study demonstrates that acute exogenous TSH administration has a suppressive effect on ghrelin secretion independent from changes in thyroid status. Frontiers Research Foundation 2011-12-16 /pmc/articles/PMC3356021/ /pubmed/22654834 http://dx.doi.org/10.3389/fendo.2011.00094 Text en Copyright © 2011 Ciuoli, Brusco, Theodoropoulou, Castagna, Neri, Pasqui and Pacini. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Endocrinology Ciuoli, Cristina Brusco, Lucia Theodoropoulou, Alexandra Castagna, Maria Grazia Neri, Ornella Pasqui, Letizia Pacini, Furio Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels |
title | Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels |
title_full | Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels |
title_fullStr | Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels |
title_full_unstemmed | Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels |
title_short | Effects of Acute Recombinant Human TSH on Serum Ghrelin Levels |
title_sort | effects of acute recombinant human tsh on serum ghrelin levels |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3356021/ https://www.ncbi.nlm.nih.gov/pubmed/22654834 http://dx.doi.org/10.3389/fendo.2011.00094 |
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