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Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function

Although it has been well established that thyroid hormones increase β-adrenergic receptors of various tissues in the animal studies, there are controversies about the β-adrenergic receptor changes of human mononuclear cells and polymorphonuclear cells. The present study was performed to analyze the...

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Autores principales: Lee, Jong Do, You, Myung Hee, Kim, Young Seol, Kim, Jin Woo, Kim, Kwang Won, Kim, Sun Woo, Choi, Young Kil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1986
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534902/
https://www.ncbi.nlm.nih.gov/pubmed/15759381
http://dx.doi.org/10.3904/kjim.1986.1.1.78
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author Lee, Jong Do
You, Myung Hee
Kim, Young Seol
Kim, Jin Woo
Kim, Kwang Won
Kim, Sun Woo
Choi, Young Kil
author_facet Lee, Jong Do
You, Myung Hee
Kim, Young Seol
Kim, Jin Woo
Kim, Kwang Won
Kim, Sun Woo
Choi, Young Kil
author_sort Lee, Jong Do
collection PubMed
description Although it has been well established that thyroid hormones increase β-adrenergic receptors of various tissues in the animal studies, there are controversies about the β-adrenergic receptor changes of human mononuclear cells and polymorphonuclear cells. The present study was performed to analyze the change of β-adrenergic receptor of those cells according to the thyroid functional status and to evaluate their usefulness in assessment of sympathetic hyperactivity. We measured [(3)H]-dihydroalprenolol binding to circulating mononuclear and polymorphonuclear cells from 18 patients with hyperthyrodism, 7 with hypothyroidism, 8 with euthyroid goiter and 21 normal controls. Only with polymorphonuclear cells the receptor concentration was significantly higher (P<0.01) in hyperthyroidism (46.07±4.78 fmol/mg protein) than in the normal control (28.42±2.06 fmol/mg protein) and the affinity constants of both cells were comparable to normal control values. And serum concentrations of T(3) were not correlated well with the changes of receptor concentrations in hyperthyroidism. The patients with hypothyroidism and euthyroid goiter showed no significant difference in the receptor concentration and the affinity constants with both cell binding assays. These results indicate that thyroid hormones increase the receptor concentration in polymorphonuclear cells which might be responsible for the symptoms of sympathetic hyperactivity and the polymorphornuclear cells are useful for β-adrenergic receptor assay.
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spelling pubmed-45349022015-10-02 Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function Lee, Jong Do You, Myung Hee Kim, Young Seol Kim, Jin Woo Kim, Kwang Won Kim, Sun Woo Choi, Young Kil Korean J Intern Med Original Article Although it has been well established that thyroid hormones increase β-adrenergic receptors of various tissues in the animal studies, there are controversies about the β-adrenergic receptor changes of human mononuclear cells and polymorphonuclear cells. The present study was performed to analyze the change of β-adrenergic receptor of those cells according to the thyroid functional status and to evaluate their usefulness in assessment of sympathetic hyperactivity. We measured [(3)H]-dihydroalprenolol binding to circulating mononuclear and polymorphonuclear cells from 18 patients with hyperthyrodism, 7 with hypothyroidism, 8 with euthyroid goiter and 21 normal controls. Only with polymorphonuclear cells the receptor concentration was significantly higher (P<0.01) in hyperthyroidism (46.07±4.78 fmol/mg protein) than in the normal control (28.42±2.06 fmol/mg protein) and the affinity constants of both cells were comparable to normal control values. And serum concentrations of T(3) were not correlated well with the changes of receptor concentrations in hyperthyroidism. The patients with hypothyroidism and euthyroid goiter showed no significant difference in the receptor concentration and the affinity constants with both cell binding assays. These results indicate that thyroid hormones increase the receptor concentration in polymorphonuclear cells which might be responsible for the symptoms of sympathetic hyperactivity and the polymorphornuclear cells are useful for β-adrenergic receptor assay. Korean Association of Internal Medicine 1986-01 /pmc/articles/PMC4534902/ /pubmed/15759381 http://dx.doi.org/10.3904/kjim.1986.1.1.78 Text en © 1986 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Jong Do
You, Myung Hee
Kim, Young Seol
Kim, Jin Woo
Kim, Kwang Won
Kim, Sun Woo
Choi, Young Kil
Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function
title Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function
title_full Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function
title_fullStr Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function
title_full_unstemmed Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function
title_short Studies on Changes of β-Adrenergic Receptors in Polymorphonuclear Cell and Mononuclear Cell with the Changes of Thyroid Function
title_sort studies on changes of β-adrenergic receptors in polymorphonuclear cell and mononuclear cell with the changes of thyroid function
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534902/
https://www.ncbi.nlm.nih.gov/pubmed/15759381
http://dx.doi.org/10.3904/kjim.1986.1.1.78
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