Literature DB >> 4086465

An improved assay method for thyroid peroxidase applicable for a few milligrams of abnormal human thyroid tissues.

T Hosoya, I Sato, Y Hiyama, H Yoshimura, H Niimi, O Tarutani.   

Abstract

A peroxidase assay method (Mini assay method) which is applicable for a minute amount (as small as a few mg) of thyroid tissue was developed, employing guaiacol or iodide as the second substrate. This method is a modification of the previous one (Ordinary assay method): the volume of the reaction mixture was reduced to about one-tenth with prior solubilization of the enzyme. The correlation between the Mini assay and Ordinary assay methods, and between the guaiacol and iodide assays by both methods were satisfactorily good, but the iodine content of thyroglobulin was found to be not directly correlated to the peroxidase activities. Protein-based specific activities of peroxidase from normal human thyroid tissue were about 0.030 guaiacol units/mg protein and 0.0066 iodide units/mg protein, which were slightly higher than those of porcine thyroid tissue. The Mini assay method developed in the present study was used for the determination of peroxidase activity in a small amount (1-8 mg) of thyroid tissue obtained by means of a needle biopsy from patients with thyroid disorders. One specimen (goitrous cretinism) showed no peroxidase activity in both the guaiacol and iodide assays, and three specimens (two chronic thyroiditis, one familial nontoxic goiter) possessed no ability to catalyze the oxidation of iodide in spite of the high reactivity towards guaiacol, suggesting the presence of an abnormal peroxidase in these tissues.

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Year:  1985        PMID: 4086465     DOI: 10.1093/oxfordjournals.jbchem.a135320

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  7 in total

1.  Improved assay method for activity of thyroid peroxidase-catalysed coupling of iodotyrosine residues of thyroglobulin utilizing h.p.l.c. for analysis of iodothyronines.

Authors:  T Ohmori; O Tarutani; T Hosoya
Journal:  Biochem J       Date:  1989-08-15       Impact factor: 3.857

2.  Human thyroid peroxidase: complete cDNA and protein sequence, chromosome mapping, and identification of two alternately spliced mRNAs.

Authors:  S Kimura; T Kotani; O W McBride; K Umeki; K Hirai; T Nakayama; S Ohtaki
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

3.  Anti-thyroid peroxidase antibodies in sera from healthy subjects and from patients with chronic thyroiditis: differences in the ability to inhibit thyroid peroxidase activities.

Authors:  Y Kohno; F Yamaguchi; K Saito; H Niimi; T Nishikawa; T Hosoya
Journal:  Clin Exp Immunol       Date:  1991-09       Impact factor: 4.330

4.  Anti-thyroglobulin autoantibodies in sera from patients with chronic thyroiditis and from healthy subjects: differences in cross-reactivity with thyroid peroxidase.

Authors:  N Naito; K Saito; T Hosoya; O Tarutani; S Sakata; T Nishikawa; H Niimi; H Nakajima; Y Kohno
Journal:  Clin Exp Immunol       Date:  1990-04       Impact factor: 4.330

5.  Autoantibodies to the thyroid microsomal/thyroid peroxidase antigen are polyclonal and directed to several distinct antigenic sites.

Authors:  N D Doble; J P Banga; R Pope; E Lalor; P Kilduff; A M McGregor
Journal:  Immunology       Date:  1988-05       Impact factor: 7.397

6.  Autoantibodies to thyroid peroxidase in patients with chronic thyroiditis: effect of antibody binding on enzyme activities.

Authors:  Y Kohno; Y Hiyama; N Shimojo; H Niimi; H Nakajima; T Hosoya
Journal:  Clin Exp Immunol       Date:  1986-09       Impact factor: 4.330

7.  Type of sweet flavour carrier affects thyroid axis activity in male rats.

Authors:  Ewelina Pałkowska-Goździk; Anna Bigos; Danuta Rosołowska-Huszcz
Journal:  Eur J Nutr       Date:  2016-12-31       Impact factor: 5.614

  7 in total

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