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      Thyroxine increases Serca2 and Ryr2 gene expression in heart failure rats with euthyroid sick syndrome

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          ABSTRACT

          Objective

          The current study was aimed at analyzing sarcoplasmic reticulum Ca 2+ ATPase (Serca2) and ryanodine receptor type 2 ( Ryr2) gene expression in rats subjected to surgery that induced HF and were subsequently treated with T4 using physiological doses.

          Materials and methods

          HF was induced in 18 male Wistar rats by clipping the ascending thoracic aorta to generate aortic stenosis (HFS group), while the control group (9-sham) underwent thoracotomy. After 21 weeks, the HFS group was subdivided into two subgroups. One group (9 Wistar rats) with HF received 1.0 µg of T4/100 g of body weight for five consecutive days (HFS/T4); the other group (9 Wistar rats) received isotonic saline solution (HFS/S). The animals were sacrificed after this treatment and examined for signs of HF. Samples from the left ventricles of these animals were analyzed by RT-qPCR for the expression of Serca2 and Ryr2 genes.

          Results

          Rats with HF developed euthyroid sick syndrome (ESS) and treatment with T4 restored the T3 values to the Sham level and increased Serca2 and Ryr2 gene expression, thereby demonstrating a possible benefit of T4 treatment for heart function in ESS associated with HF.

          Conclusion

          The T4 treatment can potentially normalize the levels of T3 as well elevated Serca2 and Ryr2 gene expression in the myocardium in heart failure rats with euthyroid sick syndrome.

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          Most cited references30

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            Biostatistical Analysis

            Designed for one/two-semester, junior/graduate-level courses in Biostatistics, Biometry, Quantitative Biology, or Statistics, the latest edition of this best-selling biostatistics text is both comprehensive and easy to read. It provides a broad and practical overview of the statistical analysis methods used by researchers to collect, summarize, analyze, and draw conclusions from biological research data. The Fourth Edition can serve as either an introduction to the discipline for beginning students or a comprehensive procedural reference for today's practitioners.
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              Non-thyroidal illness in the ICU: a syndrome with different faces.

              Critically ill patients typically present with low or low-normal plasma thyroxine, low plasma triiodothyronine (T3), increased plasma reverse T3 (rT3) concentrations, in the absence of a rise in thyrotropin (TSH). This constellation is referred to as nonthyroidal illness syndrome (NTI). Although it is long known that the severity of NTI is associated with risk of poor outcomes of critical illness, the causality in this association has not been well investigated.
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                Author and article information

                Journal
                Arch Endocrinol Metab
                Arch Endocrinol Metab
                aem
                Archives of Endocrinology and Metabolism
                Sociedade Brasileira de Endocrinologia e Metabologia
                2359-3997
                2359-4292
                26 September 2016
                Nov-Dec 2016
                : 60
                : 6
                : 582-586
                Affiliations
                [1 ] orgdiv2Unidade de Pesquisa Experimental orgdiv1Faculdade de Medicina de Botucatu orgnameUniversidade Estadual Paulista Botucatu SP Brasil original Departamento de Clínica Médica, Unidade de Pesquisa Experimental (Unipex), Faculdade de Medicina de Botucatu, Universidade Estadual Paulista (Unesp), Botucatu, SP, Brasil
                [2 ] orgdiv1Instituto de Ciências da Saúde orgnameUniversidade Federal de Mato Grosso Sinop MT Brasil originalInstituto de Ciências da Saúde, Universidade Federal de Mato Grosso (UFMT), Sinop, MT, Brasil
                [3 ] orgdiv2Departamento de Bioestatística orgdiv1Instituto de Biociências orgnameUniversidade Estadual Paulista Botucatu SP Brasil originalDepartamento de Bioestatística, Instituto de Biociências, Universidade Estadual Paulista (Unesp), Botucatu, SP, Brasil
                Author notes
                Correspondence to: Célia R. Nogueira. Faculdade de Medicina de Botucatu, Universidade Estadual Paulista. Distrito de Rubião Jr s/n. 18618-000 – Botucatu, SP, Brasil. nogueira@ 123456fmb.unesp.br

                Disclosure: no potential conflict of interest relevant to this article was reported.

                Article
                10.1590/2359-3997000000208
                10522172
                27737323
                011257d0-707d-4793-aac9-33c38cdd25cf

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 November 2015
                : 11 April 2016
                Page count
                Figures: 2, Tables: 2, Equations: 0, References: 30, Pages: 1
                Funding
                Funded by: Fapesp
                Award ID: 2007/55902-8
                Categories
                Articles

                reverse triiodothyronine,heart failure,therapeutic use,calcium channels,triiodothyronine

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