Sex impacts cardiac function and the proteome response to thyroid hormone in aged mice
Autor: | Wei Zhong Zhu, Aaron K Olson, Dolena R Ledee, Michael A. Portman |
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Rok vydání: | 2020 |
Předmět: |
Proteomics
Cardiac function curve Sex-based endocrine system medicine.medical_specialty endocrine system diseases 030204 cardiovascular system & hematology Biochemistry 03 medical and health sciences 0302 clinical medicine Internal medicine Heart rate medicine Euthyroid lcsh:QH573-671 Molecular Biology Aged 030304 developmental biology 0303 health sciences lcsh:Cytology business.industry Research Thyroid Heart Thyroid hormone medicine.anatomical_structure Endocrinology Proteome Thyroid function business Hormone |
Zdroj: | Proteome Science Proteome Science, Vol 18, Iss 1, Pp 1-13 (2020) |
ISSN: | 1477-5956 |
Popis: | BackgroundSex and age have substantial influence on thyroid function. Sex influences the risk and clinical expression of thyroid disorders (TDs), with age a proposed trigger for the development of TDs. Cardiac function is affected by thyroid hormone levels with gender differences. Accordingly, we investigated the proteomic changes involved in sex based cardiac responses to thyroid dysfunction in elderly mice.MethodsAged (18–20 months) male and female C57BL/6 mice were fed diets to create euthyroid, hypothyroid, or hyperthyroid states. Serial echocardiographs were performed to assess heart function. Proteomic changes in cardiac protein profiles were assessed by 2-D DIGE and LC-MS/MS, and a subset confirmed by immunoblotting.ResultsSerial echocardiographs showed ventricular function remained unchanged regardless of treatment. Heart rate and size increased (hyperthyroid) or decreased (hypothyroid) independent of sex. Pairwise comparison between the six groups identified 55 proteins (≥ 1.5-fold difference andp ConclusionWe identified both predicted and novel proteins with gender specific differential expression in response to thyroid hormone status, providing a catalogue of proteins associated with thyroid dysfunction. Pursuit of these proteins and their involvement in cardiac function will expand our understanding of mechanisms involved in sex-based cardiac response to thyroid dysfunction. |
Databáze: | OpenAIRE |
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