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Co-administration of Apelin and T4 Protects Inotropic and Chronotropic Changes Occurring in Hypothyroid Rats
BACKGROUND: One of the most important thyroid hormone targets is the cardiovascular system. Hemodynamic changes, such as decreased resting heart rate (HR), myocardial contractility, and cardiac output, and increased diastolic pressure and systemic vascular resistance, have been observed in hypothyro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592171/ https://www.ncbi.nlm.nih.gov/pubmed/26247243 http://dx.doi.org/10.5935/abc.20150086 |
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author | Akhondali, Zahra Badavi, Mohammad Dianat, Mahin Faraji, Farzaneh |
author_facet | Akhondali, Zahra Badavi, Mohammad Dianat, Mahin Faraji, Farzaneh |
author_sort | Akhondali, Zahra |
collection | PubMed |
description | BACKGROUND: One of the most important thyroid hormone targets is the cardiovascular system. Hemodynamic changes, such as decreased resting heart rate (HR), myocardial contractility, and cardiac output, and increased diastolic pressure and systemic vascular resistance, have been observed in hypothyroid patients. Moreover, in these patients, ECG changes include sinus bradycardia and low voltage complexes (P waves or QRS complexes). OBJECTIVE: This study aimed at evaluating the prophylactic effect of apelin on HR changes and QRS voltage that occur in propylthiouracil (PTU)-induced hypothyroid rats. METHOD: In this study, 48 adult male Wistar rats weighing 170-235g were randomly divided into 6 groups: Control group (normal saline ip injection + tap water gavage); P group (PTU 0.05%, in drinking water); A group (apelin 200 µg.kg(-1).day(-1), ip); PA group [co-administration of PTU and apelin]; PT group [co-administration of PTU + T4 (0.2 mg/g per day, gavage)]; and PAT group (co-administration of PTU, apelin and T4). All experiments were performed for 28 consecutive days, and then the animals were anesthetized with an ip injection of ketamine (80 mg/kg) and xylazine (12 mg/kg). Lead II electrocardiogram was recorded to calculate HR and QRS voltage. RESULTS: Heart rate and QRS voltage increased more significantly in the hypothyroid group that consumed both apelin and T4 (201 ± 4 beat/min, 0.71 ± 0.02 mv vs. hypothyroid 145 ± 9 beat/min, 0.563 ± 0.015 mv; respectively). CONCLUSION: The co-administration of apelin and T4 showed a protective effect on QRS voltage and HR in PTU‑induced hypothyroid rats. |
format | Online Article Text |
id | pubmed-4592171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Sociedade Brasileira de Cardiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-45921712015-10-14 Co-administration of Apelin and T4 Protects Inotropic and Chronotropic Changes Occurring in Hypothyroid Rats Akhondali, Zahra Badavi, Mohammad Dianat, Mahin Faraji, Farzaneh Arq Bras Cardiol Original Article BACKGROUND: One of the most important thyroid hormone targets is the cardiovascular system. Hemodynamic changes, such as decreased resting heart rate (HR), myocardial contractility, and cardiac output, and increased diastolic pressure and systemic vascular resistance, have been observed in hypothyroid patients. Moreover, in these patients, ECG changes include sinus bradycardia and low voltage complexes (P waves or QRS complexes). OBJECTIVE: This study aimed at evaluating the prophylactic effect of apelin on HR changes and QRS voltage that occur in propylthiouracil (PTU)-induced hypothyroid rats. METHOD: In this study, 48 adult male Wistar rats weighing 170-235g were randomly divided into 6 groups: Control group (normal saline ip injection + tap water gavage); P group (PTU 0.05%, in drinking water); A group (apelin 200 µg.kg(-1).day(-1), ip); PA group [co-administration of PTU and apelin]; PT group [co-administration of PTU + T4 (0.2 mg/g per day, gavage)]; and PAT group (co-administration of PTU, apelin and T4). All experiments were performed for 28 consecutive days, and then the animals were anesthetized with an ip injection of ketamine (80 mg/kg) and xylazine (12 mg/kg). Lead II electrocardiogram was recorded to calculate HR and QRS voltage. RESULTS: Heart rate and QRS voltage increased more significantly in the hypothyroid group that consumed both apelin and T4 (201 ± 4 beat/min, 0.71 ± 0.02 mv vs. hypothyroid 145 ± 9 beat/min, 0.563 ± 0.015 mv; respectively). CONCLUSION: The co-administration of apelin and T4 showed a protective effect on QRS voltage and HR in PTU‑induced hypothyroid rats. Sociedade Brasileira de Cardiologia 2015-09 /pmc/articles/PMC4592171/ /pubmed/26247243 http://dx.doi.org/10.5935/abc.20150086 Text en http://creativecommons.org/licenses/by/4.0/ 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. |
spellingShingle | Original Article Akhondali, Zahra Badavi, Mohammad Dianat, Mahin Faraji, Farzaneh Co-administration of Apelin and T4 Protects Inotropic and Chronotropic Changes Occurring in Hypothyroid Rats |
title | Co-administration of Apelin and T4 Protects Inotropic and Chronotropic
Changes Occurring in Hypothyroid Rats |
title_full | Co-administration of Apelin and T4 Protects Inotropic and Chronotropic
Changes Occurring in Hypothyroid Rats |
title_fullStr | Co-administration of Apelin and T4 Protects Inotropic and Chronotropic
Changes Occurring in Hypothyroid Rats |
title_full_unstemmed | Co-administration of Apelin and T4 Protects Inotropic and Chronotropic
Changes Occurring in Hypothyroid Rats |
title_short | Co-administration of Apelin and T4 Protects Inotropic and Chronotropic
Changes Occurring in Hypothyroid Rats |
title_sort | co-administration of apelin and t4 protects inotropic and chronotropic
changes occurring in hypothyroid rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592171/ https://www.ncbi.nlm.nih.gov/pubmed/26247243 http://dx.doi.org/10.5935/abc.20150086 |
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