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Biochemical and histological changes in the heart of post-partum rats exposed to Natron

BACKGROUND: The customary puerperal practice of Natron consumption has been identified as one of the predisposing factors in the etiology of peripartum cardiomyopathy (PPCM). This study was designed to investigate the effect of Natron in postpartum Wistar albino rats. METHODS: A total of 30 postpart...

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Autores principales: Saidu, Yusuf, Usman, Maimuna Jumai, Isa, Suleiman Ahmed, Isezuo, Simeon Alabi, Bilbis, Lawal Suleiman, Sahabi, Saddiku Malam, Bello, Ahmad, Muhammad, Suleiman Alhaji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306309/
https://www.ncbi.nlm.nih.gov/pubmed/30580861
http://dx.doi.org/10.1016/j.ihj.2017.12.002
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author Saidu, Yusuf
Usman, Maimuna Jumai
Isa, Suleiman Ahmed
Isezuo, Simeon Alabi
Bilbis, Lawal Suleiman
Sahabi, Saddiku Malam
Bello, Ahmad
Muhammad, Suleiman Alhaji
author_facet Saidu, Yusuf
Usman, Maimuna Jumai
Isa, Suleiman Ahmed
Isezuo, Simeon Alabi
Bilbis, Lawal Suleiman
Sahabi, Saddiku Malam
Bello, Ahmad
Muhammad, Suleiman Alhaji
author_sort Saidu, Yusuf
collection PubMed
description BACKGROUND: The customary puerperal practice of Natron consumption has been identified as one of the predisposing factors in the etiology of peripartum cardiomyopathy (PPCM). This study was designed to investigate the effect of Natron in postpartum Wistar albino rats. METHODS: A total of 30 postpartum Wistar rats were exposed to different doses (50 mg/kg, 100 mg/kg, 200 mg/kg and 300 mg/kg) of Natron for 28 days. After the treatment, we carried out biochemical analyses and histological evaluations of kidney, liver and heart. RESULTS: The study revealed that the exposure of postpartum rats to 100 mg/kg of Natron and above significantly (p < 0.05) increase the cardiac markers; myoglobin, creatine kinase-MB, troponin I and T as compared with control. The result of liver function indicated no significant difference in alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, albumin and total protein of the Natron treated groups as compared with control. However, at higher doses, the levels of total protein, globulin and alkaline phosphatase activity were significantly increased in comparison to the control. There was no significant difference in the kidney function markers of the treatment groups as compared with control. Histological examinations revealed no changes in the kidney of the treated groups. Mild portal triaditis was observed in the liver of the treated rats. The heart of the rats administered ≥100 mg/kg of Natron showed myocyte hypertrophy. CONCLUSION: The study demonstrated that the administration of Natron for 28 days caused changes in the heart of postpartum rats and thus may contribute to the pathogenesis of PPCM.
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spelling pubmed-63063092019-11-01 Biochemical and histological changes in the heart of post-partum rats exposed to Natron Saidu, Yusuf Usman, Maimuna Jumai Isa, Suleiman Ahmed Isezuo, Simeon Alabi Bilbis, Lawal Suleiman Sahabi, Saddiku Malam Bello, Ahmad Muhammad, Suleiman Alhaji Indian Heart J Pre-clinical BACKGROUND: The customary puerperal practice of Natron consumption has been identified as one of the predisposing factors in the etiology of peripartum cardiomyopathy (PPCM). This study was designed to investigate the effect of Natron in postpartum Wistar albino rats. METHODS: A total of 30 postpartum Wistar rats were exposed to different doses (50 mg/kg, 100 mg/kg, 200 mg/kg and 300 mg/kg) of Natron for 28 days. After the treatment, we carried out biochemical analyses and histological evaluations of kidney, liver and heart. RESULTS: The study revealed that the exposure of postpartum rats to 100 mg/kg of Natron and above significantly (p < 0.05) increase the cardiac markers; myoglobin, creatine kinase-MB, troponin I and T as compared with control. The result of liver function indicated no significant difference in alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, albumin and total protein of the Natron treated groups as compared with control. However, at higher doses, the levels of total protein, globulin and alkaline phosphatase activity were significantly increased in comparison to the control. There was no significant difference in the kidney function markers of the treatment groups as compared with control. Histological examinations revealed no changes in the kidney of the treated groups. Mild portal triaditis was observed in the liver of the treated rats. The heart of the rats administered ≥100 mg/kg of Natron showed myocyte hypertrophy. CONCLUSION: The study demonstrated that the administration of Natron for 28 days caused changes in the heart of postpartum rats and thus may contribute to the pathogenesis of PPCM. Elsevier 2018 2017-12-11 /pmc/articles/PMC6306309/ /pubmed/30580861 http://dx.doi.org/10.1016/j.ihj.2017.12.002 Text en © 2017 Published by Elsevier B.V. on behalf of Cardiological Society of India. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Pre-clinical
Saidu, Yusuf
Usman, Maimuna Jumai
Isa, Suleiman Ahmed
Isezuo, Simeon Alabi
Bilbis, Lawal Suleiman
Sahabi, Saddiku Malam
Bello, Ahmad
Muhammad, Suleiman Alhaji
Biochemical and histological changes in the heart of post-partum rats exposed to Natron
title Biochemical and histological changes in the heart of post-partum rats exposed to Natron
title_full Biochemical and histological changes in the heart of post-partum rats exposed to Natron
title_fullStr Biochemical and histological changes in the heart of post-partum rats exposed to Natron
title_full_unstemmed Biochemical and histological changes in the heart of post-partum rats exposed to Natron
title_short Biochemical and histological changes in the heart of post-partum rats exposed to Natron
title_sort biochemical and histological changes in the heart of post-partum rats exposed to natron
topic Pre-clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306309/
https://www.ncbi.nlm.nih.gov/pubmed/30580861
http://dx.doi.org/10.1016/j.ihj.2017.12.002
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