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Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus
Growing evidence suggests that oxytocin (OT) plays an important factor for the control of food intake, body weight, and energy metabolism in human and non-human animals. It has reported previously, the downregulation in oxytocin receptors (OTRs) expression is linked with the development of obesity,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603196/ https://www.ncbi.nlm.nih.gov/pubmed/34825159 http://dx.doi.org/10.1016/j.metop.2021.100146 |
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author | Thakur, Pratibha Shrivastava, Renu Shrivastava, Vinoy K. |
author_facet | Thakur, Pratibha Shrivastava, Renu Shrivastava, Vinoy K. |
author_sort | Thakur, Pratibha |
collection | PubMed |
description | Growing evidence suggests that oxytocin (OT) plays an important factor for the control of food intake, body weight, and energy metabolism in human and non-human animals. It has reported previously, the downregulation in oxytocin receptors (OTRs) expression is linked with the development of obesity, but exogenous OT reverse body weight and food intake in obese animal model. It is important to know that, whether intraperitoneal administration crosses blood brain barrier. Therefore, in the present experiment, we study the impact of intraperitoneal administration of synthetic OT 0.0116 mg/kg and antagonist atosiban (OTA) 1 mg/kg on food intake, and body weight of female mice, Mus musculus for different duration i.e. 30, 60, and 90 days. In this study, it was observed that there was significant decrease (p<0.001, one-way analysis of variance [ANOVA]) in the body weight (BW), food intake, and gonadosmatic indices (GSI) after the intraperitoneal exposure of OT at dose 0.0116 mg/kg up to 90 days and inhibits via antagonist atosiban. These results indicates that intraperitoneal administration of OT can be used for treatment for longer duration without any side effects and maintains homeostasis in physiologic system regulates body weight and gonadal weight in female mice, which represent an important therapeutic tool for the obesity and metabolic disorder in female. |
format | Online Article Text |
id | pubmed-8603196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86031962021-11-24 Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus Thakur, Pratibha Shrivastava, Renu Shrivastava, Vinoy K. Metabol Open Original Research Paper Growing evidence suggests that oxytocin (OT) plays an important factor for the control of food intake, body weight, and energy metabolism in human and non-human animals. It has reported previously, the downregulation in oxytocin receptors (OTRs) expression is linked with the development of obesity, but exogenous OT reverse body weight and food intake in obese animal model. It is important to know that, whether intraperitoneal administration crosses blood brain barrier. Therefore, in the present experiment, we study the impact of intraperitoneal administration of synthetic OT 0.0116 mg/kg and antagonist atosiban (OTA) 1 mg/kg on food intake, and body weight of female mice, Mus musculus for different duration i.e. 30, 60, and 90 days. In this study, it was observed that there was significant decrease (p<0.001, one-way analysis of variance [ANOVA]) in the body weight (BW), food intake, and gonadosmatic indices (GSI) after the intraperitoneal exposure of OT at dose 0.0116 mg/kg up to 90 days and inhibits via antagonist atosiban. These results indicates that intraperitoneal administration of OT can be used for treatment for longer duration without any side effects and maintains homeostasis in physiologic system regulates body weight and gonadal weight in female mice, which represent an important therapeutic tool for the obesity and metabolic disorder in female. Elsevier 2021-11-02 /pmc/articles/PMC8603196/ /pubmed/34825159 http://dx.doi.org/10.1016/j.metop.2021.100146 Text en © 2021 Published by Elsevier Inc. https://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 | Original Research Paper Thakur, Pratibha Shrivastava, Renu Shrivastava, Vinoy K. Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus |
title | Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus |
title_full | Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus |
title_fullStr | Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus |
title_full_unstemmed | Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus |
title_short | Effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, Mus musculus |
title_sort | effects of oxytocin and antagonist antidote atosiban on body weight and food intake of female mice, mus musculus |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8603196/ https://www.ncbi.nlm.nih.gov/pubmed/34825159 http://dx.doi.org/10.1016/j.metop.2021.100146 |
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