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Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor
Since 5-HT(6) receptors play role in controlling feeding and satiety and dopamine is essential for normal feeding behavior, we evaluated the ability of EMD 386088—5-HT(6) receptor partial agonist and dopamine transporter inhibitor—to reduce body weight in obese rats, as well as its anorectic propert...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296348/ https://www.ncbi.nlm.nih.gov/pubmed/28228713 http://dx.doi.org/10.3389/fnins.2017.00050 |
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author | Kotańska, Magdalena Śniecikowska, Joanna Jastrzębska-Więsek, Magdalena Kołaczkowski, Marcin Pytka, Karolina |
author_facet | Kotańska, Magdalena Śniecikowska, Joanna Jastrzębska-Więsek, Magdalena Kołaczkowski, Marcin Pytka, Karolina |
author_sort | Kotańska, Magdalena |
collection | PubMed |
description | Since 5-HT(6) receptors play role in controlling feeding and satiety and dopamine is essential for normal feeding behavior, we evaluated the ability of EMD 386088—5-HT(6) receptor partial agonist and dopamine transporter inhibitor—to reduce body weight in obese rats, as well as its anorectic properties (calorie intake reduction) in rat model of excessive eating and the influence on metabolism (plasma glucose and glycerol levels). We also determined the effect of the studied compound on pica behavior in rats and its influence on blood pressure after single administration. EMD 386088 reduced body weight in obese rats fed high-fat diet and decreased calorie intake in both models applied (rat model of obesity and of excessive eating). In both models EMD 386088 regulated plasma glucose and increased plasma glycerol levels. The latter proves that the compound reduced body fat. We think that it might have increased lipolysis, but this requires further studies. The reduction in glucose levels is the first symptom of metabolic disorders compensation. EMD 386088 did not cause pica behavior in rats but increased blood pressure after single administration. We think that partial 5-HT(6) agonists might have potential in the treatment of obesity. Thus, EMD 386088 requires extended studies. |
format | Online Article Text |
id | pubmed-5296348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52963482017-02-22 Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor Kotańska, Magdalena Śniecikowska, Joanna Jastrzębska-Więsek, Magdalena Kołaczkowski, Marcin Pytka, Karolina Front Neurosci Neuroscience Since 5-HT(6) receptors play role in controlling feeding and satiety and dopamine is essential for normal feeding behavior, we evaluated the ability of EMD 386088—5-HT(6) receptor partial agonist and dopamine transporter inhibitor—to reduce body weight in obese rats, as well as its anorectic properties (calorie intake reduction) in rat model of excessive eating and the influence on metabolism (plasma glucose and glycerol levels). We also determined the effect of the studied compound on pica behavior in rats and its influence on blood pressure after single administration. EMD 386088 reduced body weight in obese rats fed high-fat diet and decreased calorie intake in both models applied (rat model of obesity and of excessive eating). In both models EMD 386088 regulated plasma glucose and increased plasma glycerol levels. The latter proves that the compound reduced body fat. We think that it might have increased lipolysis, but this requires further studies. The reduction in glucose levels is the first symptom of metabolic disorders compensation. EMD 386088 did not cause pica behavior in rats but increased blood pressure after single administration. We think that partial 5-HT(6) agonists might have potential in the treatment of obesity. Thus, EMD 386088 requires extended studies. Frontiers Media S.A. 2017-02-08 /pmc/articles/PMC5296348/ /pubmed/28228713 http://dx.doi.org/10.3389/fnins.2017.00050 Text en Copyright © 2017 Kotańska, Śniecikowska, Jastrzębska-Więsek, Kołaczkowski and Pytka. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Kotańska, Magdalena Śniecikowska, Joanna Jastrzębska-Więsek, Magdalena Kołaczkowski, Marcin Pytka, Karolina Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor |
title | Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor |
title_full | Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor |
title_fullStr | Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor |
title_full_unstemmed | Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor |
title_short | Metabolic and Cardiovascular Benefits and Risks of EMD386088—A 5-HT(6) Receptor Partial Agonist and Dopamine Transporter Inhibitor |
title_sort | metabolic and cardiovascular benefits and risks of emd386088—a 5-ht(6) receptor partial agonist and dopamine transporter inhibitor |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5296348/ https://www.ncbi.nlm.nih.gov/pubmed/28228713 http://dx.doi.org/10.3389/fnins.2017.00050 |
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