Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C

Overweight and obesity is a growing global health concern. Current management of obesity includes lifestyle intervention, bariatric surgery and medication. The serotonin receptor, 5-HT2C, is known to mediate satiety, appetite and consumption behaviour. Lorcaserin, an appetite control drug, has demon...

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Main Authors: Heidi Yuen, Andrew Hung, Angela Wei Hong Yang, George Binh Lenon
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/4/1326
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spelling doaj-55eeaaa547c94f109287a341b58cc7bc2020-11-25T02:17:32ZengMDPI AGInternational Journal of Molecular Sciences1422-00672020-02-01214132610.3390/ijms21041326ijms21041326Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2CHeidi Yuen0Andrew Hung1Angela Wei Hong Yang2George Binh Lenon3School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria 3083, AustraliaSchool of Science, RMIT University, Melbourne, Victoria 3000, AustraliaSchool of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria 3083, AustraliaSchool of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria 3083, AustraliaOverweight and obesity is a growing global health concern. Current management of obesity includes lifestyle intervention, bariatric surgery and medication. The serotonin receptor, 5-HT2C, is known to mediate satiety, appetite and consumption behaviour. Lorcaserin, an appetite control drug, has demonstrated efficacy in appetite control by targeting 5-HT2C but causes undesirable side effects. This study aimed to explore the potential usage of Cassiae semen (CS), a well-known traditional Chinese medicine used to treat obesity. A computational molecular docking study was performed to determine the binding mechanism of CS compounds to the 5-HT2C receptors in both active, agonist-bound and inactive, antagonist-bound conformations. By comparing binding poses and predicted relative binding affinities towards the active or inactive forms of the receptor, we hypothesise that two of the CS compounds studied may be potent agonists which may mimic the appetite suppression effects of lorcaserin: obtusifoliol and cassiaside B2. Furthermore, two ligands, beta-sitosterol and juglanin, were predicted to bind favourably to 5-HT2C outside of the known agonist binding pocket in the active receptor, suggesting that such ligands may serve as positive allosteric modulators of 5-HT2C receptor function. Overall, this study proposed several CS compounds which may be responsible for exerting anti-obesity effects via appetite suppression by 5-HT2C receptor activation.https://www.mdpi.com/1422-0067/21/4/1326obesityoverweightweight lossappetite suppressionherbal medicinenatural productin silico analysis
collection DOAJ
language English
format Article
sources DOAJ
author Heidi Yuen
Andrew Hung
Angela Wei Hong Yang
George Binh Lenon
spellingShingle Heidi Yuen
Andrew Hung
Angela Wei Hong Yang
George Binh Lenon
Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C
International Journal of Molecular Sciences
obesity
overweight
weight loss
appetite suppression
herbal medicine
natural product
in silico analysis
author_facet Heidi Yuen
Andrew Hung
Angela Wei Hong Yang
George Binh Lenon
author_sort Heidi Yuen
title Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C
title_short Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C
title_full Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C
title_fullStr Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C
title_full_unstemmed Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C
title_sort mechanisms of action of cassiae semen for weight management: a computational molecular docking study of serotonin receptor 5-ht2c
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2020-02-01
description Overweight and obesity is a growing global health concern. Current management of obesity includes lifestyle intervention, bariatric surgery and medication. The serotonin receptor, 5-HT2C, is known to mediate satiety, appetite and consumption behaviour. Lorcaserin, an appetite control drug, has demonstrated efficacy in appetite control by targeting 5-HT2C but causes undesirable side effects. This study aimed to explore the potential usage of Cassiae semen (CS), a well-known traditional Chinese medicine used to treat obesity. A computational molecular docking study was performed to determine the binding mechanism of CS compounds to the 5-HT2C receptors in both active, agonist-bound and inactive, antagonist-bound conformations. By comparing binding poses and predicted relative binding affinities towards the active or inactive forms of the receptor, we hypothesise that two of the CS compounds studied may be potent agonists which may mimic the appetite suppression effects of lorcaserin: obtusifoliol and cassiaside B2. Furthermore, two ligands, beta-sitosterol and juglanin, were predicted to bind favourably to 5-HT2C outside of the known agonist binding pocket in the active receptor, suggesting that such ligands may serve as positive allosteric modulators of 5-HT2C receptor function. Overall, this study proposed several CS compounds which may be responsible for exerting anti-obesity effects via appetite suppression by 5-HT2C receptor activation.
topic obesity
overweight
weight loss
appetite suppression
herbal medicine
natural product
in silico analysis
url https://www.mdpi.com/1422-0067/21/4/1326
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