Cargando…

Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets

Lorcaserin is a serotonergic agonist specific to the 5-hydroxytryptamine 2c receptor (5-HT(2C)R) that is FDA approved for the long-term management of obesity with or without at least one weight-related comorbidity. Lorcaserin can restrain patients’ appetite and improve insulin sensitivity and hyperi...

Descripción completa

Detalles Bibliográficos
Autores principales: Jing, Muhan, Wang, Shanshan, Li, Ding, Wang, Zeyu, Li, Ziwen, Lu, Yichen, Sun, Tong, Qiu, Chen, Chen, Fang, Yu, Haijuan, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602196/
https://www.ncbi.nlm.nih.gov/pubmed/34803706
http://dx.doi.org/10.3389/fphar.2021.761966
_version_ 1784601526899048448
author Jing, Muhan
Wang, Shanshan
Li, Ding
Wang, Zeyu
Li, Ziwen
Lu, Yichen
Sun, Tong
Qiu, Chen
Chen, Fang
Yu, Haijuan
Zhang, Wei
author_facet Jing, Muhan
Wang, Shanshan
Li, Ding
Wang, Zeyu
Li, Ziwen
Lu, Yichen
Sun, Tong
Qiu, Chen
Chen, Fang
Yu, Haijuan
Zhang, Wei
author_sort Jing, Muhan
collection PubMed
description Lorcaserin is a serotonergic agonist specific to the 5-hydroxytryptamine 2c receptor (5-HT(2C)R) that is FDA approved for the long-term management of obesity with or without at least one weight-related comorbidity. Lorcaserin can restrain patients’ appetite and improve insulin sensitivity and hyperinsulinemia mainly through activating 5-HT(2C)R in the hypothalamus. It is known that the mCPP, a kind of 5-HT(2C)R agonist, decreases plasma insulin concentration in mice and previous research in our laboratory found that mCPP inhibited glucose-stimulated insulin secretion (GSIS) by activating 5-HT(2C)R on the β cells. However, the effect of lorcaserin on GSIS of pancreatic β cell has not been studied so far. The present study found that 5-HT(2C)R was expressed in both mouse pancreatic β cells and β-cell–derived MIN6 cells. Dose-dependent activation of 5-HT(2C)R by lorcaserin suppressed GSIS and SB242084 or knockdown of 5-HT(2C)R abolished lorcaserin’s effect in vitro. Additionally, lorcaserin also suppressed GSIS in high-fat diet (HFD)-fed mice in dose-dependent manner. Lorcaserin did not change insulin synthesis ATP content, but lorcaserin decrease cytosolic free calcium level [(Ca(2+))i] in MIN6 cells stimulated with glucose and also inhibit insulin secretion and (Ca(2+))i in MIN6 treated with potassium chloride. Furthermore, stimulation with the L-type channel agonist, Bay K8644 did not restore GSIS in MIN6 exposed to lorcaserin. Lorcaserin inhibits the cAMP generation of MIN6 cells and pretreatment with the Gα i/o inhibitor pertussis toxin (PTX), abolished lorcaserin-induced suppression of GSIS in β cells, while membrane-permeable cAMP analogue db-cAMP had same effect as PTX. These date indicated lorcaserin coupled to PTX-sensitive Gα i/o proteins in β cells reduced intracellular cAMP level and Ca(2+) influx, thereby causing GSIS dysfunction of β cell. These results highlight a novel signaling mechanism of lorcaserin and provide valuable insights into the further investigation of 5-HT(2C)R functions in β-cell biology and it also provides guidance for the clinical application of lorcaserin.
format Online
Article
Text
id pubmed-8602196
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-86021962021-11-20 Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets Jing, Muhan Wang, Shanshan Li, Ding Wang, Zeyu Li, Ziwen Lu, Yichen Sun, Tong Qiu, Chen Chen, Fang Yu, Haijuan Zhang, Wei Front Pharmacol Pharmacology Lorcaserin is a serotonergic agonist specific to the 5-hydroxytryptamine 2c receptor (5-HT(2C)R) that is FDA approved for the long-term management of obesity with or without at least one weight-related comorbidity. Lorcaserin can restrain patients’ appetite and improve insulin sensitivity and hyperinsulinemia mainly through activating 5-HT(2C)R in the hypothalamus. It is known that the mCPP, a kind of 5-HT(2C)R agonist, decreases plasma insulin concentration in mice and previous research in our laboratory found that mCPP inhibited glucose-stimulated insulin secretion (GSIS) by activating 5-HT(2C)R on the β cells. However, the effect of lorcaserin on GSIS of pancreatic β cell has not been studied so far. The present study found that 5-HT(2C)R was expressed in both mouse pancreatic β cells and β-cell–derived MIN6 cells. Dose-dependent activation of 5-HT(2C)R by lorcaserin suppressed GSIS and SB242084 or knockdown of 5-HT(2C)R abolished lorcaserin’s effect in vitro. Additionally, lorcaserin also suppressed GSIS in high-fat diet (HFD)-fed mice in dose-dependent manner. Lorcaserin did not change insulin synthesis ATP content, but lorcaserin decrease cytosolic free calcium level [(Ca(2+))i] in MIN6 cells stimulated with glucose and also inhibit insulin secretion and (Ca(2+))i in MIN6 treated with potassium chloride. Furthermore, stimulation with the L-type channel agonist, Bay K8644 did not restore GSIS in MIN6 exposed to lorcaserin. Lorcaserin inhibits the cAMP generation of MIN6 cells and pretreatment with the Gα i/o inhibitor pertussis toxin (PTX), abolished lorcaserin-induced suppression of GSIS in β cells, while membrane-permeable cAMP analogue db-cAMP had same effect as PTX. These date indicated lorcaserin coupled to PTX-sensitive Gα i/o proteins in β cells reduced intracellular cAMP level and Ca(2+) influx, thereby causing GSIS dysfunction of β cell. These results highlight a novel signaling mechanism of lorcaserin and provide valuable insights into the further investigation of 5-HT(2C)R functions in β-cell biology and it also provides guidance for the clinical application of lorcaserin. Frontiers Media S.A. 2021-11-05 /pmc/articles/PMC8602196/ /pubmed/34803706 http://dx.doi.org/10.3389/fphar.2021.761966 Text en Copyright © 2021 Jing, Wang, Li, Wang, Li, Lu, Sun, Qiu, Chen, Yu and Zhang. https://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) and the copyright owner(s) 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 Pharmacology
Jing, Muhan
Wang, Shanshan
Li, Ding
Wang, Zeyu
Li, Ziwen
Lu, Yichen
Sun, Tong
Qiu, Chen
Chen, Fang
Yu, Haijuan
Zhang, Wei
Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets
title Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets
title_full Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets
title_fullStr Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets
title_full_unstemmed Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets
title_short Lorcaserin Inhibit Glucose-Stimulated Insulin Secretion and Calcium Influx in Murine Pancreatic Islets
title_sort lorcaserin inhibit glucose-stimulated insulin secretion and calcium influx in murine pancreatic islets
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602196/
https://www.ncbi.nlm.nih.gov/pubmed/34803706
http://dx.doi.org/10.3389/fphar.2021.761966
work_keys_str_mv AT jingmuhan lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT wangshanshan lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT liding lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT wangzeyu lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT liziwen lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT luyichen lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT suntong lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT qiuchen lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT chenfang lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT yuhaijuan lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets
AT zhangwei lorcaserininhibitglucosestimulatedinsulinsecretionandcalciuminfluxinmurinepancreaticislets