Lysophosphatidylcholine and its phosphorothioate analogues potentiate insulin secretion via GPR40 (FFAR1), GPR55 and GPR119 receptors in a different manner-Reference-Cited by-同舟云学术

Lysophosphatidylcholine and its phosphorothioate analogues potentiate insulin secretion via GPR40 (FFAR1), GPR55 and GPR119 receptors in a different manner

Published:2018-09 Issue: Volume:472 Page:117-125
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Drzazga Anna,Kristinsson Hjalti,Sałaga Maciej,Zatorski Hubert,Koziołkiewicz Maria,Gendaszewska-Darmach Edyta^ORCID,Bergsten Peter

Funder

Polish National Science Centre

European Commission FP7 Project Beta-JUDO

European Union EIT Health project DeTecT2D

Swedish Diabetes Association

Family Ernfors Foundation

Swedish Society for Diabetology and the Regional Research Council Uppsala

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference62 articles.

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2. Plasma lysophosphatidylcholine levels are reduced in obesity and type 2 diabetes;Barber;Plos One,2012

3. Glucose-induced amplitude regulation of pulsatile insulin secretion from individual pancreatic islets;Bergsten;Diabetes,1993

4. The orphan G protein-coupled receptor GPR40 is activated by medium and long chain fatty acids;Briscoe;J. Biol. Chem.,2003

5. Pharmacological regulation of insulin secretion in MIN6 cells through the fatty acid receptor GPR40: identification of agonist and antagonist small molecules;Briscoe;Brit J. Pharmacol.,2006

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