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                  <mods:namePart>Tabarin, Antoine</mods:namePart>
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                  <mods:namePart>Marsicano, Giovanni</mods:namePart>
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                  <mods:namePart>Cota, Daniela</mods:namePart>
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               <mods:identifier type="citation">Francisco J. Bermudez-Silva, Silvana Y. Romero-Zerbo, Magalie Haissaguerre, Inmaculada Ruz-Maldonado, Said Lhamyani, Rajaa El Bekay, Antoine Tabarin, Giovanni Marsicano, Daniela Cota; The cannabinoid CB1 receptor and mTORC1 signalling pathways interact to modulate glucose homeostasis in mice. Dis Model Mech 1 January 2016; 9 (1): 51–61. doi: https://doi.org/10.1242/dmm.020750</mods:identifier>
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               <mods:identifier type="doi">10.1242/dmm.020750</mods:identifier>
               <mods:abstract>The endocannabinoid system (ECS) is an intercellular signalling&#xd;
mechanism that is present in the islets of Langerhans and plays a&#xd;
role in the modulation of insulin secretion and expansion of the β-cell&#xd;
mass. The downstream signalling pathways mediating these effects&#xd;
are poorly understood. Mammalian target of rapamycin complex 1&#xd;
(mTORC1) signalling is a key intracellular pathway involved in&#xd;
energy homeostasis and is known to importantly affect the&#xd;
physiology of pancreatic islets. We investigated the possible&#xd;
relationship between cannabinoid type 1 (CB1) receptor signalling&#xd;
and the mTORC1 pathway in the endocrine pancreas of mice by&#xd;
using pharmacological analysis as well as mice genetically lacking&#xd;
the CB1 receptor or the downstream target of mTORC1, the kinase&#xd;
p70S6K1. In vitro static secretion experiments on islets, western&#xd;
blotting, and in vivo glucose and insulin tolerance tests were&#xd;
performed. The CB1 receptor antagonist rimonabant decreased&#xd;
glucose-stimulated insulin secretion (GSIS) at 0.1 µM while&#xd;
increasing phosphorylation of p70S6K1 and ribosomal protein S6&#xd;
(rpS6) within the islets. Specific pharmacological blockade of&#xd;
mTORC1 by 3 nM rapamycin, as well as genetic deletion of&#xd;
p70S6K1, impaired the CB1-antagonist-mediated decrease in&#xd;
GSIS. In vivo experiments showed that 3 mg/kg body weight&#xd;
rimonabant decreased insulin levels and induced glucose&#xd;
intolerance in lean mice without altering peripheral insulin&#xd;
sensitivity; this effect was prevented by peripheral administration&#xd;
of low doses of rapamycin (0.1 mg/kg body weight), which increased&#xd;
insulin sensitivity. These findings suggest a functional interaction&#xd;
between the ECS and the mTORC1 pathway within the endocrine&#xd;
pancreas and at the whole-organism level, which could have&#xd;
implications for the development of new therapeutic approaches&#xd;
for pancreatic β-cell diseases.</mods:abstract>
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               </mods:language>
               <mods:accessCondition type="useAndReproduction">Atribución 4.0 Internacional</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Insulina</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>The cannabinoid CB1 receptor and mTORC1 signalling pathways interact to modulate glucose homeostasis in mice</mods:title>
               </mods:titleInfo>
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