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Copyright ©The Author(s) 2017.
World J Gastroenterol. Jul 7, 2017; 23(25): 4500-4507
Published online Jul 7, 2017. doi: 10.3748/wjg.v23.i25.4500
Table 1 Literature assessing metabotropic glutamate 5 receptor localization in the gastrointestinal tract and accessory digestive organs
OrgansRole/disorderAnimal/human studyMeasurement/observationRef.
MouthMechanical allodyniaRatsAntagonists block allodynia[11-13]
MouthInflammation/painRatsUpregulation of receptor expression[10]
MouthInflammationHuman pulpReceptor-mediated inflammatory nociception.[14]
MouthOral cancerHuman tissueTumor progression, cell migration[16]
Esophagus/stomachTLESR (transient lower sphincter relaxation)FerretsReduction in reflux[17,20]
Esophagus/stomachTLESRHumansReduction in reflux[22-24]
Esophagus/stomachTLESRHumansReduction in reflux[25]
IntestineIntestinal inflammationPigs and miceDecreased mGluR5 expression[30]
IntestineVisceral painRats and micemGluR5 antagonists inhibit colorectal distension-evoked visceromotor (VMR)[31]
IntestineEpithelial barrier functionMicemGluR5 antagonists improve the epithelial barrier function[32]
TongueInflammationRatsMechanical and heat hypersensitivity[33]
TongueCancerHuman cell linesAntagonists block tumor cell migration and invasion[16]
TongueCancerMiceAntagonists block tumor cell migration[34]
LiverHypoxiaRats and miceNecrosis, reactive oxygen species (ROS)[36,37]
LiverAcetaminophen damageMiceROS iNOS[42]
LiverCancerMiceTumor reduction[47]
LiverFulminant hepatitisMiceMortality, Lipid peroxidation[44]
LiverMitochondrial damageRatsMitochondrial membrane potential[46]
ROS production
PancreasInsulin releaseRatsChange in glucose concentration[48]
PancreasInsulin secretionRats and miceGlucose-stimulated intracellular Ca2+[5]