2008
DOI: 10.1016/j.coph.2008.08.005
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Reflux inhibitors: a new approach for GERD?

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Cited by 23 publications
(22 citation statements)
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“…Considering transient lower esophageal sphincter relaxations account for the vast majority of reflux events [5], it is predictable that baclofen may be helpful for refractory GERC by the inhibition of both acid and nonacid reflux. The limited studies have shown that it decreased the frequency of transient lower esophageal sphincter relaxations by 40-60% and acid or non-acid reflux episodes by 43% [6][7][8].…”
Section: Discussionmentioning
confidence: 99%
“…Considering transient lower esophageal sphincter relaxations account for the vast majority of reflux events [5], it is predictable that baclofen may be helpful for refractory GERC by the inhibition of both acid and nonacid reflux. The limited studies have shown that it decreased the frequency of transient lower esophageal sphincter relaxations by 40-60% and acid or non-acid reflux episodes by 43% [6][7][8].…”
Section: Discussionmentioning
confidence: 99%
“…29 The clinical use of baclofen is, however, limited by its adverse effects on the central nervous system, which include dizziness and somnolence. In a recent proof-of-concept study, the newly developed GABA B receptor agonist lesogaberan, which appears to act predominantly in the periphery, significantly reduced reflux symptoms in patients with GERD with symptoms despite PPI therapy, and was well tolerated.…”
Section: Discussionmentioning
confidence: 99%
“…30 Another potential approach is treatment with a metabotropic glutamate receptor 5 (mGluR5) antagonist, which has been shown to inhibit TLESRs in animal studies. 29 The mGluR5 negative allosteric modulator ADX10059 significantly reduced the number of symptomatic reflux episodes in patients with GERD in clinical trials. 31 However, as with baclofen, clinical use of ADX10059 may be limited by commonly occurring adverse effects on the central nervous system, including dizziness and nausea.…”
Section: Discussionmentioning
confidence: 99%
“…Transient lower oesophageal sphincter relaxations are controlled by a vago-vagal reflex pathway, which is triggered by gastric distention, integrated in the brainstem and induces release of nitric oxide from intrinsic nerves at the LES. [36][37][38] Endocannabinoids can potentially control this vago-vagal reflex pathway at many points as CB1 receptors are expressed on vagal afferents, in the brain stem, on interneurons in the wall of the gastrointestinal tract and on postganglionic fibres innervating smooth muscle in the gastrointestinal tract. [39][40][41][42] In the dog, rimonabant only increased the number of TLESRs, whereas their characteristics and oesophageal motility were unchanged, and this was considered an argument in favour of a central site of action.…”
Section: Discussionmentioning
confidence: 99%