2000
DOI: 10.1016/s0016-5107(00)14669-3
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6998 Effects of synthetic prostaglandins e1 and f2a on motility of the sphincter of oddi in humans.

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Cited by 2 publications
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“…Dysfunction of Oddi's sphincter could be the outcome of loss of myenteric inhibitory neurones resulting in opposing cholinergic tone. The somatostatin analogue, octreotide, and the synthetic prostaglandin E 1 analogue, alprostadil alfadex, reduce the pressure of Oddi's sphincter and might be valuable in the management of the postcholecystectomy syndrome (Fazel et al 2002; Koshitani et al 2002).…”
Section: The Gall Bladdermentioning
confidence: 99%
“…Dysfunction of Oddi's sphincter could be the outcome of loss of myenteric inhibitory neurones resulting in opposing cholinergic tone. The somatostatin analogue, octreotide, and the synthetic prostaglandin E 1 analogue, alprostadil alfadex, reduce the pressure of Oddi's sphincter and might be valuable in the management of the postcholecystectomy syndrome (Fazel et al 2002; Koshitani et al 2002).…”
Section: The Gall Bladdermentioning
confidence: 99%
“…PGE 1 and PGE 2 induce relaxation of the SO in animals, whereas PGF 2␣ evokes contraction, probably a pharmacologic action. A synthetic prostaglandin E 1 , alprostadil alfadex, markedly reduces sphincter tone and contractile activity in humans undergoing ERCP [28]. This agent may therefore find a therapeutic use in biliary endoscopy or for SO dysfunction.…”
Section: Prostaglandins and L-type Calcium Channel Antagonistsmentioning
confidence: 99%