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Neurogastroenterol Motil ; 22(11): 1183-90, e314, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20584263

RESUMO

BACKGROUND: It is widely reported that hexose sugars slow gastric emptying (GE) via osmoreceptor stimulation but this remains uncertain. We evaluated the effects of a panel of hexoses of differing molecular structure, assessing the effects of osmolality, intra-individual reproducibility and the role of the CCK(1) receptor, in the regulation of GE by hexoses. METHODS: Thirty one healthy non-obese male and female subjects were studied in a series of protocols, using a (13) C-acetate breath test to evaluate GE of varying concentrations of glucose, galactose, fructose and tagatose, with water, NaCl and lactulose as controls. GE was further evaluated following the administration of a CCK(1) receptor antagonist. Three subjects underwent repeated studies to evaluate intra-individual reproducibility. KEY RESULTS: At 250 mOsmol, a hexose-specific effect was apparent: tagatose slowed GE more potently than water, glucose and fructose (P < 0.05). Fructose (P < 0.05) also slowed GE, but with substantial inter-, but not intra-, individual differences. As osmolality increased further the hexose-specific differences were lost. At 500 mOsmol, all hexoses slowed GE compared with water (P < 0.05), whereas lactulose and saline did not. The slowing of GE by hexose sugars appeared to be CCK(1) receptor-dependent. CONCLUSIONS & INFERENCES: The effects of hexose sugars on GE appear related to their molecular structure rather than osmolality per se, and are, at least in part, CCK(1) receptor-dependent.


Assuntos
Esvaziamento Gástrico/efeitos dos fármacos , Hexoses/química , Hexoses/farmacologia , Receptor de Colecistocinina A/fisiologia , Acetatos/metabolismo , Adulto , Área Sob a Curva , Dióxido de Carbono/metabolismo , Feminino , Esvaziamento Gástrico/fisiologia , Trânsito Gastrointestinal/efeitos dos fármacos , Hexoses/metabolismo , Humanos , Masculino , Concentração Osmolar , Técnicas de Patch-Clamp , Ácidos Pentanoicos/farmacologia , Receptor de Colecistocinina A/antagonistas & inibidores , Reprodutibilidade dos Testes , Relação Estrutura-Atividade
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