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Clin Gastroenterol Hepatol ; 5(11): 1291-9, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17920338

RESUMO

BACKGROUND & AIMS: Orlistat is a weight management agent that selectively inhibits gastrointestinal lipase activity. Because of orlistat's mode of action, increased fecal fat is presented to the colonic mucosa, and fecal bile acid and free fatty acid composition may be altered during treatment. Our aim was to assess the effect of treatment of obese subjects with orlistat 120 mg 3 times a day for 6 weeks on fecal lipid and bile acid parameters and colonic mucosal cell proliferation. METHODS: Twenty-four obese (body mass index, 30-40 kg/m2) but otherwise healthy male and female subjects were enrolled in a single-center, randomized, double-blind, placebo-controlled, parallel-group study. Participants were hospitalized during days 1-3 and 33-42 of treatment and were treated as outpatients for the remaining days. RESULTS: Treatment with orlistat for 6 weeks resulted in significantly greater increases in fecal weight, total fecal fat, and fecal free fatty acids than placebo. Total fecal bile acid amounts decreased slightly with orlistat, and increased significantly with placebo treatment (P < .05 between-group difference). Orlistat did not alter colonic cell proliferation as assessed by the 3 proliferative indices (5-bromo-2-deoxyuridine, whole crypt mitotic count, and proliferating cell nuclear antigen). CONCLUSIONS: Biochemical changes in fecal composition related to the pharmacodynamic mode of action of orlistat are not accompanied by altered colonic cell proliferation, a putative biomarker of colon cancer risk.


Assuntos
Fármacos Antiobesidade/farmacologia , Ácidos e Sais Biliares/metabolismo , Gorduras na Dieta/metabolismo , Ácidos Graxos/metabolismo , Fezes/química , Lactonas/farmacologia , Obesidade/tratamento farmacológico , Adulto , Idoso , Fármacos Antiobesidade/uso terapêutico , Biópsia , Bromodesoxiuridina/metabolismo , Proliferação de Células , Colo/metabolismo , Colo/patologia , Dieta com Restrição de Gorduras , Método Duplo-Cego , Feminino , Humanos , Lactonas/uso terapêutico , Masculino , Pessoa de Meia-Idade , Índice Mitótico , Obesidade/metabolismo , Orlistate , Antígeno Nuclear de Célula em Proliferação/metabolismo
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