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全剂量与分剂量奥利司他对膳食脂肪吸收抑制作用的比较。

Comparison of the inhibition of dietary fat absorption by full versus divided doses of orlistat.

作者信息

Hussain Y, Güzelhan C, Odink J, van der Beek E J, Hartmann D

机构信息

Pharma Clinical Research, F. Hoffmann-La Roche, Ltd. Basel, Switzerland.

出版信息

J Clin Pharmacol. 1994 Nov;34(11):1121-5. doi: 10.1002/j.1552-4604.1994.tb01990.x.

DOI:10.1002/j.1552-4604.1994.tb01990.x
PMID:7876405
Abstract

Orlistat is a potent and selective inhibitor of gastrointestinal lipases. The drug is designed for the treatment of obesity. The effect on dietary fat absorption of orlistat after administration of divided doses spread over 2 hours from mid-meal, in comparison with that after administration of a full dose mid-meal, was investigated in a randomized, single-blind study including 16 hospitalized healthy males. After a 5-day run-in, to accustom the subjects to a diet of 2350 kcal and 76 g fat per day and to establish baseline fecal fat excretion, subjects received, in two parallel groups of eight over 8 days, three times a day 80 mg orlistat at mid-meal, and placebo at mid-meal and 0.5, 1, and 2 hr after mid-meal (group A), or placebo at mid-meal, and 20 mg orlistat at mid-meal and 0.5, 1, and 2 hr after mid-meal (group B). Feces were collected to measure total fat excretion. The mean (SD) of fecal fat in percent of dietary fat, after deduction of pretreatment fecal fat, was (%) 36.1 (4.2) and 37.0 (9.3) in groups A and B, respectively. Changing the mode of administration of orlistat, within the dose regimens investigated, does not affect its pharmacologic efficacy.

摘要

奥利司他是一种强效且具有选择性的胃肠道脂肪酶抑制剂。该药物用于治疗肥胖症。在一项包括16名住院健康男性的随机、单盲研究中,研究了从餐中开始分剂量在2小时内给药的奥利司他与餐中给予全剂量后对饮食中脂肪吸收的影响。经过5天的导入期,为使受试者适应每天2350千卡热量和76克脂肪的饮食并建立粪便脂肪排泄基线,在8天内将受试者分为两组,每组8人,一组在餐中每天三次服用80毫克奥利司他,餐中及餐后0.5、1和2小时服用安慰剂(A组),另一组餐中服用安慰剂,餐中及餐后0.5、1和2小时服用20毫克奥利司他(B组)。收集粪便以测量总脂肪排泄量。扣除预处理粪便脂肪后,A组和B组粪便脂肪占饮食脂肪的百分比均值(标准差)分别为(%)36.1(4.2)和37.0(9.3)。在所研究的剂量方案范围内,改变奥利司他的给药方式不会影响其药理疗效。

相似文献

1
Comparison of the inhibition of dietary fat absorption by full versus divided doses of orlistat.全剂量与分剂量奥利司他对膳食脂肪吸收抑制作用的比较。
J Clin Pharmacol. 1994 Nov;34(11):1121-5. doi: 10.1002/j.1552-4604.1994.tb01990.x.
2
Effect on dietary fat absorption of orlistat, administered at different times relative to meal intake.相对于进餐时间,在不同时间服用奥利司他对膳食脂肪吸收的影响。
Br J Clin Pharmacol. 1993 Sep;36(3):266-70. doi: 10.1111/j.1365-2125.1993.tb04228.x.
3
The interaction of the lipase inhibitor orlistat with ethanol in healthy volunteers.健康志愿者中脂肪酶抑制剂奥利司他与乙醇的相互作用。
Eur J Clin Pharmacol. 1998 Nov-Dec;54(9-10):773-7. doi: 10.1007/s002280050550.
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Influence of dietary composition on the inhibition of fat absorption by orlistat.饮食成分对奥利司他抑制脂肪吸收的影响。
J Int Med Res. 1994 Sep-Oct;22(5):255-65. doi: 10.1177/030006059402200502.
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Reduction of dietary fat absorption by the novel gastrointestinal lipase inhibitor cetilistat in healthy volunteers.新型胃肠道脂肪酶抑制剂西替利司他对健康志愿者膳食脂肪吸收的影响
Br J Clin Pharmacol. 2009 Mar;67(3):309-15. doi: 10.1111/j.1365-2125.2008.03311.x. Epub 2008 Sep 19.
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Retrospective population-based analysis of the dose-response (fecal fat excretion) relationship of orlistat in normal and obese volunteers.基于人群的回顾性分析:奥利司他在正常和肥胖志愿者中的剂量反应(粪便脂肪排泄)关系。
Clin Pharmacol Ther. 1994 Jul;56(1):82-5. doi: 10.1038/clpt.1994.104.
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Pharmacodynamic equivalence of two orlistat capsule formulations in healthy volunteers under fed conditions.两种奥利司他胶囊制剂在进食条件下对健康志愿者的药效学等效性。
Int J Clin Pharmacol Ther. 2008 Jun;46(6):319-26. doi: 10.5414/cpp46319.
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Influence of orlistat on the regulation of gallbladder contraction in man: a randomized double-blind placebo-controlled crossover study.奥利司他对人体胆囊收缩调节的影响:一项随机双盲安慰剂对照交叉研究。
Dig Dis Sci. 1996 Dec;41(12):2404-8. doi: 10.1007/BF02100135.
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Lipase inhibition attenuates the acute inhibitory effects of oral fat on food intake in healthy subjects.脂肪酶抑制可减弱口服脂肪对健康受试者食物摄入量的急性抑制作用。
Br J Nutr. 2003 Nov;90(5):849-52. doi: 10.1079/bjn2003971.
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Effect of orlistat on fecal fat, fecal biliary acids, and colonic cell proliferation in obese subjects.奥利司他对肥胖受试者粪便脂肪、粪便胆汁酸及结肠细胞增殖的影响。
Clin Gastroenterol Hepatol. 2007 Nov;5(11):1291-9. doi: 10.1016/j.cgh.2007.07.009. Epub 2007 Oct 24.

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