• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Studies on the antiobesity activity of tetrahydrolipstatin, a potent and selective inhibitor of pancreatic lipase.

作者信息

Hogan S, Fleury A, Hadvary P, Lengsfeld H, Meier M K, Triscari J, Sullivan A C

机构信息

Hoffmann-La Roche Inc., Nutley, NJ 07110.

出版信息

Int J Obes. 1987;11 Suppl 3:35-42.

PMID:3440690
Abstract

In summary, THL is a potent inhibitor of pancreatic lipase, which is both selective and irreversible in its action in vitro. It is also likely that THL inhibits pancreatic lipase in vivo, since its acute administration to mice and squirrel monkeys suppresses absorption of dietary triglycerides, without an apparent alteration in the absorption of fatty acids. The marked loss in body weight and carcass fat of DIO rats with subchronic administration of THL strongly suggests that inhibition of pancreatic lipase is a feasible strategy for the treatment of obesity. Whether obese humans will overeat in response to a reduction in body energy stores is not known. However, it is probable that compliance to a therapy which maintains the present level of food intake while inducing excretion of dietary fat, will be greater than a reducing diet alone or conjunction with the currently available antiobesity drugs.

摘要

相似文献

1
Studies on the antiobesity activity of tetrahydrolipstatin, a potent and selective inhibitor of pancreatic lipase.
Int J Obes. 1987;11 Suppl 3:35-42.
2
Antiobesity potential of ursolic acid stearoyl glucoside by inhibiting pancreatic lipase.熊果酸硬脂酰葡萄糖苷通过抑制胰脂肪酶发挥其抗肥胖潜力。
Eur J Pharmacol. 2013 Jun 5;709(1-3):28-36. doi: 10.1016/j.ejphar.2013.02.032. Epub 2013 Mar 13.
3
The 2',4',6'-trihydroxyacetophenone isolated from Myrcia multiflora has antiobesity and mixed hypolipidemic effects with the reduction of lipid intestinal absorption.从桃金娘科复蕊木中分离得到的 2',4',6'-三羟基苯乙酮具有抗肥胖作用和混合降血脂作用,能减少脂质的肠道吸收。
Planta Med. 2011 Sep;77(14):1569-74. doi: 10.1055/s-0030-1270956. Epub 2011 Apr 6.
4
Anti-obesity effects in rodents of dietary teasaponin, a lipase inhibitor.脂肪酶抑制剂——茶皂素对啮齿动物的抗肥胖作用。
Int J Obes Relat Metab Disord. 2001 Oct;25(10):1459-64. doi: 10.1038/sj.ijo.0801747.
5
Effects of tetrahydrolipstatin, a lipase inhibitor, on absorption of fat from the intestine of the rat.脂肪酶抑制剂四氢脂抑素对大鼠肠道脂肪吸收的影响。
Biochim Biophys Acta. 1989 Feb 20;1001(3):249-55. doi: 10.1016/0005-2760(89)90107-0.
6
Cetilistat (ATL-962), a novel pancreatic lipase inhibitor, ameliorates body weight gain and improves lipid profiles in rats.西替利司他(ATL-962)是一种新型的胰脂肪酶抑制剂,可改善大鼠体重增加并改善血脂情况。
Horm Metab Res. 2008 Aug;40(8):539-43. doi: 10.1055/s-2008-1076699. Epub 2008 May 21.
7
Initial studies in humans with the novel gastrointestinal lipase inhibitor Ro 18-0647 (tetrahydrolipstatin).对新型胃肠道脂肪酶抑制剂Ro 18 - 0647(四氢脂抑素)进行的人体初步研究。
Am J Clin Nutr. 1992 Jan;55(1 Suppl):309S-313S. doi: 10.1093/ajcn/55.1.309s.
8
Inhibition of pancreatic lipase by poloxamer 407 may provide an adjunct treatment strategy for weight loss.
J Pharm Pharmacol. 2006 Aug;58(8):1099-105. doi: 10.1211/jpp.58.8.0011.
9
Reduction of fat storage in mice fed a high-fat diet long term by treatment with saponins prepared from Kochia scoparia fruit.通过用地肤果实制备的皂苷处理长期喂食高脂饮食的小鼠来减少脂肪储存。
Phytother Res. 2006 Oct;20(10):877-82. doi: 10.1002/ptr.1981.
10
Antiobesity action of epsilon-polylysine, a potent inhibitor of pancreatic lipase.ε-聚赖氨酸(一种有效的胰脂肪酶抑制剂)的抗肥胖作用
J Lipid Res. 2006 Aug;47(8):1852-8. doi: 10.1194/jlr.M600168-JLR200. Epub 2006 May 24.

引用本文的文献

1
Functionally overlapping intra- and extralysosomal pathways promote bis(monoacylglycero)phosphate synthesis in mammalian cells.功能上重叠的内溶酶体和外溶酶体途径促进了哺乳动物细胞中双(单酰基甘油)磷酸的合成。
Nat Commun. 2024 Nov 16;15(1):9937. doi: 10.1038/s41467-024-54213-1.
2
Orlistat for the treatment of antipsychotic-induced weight gain: an eight-week multicenter, randomized, placebo-controlled, double-blind trial.奥利司他治疗抗精神病药引起的体重增加:一项为期 8 周的多中心、随机、安慰剂对照、双盲试验。
Lipids Health Dis. 2024 Jul 24;23(1):225. doi: 10.1186/s12944-024-02214-w.
3
Selective measurement of NAPE-PLD activity via a PLA-resistant fluorogenic N-acyl-phosphatidylethanolamine analog.
通过一种 PLA 抗性荧光 N-酰基磷脂酰乙醇胺类似物选择性测量 NAPE-PLD 活性。
J Lipid Res. 2022 Jan;63(1):100156. doi: 10.1016/j.jlr.2021.100156. Epub 2021 Nov 26.
4
A stereoselective synthesis of (-)-tetrahydrolipstatin.(-)-四氢脂抑素的立体选择性合成。
Chem Commun (Camb). 1999;1999(17):1743-1744. doi: 10.1039/A904533C.
5
Obesity: Current and potential pharmacotherapeutics and targets.肥胖症:当前及潜在的药物治疗方法与靶点
Pharmacol Ther. 2017 Feb;170:116-147. doi: 10.1016/j.pharmthera.2016.10.015. Epub 2016 Oct 20.
6
Endoplasmic Reticulum Lipid Flux Influences Enterocyte Nuclear Morphology and Lipid-dependent Transcriptional Responses.内质网脂质通量影响肠上皮细胞核形态及脂质依赖性转录反应。
J Biol Chem. 2016 Nov 4;291(45):23804-23816. doi: 10.1074/jbc.M116.749358. Epub 2016 Sep 21.
7
Fatty Acids and Breast Cancer: Make Them on Site or Have Them Delivered.脂肪酸与乳腺癌:原位生成还是外源性供给。
J Cell Physiol. 2016 Oct;231(10):2128-41. doi: 10.1002/jcp.25332. Epub 2016 Feb 16.
8
Benefit-risk assessment of orlistat in the treatment of obesity.奥利司他治疗肥胖症的获益-风险评估。
Drug Saf. 2014 Aug;37(8):597-608. doi: 10.1007/s40264-014-0210-7.
9
A genome scale overexpression screen to reveal drug activity in human cells.一种在人类细胞中揭示药物活性的全基因组过表达筛选。
Genome Med. 2014 Apr 29;6(4):32. doi: 10.1186/gm549. eCollection 2014.
10
Critical role of neutral cholesteryl ester hydrolase 1 in cholesteryl ester hydrolysis in murine macrophages.中性胆固醇酯水解酶1在小鼠巨噬细胞胆固醇酯水解中的关键作用
J Lipid Res. 2014 Oct;55(10):2033-40. doi: 10.1194/jlr.M047787. Epub 2014 May 27.