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组胺 H 受体反向激动剂匹哚尼沙明可降低肥胖小鼠的体重。

The histamine H receptor inverse agonist pitolisant reduces body weight in obese mice.

机构信息

Department of Pharmacodynamics, Jagiellonian University Medical College, 9 Medyczna Street, 30-688, Krakow, Poland.

Department of Technology and Biotechnology of Drugs, Faculty of Pharmacy, Jagiellonian University Medical College, Krakow, Poland.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2018 Aug;391(8):875-881. doi: 10.1007/s00210-018-1516-2. Epub 2018 May 25.

Abstract

The pharmacological profile of pitolisant, a histamine H receptor antagonist/inverse agonist, indicates that this compound might reduce body weight and metabolic disturbances. Therefore, we studied the influence of pitolisant on body weight, water and sucrose intake as well as metabolic disturbances in the high-fat and high-sugar diet-induced obesity model in mice. To induce obesity, male CD-1 mice were fed a high-fat diet consisting of 40% fat blend for 14 weeks, water and 30% sucrose solution available ad libitum. Glucose tolerance test was performed at the beginning of week 15. Insulin tolerance was tested the day after. At the end of study, plasma levels of triglycerides and cholesterol were determined. Pitolisant at dose of 10 mg/kg bw (ip) was administrated during 14 days, starting from the beginning of week 13. Metformin at dose of 100 mg/kg bw (ip) was used as reference drug. Mice fed with high-fat diet and sucrose solution showed more weight gain throughout the 12-week period of inducing obesity. Animals fed with high-fat diet and treated with pitolisant (for the next 14 days) showed significantly less weight gain than mice from the control group consuming a high-fat feed. In the group treated with pitolisant, glucose levels were significantly lower than glucose levels of control obese mice after glucose load. The plasma triglyceride levels in pitolisant-treated mice were significantly lower compared with those in control obese group. In conclusion, pitolisant has a favorable influence of body weight and improves glucose tolerance and the lipid profile in obese mice.

摘要

匹哚沙明是一种组胺 H 受体拮抗剂/反向激动剂,其药理学特性表明,这种化合物可能会降低体重和代谢紊乱。因此,我们研究了匹哚沙明对高脂肪和高糖饮食诱导肥胖模型中小鼠体重、水和蔗糖摄入量以及代谢紊乱的影响。为了诱导肥胖,雄性 CD-1 小鼠喂食高脂肪饮食,其中包含 40%的脂肪混合物,持续 14 周,同时可自由摄取水和 30%的蔗糖溶液。在第 15 周开始时进行葡萄糖耐量测试,次日进行胰岛素耐量测试。在研究结束时,测定血浆中甘油三酯和胆固醇的水平。从第 13 周开始,14 天内每天腹腔注射 10mg/kg bw 的匹哚沙明。将 100mg/kg bw 的二甲双胍作为参考药物。在 12 周的肥胖诱导期内,喂食高脂肪和蔗糖溶液的小鼠体重明显增加。与喂食高脂肪饲料的对照组相比,喂食高脂肪饮食并接受匹哚沙明治疗(在接下来的 14 天内)的动物体重增加明显减少。在接受匹哚沙明治疗的组中,与肥胖对照组相比,葡萄糖负荷后血糖水平明显降低。与肥胖对照组相比,接受匹哚沙明治疗的小鼠的血浆甘油三酯水平明显降低。总之,匹哚沙明对体重有有利影响,并改善肥胖小鼠的葡萄糖耐量和血脂谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60cb/6061715/05272c4f281f/210_2018_1516_Fig1_HTML.jpg

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