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饮食诱导的大麻素 2 型受体敲除小鼠和大麻素受体 1/2 双敲除小鼠肥胖。

Diet-Induced Obesity in Cannabinoid-2 Receptor Knockout Mice and Cannabinoid Receptor 1/2 Double-Knockout Mice.

机构信息

Department of Family Medicine, Michigan State University, East Lansing, Michigan, USA.

Department of Physiology, Michigan State University, East Lansing, Michigan, USA.

出版信息

Obesity (Silver Spring). 2019 Mar;27(3):454-461. doi: 10.1002/oby.22403. Epub 2019 Jan 30.

Abstract

OBJECTIVE

Evidence suggests that cannabinoid-1 receptor (CB1R) activation is associated with increased food intake and body weight gain. Human epidemiological studies, however, show decreased prevalence of obesity in cannabis users. Given the overlapping and complementary functions of the cannabinoid receptors (CB1R and CB2R), mice lacking CB2R and mice lacking both CB1R and CB2R were studied.

METHODS

A high-fat diet was used to study metabolic changes in male mice lacking CB2R (CB2 ) or lacking both CB1R and CB2R (double-knockout [CB-DKO]) compared with wild-type mice.

RESULTS

When CB2 mice were maintained on a high-fat diet, their weight gain was not different from wild-type mice (gaining 19 and 21 g, respectively), whereas CB-DKO mice gained only 5 g. There were no significant differences in food intake or locomotor activity between the three groups. Respiratory exchange rate and heat production were elevated in CB-DKO mice, with upregulation of adipose tissue thermogenic genes. Glucose tolerance test and insulin levels indicated increased insulin sensitivity in CB-DKO mice, whereas CB2 displayed signs of impaired glucose clearance.

CONCLUSIONS

These results indicate that lacking both CB1R and CB2R protected mice from diet-induced obesity, possibly through the prominent role of CB1R in obesity or through an interactive effect of both receptors.

摘要

目的

有证据表明,大麻素-1 型受体(CB1R)的激活与食物摄入增加和体重增加有关。然而,人类流行病学研究表明,大麻使用者中肥胖的患病率降低。鉴于大麻素受体(CB1R 和 CB2R)的重叠和互补功能,研究了缺乏 CB2R 的小鼠和缺乏 CB1R 和 CB2R 的双敲除(CB-DKO)小鼠。

方法

使用高脂肪饮食研究缺乏 CB2R(CB2)或缺乏 CB1R 和 CB2R(双敲除 [CB-DKO])的雄性小鼠与野生型小鼠相比代谢变化。

结果

当 CB2 小鼠维持在高脂肪饮食时,它们的体重增加与野生型小鼠没有区别(分别增加 19 和 21g),而 CB-DKO 小鼠仅增加 5g。三组之间的食物摄入量或运动活性没有显着差异。呼吸交换率和产热在 CB-DKO 小鼠中升高,脂肪组织产热基因上调。葡萄糖耐量试验和胰岛素水平表明 CB-DKO 小鼠胰岛素敏感性增加,而 CB2 显示葡萄糖清除受损的迹象。

结论

这些结果表明,缺乏 CB1R 和 CB2R 可防止小鼠因饮食引起的肥胖,这可能是由于 CB1R 在肥胖中的突出作用,或者是由于两种受体的相互作用。

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