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在极度肥胖的大鼠中,胰岛淀粉样多肽/瘦素协同作用缺失,且热量限制诱导的体重减轻也无法恢复这种协同作用。

Amylin/leptin synergy is absent in extreme obesity and not restored by calorie restriction-induced weight loss in rats.

作者信息

Trevaskis J L, Wittmer C, Athanacio J, Griffin P S, Parkes D G, Roth J D

机构信息

Present address: MedImmune, Gaithersburg MD USA.

Amylin Pharmaceuticals San Diego CA USA.

出版信息

Obes Sci Pract. 2016 Dec;2(4):385-391. doi: 10.1002/osp4.62. Epub 2016 Sep 7.

Abstract

OBJECTIVE

Co-administration of amylin and leptin induces synergistic and clinically meaningful (>10%) weight loss that is attenuated as the degree of obesity increases. We explored whether calorie restriction (CR) could restore amylin/leptin synergy in very obese rats.

METHODS

Sprague Dawley rats on high-fat diet (696 ± 8 g,  = 72) were randomized to three cohorts (C1-C3). Rats in C1 were administered vehicle, rat amylin (50 µg kg d), murine leptin (125 µg kg d) or amylin and leptin for 28 days ( = 6 per group) via subcutaneous minipump. Simultaneously, C2 and C3 rats initiated CR. After moderate (12.4 ± 0.3%, 86.7 ± 2.8 g; C2) or severe (24.9 ± 0.3%, 172.7 ± 4.7 g; C3) weight loss, amylin and/or leptin was administered as described.

RESULTS

In C1, leptin did not alter weight, and amylin induced 40.2 ± 6.1 g weight loss (-6.0 ± 0.9%), which was not enhanced by leptin (44.4 ± 4.9 g, -6.1 ± 0.8%). In C2, vehicle-treated (75.1 ± 7.8 g weight change from start of treatment, 1.1 ± 0.8% difference from start of pre-CR phase) and leptin-treated rats (68.6 ± 9.2 g, -1.3 ± 1.0%) rebounded to pre-restriction weight that was attenuated by amylin (29.2 ± 11.4 g, -6.2 ± 0.7%). Leptin did not enhance the effect of amylin (22.8 ± 11.7 g, -8.3 ± 1.5%). In C3, vehicle-treated and leptin-treated rats regained most of their weight (161.9 ± 11.8, -2.3 ± 0.8% and 144.6 ± 9.5 g, -2.3 ± 0.9%, respectively), which was attenuated by amylin (91.1 ± 16.8 g, -11.2 ± 0.7%), but not enhanced by leptin (83.0 ± 7.6 g, -10.7 ± 0.8%).

CONCLUSIONS

Extreme obesity associated with leptin resistance perturbs amylin/leptin weight loss synergy in rats, which cannot be restored by pre-treatment weight loss.

摘要

目的

共施用胰岛淀粉样多肽和瘦素可诱导协同且具有临床意义(>10%)的体重减轻,且随着肥胖程度的增加,这种体重减轻作用会减弱。我们探究了热量限制(CR)是否能恢复极肥胖大鼠体内胰岛淀粉样多肽/瘦素的协同作用。

方法

将高脂饮食的斯普拉格-道利大鼠(696±8 g,n = 72)随机分为三组(C1 - C3)。C1组大鼠通过皮下微型泵接受赋形剂、大鼠胰岛淀粉样多肽(50 μg·kg·d)、小鼠瘦素(125 μg·kg·d)或胰岛淀粉样多肽与瘦素治疗28天(每组n = 6)。同时,C2组和C3组大鼠开始进行热量限制。在体重适度减轻(12.4±0.3%,86.7±2.8 g;C2组)或严重减轻(24.9±0.3%,172.7±4.7 g;C3组)后,按上述方法给予胰岛淀粉样多肽和/或瘦素。

结果

在C1组中,瘦素未改变体重,胰岛淀粉样多肽诱导体重减轻40.2±6.1 g(-6.0±0.9%),瘦素未增强此效果(44.4±4.9 g,-6.1±0.8%)。在C2组中,接受赋形剂治疗的大鼠(治疗开始后体重变化75.1±7.8 g,与热量限制前阶段开始时相比差异为1.1±0.8%)和接受瘦素治疗的大鼠(68.6±9.2 g,-1.3±1.0%)体重反弹至限制前水平,而胰岛淀粉样多肽减轻了体重反弹(29.2±11.4 g,-6.2±0.7%)。瘦素未增强胰岛淀粉样多肽的作用(22.8±11.7 g,-8.3±1.5%)。在C3组中,接受赋形剂治疗和瘦素治疗的大鼠体重大部分恢复(分别为161.9±11.8 g,-2.3±0.8%和144.6±9.5 g,-2.3±0.9%),胰岛淀粉样多肽减轻了体重恢复(91.1±16.8 g,-11.2±0.7%),但瘦素未增强此效果(83.0±7.6 g,-10.7±0.8%)。

结论

与瘦素抵抗相关的极度肥胖扰乱了大鼠体内胰岛淀粉样多肽/瘦素的体重减轻协同作用,且这种协同作用无法通过预处理减重来恢复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/404e/5523720/9aa022362e2b/OSP4-2-385-g001.jpg

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