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本文引用的文献

1
Activation of the cholinergic antiinflammatory pathway ameliorates obesity-induced inflammation and insulin resistance.胆碱能抗炎通路的激活可改善肥胖引起的炎症和胰岛素抵抗。
Endocrinology. 2011 Mar;152(3):836-46. doi: 10.1210/en.2010-0855. Epub 2011 Jan 14.
2
Associations of smoking cessation with visceral fat area and prevalence of metabolic syndrome in men: the Hitachi health study.吸烟与男性内脏脂肪面积和代谢综合征患病率的关联:日立健康研究。
Obesity (Silver Spring). 2011 Mar;19(3):647-51. doi: 10.1038/oby.2010.237. Epub 2010 Oct 21.
3
High fat diet altered the mechanism of energy homeostasis induced by nicotine and withdrawal in C57BL/6 mice.高脂饮食改变了尼古丁诱导和戒断引起的 C57BL/6 小鼠能量平衡的机制。
Mol Cells. 2010 Sep;30(3):219-26. doi: 10.1007/s10059-010-0110-3. Epub 2010 Aug 23.
4
Smoking expectancies, weight concerns, and dietary behaviors in adolescence.青少年的吸烟预期、体重担忧和饮食行为。
Pediatrics. 2010 Jul;126(1):e66-72. doi: 10.1542/peds.2009-2381. Epub 2010 Jun 14.
5
Cigarette smoking exacerbates nonalcoholic fatty liver disease in obese rats.吸烟可使肥胖大鼠的非酒精性脂肪肝病情恶化。
Hepatology. 2010 May;51(5):1567-76. doi: 10.1002/hep.23516.
6
Prevalence and trends in obesity among US adults, 1999-2008.美国成年人肥胖率的流行趋势及变化,1999-2008 年。
JAMA. 2010 Jan 20;303(3):235-41. doi: 10.1001/jama.2009.2014. Epub 2010 Jan 13.
7
The effects of chronic nicotine on meal patterns, food intake, metabolism and body weight of male rats.慢性尼古丁对雄性大鼠的进食模式、食物摄入、代谢和体重的影响。
Pharmacol Biochem Behav. 2010 Mar;95(1):92-9. doi: 10.1016/j.pbb.2009.12.012. Epub 2009 Dec 24.
8
Second-hand smoke stimulates lipid accumulation in the liver by modulating AMPK and SREBP-1.二手烟通过调节 AMPK 和 SREBP-1 刺激肝脏脂质积累。
J Hepatol. 2009 Sep;51(3):535-47. doi: 10.1016/j.jhep.2009.03.026. Epub 2009 May 18.
9
Multimodality rodent imaging chambers for use under barrier conditions with gas anesthesia.用于屏障条件下气体麻醉的多模态啮齿动物成像室。
Mol Imaging Biol. 2009 Mar-Apr;11(2):100-6. doi: 10.1007/s11307-008-0165-0. Epub 2008 Aug 5.
10
Long-term cigarette smoke exposure increases uncoupling protein expression but reduces energy intake.长期接触香烟烟雾会增加解偶联蛋白的表达,但会减少能量摄入。
Brain Res. 2008 Sep 4;1228:81-8. doi: 10.1016/j.brainres.2008.06.067. Epub 2008 Jun 26.

尼古丁对小鼠体成分的影响。

Effect of nicotine on body composition in mice.

机构信息

Division of Endocrinology, Department of Medicine, Charles R. Drew University of Medicine and Sciences-UCLA School of Medicine, 1731 East 120th Street, Los Angeles, California 90059, USA.

出版信息

J Endocrinol. 2012 Mar;212(3):317-26. doi: 10.1530/JOE-11-0350. Epub 2011 Dec 2.

DOI:10.1530/JOE-11-0350
PMID:22138237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3444240/
Abstract

Nicotine induces weight loss in both humans and rodents consuming a regular diet; however, the effect of nicotine on body weight and fat composition in rodents consuming a high-fat diet (HFD) has not been well studied. Thus, this study examined the effect of nicotine vs saline on body weight and fat composition in mice fed with either an HFD (62% of kcal from fat) or a standard normal chow diet (NCD) for 7 weeks. Nicotine dose dependently reduced body weight gain in mice that consumed both diets, but this effect was significantly greater in mice on the HFD. Caloric intake was decreased in nicotine-treated mice. Estimates of energy intake suggested that decreased caloric intake accounted for all the reduced weight gain in mice on an NCD and 66% of the reduced weight gain on an HFD. Computed tomography analysis for fat distribution demonstrated that nicotine was effective in reducing abdominal fat in mice that consumed the HFD, with nicotine treatment leading to lower visceral fat. The effect of nicotine on weight loss in mice on an HFD was completely blocked by mecamylamine, a nonselective nicotinic acetylcholine receptor (nAChR) antagonist, but only partially blocked by the α4β2 nAChR partial agonist/antagonist, varenicline. We conclude that nicotine is effective in preventing HFD-induced weight gain and abdominal fat accumulation.

摘要

尼古丁会导致食用常规饮食的人类和啮齿动物体重减轻;然而,尼古丁对食用高脂肪饮食(HFD)的啮齿动物体重和脂肪组成的影响尚未得到充分研究。因此,本研究检查了尼古丁与盐水对 7 周内分别喂食高脂肪饮食(62%的卡路里来自脂肪)或标准正常饮食(NCD)的小鼠体重和脂肪组成的影响。尼古丁剂量依赖性地降低了两种饮食的小鼠体重增加,但在 HFD 饮食的小鼠中这种作用更为明显。尼古丁处理的小鼠的热量摄入减少。能量摄入的估计表明,减少的热量摄入解释了 NCD 组小鼠体重减轻的全部原因,以及 HFD 组小鼠体重减轻的 66%。用于脂肪分布的计算机断层扫描分析表明,尼古丁可有效减少 HFD 饮食小鼠的腹部脂肪,尼古丁治疗导致内脏脂肪减少。美加仑胺,一种非选择性烟碱型乙酰胆碱受体(nAChR)拮抗剂,完全阻断了尼古丁在 HFD 饮食的小鼠中减轻体重的作用,但仅部分阻断了 α4β2 nAChR 部分激动剂/拮抗剂伐尼克兰的作用。我们得出的结论是,尼古丁有效预防 HFD 引起的体重增加和腹部脂肪堆积。