The antidepressant trans-2-phenylcyclopropylamine protects mice from high-fat-diet-induced obesity.

The antidepressant trans-2-phenylcyclopropylamine protects mice from high-fat-diet-induced obesity.
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DOI:
10.1371/journal.pone.0089199
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发表时间:
2014
期刊:
影响因子:
3.7
通讯作者:
Zong H
Zong H
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Shemesh A;Abdulla A;Yang F;Chua SC;Pessin JE;Zong H

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Mice treated with the antidepressant trans-2-phenylcyclopropylamine (2-PCPA) were protected against diet-induced-obesity, and adiposity was reversed in pre-established diet-induced obese mice. Contrary to a recent report that inhibition of lysine-specific demethylase-1 by 2-PCPA results in increased energy expenditure, long-term 2-PCPA treatment had no such effect but its protection against obesity was associated with increased spontaneous locomotor activity, Moreover, pair feeding to assure equal caloric intake in wild type mice as well as in genetic hyperphagic mice (ob/ob) also resulted in weight reduction in 2-PCPA treated mice that correlated with increased activity but no change in energy expenditure. Similarly, short-term intraperitoneal injections of 2-PCPA did not affect food intake but caused a substantial increase in locomotor activity in the light cycle that correlated with increased energy expenditure, whereas activity and energy expenditure were unchanged in the dark cycle. Lastly, 2-PCPA was also effective in reducing obesity in genetic UCP1 null mice. These data suggest that 2-PCPA can reduce obesity by decreasing food intake in the long term while increasing activity in the short-term. However, the protective and weight loss effects of 2-PCPA are independent of UCP1-regulated thermogenesis or basal energy expenditure.
DOI: 10.1007/bf00403623
发表时间: 1971-01-01
期刊: PSYCHOPHARMACOLOGIA
影响因子: --
作者:
HOLTZMAN, S;JEWETT, RE
通讯作者: JEWETT, RE
DOI: 10.1016/0006-8993(72)90789-5
发表时间: 1972-01-01
期刊: BRAIN RESEARCH
影响因子: 2.9
作者:
JONES, BE
通讯作者: JONES, BE
DOI: 10.1016/0014-5793(84)80120-9
发表时间: 1984-01-01
期刊: FEBS LETTERS
影响因子: 3.5
作者:
MORY, G;BOUILLAUD, F;RICQUIER, D
通讯作者: RICQUIER, D
DOI: 10.1079/bjn19840087
发表时间: 1984-01-01
影响因子: 3.6
作者:
DULLOO, AG;MILLER, DS
通讯作者: MILLER, DS
DOI: 10.1038/ncomms1755
发表时间: 2012-03-27
影响因子: 16.6
作者:
通讯作者: --