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缺乏溶血磷脂酸受体-1的小鼠改变了食物的消耗。

Altered food consumption in mice lacking lysophosphatidic acid receptor-1.

机构信息

Institut de Médecine Moléculaire de Rangueil, INSERM U858, IFR31, Université Paul Sabatier, BP 84225, F-31432, Toulouse cedex 4, France.

出版信息

J Physiol Biochem. 2009 Dec;65(4):345-50. doi: 10.1007/BF03185929.

Abstract

The release of lysophosphatidic acid (LPA) by adipocytes has previously been proposed to play a role in obesity and associated pathologies such as insulin resistance and diabetes. In the present work, the sensitivity to diet-induced obesity was studied in mice lacking one of the LPA receptor subtype (LPA1R). Conversely to what was observed in wild type (WT) mice, LPA1R-KO-mice fed a high fat diet (HFD) showed no significant increase in body weight or fat mass when compared to low fat diet (LFD). In addition, in contrast to what was observed in WT mice, LPA1R-KO mice did not exhibit over-consumption of food associated with HFD. Surprisingly, when fed a LFD, LPA1R-KO mice exhibited significant higher plasma leptin concentration and higher level of adipocyte leptin mRNA than WT mice. In conclusion, LPA1R-KO mice were found to be resistant to diet-induced obesity consecutive to a resistance to fat-induced over-consumption of food that may result at least in part from alterations in leptin expression and production.

摘要

先前有研究提出,脂肪细胞释放的溶血磷脂酸(LPA)在肥胖及其相关病症(如胰岛素抵抗和糖尿病)中发挥作用。在本研究中,研究人员研究了缺乏 LPA 受体亚型之一(LPA1R)的小鼠对饮食诱导肥胖的敏感性。与野生型(WT)小鼠不同的是,与低脂饮食(LFD)相比,高脂饮食(HFD)喂养的 LPA1R-KO 小鼠的体重或脂肪量没有明显增加。此外,与 WT 小鼠不同的是,LPA1R-KO 小鼠没有出现与 HFD 相关的过度摄食。令人惊讶的是,当喂食 LFD 时,LPA1R-KO 小鼠的血浆瘦素浓度和脂肪细胞瘦素 mRNA 水平明显高于 WT 小鼠。总之,LPA1R-KO 小鼠对饮食诱导的肥胖具有抗性,这种抗性可能与脂肪诱导的过度摄食有关,而脂肪诱导的过度摄食至少部分是由于瘦素表达和产生的改变所致。

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