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饮食诱导的肥胖以组织特异性方式上调GPR43和GPR120的丰度。

Diet-induced obesity up-regulates the abundance of GPR43 and GPR120 in a tissue specific manner.

作者信息

Cornall Lauren M, Mathai Michael L, Hryciw Deanne H, McAinch Andrew J

机构信息

Biomedical and Lifestyle Diseases Unit, School of Biomedical and Health Sciences, Victoria University, Melbourne, Australia.

出版信息

Cell Physiol Biochem. 2011;28(5):949-58. doi: 10.1159/000335820. Epub 2011 Dec 15.

Abstract

BACKGROUND/AIMS: GPR43 and GPR120 have recently been deorphanised as receptors for fatty acids. Fatty acids mediate a variety of metabolic processes in the body, however, the effect these receptors have on metabolism is not fully understood. Here, we characterise the effect of diet-induced obesity on the expression of GPR43 and GPR120 in tissues important in maintaining metabolic health.

METHODS

Six-week old male Sprague Dawley rats were fed either a high fat diet (HFD; 22% fat) or control diet (5% fat; n = 8-9/group) for 12 weeks. Rats were euthanized and the heart, liver, soleus and extensor digitorum longus (EDL) skeletal muscles were excised. GPR43 and GPR120 receptor abundance was quantified by 'real-time' PCR.

RESULTS

GPR43 mRNA abundance was significantly up-regulated by a HFD in liver and soleus and EDL skeletal muscles compared to control (p ≤ 0.05). Whilst a HFD significantly up-regulated GPR120 gene transcripts in cardiac tissue and EDL skeletal muscle when compare to control (p ≤ 0.05).

CONCLUSION

We have shown for the first time that up-regulation of GPR43 and GPR120 in response to a HFD, is tissue specific. This suggests these receptors have different roles in mediating metabolic function in a number of tissues in the human body.

摘要

背景/目的:GPR43和GPR120最近已被鉴定为脂肪酸受体。脂肪酸介导体内多种代谢过程,然而,这些受体对代谢的影响尚未完全了解。在此,我们研究饮食诱导的肥胖对维持代谢健康重要组织中GPR43和GPR120表达的影响。

方法

六周龄雄性Sprague Dawley大鼠分别喂食高脂饮食(HFD;22%脂肪)或对照饮食(5%脂肪;每组n = 8 - 9只)12周。对大鼠实施安乐死后,切除心脏、肝脏、比目鱼肌和趾长伸肌(EDL)骨骼肌。通过“实时”PCR定量GPR43和GPR120受体丰度。

结果

与对照组相比,高脂饮食显著上调肝脏、比目鱼肌和EDL骨骼肌中GPR43 mRNA丰度(p≤0.05)。与对照组相比,高脂饮食显著上调心脏组织和EDL骨骼肌中GPR120基因转录本(p≤0.05)。

结论

我们首次表明,高脂饮食引起的GPR43和GPR120上调具有组织特异性。这表明这些受体在介导人体多种组织的代谢功能中具有不同作用。

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