Mechaly Alejandro S, Richardson Ebony, Rinkwitz Silke
Dept. of Physiology, Sydney Medical School, University of Sydney, Camperdown 2050, Australia.
Dept. of Physiology, Sydney Medical School, University of Sydney, Camperdown 2050, Australia.
Gen Comp Endocrinol. 2017 May 15;246:233-240. doi: 10.1016/j.ygcen.2016.12.013. Epub 2016 Dec 29.
Serotonin has been implicated in the inhibition of food intake in vertebrates. However, the mechanisms through which serotonin acts has yet to be elucidated. Recently, ETV5 (ets variant gene 5) has been associated with obesity and food intake control mechanisms in mammals. We have analyzed a putative physiological function of the two etv5 paralogous genes (etv5a and etv5b) in neuronal food intake control in adult zebrafish that have been exposed to different nutritional conditions. A feeding assay was established and fluoxetine, a selective serotonin re-uptake inhibitor (SSRI), was applied. Gene expression changes in the hypothalamus were determined using real-time PCR. Fasting induced an up-regulation of etv5a and etv5b in the hypothalamus, whereas increased serotonin levels in the fasted fish counteracted the increase in expression. To investigate potential mechanisms the expression of further food intake control genes was determined. The results show that an increase of serotonin in fasting fish causes a reduction in the activity of genes stimulating food intake. This is in line with a previously demonstrated anorexigenic function of serotonin. Our results suggest that obesity-associated ETV5 has a food intake stimulating function and that this function is modulated through serotonin.
血清素与脊椎动物的食物摄入抑制有关。然而,血清素发挥作用的机制尚未阐明。最近,ETV5(ETS变异基因5)已与哺乳动物的肥胖和食物摄入控制机制相关联。我们分析了成年斑马鱼在暴露于不同营养条件下,两个etv5旁系同源基因(etv5a和etv5b)在神经元食物摄入控制中的假定生理功能。建立了喂食试验,并应用了选择性血清素再摄取抑制剂(SSRI)氟西汀。使用实时PCR测定下丘脑的基因表达变化。禁食诱导下丘脑etv5a和etv5b上调,而禁食鱼血清素水平升高抵消了表达的增加。为了研究潜在机制,测定了其他食物摄入控制基因的表达。结果表明,禁食鱼血清素增加会导致刺激食物摄入的基因活性降低。这与先前证明的血清素的厌食功能一致。我们的结果表明,与肥胖相关的ETV5具有刺激食物摄入的功能,并且该功能通过血清素调节。