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Astrocytes Regulate GLP-1 Receptor-Mediated Effects on Energy Balance

机译:星形胶质细胞调节能量平衡的GLP-1受体介导的作用。

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摘要

Astrocytes are well established modulators of extracellular glutamate, but their direct influence on energy balance-relevant behaviors is largely understudied. As the anorectic effects of glucagon-like peptide-1 receptor (GLP-1R) agonists are partly mediated by central modulation of glutamatergic signaling, we tested the hypothesis that astrocytic GLP-1R signaling regulates energy balance in rats. Central or peripheral administration of a fluorophore-labeled GLP-1R agonist, exendin-4, localizes within astrocytes and neurons in the nucleus tractus solitarius (NTS), a hindbrain nucleus critical for energy balance control. This effect is mediated by GLP-1R, as the uptake of systemically administered fluorophore-tagged exendin-4 was blocked by central pretreatment with the competitive GLP-1R antagonist exendin-(9–39). Ex vivo analyses show prolonged exendin-4-induced activation (live cell calcium signaling) of NTS astrocytes and neurons; these effects are also attenuated by exendin-(9–39), indicating mediation by the GLP-1R. In vitro analyses show that the application of GLP-1R agonists increases cAMP levels in astrocytes. Immunohistochemical analyses reveal that endogenous GLP-1 axons form close synaptic apposition with NTS astrocytes. Finally, pharmacological inhibition of NTS astrocytes attenuates the anorectic and body weight-suppressive effects of intra-NTS GLP-1R activation. Collectively, data demonstrate a role for NTS astrocytic GLP-1R signaling in energy balance control.>SIGNIFICANCE STATEMENT Glucagon-like peptide-1 receptor (GLP-1R) agonists reduce food intake and are approved by the Food and Drug Administration for the treatment of obesity, but the cellular mechanisms underlying the anorectic effects of GLP-1 require further investigation. Astrocytes represent a major cellular population in the CNS that regulates neurotransmission, yet the role of astrocytes in mediating energy balance is largely unstudied. The current data provide novel evidence that astrocytes within the NTS are relevant for energy balance control by GLP-1 signaling. Here, we report that GLP-1R agonists activate and internalize within NTS astrocytes, while behavioral data suggest the pharmacological relevance of NTS astrocytic GLP-1R activation for food intake and body weight. These findings support a previously unknown role for CNS astrocytes in energy balance control by GLP-1 signaling.
机译:星形胶质细胞是细胞外谷氨酸的成熟调节剂,但其对能量平衡相关行为的直接影响却被大大研究。由于胰高血糖素样肽1受体(GLP-1R)激动剂的厌食作用部分是由谷氨酸能信号传导的中枢调节介导的,因此我们测试了星形细胞GLP-1R信号传导调节大鼠能量平衡的假设。荧光团标记的GLP-1R激动剂exendin-4的中央或外围给药位于孤束核(NTS)的星形胶质细胞和神经元内,后者是对能量平衡控制至关重要的后脑核。这种作用是由GLP-1R介导的,因为用竞争性GLP-1R拮抗剂exendin-(9-39)进行的中央预处理可阻止全身施用荧光团标记的exendin-4的摄取。离体分析显示,NTS星形胶质细胞和神经元的exendin-4诱导的激活时间延长(活细胞钙信号传导);这些作用也被exendin-(9-39)减弱,表明由GLP-1R介导。体外分析表明,应用GLP-1R激动剂可增加星形胶质细胞中的cAMP水平。免疫组织化学分析显示,内源性GLP-1轴突与NTS星形胶质细胞形成紧密的突触并置。最后,对NTS星形胶质细胞的药理抑制作用会减弱NTS内GLP-1R激活的厌食和体重抑制作用。总体而言,数据证明了NTS星形细胞GLP-1R信号传导在能量平衡控制中的作用。>意义声明胰高血糖素样肽1受体(GLP-1R)激动剂可减少食物摄入,并得到了食品和药物管理局的批准药物管理局用于治疗肥胖症,但GLP-1的厌食作用所依据的细胞机制尚需进一步研究。星形胶质细胞是中枢神经系统中调节神经传递的主要细胞群,但在很大程度上尚未研究星形胶质细胞在介导能量平衡中的作用。当前数据提供了新的证据,表明NTS中的星形胶质细胞与通过GLP-1信号传导进行能量平衡控制有关。在这里,我们报道GLP-1R激动剂在NTS星形胶质细胞内激活和内在化,而行为数据表明NTS星形细胞GLP-1R激活对食物摄入和体重的药理学意义。这些发现支持了中枢神经系统星形胶质细胞在通过GLP-1信号进行能量平衡控制中的未知角色。

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