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首页> 外文期刊>Cell >SIRT1 activates MAO-A in the brain to mediate anxiety and exploratory drive
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SIRT1 activates MAO-A in the brain to mediate anxiety and exploratory drive

机译:SIRT1激活大脑中的MAO-A以介导焦虑和探索性驱动

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摘要

SIRT1 is a NAD~+-dependent deacetylase that governs a number of genetic programs to cope with changes in the nutritional status of cells and organisms. Behavioral responses to food abundance are important for the survival of higher animals. Here we used mice with increased or decreased brain SIRT1 to show that this sirtuin regulates anxiety and exploratory drive by activating transcription of the gene encoding the monoamine oxidase A (MAO-A) to reduce serotonin levels in the brain. Indeed, treating animals with MAO-A inhibitors or selective serotonin reuptake inhibitors (SSRIs) normalized anxiety differences between wild-type and mutant animals. SIRT1 deacetylates the brain-specific helix-loop-helix transcription factor NHLH2 on lysine 49 to increase its activation of the MAO-A promoter. Both common and rare variations in the SIRT1 gene were shown to be associated with risk of anxiety in human population samples. Together these data indicate that SIRT1 mediates levels of anxiety, and this regulation may be adaptive in a changing environment of food availability.
机译:SIRT1是一种NAD〜+依赖性脱乙酰基酶,可控制许多遗传程序来应对细胞和生物体营养状况的变化。对食物丰富的行为反应对于高等动物的生存很重要。在这里,我们使用具有增加或减少的大脑SIRT1的小鼠来表明,这种沉默调节蛋白通过激活编码单胺氧化酶A(MAO-A)的基因的转录来调节大脑中的血清素水平,从而调节焦虑和探索性驱动。确实,用MAO-A抑制剂或选择性5-羟色胺再摄取抑制剂(SSRIs)治疗动物可正常化野生型和突变型动物之间的焦虑差异。 SIRT1使赖氨酸49上的大脑特异性螺旋-环-螺旋转录因子NHLH2脱乙酰基化,以增加其对MAO-A启动子的激活。在人群样本中,SIRT1基因的常见变异和稀有变异均与焦虑风险相关。这些数据加在一起表明SIRT1介导了焦虑水平,并且这种调节可能在不断变化的食物供应环境中具有适应性。

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