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The Suprachiasmatic Nucleus Modulates the Sensitivity of Arcuate Nucleus to Hypoglycemia in the Male Rat

机译:视交叉上核调节弓形核对雄性大鼠低血糖的敏感性

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摘要

The suprachiasmatic nucleus (SCN) and arcuate nucleus (ARC) have reciprocal connections; catabolic metabolic information activates the ARC and inhibits SCN neuronal activity. Little is known about the influence of the SCN on the ARC. Here, we investigated whether the SCN modulated the sensitivity of the ARC to catabolic metabolic conditions. ARC neuronal activity, as determined by c-Fos immunoreactivity, was increased after a hypoglycemic stimulus by 2-deoxyglucose (2DG). The highest ARC neuronal activity after 2DG was found at the end of the light period (zeitgeber 11, ZT11) with a lower activity in the beginning of the light period (zeitgeber 2, ZT2), suggesting the involvement of the SCN. The higher activation of ARC neurons after 2DG at ZT11 was associated with higher 2DG induced blood glucose levels as compared with ZT2. Unilateral SCN-lesioned animals, gave a mainly ipsilateral activation of ARC neurons at the lesioned side, suggesting an inhibitory role of the SCN on ARC neurons. The 2DG-induced counterregulatory glucose response correlated with increased ARC neuronal activity and was significantly higher in unilateral SCN-lesioned animals. Finally, the ARC as site where 2DG may, at least partly, induce a counterregulatory response was confirmed by local microdialysis of 2DG. 2DG administration in the ARC produced a higher increase in circulating glucose compared with 2DG administration in surrounding areas such as the ventromedial nucleus of the hypothalamus (VMH). We conclude that the SCN uses neuronal pathways to the ARC to gate sensory metabolic information to the brain, regulating ARC glucose sensitivity and counterregulatory responses to hypoglycemic conditions
机译:视交叉上核(SCN)和弓状核(ARC)具有相互连接。分解代谢信息激活ARC并抑制SCN神经元活性。关于SCN对ARC的影响知之甚少。在这里,我们调查了SCN是否调节了ARC对分解代谢代谢条件的敏感性。由c-Fos免疫反应性确定的ARC神经元活性在2-脱氧葡萄糖(2DG)降糖刺激后增加。在2DG之后,在光照期结束时(zeitgeber 11,ZT11)发现了最高的ARC神经元活性,而在光照期开始时(zeitgeber 2,ZT2)却发现了较低的活性,表明SCN参与其中。与ZT2相比,ZT11的2DG后ARC神经元的更高激活与更高的2DG诱导的血糖水平相关。单侧SCN病变的动物在病变侧主要引起ARC神经元的同侧激活,表明SCN对ARC神经元具有抑制作用。 2DG诱导的反调节葡萄糖反应与ARC神经元活性增加有关,并且在单侧SCN病变动物中明显更高。最后,通过2DG的局部微透析证实了ARC作为2DG可能至少部分诱导反调节反应的部位。与2DG给药相比,在下丘脑腹侧核(VMH)周围,与DG给药相比,ARC中的2DG产生的循环葡萄糖升高更高。我们得出的结论是,SCN使用通往ARC的神经通路来控制通往大脑的感觉代谢信息,调节ARC葡萄糖敏感性和对低血糖状况的反调节反应

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