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首页> 外文期刊>Peptides: An International Journal >Repeated glucoprivation delayed hyperphagic responses while activating neuropeptide Y neurons in rats.
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Repeated glucoprivation delayed hyperphagic responses while activating neuropeptide Y neurons in rats.

机译:重复的糖缺乏会在激活大鼠神经肽Y神经元的同时延迟高吞噬反应。

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It is well known that glucoprivation induces the release of counterregulatory hormones such as glucagon, and that the response is attenuated when the stimuli are repeated. Glucoprivation also activates orexigenic neurons and induces hyperphagic responses, although it remains unclear whether these responses are attenuated in repeated glucoprivation. In this study, we examined time course changes in feeding as well as activities of orexigenic neuropeptide Y (NPY) neurons in repeated glucoprivation in rats. Either 2-deoxy-d-glucose (2DG), which blocks glucose utilization, or isotonic saline (control) was injected subcutaneously to rats for 14 days, and food consumption for 1 and 2h after injection was monitored throughout the experiment. While 2DG injection induced robust feeding responses during the first 1h after injection, the response was gradually attenuated and the food consumption was significantly less on days 12-14 compared to that on day 1. On the other hand, food consumption during 2h after 2DG injection was not changed significantly for 14 days. The transcriptional activities of NPY neurons in the arcuate nucleus and C1/A1 region of the hindbrain, measured by intronic in situ hybridization, were significantly enhanced after repeated 2DG injection for 14 days, while the feeding responses to intracerebroventricular injection of NPY were significantly less in the 2DG-repeated group compared to the saline-repeated group. It is thus demonstrated that repeated glucoprivation delayed hyperphagic responses while activating NPY neurons in rats. Our data also suggest that decreased feeding responses to NPY might be at least partially responsible for the delayed response.
机译:众所周知,糖缺乏会诱导释放反调节激素,例如胰高血糖素,并且当重复刺激时反应会减弱。尽管尚不清楚在重复的糖剥夺中这些反应是否减弱,但糖剥夺也激活食源性神经元并诱导高吞噬反应。在这项研究中,我们检查了大鼠反复进食糖缺乏时进食的时程变化以及致食性神经肽Y(NPY)神经元的活动。向大鼠皮下注射能阻止葡萄糖利用的2-deoxy-d-葡萄糖(2DG)或等渗盐水(对照),持续14天,并在整个实验过程中监测注射后1和2h的食物消耗。尽管2DG注射在注射后的前1h引起强烈的进食反应,但与第1天相比,该反应在12-14天逐渐减弱,食物消耗显着减少。另一方面,2DG注射后2h的食物消耗14天没有明显变化。内含子原位杂交测定,重复2DG注射14天后,弓形核和后脑C1 / A1区NPY神经元的转录活性显着增强,而脑室内注射NPY的进食反应显着降低。 2DG重复组与盐水重复组相比。因此证明了重复的糖缺乏会在激活大鼠中的NPY神经元的同时延迟高吞噬反应。我们的数据还表明,对NPY的饲喂反应减少可能至少部分是造成延迟反应的原因。

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