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Orexins and adipoinsular axis function in the rat.

机译:食欲素和大鼠腹窦轴功能。

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Orexin A and B are recently identified as peptides that are derived from the same precursor and their expression is highly specifically localized in neurons located in the lateral hypothalamic area, a region implicated in the feeding behaviour. These peptides appear to be a part of a complex circuit that integrates the aspects of energy metabolism, cardiovascular function, hormone homeostasis and sleep/wake behaviours. The functional linking of orexins with leptin and insulin suggests the possibility of its involvement in the regulation of the adipoinsular axis, and the present investigation was designed to examine the potential role of orexins in this axis regulation. In all the tested doses (8, 16 and 40 nmol/kg body weight (b.w.)), subcutaneous (s.c.) injections of orexin A caused the significant increase in insulin and leptin blood levels. These elevations were observed 60 and 120 min after peptide administration. On the other hand, after the orexin B administration, elevated insulin and leptin blood concentrations were found only at 60 min of the experiment, and in that time point, the increases were comparable to that evoked by orexin A. In comparison with the control animals, the administration of orexins for 7 days resulted in a significant gain in body weight. Prolonged administration of either orexin A or orexin B significantly elevated insulin and leptin blood concentrations. Under these conditions, the orexin A effect on the leptin secretion was more marked than on the insulin secretion, and this difference is reflected by the lowered insulin/leptin molar ratio. These results suggest that orexins play an important role in the adipoinsular axis function and may be a significant regulator of both insulin and leptin secretion. In this regard, we suggest the updated functional model of Kieffer and Habener [Am. J. Physiol.: Endocrinol. Metab. 27 (2000) E1] that proposed the adipoinsular axis. Our model is extended by the probable humoral links between orexins and leptin and orexins and insulin and points on the dependence of the effects evoked by orexins, leptin and insulin on the blood glucose levels.
机译:食欲素A和B最近被鉴定为衍生自相同前体的肽,它们的表达高度特异地位于下丘脑外侧区域的神经元中,该区域与进食行为有关。这些肽似乎是复杂回路的一部分,该回路整合了能量代谢,心血管功能,激素稳态和睡眠/苏醒行为。食欲肽与瘦素和胰岛素的功能性连接暗示了其可能参与脂多糖轴的调控,并且本研究旨在检验食欲肽在该轴调控中的潜在作用。在所有测试剂量(8、16和40 nmol / kg体重(b.w.))中,皮下注射(s.c.)注射orexin A导致胰岛素和瘦素血液水平显着增加。在肽给药后60和120分钟观察到这些升高。另一方面,在使用orexin B后,仅在实验60分钟时发现胰岛素和瘦素的血药浓度升高,并且在那个时间点,其增加量与orexin A引起的增加相当。与对照动物相比,服用orexins 7天导致体重显着增加。长时间服用orexin A或orexin B会显着提高胰岛素和瘦素的血药浓度。在这些条件下,食欲素A对瘦素分泌的作用比对胰岛素分泌的作用更显着,并且这种差异通过降低的胰岛素/瘦素摩尔比反映出来。这些结果表明,食欲素在脂肪链轴功能中起重要作用,并且可能是胰岛素和瘦素分泌的重要调节剂。在这方面,我们建议Kieffer和Habener [Am。 J.生理学:内分泌醇。代谢27(2000)E1]提出了腹窦轴。我们的模型通过食欲素和瘦素以及食欲素和胰岛素之间可能的体液联系而得到扩展,并指出了食欲素,瘦素和胰岛素对血糖水平的影响。

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