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在调节弓状核神经肽Y神经元的Ca2+信号传导过程中,瘦素对胃饥饿素具有短暂的拮抗作用,而对食欲素具有持久的拮抗作用。

Leptin transiently antagonizes ghrelin and long-lastingly orexin in regulation of Ca2+ signaling in neuropeptide Y neurons of the arcuate nucleus.

作者信息

Kohno Daisuke, Suyama Shigetomo, Yada Toshihiko

机构信息

Division of Integrative Physiology, Department of Physiology, Jichi Medical University, School of Medicine, Tochigi 329-0498, Japan.

出版信息

World J Gastroenterol. 2008 Nov 7;14(41):6347-54. doi: 10.3748/wjg.14.6347.

Abstract

AIM

To explore the mechanism for interactions of leptin with ghrelin and orexin in the arcuate nucleus (ARC) activating neuropeptide Y (NPY) neurons during physiological regulation of feeding.

METHODS

Single neurons from ARC of adult rats with matured feeding function were isolated. [Ca2+]i was measured to monitor their activities. The time course of leptin effects on ghrelin-induced versus orexin-induced [Ca2+]i increases in NPY neurons was studied.

RESULTS

Administration of ghrelin or orexin-A at 10(-10) mol/L increased cytosolic Ca2+ concentration ([Ca2+]i) in NPY neurons isolated from the ARC of adult rats. Upon administration of leptin at 10(-14)-10(-12) mol/L, ghrelin-induced [Ca2+]i increases were initially (<10 min) inhibited but later restored, exhibiting a transient pattern of inhibition. In contrast, orexin-induced [Ca2+]i increases were inhibited by leptin in a long-lasting manner. Furthermore, a prior administration of leptin inhibited orexin action but not ghrelin action to increase [Ca2+]i.

CONCLUSION

Leptin counteracted ghrelin effects transiently and orexin effects long-lastingly in NPY neurons. The transient property with which leptin counteracts ghrelin action in NPY neurons may allow the fasting-associated increase in ghrelin levels to activate NPY neurons in the presence of physiological leptin and to stimulate feeding.

摘要

目的

探讨在进食的生理调节过程中,瘦素与胃饥饿素及食欲素在弓状核(ARC)相互作用激活神经肽Y(NPY)神经元的机制。

方法

分离具有成熟进食功能的成年大鼠弓状核的单个神经元。测量[Ca2+]i以监测其活性。研究了瘦素对胃饥饿素诱导的与食欲素诱导的NPY神经元[Ca2+]i升高的作用时程。

结果

给予10^(-10) mol/L的胃饥饿素或食欲素-A可使成年大鼠弓状核分离出的NPY神经元胞质Ca2+浓度([Ca2+]i)升高。给予10^(-14)-10^(-12) mol/L的瘦素后,胃饥饿素诱导的[Ca2+]i升高最初(<10分钟)受到抑制,但随后恢复,呈现出短暂的抑制模式。相比之下,瘦素以持久的方式抑制食欲素诱导的[Ca2+]i升高。此外,预先给予瘦素可抑制食欲素增加[Ca2+]i的作用,但不抑制胃饥饿素的作用。

结论

在NPY神经元中,瘦素对胃饥饿素的作用具有短暂的拮抗作用,而对食欲素的作用具有持久的拮抗作用。瘦素在NPY神经元中对胃饥饿素作用的短暂特性可能使与禁食相关的胃饥饿素水平升高在生理水平的瘦素存在时激活NPY神经元并刺激进食。

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