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神经肽可使哺乳动物的昼夜节律起搏器发生相位转移。

Neuropeptides phase shift the mammalian circadian pacemaker.

作者信息

Piggins H D, Antle M C, Rusak B

机构信息

Department of Psychology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

J Neurosci. 1995 Aug;15(8):5612-22. doi: 10.1523/JNEUROSCI.15-08-05612.1995.

Abstract

We studied the influence on circadian rhythms of peptides that have been reported to be colocalized in suprachiasmatic nucleus (SCN) neurons. Gastrin-releasing peptide (GRP1-27), peptide histidine isoleucine (PHI), and vasoactive intestinal polypeptide (VIP) were microinjected into the suprachiasmatic nucleus (SCN) region of Syrian hamsters free running under three different constant lighting conditions. All peptide injections caused phase-dependent phase shifts of hamster locomotor activity rhythms which were unaffected by constant lighting conditions. GRP1-27 (150 pmol) caused large phase delays when injected at circadian times (CT) 12-16, modest phase advances when administered at CT20-24, and few shifts during the subjective day. Injections of saline vehicle at any of these phases caused only very small phase shifts. Phase delays induced by GRP1-27 at CT12-14 were dose dependent, unrelated to injection volume (at a constant dose), and attenuated by pretreatment with the BN/GRP-preferring receptor antagonist BIM 26226. VIP (150 pmol) caused moderate phase delays at CT12-14 and moderate phase advances at CT20-24. PHI (150 pmol) caused moderate phase delays at CT12-14 only. Coadministration of 150 pmol of GRP1-27, PHI, and VIP in an equimolar neuropeptide cocktail (50 pmol of each peptide) caused phase delays at CT12-14 and phase advances at CT20-24 which did not differ from those induced by 150 pmol of GRP1-27 alone at these phases. The shifts induced by 150 pmol of the peptide cocktail were smaller than the sum of the shifts induced by 50 pmol doses of each peptide administered separately at those phases. Since the phase-delaying effects of the cocktail were weaker than the summed effects of the component 50 pmol doses of the peptides, these data demonstrate a lack of synergism among the effects of these peptides. Since GRP1-27 (150 pmol) evoked shifts similar in magnitude to those of the cocktail, there is no evidence that these apparently colocalized neuropeptides must interact to exert maximal effects on the circadian pacemaker.

摘要

我们研究了据报道在视交叉上核(SCN)神经元中共定位的肽对昼夜节律的影响。将胃泌素释放肽(GRP1 - 27)、肽组氨酸异亮氨酸(PHI)和血管活性肠肽(VIP)微量注射到在三种不同恒定光照条件下自由活动的叙利亚仓鼠的视交叉上核(SCN)区域。所有肽注射均引起仓鼠运动活动节律的相位依赖性相移,且不受恒定光照条件的影响。GRP1 - 27(150 pmol)在昼夜时间(CT)12 - 16注射时引起大的相位延迟,在CT20 - 24给药时引起适度的相位提前,在主观白天期间引起的相移很少。在这些相位的任何一个时间注射生理盐水载体仅引起非常小的相移。GRP1 - 27在CT12 - 14引起的相位延迟是剂量依赖性的,与注射体积无关(在恒定剂量下),并且通过用BN/GRP偏好受体拮抗剂BIM 26226预处理而减弱。VIP(150 pmol)在CT12 - 14引起适度的相位延迟,在CT20 - 24引起适度的相位提前。PHI(150 pmol)仅在CT12 - 14引起适度的相位延迟。将150 pmol的GRP1 - 27、PHI和VIP以等摩尔神经肽混合物(每种肽50 pmol)共同给药,在CT12 - 14引起相位延迟,在CT20 - 24引起相位提前,这与在这些相位单独注射150 pmol的GRP1 - 27所诱导的相移没有差异。150 pmol的肽混合物诱导的相移小于在这些相位分别给予50 pmol剂量的每种肽所诱导的相移之和。由于混合物的相位延迟效应比各肽50 pmol剂量的相加效应弱,这些数据表明这些肽的效应之间缺乏协同作用。由于GRP1 - 27(150 pmol)引起的相移幅度与混合物相似,没有证据表明这些明显共定位的神经肽必须相互作用才能对昼夜节律起搏器发挥最大作用。

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