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本文引用的文献

1
Differential effects of metoprolol and atenolol to neuropeptide Y blockade in coronary artery disease.美托洛尔和阿替洛尔对冠心病神经肽 Y 阻断的差异作用。
Scand Cardiovasc J. 2012 Feb;46(1):23-31. doi: 10.3109/14017431.2011.624195. Epub 2011 Oct 24.
2
NPY receptors as potential targets for anti-obesity drug development.神经肽 Y 受体作为抗肥胖药物开发的潜在靶点。
Br J Pharmacol. 2011 Jul;163(6):1170-202. doi: 10.1111/j.1476-5381.2011.01363.x.
3
Of mice and men: neuropeptide Y and its receptors are associated with atherosclerotic lesion burden and vulnerability.从老鼠到人:神经肽 Y 及其受体与动脉粥样硬化病变负担和易损性有关。
J Cardiovasc Transl Res. 2011 Jun;4(3):351-62. doi: 10.1007/s12265-011-9271-5. Epub 2011 Apr 6.
4
Metoprolol, but not atenolol, reduces stress induced neuropeptide Y release in pigs.美托洛尔而非阿替洛尔可减少应激诱导的猪神经肽 Y 释放。
Scand Cardiovasc J. 2010 Oct;44(5):273-8. doi: 10.3109/14017431.2010.498923.
5
Adrenal responses to stress.肾上腺对压力的反应。
Cell Mol Neurobiol. 2010 Nov;30(8):1433-40. doi: 10.1007/s10571-010-9606-9.
6
Therapeutic potential of neuropeptide Y (NPY) receptor ligands.神经肽 Y(NPY)受体配体的治疗潜力。
EMBO Mol Med. 2010 Nov;2(11):429-39. doi: 10.1002/emmm.201000100.
7
Neuropeptide Y is a mediator of chronic vascular and metabolic maladaptations to stress and hypernutrition.神经肽 Y 是慢性血管和代谢适应应激和高营养的介质。
Exp Biol Med (Maywood). 2010 Oct;235(10):1179-84. doi: 10.1258/ebm.2010.009136.
8
Brain neuropeptide Y and corticotropin-releasing hormone in mediating stress and anxiety.脑内神经肽 Y 和促肾上腺皮质激素释放激素在介导应激和焦虑中的作用。
Exp Biol Med (Maywood). 2010 Oct;235(10):1163-7. doi: 10.1258/ebm.2010.009331.
9
Adaptation to extreme stress: post-traumatic stress disorder, neuropeptide Y and metabolic syndrome.适应极端压力:创伤后应激障碍、神经肽 Y 和代谢综合征。
Exp Biol Med (Maywood). 2010 Oct;235(10):1150-62. doi: 10.1258/ebm.2010.009334.
10
Noradrenaline and ATP as cotransmitters in sympathetic nerves.去甲肾上腺素和三磷酸腺苷作为交感神经中的共递质。
Neurochem Int. 1990;17(2):357-68. doi: 10.1016/0197-0186(90)90158-p.

30 年后的 NPY 与压力:外周观点。

NPY and stress 30 years later: the peripheral view.

机构信息

Department of Integrative Biology and Physiology, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Cell Mol Neurobiol. 2012 Jul;32(5):645-59. doi: 10.1007/s10571-011-9793-z. Epub 2012 Jan 24.

DOI:10.1007/s10571-011-9793-z
PMID:22271177
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3492947/
Abstract

Almost 30 years ago, neuropeptide Y (NPY) was discovered as a sympathetic co-transmitter and one of the most evolutionarily conserved peptides abundantly present all over the body. Soon afterward, NPY's multiple receptors were characterized and cloned, and the peptide's role in stress was first documented. NPY has proven to be pivotal for maintaining many stress responses. Most notably, NPY is known for activating long-lasting vasoconstriction in many vascular beds, including coronary arteries. More recently, NPY was found to play a role in stress-induced accretion of adipose tissue which many times can lead to detrimental metabolic changes. It is however due to its prominent actions in the brain, one of which is its powerful ability to stimulate appetite as well as its anxiolytic activities that NPY became a peptide of importance in neuroscience. In contrast, its actions in the rest of the body, including its role as a stress mediator, remained, surprisingly underappreciated and not well understood. Our research has focused on that other, "peripheral" side of NPY. In this review, we will discuss those actions of NPY on the cardiovascular system and metabolism, as they relate to adaptation to stress, and attempt to both distinguish NPY's effects from and integrate them with the effects of the classical stress mediators, glucocorticoids, and catecholamines. To limit the bias of someone (ZZ) who has viewed the world of stress through the eyes of NPY for over 20 years, fresh insight (DH) has been solicited to more objectively assess NPY's contributions to stress-related diseases and the body's ability to adapt to stress.

摘要

大约 30 年前,神经肽 Y(NPY)被发现是一种交感神经递质,也是体内广泛存在的最具进化保守性的肽类之一。此后不久,NPY 的多种受体被鉴定和克隆,其在应激中的作用也首次被记录。事实证明,NPY 对维持多种应激反应至关重要。最值得注意的是,NPY 已知可在许多血管床(包括冠状动脉)中引发持久的血管收缩。最近,人们发现 NPY 在应激诱导的脂肪组织堆积中发挥作用,而这种情况往往会导致有害的代谢变化。然而,由于其在大脑中的突出作用,包括其刺激食欲以及抗焦虑的强大能力,NPY 成为神经科学中重要的肽类。相比之下,其在身体其他部位的作用,包括作为应激介质的作用,仍然令人惊讶地被低估和不被理解。我们的研究集中在 NPY 的“外周”作用上。在这篇综述中,我们将讨论 NPY 对心血管系统和代谢的作用,因为它们与应激适应有关,并试图区分 NPY 的作用,并将其与经典应激介质(糖皮质激素和儿茶酚胺)的作用整合起来。为了避免某人(ZZ)因 20 多年来一直从 NPY 的角度看待应激世界而产生偏见,我们还征求了新的见解(DH),以更客观地评估 NPY 对应激相关疾病和身体适应应激的贡献。