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本文引用的文献

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Bis(31/31')[[Cys(31), Nva(34)]NPY(27-36)-NH(2)]: a neuropeptide Y (NPY) Y(5) receptor selective agonist with a latent stimulatory effect on food intake in rats.双(31/31')[[半胱氨酸(31),β-氨基正缬氨酸(34)]神经肽Y(NPY)(27 - 36)-NH₂]:一种对大鼠食物摄入量具有潜在刺激作用的神经肽Y(NPY)Y₅受体选择性激动剂。
Peptides. 2002 Aug;23(8):1485-90. doi: 10.1016/s0196-9781(02)00086-4.
2
Gut hormone PYY(3-36) physiologically inhibits food intake.肠道激素PYY(3-36)在生理上抑制食物摄入。
Nature. 2002 Aug 8;418(6898):650-4. doi: 10.1038/nature00887.
3
Selective antagonism of the NPY Y5 receptor does not have a major effect on feeding in rats.神经肽Y Y5受体的选择性拮抗作用对大鼠进食没有主要影响。
Diabetes. 2002 Aug;51(8):2441-9. doi: 10.2337/diabetes.51.8.2441.
4
Receptor subtypes Y1 and Y5 mediate neuropeptide Y induced feeding in the guinea-pig.受体亚型Y1和Y5介导神经肽Y诱导的豚鼠进食。
Br J Pharmacol. 2002 Apr;135(8):2029-37. doi: 10.1038/sj.bjp.0704667.
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Appetite suppression based on selective inhibition of NPY receptors.基于对神经肽Y受体的选择性抑制的食欲抑制。
Int J Obes Relat Metab Disord. 2002 Mar;26(3):281-98. doi: 10.1038/sj.ijo.0801948.
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Identification of potent and selective neuropeptide Y Y(1) receptor agonists with orexigenic activity in vivo.体内具有促食欲活性的强效和选择性神经肽Y Y(1)受体激动剂的鉴定。
Mol Pharmacol. 2001 Sep;60(3):534-40.
7
Interactions between orexin A, NPY and galanin in the control of food intake of the goldfish, Carassius auratus.食欲肽A、神经肽Y和甘丙肽在金鱼(Carassius auratus)摄食控制中的相互作用
Regul Pept. 2001 Sep 15;101(1-3):59-72. doi: 10.1016/s0167-0115(01)00261-0.
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Novel analogues of neuropeptide Y with a preference for the Y1-receptor.对Y1受体具有选择性的神经肽Y新型类似物。
Eur J Biochem. 2001 May;268(10):2828-37. doi: 10.1046/j.1432-1327.2001.02161.x.
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Cloning and characterization of the guinea pig neuropeptide Y receptor Y5.豚鼠神经肽Y受体Y5的克隆与特性分析
Peptides. 2001 Mar;22(3):357-63. doi: 10.1016/s0196-9781(01)00338-2.
10
Reduced food intake in response to CGP 71683A may be due to mechanisms other than NPY Y5 receptor blockade.对CGP 71683A作出反应时食物摄入量减少可能是由于除NPY Y5受体阻断以外的机制。
Int J Obes Relat Metab Disord. 2001 Jan;25(1):84-94. doi: 10.1038/sj.ijo.0801472.

神经肽Y受体Y1和Y5的激动剂刺激豚鼠进食的不同阶段。

Agonists for neuropeptide Y receptors Y1 and Y5 stimulate different phases of feeding in guinea pigs.

作者信息

Lecklin Anne, Lundell Ingrid, Salmela Suvi, Männistö Pekka T, Beck-Sickinger Annette G, Larhammar Dan

机构信息

Department of Neuroscience, Unit of Pharmacology, Uppsala University, Box 593, S-75124 Uppsala, Sweden.

出版信息

Br J Pharmacol. 2003 Aug;139(8):1433-40. doi: 10.1038/sj.bjp.0705389.

DOI:10.1038/sj.bjp.0705389
PMID:12922930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1573983/
Abstract
  1. The stimulatory effect of neuropeptide Y (NPY) on food intake is well established but the roles of the receptor subtypes Y(1) and Y(5) have been difficult to define. We have studied the effects of two novel Y(1)-preferring and two Y(5)-preferring agonists on feeding in guinea pigs. 2. The Y(1)-preferring receptor agonists [Arg(6),Pro(34)]pNPY and [Phe(7),Pro(34)]pNPY had high affinity for the Y(1) receptor (K(i) values 0.07 and 0.04 nM, respectively) and nanomolar affinity for the Y(5) receptor. Administration of either compound into the third brain ventricle increased food intake equally to NPY. 3. The Y(5) agonist [Ala(31),Aib(32)]pNPY displayed a moderate affinity for the Y(5) receptor (K(i) 7.42 nM) and a low affinity for Y(1) (K(i) 1.7 micro M). This compound had only a modest effect on feeding. 4. The other Y(5)-preferring peptide [cPP(1-7),NPY(19-23),Ala(31),Aib(32),Gln(34)]hPP had a higher affinity at the Y(5) receptor (K(i) 1.32 nM) and also at the Y(1) receptor (K(i) 85 nM). It potently stimulated feeding: the food consumption after administration of this peptide was two-fold compared to NPY. 5. Our results support the view that both the receptor subtypes Y(1) and Y(5) are involved in the stimulation of feeding. As the action profiles of the Y(1) and Y(5) agonists on feeding parameters were different, it seems that they influence different phases of eating.
摘要
  1. 神经肽Y(NPY)对食物摄入的刺激作用已得到充分证实,但其Y(1)和Y(5)受体亚型的作用却难以界定。我们研究了两种新型的偏好Y(1)的激动剂和两种偏好Y(5)的激动剂对豚鼠进食的影响。2. 偏好Y(1)的受体激动剂[Arg(6),Pro(34)]pNPY和[Phe(7),Pro(34)]pNPY对Y(1)受体具有高亲和力(K(i)值分别为0.07和0.04 nM),对Y(5)受体具有纳摩尔亲和力。将这两种化合物中的任何一种注入第三脑室,均可使食物摄入量增加,与NPY的作用相当。3. Y(5)激动剂[Ala(31),Aib(32)]pNPY对Y(5)受体表现出中等亲和力(K(i) 7.42 nM),对Y(1)受体表现出低亲和力(K(i) 1.7 μM)。该化合物对进食仅有适度影响。4. 另一种偏好Y(5)的肽[cPP(1 - 7),NPY(19 - 23),Ala(31),Aib(32),Gln(34)]hPP对Y(5)受体具有更高的亲和力(K(i) 1.32 nM),对Y(1)受体也具有一定亲和力(K(i) 85 nM)。它能有效刺激进食:给予该肽后食物消耗量是给予NPY后的两倍。5. 我们的结果支持这样的观点,即Y(1)和Y(5)受体亚型均参与进食的刺激过程。由于Y(1)和Y(5)激动剂对进食参数的作用模式不同,似乎它们影响进食的不同阶段。