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本文引用的文献

1
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.
2
Important role of hypothalamic Y2 receptors in body weight regulation revealed in conditional knockout mice.条件性基因敲除小鼠揭示了下丘脑Y2受体在体重调节中的重要作用。
Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8938-43. doi: 10.1073/pnas.132043299. Epub 2002 Jun 18.
3
Blockade of neuropeptide Y(2) receptors and suppression of NPY's anti-epileptic actions in the rat hippocampal slice by BIIE0246.BIIE0246对大鼠海马切片中神经肽Y(2)受体的阻断及神经肽Y抗癫痫作用的抑制
Br J Pharmacol. 2002 Jun;136(4):502-9. doi: 10.1038/sj.bjp.0704751.
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Autoinhibitory function of the sympathetic prejunctional neuropeptide Y Y(2) receptor evidenced by BIIE0246.BIIE0246证明的交感神经节前神经肽Y Y(2)受体的自身抑制功能
Eur J Pharmacol. 2002 Mar 29;439(1-3):113-9. doi: 10.1016/s0014-2999(02)01371-7.
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Hypothalamic Y2 receptors regulate bone formation.下丘脑Y2受体调节骨形成。
J Clin Invest. 2002 Apr;109(7):915-21. doi: 10.1172/JCI14588.
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Neuropeptide Y, Y1, Y2 and Y4 receptors mediate Y agonist responses in isolated human colon mucosa.神经肽Y、Y1、Y2和Y4受体介导了离体人结肠黏膜中Y激动剂的反应。
Br J Pharmacol. 2002 Mar;135(6):1505-12. doi: 10.1038/sj.bjp.0704604.
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Role of neuropeptide Y Y(2) receptors in modulation of cardiac parasympathetic neurotransmission.神经肽Y Y(2)受体在调节心脏副交感神经传递中的作用。
Regul Pept. 2002 Feb 15;103(2-3):105-11. doi: 10.1016/s0167-0115(01)00368-8.
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Modulation of intracellular calcium changes and glutamate release by neuropeptide Y1 and Y2 receptors in the rat hippocampus: differential effects in CA1, CA3 and dentate gyrus.神经肽Y1和Y2受体对大鼠海马细胞内钙变化和谷氨酸释放的调节作用:在CA1、CA3和齿状回中的差异效应
J Neurochem. 2001 Oct;79(2):286-96. doi: 10.1046/j.1471-4159.2001.00560.x.
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Emerging functions of neuropeptide Y Y(2) receptors in the brain.神经肽Y Y(2)受体在大脑中的新功能
Peptides. 2001 Mar;22(3):501-6. doi: 10.1016/s0196-9781(01)00362-x.
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Multiple Y receptors mediate pancreatic polypeptide responses in mouse colon mucosa.多种Y受体介导小鼠结肠黏膜中的胰多肽反应。
Peptides. 2001 Mar;22(3):445-52. doi: 10.1016/s0196-9781(01)00355-2.

神经肽Y Y2受体敲除及Y2拮抗在小鼠和人类结肠组织中的功能后果

Functional consequences of neuropeptide Y Y 2 receptor knockout and Y2 antagonism in mouse and human colonic tissues.

作者信息

Hyland Niall P, Sjöberg Frida, Tough Iain R, Herzog Herbert, Cox Helen M

机构信息

Centre for Neuroscience Research, King's College London, GKT School of Biomedical Sciences, Guy's Campus, London SE1 1UL, UK.

出版信息

Br J Pharmacol. 2003 Jun;139(4):863-71. doi: 10.1038/sj.bjp.0705298.

DOI:10.1038/sj.bjp.0705298
PMID:12813010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1573894/
Abstract

1 Neuropeptide Y (NPY), peptide YY (PYY) and pancreatic polypeptide (PP) differentially activate three Y receptors (Y(1), Y(2) and Y(4)) in mouse and human isolated colon. 2 The aim of this study was to characterise Y(2) receptor-mediated responses in colon mucosa and longitudinal smooth muscle preparations from wild type (Y(2)+/+) and knockout (Y(2)-/-) mice and to compare the former with human mucosal Y agonist responses. Inhibition of mucosal short-circuit current and increases in muscle tone were monitored in colonic tissues from Y(2)+/+ and Y(2)-/- mice+/-Y(1) ((R)-N-[[4-(aminocarbonylaminomethyl)phenyl)methyl]-N(2)-(diphenylacetyl)-argininamide-trifluoroacetate (BIBO3304) or Y(2) (S)-N(2)-[[1-[2-[4-[(R,S)-5,11-dihydro-6(6H)-oxodibenz[b,e]azepin-11-yl]-1-piperazinyl]-2-oxoethyl]cyclopentyl]acetyl]-N-[2-[1,2-dihydro-3,5(4H)-dioxo-1,2-diphenyl-3H-1,2,4-triazol-4-yl]ethyl]-argininamide (BIIE0246) antagonists. 3 Predictably, Y(2)-/- tissues were insensitive to Y(2)-preferred agonist PYY(3-36) (</=100 nM), but unexpectedly Y(4)-preferred PP responses were right-shifted probably as a consequence of elevated circulating PP levels, particularly in male Y(2)-/- mice (Sainsbury et al., 2002). 4 BIBO3304 and BIIE0246 elevated mucosal ion transport, indicating blockade of inhibitory mucosal tone in Y(2)+/+ tissue. While BIBO3304 effects were unchanged, those to BIIE0246 were absent in Y(2)-/- mucosae. Neither antagonist altered muscle tone; however, BIIE0246 blocked NPY and PYY(3-36) increases in Y(2)+/+ basal tone. BIBO3304 abolished residual Y(1)-mediated NPY responses in Y(2)-/- smooth muscle. 5 Tetrodotoxin significantly reduced BIIE0246 and PYY(3-36) effects in Y(2)+/+ mouse and human mucosae, but had no effect upon Y-agonist contractile responses, indicating that Y(2) receptors are located on submucosal, but not myenteric neurones. 6 Tonic activation of submucosal Y(2) receptors by endogenous NPY, PYY or PYY(3-36) could indirectly reduce mucosal ion transport in murine and human colon, while direct activation of Y(2) receptors on longitudinal muscle results in contraction.

摘要

1 神经肽Y(NPY)、肽YY(PYY)和胰多肽(PP)在小鼠和人离体结肠中对三种Y受体(Y(1)、Y(2)和Y(4))的激活作用存在差异。2 本研究的目的是表征野生型(Y(2)+/+)和基因敲除(Y(2)-/-)小鼠结肠黏膜和纵行平滑肌制剂中Y(2)受体介导的反应,并将前者与人类黏膜Y激动剂反应进行比较。在来自Y(2)+/+和Y(2)-/-小鼠的结肠组织中监测黏膜短路电流的抑制和肌张力的增加,这些组织±Y(1) ((R)-N-[[4-(氨基羰基氨基甲基)phenyl)甲基]-N(2)-(二苯基乙酰基)-精氨酰胺-三氟乙酸盐(BIBO3304)或Y(2) (S)-N(2)-[[1-[2-[4-[(R,S)-5,11-二氢-6(6H)-氧代二苯并[b,e]氮杂卓-11-基]-1-哌嗪基]-2-氧代乙基]环戊基]乙酰基]-N-[2-[1,2-二氢-3,5(4H)-二氧代-1,2-二苯基-3H-1,2,4-三唑-4-基]乙基]-精氨酰胺(BIIE0246)拮抗剂)。3 不出所料,Y(2)-/-组织对Y(2)偏好的激动剂PYY(3-36)(≤100 nM)不敏感,但出乎意料的是,Y(4)偏好的PP反应向右偏移,这可能是循环PP水平升高的结果,尤其是在雄性Y(2)-/-小鼠中(Sainsbury等人,2002年)。4 BIBO3304和BIIE0246提高了黏膜离子转运,表明在Y(2)+/+组织中抑制性黏膜张力被阻断。虽然BIBO3304的作用未改变,但在Y(2)-/-黏膜中对BIIE0246的作用不存在。两种拮抗剂均未改变肌张力;然而,BIIE0246阻断了Y(2)+/+基础肌张力中NPY和PYY(3-36)的增加。BIBO3304消除了Y(2)-/-平滑肌中残余的Y(1)介导的NPY反应。5 河豚毒素显著降低了Y(2)+/+小鼠和人黏膜中BIIE0246和PYY(3-36)的作用,但对Y激动剂的收缩反应没有影响,表明Y(