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人类速激肽NK2受体:结肠与膀胱的比较研究

Human tachykinin NK2 receptor: a comparative study of the colon and urinary bladder.

作者信息

Warner Fiona J, Miller Robert C, Burcher Elizabeth

机构信息

School of Physiology and Pharmacology, University of New South Wales, Sydney, New South Wales, Australia.

出版信息

Clin Exp Pharmacol Physiol. 2003 Sep;30(9):632-9. doi: 10.1046/j.1440-1681.2003.03887.x.

DOI:10.1046/j.1440-1681.2003.03887.x
PMID:12940880
Abstract
  1. The present study compared the binding and functional characteristics of tachykinin NK2 receptors in human detrusor muscle with those in human colon circular muscle. 2. In radioligand binding studies, similar KD values were observed for tachykinin NK2 receptor radioligands [125I]-neurokinin (NK) A, [125I]-[Lys5,Tyr(I2)7,MeLeu9,Nle10,]NKA(4-10) and [3H]-SR48968 in both human colon circular muscle (0.28-1.1 nmol/L) and human bladder detrusor (0.49-0.91 nmol/L), suggesting binding was primarily to tachykinin NK2 receptors. Receptor capacity (Bmax) was greater in colon compared with detrusor muscle. 3. In functional studies of isolated smooth muscle contraction, there was an excellent positive correlation between human bladder detrusor and colon circular muscle with respect to in vitro contractile potency (r = 0.97) and maximum responses (r = 0.98) to tachykinins, selective tachykinin receptor ligands and l-Ala-substituted NKA(4-10) analogues. 4. Species differences between the human and rat tachykinin NK2 receptors were apparent as observed by a low correlation for potency (r = 0.77) and efficacy (r = 0.32) of l-Ala-substituted analogues in isolated smooth muscle contractile studies. 5. Minor differences observed in the affinity and potency of NK2 receptor agonists between colon and bladder are dependent on the tissue of interest, the receptor-effector coupling and the presence of other tachykinin receptors. Overall, the NK2 receptors of human colon and urinary bladder smooth muscle appear pharmacologically identical.
摘要
  1. 本研究比较了人逼尿肌和人结肠环行肌中速激肽NK2受体的结合特性和功能特性。2. 在放射性配体结合研究中,在人结肠环行肌(0.28 - 1.1 nmol/L)和人膀胱逼尿肌(0.49 - 0.91 nmol/L)中,速激肽NK2受体放射性配体[125I] - 神经激肽(NK)A、[125I] - [Lys5,Tyr(I2)7,MeLeu9,Nle10,]NKA(4 - 10)和[3H] - SR48968观察到相似的KD值,表明结合主要是与速激肽NK2受体。与逼尿肌相比,结肠中的受体容量(Bmax)更大。3. 在离体平滑肌收缩功能研究中,人膀胱逼尿肌和结肠环行肌在对速激肽、选择性速激肽受体配体和l - Ala取代的NKA(4 - 10)类似物的体外收缩效力(r = 0.97)和最大反应(r = 0.98)方面存在极好的正相关。4. 在离体平滑肌收缩研究中,观察到l - Ala取代类似物的效力(r = 0.77)和效能(r = 0.32)相关性较低,表明人和大鼠速激肽NK2受体之间存在明显的种属差异。5. 在结肠和膀胱之间观察到的NK2受体激动剂亲和力和效力的微小差异取决于所关注的组织、受体 - 效应器偶联以及其他速激肽受体的存在。总体而言,人结肠和膀胱平滑肌的NK2受体在药理学上似乎是相同的。

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