Bellucci F, Cucchi P, Santicioli P, Lazzeri M, Turini D, Meini S
Pharmacology Department, Menarini Ricerche S.p.A., Florence, Italy.
Br J Pharmacol. 2007 Jan;150(2):192-9. doi: 10.1038/sj.bjp.0706976. Epub 2006 Dec 18.
Kinins have an important role in inflammatory cystitis and in animal pathophysiological models, by acting on epithelium, fibroblasts, sensory innervation and smooth muscle. The aim of this study was to characterize the receptors responsible for direct motor responses induced by kinins on human detrusor.
Human detrusor cells from biopsies were isolated and maintained in culture. B(1) and B(2) kinin receptors were characterized by means of radioligand and functional experiments (PI accumulation and PGE(2) release).
[(3)H]-[desArg(9)]-Lys-BK and [(3)H]-BK saturation studies indicated receptor density (B(max)) and K (d) values of 19 or 113 fmol mg(-1), and 0.16 or 0.11 nM for the B(1) or B(2) receptors, respectively. Inhibition binding studies indicated the selectivity of the B(1) receptor antagonist [desArg(9)Leu(8)]-Lys-BK and of the B(2) receptor antagonists Icatibant and MEN16132. [DesArg(9)]-Lys-BK and BK induced PI accumulation with an EC(50) of 1.6 and 1.4 nM and different maximal responses (E(max) of [desArg(9)]-Lys-BK was 10% of BK). BK also induced prostaglandin E(2) release (EC(50) 2.3 nM), whereas no response was detected with the B(1) receptor agonist. The incubation of detrusor smooth muscle cells with interleukin 1beta (IL-1beta) or tumour necrosis factor-alpha (TNF-alpha) (10 ng ml(-1)) induced a time-dependent increase in radioligand-specific binding, which was greater for the B(1) than for the B(2) receptor.
Human detrusor smooth muscle cells in culture retain kinin receptors, and represent a suitable model to investigate the mechanisms and changes that occur under chronic inflammatory conditions.
激肽通过作用于上皮细胞、成纤维细胞、感觉神经支配及平滑肌,在炎性膀胱炎及动物病理生理模型中发挥重要作用。本研究旨在鉴定负责激肽对人逼尿肌直接运动反应的受体。
从活检组织中分离人逼尿肌细胞并进行培养。通过放射性配体及功能实验(磷脂酰肌醇积累和前列腺素E2释放)对B(1)和B(2)激肽受体进行鉴定。
[(3)H]-[去精氨酸(9)]-赖氨酸-缓激肽和[(3)H]-缓激肽饱和研究表明,B(1)或B(2)受体的受体密度(B(max))和K(d)值分别为19或113 fmol mg(-1)以及0.16或0.11 nM。抑制结合研究表明B(1)受体拮抗剂[去精氨酸(9)亮氨酸(8)]-赖氨酸-缓激肽以及B(2)受体拮抗剂依卡替班和MEN16132具有选择性。[去精氨酸(9)]-赖氨酸-缓激肽和缓激肽诱导磷脂酰肌醇积累,其半数有效浓度(EC(50))分别为1.6和1.4 nM,且最大反应不同([去精氨酸(9)]-赖氨酸-缓激肽的最大效应(E(max))为缓激肽的10%)。缓激肽还诱导前列腺素E2释放(EC(50) 2.3 nM),而B(1)受体激动剂未检测到反应。用白细胞介素1β(IL-1β)或肿瘤坏死因子-α(TNF-α)(10 ng ml(-1))孵育人逼尿肌平滑肌细胞,可导致放射性配体特异性结合随时间增加,B(1)受体增加幅度大于B(2)受体。
培养的人逼尿肌平滑肌细胞保留激肽受体,是研究慢性炎症条件下发生的机制及变化的合适模型。