Faure C, Pimoule C, Vallancien G, Langer S Z, Graham D
Synthélabo Recherche (L.E.R.S.), Bagneux, France.
Life Sci. 1994;54(21):1595-605. doi: 10.1016/0024-3205(94)90031-0.
alpha 1-Adrenoceptors (ARs) play an important role in mediating human prostatic smooth muscle contraction. In the present study cDNA fragments covering different domains of 3 alpha 1-AR subtypes (alpha 1b, alpha 1c and alpha 1d) were generated from human prostate by reverse transcription coupled to the polymerase chain reaction (RT-PCR). The reconstituted partial sequence (349 amino acids) of the human prostatic alpha 1c-AR PCR products showed 94% identity at the amino acid level with that of the corresponding region of the cloned bovine brain alpha 1c-AR. Using human alpha 1-AR subtype selective cDNA probes in Northern blot analysis, the co-expression of mRNA transcripts corresponding to alpha 1b-, alpha 1c- and alpha 1d-AR subtypes was detected in 4 different regions (apex, base, periurethra and lateral lobe) of the human prostate. Competitive inhibition experiments of [3H]-prazosin binding to membrane preparations of human prostate revealed that the non-selective alpha 1-subtype antagonist, alfuzosin, produced a monophasic inhibition curve, whereas oxymetazoline produced a 2-component inhibition curve with pKi values of 8.54 and 5.46. The high-affinity alpha 1-AR component of the oxymetazoline inhibition curve was predominant (57%-66%) and showed an affinity for oxymetazoline comparable to that of the alpha 1c-AR subtype. As such our results illustrate the expression of different alpha 1-AR subtypes in human prostate and importantly that alpha 1c represents the predominant alpha 1-AR subtype present in this tissue.
α1 - 肾上腺素能受体(ARs)在介导人类前列腺平滑肌收缩中起重要作用。在本研究中,通过逆转录聚合酶链反应(RT-PCR)从人前列腺中生成了覆盖3种α1 - AR亚型(α1b、α1c和α1d)不同结构域的cDNA片段。人前列腺α1c - AR PCR产物的重组部分序列(349个氨基酸)在氨基酸水平上与克隆的牛脑α1c - AR相应区域的序列有94%的同一性。在Northern印迹分析中使用人α1 - AR亚型选择性cDNA探针,在人前列腺的4个不同区域(尖部、基部、尿道周围和侧叶)检测到了与α1b -、α1c - 和α1d - AR亚型相对应的mRNA转录本的共表达。[3H] - 哌唑嗪与人前列腺膜制剂结合的竞争性抑制实验表明,非选择性α1 - 亚型拮抗剂阿夫唑嗪产生单相抑制曲线,而奥昔麻黄碱产生双组分抑制曲线,pKi值分别为8.54和5.46。奥昔麻黄碱抑制曲线的高亲和力α1 - AR组分占主导(57% - 66%),并且对奥昔麻黄碱的亲和力与α1c - AR亚型相当。因此,我们的结果说明了不同α1 - AR亚型在人前列腺中的表达,重要的是α1c是该组织中存在的主要α1 - AR亚型。