首页> 外文期刊>European Journal of Pharmacology: An International Journal >Lack of evidence for cross-competition between vasoactive intestinal peptide and somatostatin at their respective receptors.
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Lack of evidence for cross-competition between vasoactive intestinal peptide and somatostatin at their respective receptors.

机译:缺乏证据表明血管活性肠肽和生长抑素在各自的受体之间存在交叉竞争。

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摘要

A possible cross-competition between vasoactive intestinal peptide (VIP) and somatostatin (somatotropin release inhibiting factor; SRIF) and their respective receptors, was investigated at native or recombinant SRIF and VIP/pituitary adenylate cyclase-activating polypeptide (PACAP) receptors. The activity of VIP was examined in radioligand binding assays at mouse sst(1-5), rat sst(1-2) and human sst(1-5) receptors; or at human tumours preferentially expressing each of the five SRIF receptors. Moreover, SRIF was investigated at human tumoral tissues known to exclusively express specific VIP/PACAP receptor(s). VIP had no significant effect on any of the radioligand binding sites of the SRIF receptor family of rat, mouse or human origin tested. Conversely, SRIF did not interfere with the human VIP/PACAP binding sites tested. Taken together, the results cast reservation on the claimed cross-competition between VIP and SRIF at, specifically human sst(3) receptors, or any of the cloned SRIF or VIP/PACAP receptors recognised to date.
机译:在天然或重组SRIF和VIP /垂体腺苷酸环化酶激活多肽(PACAP)受体上研究了血管活性肠肽(VIP)和生长抑素(生长激素释放抑制因子SRIF)及其各自受体之间可能的交叉竞争。在小鼠sst(1-5),大鼠sst(1-2)和人sst(1-5)受体的放射性配体结合试验中检查了VIP的活性。或优先表达五个SRIF受体中的每一个的人类肿瘤。此外,在已知专门表达特定VIP / PACAP受体的人肿瘤组织上研究了SRIF。 VIP对测试的大鼠,小鼠或人类来源的SRIF受体家族的任何放射性配体结合位点均无明显影响。相反,SRIF不会干扰测试的人类VIP / PACAP结合位点。两者合计,结果对VIP和SRIF之间在特定的人类sst(3)受体或迄今公认的任何克隆的SRIF或VIP / PACAP受体之间的交叉竞争提出了保留。

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