WIN-64821, A NOVEL NEUROKININ ANTAGONIST PRODUCED BY AN ASPERGILLUS SP .2. BIOLOGICAL-ACTIVITY

被引:31
作者
OLEYNEK, JJ
SEDLOCK, DM
BARROW, CJ
APPELL, KC
CASIANO, F
HAYCOCK, D
WARD, SJ
KAPLITA, P
GILLUM, AM
机构
[1] STERLING WINTHROP PHARMACEUT,DEPT NAT PROD BIOL,DIV RES,COLLEGEVILLE,PA 19426
[2] STERLING WINTHROP PHARMACEUT,DEPT NAT PROD CHEM,DIV RES,COLLEGEVILLE,PA 19426
[3] STERLING WINTHROP PHARMACEUT,DEPT ENZYMOL & RECEPTOR BIOCHEM,DIV RES,COLLEGEVILLE,PA 19426
[4] STERLING WINTHROP PHARMACEUT,DEPT NEUROSCI & INFLAMMAT,DIV RES,COLLEGEVILLE,PA 19426
关键词
D O I
10.7164/antibiotics.47.399
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
WIN 64821, a secondary metabolite produced by Aspergillus sp. (ATCC 74177) was found to inhibit radiolabeled substance P (SP) binding in a variety of tissues, including those of human origin. This compound inhibited, in a competitive manner, the binding of SP with Ki values ranging from 0.24 mu M in human astrocytoma U-373 MG cells to 7.89 mu M in rat submaxillary membranes. Additionally, WIN 64821 was found to inhibit I-125-NKA binding to the NK2 receptor in human tissue at a concentration equivalent to its NK1 activity (0.26 mu M). The inhibitory activity of WIN 64821 against an NK3 selective ligand, H-3-senktide, was found to be much weaker (Ki=15.2 mu M). WIN 64821 was also evaluated in NK1 functional assays and was found to be a competitive antagonist of SP-induced contractility in the guinea pig ileum (pA(2)=6.6) as well as an inhibitor of SP-induced Ca-45(2+) efflux from human astrocytoma U-373 MG cells (IC50 =0.6 mu M). In a rat vas deferens model, WIN 64821 inhibited eledoisin-induced contractility with an IC50 of 3.4 mu M indicating functional antagonism at the NK2 receptor. The data presented in this study provide biochemical, pharmacological and functional evidence supporting WIN 64821 as a competitive neurokinin antagonist.
引用
收藏
页码:399 / 410
页数:12
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