THE NOVEL INS(1,4,5)P-3 ANALOG 3-AMINO-3-DEOXY-INS(1,4,5)P-3 - A PH-DEPENDENT INS(1,4,5)P-3 RECEPTOR PARTIAL AGONIST IN SH-SY5Y NEUROBLASTOMA-CELLS

被引:14
作者
KOZIKOWSKI, AP [1 ]
FAUQ, AH [1 ]
WILCOX, RA [1 ]
CHALLISS, RAJ [1 ]
NAHORSKI, SR [1 ]
机构
[1] UNIV LEICESTER,DEPT CELL PHYSIOL & PHARMACOL,LEICESTER LE1 9HN,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1021/jm00032a022
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We have synthesized the first amino-substituted inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] analogue, D-3-amino-3-deoxy-myo-Ins(1,4,5)P3 (9). Although 9 is a full agonist at the Ca2+ mobilizing Ins(1,4,5)P3 receptor at pH 7.2 and 7.6, it is apparently a high intrinsic activity partial agonist at pH 6.8, releasing only 80% of the Ins(1,4,5)P3-sensitive Ca2+ stores of SH-SY5Y cells. Additionally, 9 was able to fully displace [H-3]Ins(1,4,5)P3 from binding sites in rat cerebellum membranes at both pH 6.8 and 7.6, indicating a full interaction with the Ins(1,4,5)P3 receptor. The activity displayed by this amino analogue is unexpected and may be indicative of a pH-dependent conformational change in the amino acid residues comprising the Ins(1,4,5)P3 binding site.
引用
收藏
页码:868 / 872
页数:5
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