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U73122,一种氨基甾醇类磷脂酶 C 抑制剂,通过依赖于 PIP2 的机制成为一种强有力的心脏磷脂酶 D 的抑制剂。

U73122, an aminosteroid phospholipase C inhibitor, is a potent inhibitor of cardiac phospholipase D by a PIP2-dependent mechanism.

机构信息

Department of Internal Medicine II, University Hospital Schleswig-Holstein, Lübeck, Germany.

出版信息

J Cardiovasc Pharmacol. 2010 Jun;55(6):555-9. doi: 10.1097/FJC.0b013e3181d8bec5.

DOI:10.1097/FJC.0b013e3181d8bec5
PMID:20179606
Abstract

The aminosteroid 1-[6-({17beta-3-methoxyestra-1,3,5(10)-trien-17-yl}amino)hexyl]-1H-pyrrole-2,5-dione (U73122) has been extensively used as a pharmacologic inhibitor of phospholipase C (PLC). The inhibitory effect of U73122 on PLC activity is most likely the result of decreased availability of phosphatidylinositol 4,5-bisphosphate (PIP2), the substrate of the PLC signal transduction pathway, rather than direct inhibition of the enzyme. PIP2 is a phospholipid with pleiotropic cellular functions, including a pivotal role in regulating cardiac phospholipase D (PLD) signal transduction. Here, we hypothesized that U73122 acts as an inhibitor of cardiac PLD activity by interference with PIP2. U73122 concentration-dependently inhibited PLD activity in rat myocardial membranes. The inhibitory effect of U73122 was significantly attenuated when assayed on solubilized PLD activity and was completely restored if solubilized PLD activity was assayed in the presence of PIP2. U73122 had no inhibitory effect on purified PLD indicating that the substance does not interact with PLD directly. These data highlight a mechanism of action of U73122 as an inhibitor of myocardial PLD by interaction with PIP2 as a cofactor for optimal PLD activity. Hence, studies using U73122 as a specific inhibitor of PLC have to take into account that PLD may be involved in some of the effects ascribed to PLC.

摘要

氨基甾体 1-[6-({17β-3-甲氧基雌-1,3,5(10)-三烯-17-基}氨基)己基]-1H-吡咯-2,5-二酮 (U73122) 已被广泛用作磷脂酶 C (PLC) 的药理学抑制剂。U73122 对 PLC 活性的抑制作用很可能是由于可利用的磷脂酰肌醇 4,5-二磷酸 (PIP2) 减少的结果,PIP2 是 PLC 信号转导途径的底物,而不是直接抑制酶。PIP2 是一种具有多种细胞功能的磷脂,包括在调节心脏磷脂酶 D (PLD) 信号转导中起关键作用。在这里,我们假设 U73122 通过干扰 PIP2 作为心脏 PLD 活性的抑制剂起作用。U73122 浓度依赖性地抑制大鼠心肌膜中的 PLD 活性。当在可溶性 PLD 活性上进行测定时,U73122 的抑制作用显著减弱,如果在存在 PIP2 的情况下测定可溶性 PLD 活性,则完全恢复。U73122 对纯化的 PLD 没有抑制作用,表明该物质不会直接与 PLD 相互作用。这些数据突出了 U73122 作为心肌 PLD 抑制剂的作用机制,通过与 PIP2 相互作用作为最佳 PLD 活性的辅助因子。因此,使用 U73122 作为 PLC 的特异性抑制剂的研究必须考虑到 PLD 可能参与一些归因于 PLC 的作用。

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