首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Photolysis of the novel inotropes EMD 57033 and EMD 57439: evidence that Ca2+ sensitization and phosphodiesterase inhibition depend upon the same enantiomeric site.
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Photolysis of the novel inotropes EMD 57033 and EMD 57439: evidence that Ca2+ sensitization and phosphodiesterase inhibition depend upon the same enantiomeric site.

机译:新型变力剂EMD 57033和EMD 57439的光解作用:证据表明Ca2 +致敏性和磷酸二酯酶抑制作用取决于相同的对映体位点。

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摘要

1. We studied the effects of flash photolysis on the novel enantiomeric cardiac inotropes EMD 57033 (a calcium sensitizer) and EMD 57439 (a phosphodiesterase III inhibitor) in rat isolated ventricular trabeculae. 2. In skinned trabeculae, EMD 57439 had no effect on force production, consistent with lack of an active cyclic AMP system in this preparation. In contrast, EMD 57033 potentiated force at partial and maximal activation. A single flash of near u.v. light given at partial activation (30-70%) reduced force potentiation by 52.4 +/- 5.2%. No effect was produced by flashes in the presence of EMD 57439 or in the absence of either drug. 3. The time course of relaxation induced by EMD 57033 photolysis was indistinguishable from that obtained on deactivating the muscle by rapidly lowering Ca2+ using photolysis of the caged chelator of calcium, diazo-2. 4. In intact, twitching trabeculae, EMD 57033 increased diastolic and peak force and slowed relaxation. These effects were simultaneously reduced by a light flash. In these muscles EMD 57439 reduced force, without affecting the twitch time course. These effects were also reduced by a light flash. 5. The u.v. absorbance spectra of EMD 57033 and EMD 57439 were identical. After photolysis optical density decreased substantially and the peak shifted from 320 nm to 280 nm. 6. The proton n.m.r. spectra of these compounds were identical. The main change post-photolysis was a decrease in the proton signal associated with the enantiomeric carbon atom. 7. This novel manipulation of the molecular structure of EMD 57033 and EMD 57439 within an experiment thus provides direct evidence linking calcium sensitization to a particular molecular structure. The three main effects of the sensitizer on the twitch were simultaneously abolished and may be mechanistically linked. Flash photolysis may be a useful tool for further investigations of the actions of these compounds. In particular, flash photolysis of the sensitizer represents a novel method of rapidly deactivating cardiac muscle.
机译:1.我们研究了快速光解对大鼠离体小梁中新型对映体心脏正性肌力药物EMD 57033(钙敏化剂)和EMD 57439(磷酸二酯酶III抑制剂)的影响。 2.在皮肤小梁中,EMD 57439对力的产生没有影响,这与该制剂中缺乏活性的环AMP系统一致。相反,EMD 57033在部分和最大激活时会增强作用力。一次近紫外线的闪光部分激活(30-70%)时发出的光会使力量增强降低52.4 +/- 5.2%。在有EMD 57439的情况下或在两种药物都不存在的情况下,闪光不会产生任何影响。 3. EMD 57033光解引起的弛豫的时间进程与笼罩式钙重氮2的螯合剂的光解通过迅速降低Ca2 +使肌肉失活所获得的弛豫时间进程没有区别。 4.在完整的小梁抽搐中,EMD 57033增加了舒张力和峰值力,并减慢了放松。闪光灯同时减轻了这些影响。在这些肌肉中,EMD 57439的作用力减小,而不会影响抽动时间。闪光也可以减轻这些影响。 5.紫外线EMD 57033和EMD 57439的吸收光谱相同。光解后,光密度显着降低,峰从320 nm移至280 nm。 6.质子这些化合物的光谱相同。光解后的主要变化是与对映体碳原子相关的质子信号的减少。 7.实验中对EMD 57033和EMD 57439分子结构的这种新颖操纵,提供了将钙敏化与特定分子结构相关联的直接证据。敏化剂对抽搐的三个主要作用同时被消除,并且可能是机械性的。闪光光解可能是进一步研究这些化合物作用的有用工具。特别地,敏化剂的快速光解代表了快速使心肌失活的新方法。

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