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1
Photolysis of the novel inotropes EMD 57033 and EMD 57439: evidence that Ca2+ sensitization and phosphodiesterase inhibition depend upon the same enantiomeric site.新型正性肌力药EMD 57033和EMD 57439的光解作用:钙离子致敏和磷酸二酯酶抑制作用取决于同一对映体位点的证据。
Br J Pharmacol. 1996 Aug;118(8):2037-44. doi: 10.1111/j.1476-5381.1996.tb15641.x.
2
The two mechanisms of action of racemic cardiotonic EMD 53998, calcium sensitization and phosphodiesterase inhibition, reside in different enantiomers.消旋强心剂EMD 53998的两种作用机制,即钙致敏作用和磷酸二酯酶抑制作用,分别存在于不同的对映体中。
J Cardiovasc Pharmacol. 1993 Jun;21(6):883-92. doi: 10.1097/00005344-199306000-00006.
3
The effect of EMD 57033, a novel cardiotonic agent, on the relaxation of skinned cardiac and skeletal muscle produced by photolysis of diazo-2, a caged calcium chelator.
Pflugers Arch. 1993 Oct;425(1-2):175-7. doi: 10.1007/BF00374519.
4
Novel diazinone derivatives separate myofilament Ca2+ sensitization and phosphodiesterase III inhibitory effects in guinea pig myocardium.新型二嗪农衍生物可区分豚鼠心肌中肌丝Ca2+致敏作用和磷酸二酯酶III抑制作用。
Circ Res. 1992 Jun;70(6):1081-90. doi: 10.1161/01.res.70.6.1081.
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The effects of the inotropic agent EMD 57033 on activation and relaxation kinetics in frog skinned skeletal muscle.
Pflugers Arch. 2001 May;442(2):171-7. doi: 10.1007/s004240000500.
6
In vivo evidence of positive inotropism of EMD 57033 through calcium sensitization.EMD 57033通过钙致敏产生正性肌力作用的体内证据。
J Cardiovasc Pharmacol. 1997 May;29(5):647-55. doi: 10.1097/00005344-199705000-00013.
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The thiadiazinone EMD 57033 speeds the activation of skinned cardiac muscle produced by the photolysis of nitr-5.
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Ca2+ sensitization in idiopathic dilated human myocardium. Differential in vitro effects of (+)-(5-methyl-6-phenyl)-1,3,5,6-tetrahydro-3,6-methano-1,5-benzodiazoci ne-2,4-dione, a novel purely Ca2+sensitizing agent, and (+)-5-(1-(3,4-dimethoxybenzoyl)-1,2,3,4-tetrahydroquinolin-6-yl)-6-meth yl-3, 6-dihydro-2H-1,3,4-thiadiazin-2-one on skinned fibres and isolated ventricular strips.特发性扩张型心肌病患者心肌中的钙离子致敏作用。新型纯钙离子致敏剂(+)-(5-甲基-6-苯基)-1,3,5,6-四氢-3,6-亚甲基-1,5-苯并二氮杂卓-2,4-二酮与(+)-5-(1-(3,4-二甲氧基苯甲酰基)-1,2,3,4-四氢喹啉-6-基)-6-甲基-3,6-二氢-2H-1,3,4-噻二嗪-2-酮对脱细胞纤维和离体心室肌条的体外差异作用
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9
Replacement of troponin-I in slow-twitch skeletal muscle alters the effects of the calcium sensitizer EMD 53998.慢肌骨骼肌中肌钙蛋白-I的替代改变了钙敏化剂EMD 53998的作用。
Pflugers Arch. 1998 Aug;436(3):398-406. doi: 10.1007/s004240050649.
10
Differential effects of the optical isomers of EMD 53998 on contraction and cytoplasmic Ca2+ in isolated ferret cardiac muscle.EMD 53998光学异构体对离体雪貂心肌收缩和细胞质Ca2+的不同作用。
Circ Res. 1993 Jul;73(1):61-70. doi: 10.1161/01.res.73.1.61.

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1
Effects of troponin C isoform on the action of the cardiotonic agent EMD 57033.肌钙蛋白C亚型对强心剂EMD 57033作用的影响。
Biochem J. 2005 Jun 15;388(Pt 3):905-12. doi: 10.1042/BJ20041841.

本文引用的文献

1
Interaction of cardiotonic thiadiazinone derivatives with cardiac troponin C.强心噻二嗪酮衍生物与心肌肌钙蛋白C的相互作用。
J Biol Chem. 1996 Jan 12;271(2):817-23.
2
Differential effects of the optical isomers of EMD 53998 on contraction and cytoplasmic Ca2+ in isolated ferret cardiac muscle.EMD 53998光学异构体对离体雪貂心肌收缩和细胞质Ca2+的不同作用。
Circ Res. 1993 Jul;73(1):61-70. doi: 10.1161/01.res.73.1.61.
3
Controlling cell chemistry with caged compounds.利用笼形化合物控制细胞化学。
Annu Rev Physiol. 1993;55:755-84. doi: 10.1146/annurev.ph.55.030193.003543.
4
The effect of EMD 57033, a novel cardiotonic agent, on the relaxation of skinned cardiac and skeletal muscle produced by photolysis of diazo-2, a caged calcium chelator.
Pflugers Arch. 1993 Oct;425(1-2):175-7. doi: 10.1007/BF00374519.
5
Stereoselective actions of thiadiazinones on canine cardiac myocytes and myofilaments.噻二嗪酮对犬心肌细胞和肌丝的立体选择性作用。
Circ Res. 1993 Dec;73(6):981-90. doi: 10.1161/01.res.73.6.981.
6
The thiadiazinone EMD 57033 speeds the activation of skinned cardiac muscle produced by the photolysis of nitr-5.
Pflugers Arch. 1994 Jul;427(5-6):550-2. doi: 10.1007/BF00374274.
7
The role of troponin C in modulating the Ca2+ sensitivity of mammalian skinned cardiac and skeletal muscle fibres.肌钙蛋白C在调节哺乳动物去表皮心肌和骨骼肌纤维的Ca2+敏感性中的作用。
J Physiol. 1994 Oct 1;480 ( Pt 1)(Pt 1):45-60. doi: 10.1113/jphysiol.1994.sp020339.
8
Effects of troponin-I extraction with vanadate and of the calcium sensitizer EMD 53998 on the rate of force generation in skinned cardiac muscle.
J Mol Cell Cardiol. 1995 Jan;27(1):615-23. doi: 10.1016/s0022-2828(08)80055-7.
9
The two mechanisms of action of racemic cardiotonic EMD 53998, calcium sensitization and phosphodiesterase inhibition, reside in different enantiomers.消旋强心剂EMD 53998的两种作用机制,即钙致敏作用和磷酸二酯酶抑制作用,分别存在于不同的对映体中。
J Cardiovasc Pharmacol. 1993 Jun;21(6):883-92. doi: 10.1097/00005344-199306000-00006.
10
Steady-state [Ca2+]i-force relationship in intact twitching cardiac muscle: direct evidence for modulation by isoproterenol and EMD 53998.完整的抽搐心肌中稳态[Ca2+]i-张力关系:异丙肾上腺素和EMD 53998调节的直接证据。
Biophys J. 1995 Jul;69(1):189-201. doi: 10.1016/S0006-3495(95)79889-7.

新型正性肌力药EMD 57033和EMD 57439的光解作用:钙离子致敏和磷酸二酯酶抑制作用取决于同一对映体位点的证据。

Photolysis of the novel inotropes EMD 57033 and EMD 57439: evidence that Ca2+ sensitization and phosphodiesterase inhibition depend upon the same enantiomeric site.

作者信息

Lee J A, Palmer S, Kentish J C

机构信息

Department of Pharmacology, UMDS, London.

出版信息

Br J Pharmacol. 1996 Aug;118(8):2037-44. doi: 10.1111/j.1476-5381.1996.tb15641.x.

DOI:10.1111/j.1476-5381.1996.tb15641.x
PMID:8864540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1909887/
Abstract
  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.
摘要
  1. 我们研究了闪光光解对新型对映体强心剂EMD 57033(一种钙敏化剂)和EMD 57439(一种磷酸二酯酶III抑制剂)在大鼠离体心室小梁中的作用。2. 在去表皮小梁中,EMD 57439对力的产生没有影响,这与该制剂中缺乏活性环磷酸腺苷系统一致。相比之下,EMD 57033在部分激活和最大激活时增强了力。在部分激活(30 - 70%)时给予单次近紫外光闪光可使力的增强降低52.4 +/- 5.2%。在EMD 57439存在时或两种药物都不存在时闪光均无作用。3. EMD 57033光解诱导的松弛时间进程与通过使用钙笼形螯合剂重氮-2的光解快速降低Ca2+使肌肉失活所获得的时间进程无法区分。4. 在完整的、抽搐的小梁中,EMD 57033增加舒张期和峰值力并减慢松弛。这些作用同时被一次闪光降低。在这些肌肉中,EMD 57439降低力,但不影响抽搐时间进程。这些作用也被一次闪光降低。5. EMD 57033和EMD 57439的紫外吸收光谱相同。光解后光密度大幅下降,峰值从320 nm移至280 nm。6. 这些化合物的质子核磁共振光谱相同。光解后的主要变化是与对映体碳原子相关的质子信号减少。7. 因此,在一个实验中对EMD 57033和EMD 57439分子结构的这种新颖操作提供了将钙敏化与特定分子结构联系起来的直接证据。敏化剂对抽搐的三个主要作用同时被消除,并且可能在机制上相关联。闪光光解可能是进一步研究这些化合物作用的有用工具。特别是,敏化剂的闪光光解代表了一种快速使心肌失活的新方法。