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新型Na(+)-H+交换抑制剂Hoe 694对豚鼠心室肌细胞内pH调节的作用

Effect of Hoe 694, a novel Na(+)-H+ exchange inhibitor, on intracellular pH regulation in the guinea-pig ventricular myocyte.

作者信息

Loh S H, Sun B, Vaughan-Jones R D

机构信息

University Laboratory of Physiology, Oxford.

出版信息

Br J Pharmacol. 1996 Aug;118(8):1905-12. doi: 10.1111/j.1476-5381.1996.tb15623.x.

Abstract
  1. Hoe 694 (3-methylsulphonyl-4-piperidinobenzoyl, guanidine hydrochloride) is a Na+/H+ exchange (NHE) inhibitor exhibiting cardioprotective properties during ischaemia and reperfusion in animal hearts. We have (i) tested the selectivity of Hoe 694 for NHE over other pHi-regulating mechanisms in the myocardium, and (ii) tested if the functionally important NHE isoform contributing to intracellular pH regulation in heart is NHE-1, as suggested from molecular biology studies of this protein. 2. pHi was recorded by fluorescence microscopy with carboxy SNARF-1, AM-loaded into single ventricular myocytes of guinea-pig. 3. In nominally HCO3-free media, recovery of pHi from an intracellular acid load is mediated by NHE, and was inhibited by Hoe 694, amiloride (an NHE inhibitor) or dimethyl amiloride (DMA, a high affinity NHE inhibitor) with potency values of 2.05, 87.3 and 1.96 microM respectively, giving the potency series: Hoe 694 congruent to DMA > > amiloride. This potency series, and the potency values (corrected for drug competition with extracellular Na+) match those determined previously for cloned NHE-1 expressed in mutant fibroblasts. In the absence of extracellular Na+ (to inhibit NHE), Hoe 694 had no effect on pHi. 4. In 5% CO2/HCO3(-)-buffered solution containing DMA, pHi recovery from acidosis is mediated by Na(+)-HCO3- symport and was unaffected by Hoe 694. The drug also had no effect on pHi recovery from an alkali-load, a process largely mediated by Cl(-)-HCO3- exchange. Finally, the fall of pHi upon adding extracellular Na-lactate is assisted by H(+)-lactate symport, and this too was unaffected by Hoe 694. 5. We conclude (i) Hoe 694 has no detectable inhibitory potency for pH-regulating carriers in heart other than NHE. (ii) native NHE functioning during pHi-regulation in the cardiomyocyte is the NHE-1 isoform. These data strengthen the case for NHE-1 being the receptor for mediating the cardioprotective effects of Hoe 694.
摘要
  1. Hoe 694(3-甲基磺酰基-4-哌啶基苯甲酰基盐酸胍)是一种Na⁺/H⁺交换(NHE)抑制剂,在动物心脏缺血和再灌注期间具有心脏保护特性。我们进行了以下两项研究:(i)测试了Hoe 694对心肌中NHE相对于其他调节细胞内pH机制的选择性;(ii)测试了如该蛋白分子生物学研究所暗示的,在心脏中对细胞内pH调节起重要作用的NHE同工型是否为NHE-1。2. 通过荧光显微镜记录豚鼠单个心室肌细胞中羧基SNARF-1 AM加载后的细胞内pH(pHi)。3. 在名义上无HCO₃⁻的培养基中,细胞内酸负荷后pHi的恢复由NHE介导,并被Hoe 694、氨氯地平(一种NHE抑制剂)或二甲基氨氯地平(DMA,一种高亲和力NHE抑制剂)抑制,效价分别为2.05、87.3和1.96 μM,得出效价顺序:Hoe 69₄≡DMA >>氨氯地平。该效价顺序以及效价值(校正药物与细胞外Na⁺的竞争)与先前在突变成纤维细胞中表达的克隆NHE-1所确定的结果相符。在无细胞外Na⁺(以抑制NHE)的情况下,Hoe 694对pHi无影响。4. 在含有DMA的5% CO₂/HCO₃⁻缓冲溶液中,酸中毒后pHi的恢复由Na⁺-HCO₃⁻共转运介导,且不受Hoe 694影响。该药物对碱负荷后pHi的恢复也无影响,碱负荷后pHi的恢复主要由Cl⁻-HCO₃⁻交换介导。最后,添加细胞外乳酸钠后pHi的下降由H⁺-乳酸共转运辅助,这同样不受Hoe 694影响。5. 我们得出以下结论:(i)除NHE外,Hoe 694对心脏中调节pH的载体无明显抑制作用。(ii)心肌细胞中pHi调节过程中起作用的天然NHE是NHE-1同工型。这些数据进一步证明NHE-1是介导Hoe 694心脏保护作用的受体。

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Characterization of intracellular pH regulation in the guinea-pig ventricular myocyte.豚鼠心室肌细胞内pH调节的特征
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