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钠氢交换体抑制剂无法预防山羊的心房电重构。

Inhibitors of the Na+/H+ exchanger cannot prevent atrial electrical remodeling in the goat.

作者信息

Blaauw Yuri, Beier Norbert, van der Voort Pepijn, van Hunnik Arne, Schotten Ulrich, Allessie Maurits A

机构信息

Department of Physiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht, The Netherlands.

出版信息

J Cardiovasc Electrophysiol. 2004 Apr;15(4):440-6. doi: 10.1046/j.1540-8167.2004.03498.x.

Abstract

INTRODUCTION

It has been suggested that blockade of the Na+/H+ exchanger (NHE1) can prevent atrial fibrillation (AF)-induced electrical remodeling and the development of AF.

METHODS AND RESULTS

AF was maintained by burst pacing in 10 chronically instrumented conscious goats. Intravenous and oral dosages of two NHE1 blockers (EMD87580 and EMD125021) resulted in plasma levels several magnitudes higher than required for effective NHE1 blockade. Shortening of atrial refractoriness immediately after 5 minutes of AF was not prevented by NHE1 blockade. In remodeled atria, increasing dosages of EMD87580 and EMD125021 did not reverse shortening of the atrial refractory period or reduce the duration of AF episodes. The cycle length during persistent AF also was not affected. Oral pretreatment with EMD87580 (8 mg/kg bid) starting 3 days before AF could not prevent electrical remodeling. After 24 and 48 hours of remodeling, the duration of AF paroxysms was 47 +/- 32 seconds and 135 +/- 63 seconds compared to 56 +/- 17 seconds and 136 +/- 52 seconds in placebo-treated animals (P > 0.8), respectively.

CONCLUSION

In the goat model of AF, the Na+/H+ exchanger inhibitors EMD87580 and EMD125021 did not prevent or revert AF-induced electrical remodeling. This indicates that activation of the Na+/H+ exchanger is not involved in the intracellular pathways of electrical remodeling. This does not support the suggestion that blockers of the Na+/H+ exchanger may be beneficial for prevention and treatment of AF.

摘要

引言

有人提出,阻断钠氢交换体(NHE1)可预防心房颤动(AF)诱发的电重构及房颤的发生。

方法与结果

通过对10只长期植入仪器的清醒山羊进行短阵猝发起搏来维持房颤。两种NHE1阻滞剂(EMD87580和EMD125021)的静脉和口服剂量导致血浆水平比有效阻断NHE1所需水平高几个数量级。房颤5分钟后立即出现的心房不应期缩短并未因NHE1阻断而得到预防。在重构的心房中,增加EMD87580和EMD125021的剂量并不能逆转心房不应期的缩短或减少房颤发作的持续时间。持续性房颤期间的周期长度也未受影响。在房颤发作前3天开始用EMD87580(8毫克/千克,每日两次)进行口服预处理,无法预防电重构。在重构24小时和48小时后,房颤发作的持续时间分别为47±32秒和135±63秒,而安慰剂治疗动物的相应时间分别为56±17秒和136±52秒(P>0.8)。

结论

在山羊房颤模型中,钠氢交换体抑制剂EMD87580和EMD125021不能预防或逆转房颤诱发的电重构。这表明钠氢交换体的激活不参与电重构的细胞内途径。这并不支持钠氢交换体阻滞剂可能对房颤的预防和治疗有益的观点。

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