Suppr超能文献

尼索地平与不同程度同心性狭窄的清醒猪狭窄后心肌的灌注

Nisoldipine and perfusion of post-stenotic myocardium in conscious pigs with different degrees of concentric stenosis.

作者信息

Duncker D J, Heiligers J P, Saxena P R, Verdouw P D

机构信息

Laboratory for Experimental Cardiology, Thoraxcentre, Rotterdam, The Netherlands.

出版信息

Br J Pharmacol. 1988 May;94(1):219-27. doi: 10.1111/j.1476-5381.1988.tb11518.x.

Abstract
  1. The effects of oral nisoldipine on the perfusion and wall function of a myocardial segment distal to a fixed coronary artery stenosis were studied in 2 groups of conscious pigs with different degrees of stenosis. In group 1 (n = 8) systolic wall thickening (SWT) of the post-stenotic segment was more than 15% (27 +/- 4%); in group 2 (n = 7) SWT was less than 10% (7 +/- 1%). 2. The systemic haemodynamic profiles at baseline and during nisoldipine were similar in both groups. Dose-titrations of nisoldipine (0.24 +/- 0.02 mg kg-1 and 0.47 +/- 0.04 mg kg-1) were performed to obtain increases in heart rate of 25% and 50%, respectively. These increases were accompanied by increases in cardiac output (up to 50%) and left ventricular (LV)dP/dt max (60%), while systemic vascular resistance (35%) and mean arterial blood pressure (10%) were reduced. Left ventricular systolic and end-diastolic blood pressure and stroke volume were not affected. 3. In both groups, nisoldipine caused increases in blood flow to the non-stenotic area which favoured the subepicardium more than the subendocardium. Blood flow to the post-stenotic area of group 1 was normal at baseline and was only slightly enhanced (preferentially to the subepicardium) by nisoldipine. In the post-stenotic area of group 2 transmural and subendocardial blood flow were lower at baseline compared to the control area. Nisoldipine did not affect subepicardial blood flow but reduced subendocardial blood flow. 4. In spite of the reflex-mediated positive chronotropic actions of nisoldipine, the acute poststenotic systolic wall thickening was not affected by nisoldipine in either group. 5. We conclude that, under the experimental conditions employed (concentric stenosis, no coronary collaterals and acute drug administration), nisoldipine does not have a useful effect on post-stenotic myocardial blood flow, particularly in animals with severe stenosis. In view of a possible resetting of the baroreceptors (subsiding of the tachycardia) with chronic treatment and the presence of eccentric stenosis in many patients, additional studies are warranted.
摘要
  1. 在两组患有不同程度冠状动脉狭窄的清醒猪中,研究了口服尼索地平对固定冠状动脉狭窄远端心肌节段灌注和壁功能的影响。第一组(n = 8)狭窄后节段的收缩期壁增厚(SWT)超过15%(27±4%);第二组(n = 7)SWT小于10%(7±1%)。2. 两组在基线时和尼索地平给药期间的全身血流动力学特征相似。进行尼索地平的剂量滴定(0.24±0.02 mg·kg⁻¹和0.47±0.04 mg·kg⁻¹),以使心率分别增加25%和50%。这些增加伴随着心输出量增加(高达50%)和左心室(LV)dP/dt max增加(60%),而全身血管阻力降低(35%),平均动脉血压降低(10%)。左心室收缩压和舒张压以及每搏输出量未受影响。3. 在两组中,尼索地平均使非狭窄区域的血流增加,对心外膜下的血流增加比对心内膜下的血流增加更有利。第一组狭窄后区域的血流在基线时正常,尼索地平仅使其略有增加(优先于心外膜下)。与对照组区域相比,第二组狭窄后区域的透壁血流和心内膜下血流在基线时较低。尼索地平不影响心外膜下血流,但减少心内膜下血流。4.尽管尼索地平具有反射介导的正性变时作用,但两组中尼索地平均未影响急性狭窄后收缩期壁增厚。5. 我们得出结论,在所采用的实验条件下(同心狭窄、无冠状动脉侧支和急性药物给药),尼索地平对狭窄后心肌血流没有有益影响,特别是在严重狭窄的动物中。鉴于长期治疗可能会使压力感受器重新设定(心动过速消退),并且许多患者存在偏心狭窄,因此有必要进行进一步研究。

相似文献

6
Is nisoldipine capable of reducing left ventricular preload?
Eur J Pharmacol. 1984 Feb 10;98(1):137-40. doi: 10.1016/0014-2999(84)90120-1.
9
Nisoldipine improves blood flow to skeletal muscles in conscious pigs with chronic heart failure.
Eur Heart J. 1990 Jun;11(6):552-9. doi: 10.1093/oxfordjournals.eurheartj.a059749.

本文引用的文献

1
Coronary steal-induced increase in myocardial infarct size after pharmacologic coronary vasodilation.
Am J Cardiol. 1980 Jul;46(1):83-90. doi: 10.1016/0002-9149(80)90609-8.
6
Is nisoldipine capable of reducing left ventricular preload?
Eur J Pharmacol. 1984 Feb 10;98(1):137-40. doi: 10.1016/0014-2999(84)90120-1.
8
Coronary physiology.冠状动脉生理学
Physiol Rev. 1983 Jan;63(1):1-205. doi: 10.1152/physrev.1983.63.1.1.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验