去甲肾上腺素诱发心肌病的心室功能障碍。

Circulatory shock Pub Date : 1994-07-01
F M Powers, R Pifarre, J X Thomas
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引用次数: 0

摘要

去甲肾上腺素引起的心肌病引起的心功能障碍尚未得到充分的研究。本研究评估在三个水平的去甲肾上腺素(NE)诱导的损伤中收缩和舒张功能的急性和慢性变化。将家兔分别输注生理盐水或2、4或6微克/千克/分钟NE,持续90分钟。在输注后立即评估心室功能,或在48小时使用离体无射血心脏制剂评估心室功能。用Krebs-Henseleit缓冲液以10 ml/min/g灌注心脏。基线测量后,心脏灌注NE(10(-10)至10(-7)M),在基线和各NE浓度下记录稳态左心室压(LVP)、+dP/dt和-dP/dt。NE输注急性降低左室收缩功能基线。LVP和+dP/dt的降低与NE输注剂量呈负相关。48小时时,所有NE组的LVP和+dP/dt均略有改善,但仅在输注4微克NE的兔心脏中有显著改善。灌注6微克NE后,小鼠心脏收缩功能仍然受到抑制。与生理盐水处理的心脏相比,NE输注后心脏舒张(-dP/dt)功能受损,并且在48小时内没有改善。虽然基线功能下降,但肌病心脏在10(-7)M NE时增加的心室功能与正常心脏相同。这些结果表明:a) NE输注后左室收缩和舒张功能急性受损;b) 48小时内收缩功能改善;c) NE对收缩能力的增强不受损害;d)收缩功能恢复在舒张功能改善之前。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ventricular dysfunction in norepinephrine-induced cardiomyopathy.

Cardiac dysfunction resulting from norepinephrine-induced cardiomyopathy has not been fully investigated. This study evaluates acute and chronic changes in systolic and diastolic function at three levels of norepinephrine (NE)-induced injury. Rabbits were infused with saline or 2, 4, or 6 micrograms/kg/min NE for 90 min. Ventricular function was assessed immediately after infusion or at 48 hr using the isolated non-ejecting heart preparation. Hearts were perfused at 10 ml/min/g with Krebs-Henseleit buffer. After baseline measurements, hearts were perfused with NE (10(-10) to 10(-7) M). Steady state left ventricular pressure (LVP), +dP/dt, and -dP/dt were recorded at baseline and each NE concentration. NE infusion acutely depressed baseline LV systolic function. Decreases in LVP and +dP/dt were inversely related to dose of infused NE. By 48 hr, LVP and +dP/dt improved slightly in all NE groups but improvement was significant only in hearts from rabbits infused with 4 micrograms NE. Systolic function of hearts from animals infused with 6 micrograms NE remained depressed. Diastolic (-dP/dt) function was impaired following NE infusion when compared to saline treated hearts and did not improve within 48 hr. Although baseline function is depressed, myopathic hearts increased ventricular function the same amount as normal hearts at 10(-7) M NE. These findings demonstrate a) impairment in LV systolic and diastolic function acutely after NE infusion, b) improvement in systolic function within 48 hr, c) ability to increase contractility in response to NE is not impaired, and d) recovery of systolic function precedes improvement in diastolic function.

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