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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Therapeutic Relevance of Elevated Blood Pressure After Ischemic Stroke in the Hypertensive Rats
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Therapeutic Relevance of Elevated Blood Pressure After Ischemic Stroke in the Hypertensive Rats

机译:高血压大鼠缺血性脑卒中后血压升高的治疗相关性

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摘要

Over 80% of patients exhibit an acute increase in blood pressure (BP) following stroke. Current clinical guidelines make no distinction in BP management between patients with or without prior hypertension. Spontaneously hypertensive (SH) rats were preinstrumented with telemeters to record BP, intracranial pressure, and brain tissue oxygen in the predicted ischemic penumbra for 3 days before and 10 days after transient middle cerebral artery occlusion (n=8 per group) or sham (n=5). Before stroke, BP was either left untreated or chronically treated to a normotensive level (enalapril 10 mg/kg per day). Poststroke elevations in BP were either left uncontrolled, controlled (to the prestroke baseline level), or overcontrolled (to a normotensive level) via subcutaneous infusion of labetalol. Baseline values of intracranial pressure and brain tissue oxygen were similar between all groups, whereas BP was lower in treated SH rats (144 +/- 3 versus 115 +/- 5 mm Hg; P<0.001). Following middle cerebral artery occlusion, a similar rise in BP was observed in untreated (+16 +/- 2 mm Hg; P=0.005) and treated SH rats (+13 +/- 5 mm Hg; P=0.021). Intervening to prevent BP from increasing after stroke did not worsen outcome. However, reducing BP below prestroke baseline levels was associated with higher intracranial pressure (days 1-3; P<0.001), reduced cerebral perfusion pressure (days 2-4; P<0.001), higher mortality, slower functional recovery and larger infarct volumes. Although treating to maintain BP at the prestroke baseline level was not detrimental, our results suggest that when setting BP targets after stroke, consideration must be given to the potential negative impact of inadvertent excessive BP lowering in subjects with undiagnosed or poorly controlled hypertension.
机译:超过80%的患者表现出卒中后血压(BP)的急性增加。目前的临床指南在患者之间没有区别或不含高血压的患者。自发性高血压(SH)大鼠用遥测瞬间记录预测缺血半影中的BP,颅内压力和脑组织氧3天和瞬时中脑动脉闭塞(N = 8每组)或假(n = 5)。在中风之前,BP无论是未经处理的还是长期处理到正常均衡的水平(每天烯丙醇10 mg / kg)。通过皮下注射Labetalol,BP的失败者升高无论是不受控制的,控制(对Prestroke基线水平),或过度控制(对正常血压液体)。所有基团之间的颅内压和脑组织氧的基线值相似,而在处理的SH大鼠(144 +/- 3对115 +/- 5mm Hg; P <0.001)中,BP较低。在中间脑动脉闭塞后,在未处理的(+ 16 +/- 2mm Hg; p = 0.005)和处理的SH大鼠(+13 +/- 5mm Hg; p = 0.021)中,观察到Bp的类似升高。干预以防止BP在中风没有恶化结果后增加。然而,降低PRESTROKE基线水平以下的BP与颅内压(天1-3; P <0.001天)相关,降低脑灌注压力(天2-4; P <0.001天),提高死亡率,较慢的官能恢复和较大的梗塞体积。虽然治疗PRESTROKE基线水平保持BP并不有害,但我们的结果表明,当中风后设定BP靶标时,必须考虑因未确诊或受控制的高血压受到较低的受试者的无意过量BP的潜在负面影响。

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