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成年犬逐渐诱导压力超负荷新模型中左心室功能障碍的病前决定因素

Premorbid determinants of left ventricular dysfunction in a novel model of gradually induced pressure overload in the adult canine.

作者信息

Koide M, Nagatsu M, Zile M R, Hamawaki M, Swindle M M, Keech G, DeFreyte G, Tagawa H, Cooper G, Carabello B A

机构信息

Cardiology Division, Medical University of South Carolina, Charleston 29425-2221, USA.

出版信息

Circulation. 1997 Mar 18;95(6):1601-10. doi: 10.1161/01.cir.95.6.1601.

Abstract

BACKGROUND

When a pressure overload is placed on the left ventricle, some patients develop relatively modest hypertrophy whereas others develop extensive hypertrophy. Likewise, the occurrence of contractile dysfunction also is variable. The cause of this heterogeneity is not well understood.

METHODS AND RESULTS

We recently developed a model of gradual proximal aortic constriction in the adult canine that mimicked the heterogeneity of the hypertrophic response seen in humans. We hypothesized that differences in outcome were related to differences present before banding. Fifteen animals were studied initially. Ten developed left ventricular dysfunction (dys group). Five dogs maintained normal function (nl group). At baseline, the nl group had a lower mean systolic wall stress (96 +/- 9 kdyne/cm2; dys group, 156 +/- 7 kdyne/cm2; P < .0002) and greater relative left ventricular mass (left ventricular weight [g]/body wt [kg], 5.1 +/- 0.36; dys group, 3.9 +/- 0.26; P < .02). On the basis of differences in mean systolic wall stress at baseline, we predicted outcome in the next 28 dogs by using a cutoff of 115 kdyne/cm2. Eighteen of 20 dogs with baseline mean systolic stress > 115 kdyne/cm2 developed dysfunction whereas 6 of 8 dogs with resting stress < or = 115 kdyne/cm2 maintained normal function.

CONCLUSIONS

We conclude that this canine model mimicked the heterogeneous hypertrophic response seen in humans. In the group that eventually developed dysfunction there was less cardiac mass despite 60% higher wall stress at baseline, suggesting a different set point for regulating myocardial growth in the two groups.

摘要

背景

当左心室承受压力过载时,一些患者会出现相对适度的肥厚,而另一些患者则会出现广泛的肥厚。同样,收缩功能障碍的发生情况也各不相同。这种异质性的原因尚不清楚。

方法与结果

我们最近在成年犬中建立了一种逐渐进行近端主动脉缩窄的模型,该模型模拟了人类中观察到的肥厚反应的异质性。我们假设结果的差异与缩窄前存在的差异有关。最初研究了15只动物。其中10只出现左心室功能障碍(功能障碍组)。5只狗维持正常功能(正常组)。在基线时,正常组的平均收缩期壁应力较低(96±9达因/平方厘米;功能障碍组为156±7达因/平方厘米;P<.0002),相对左心室质量较大(左心室重量[克]/体重[千克],5.1±0.36;功能障碍组为3.9±0.26;P<.02)。基于基线时平均收缩期壁应力的差异,我们使用115达因/平方厘米的临界值预测了接下来28只狗的结果。20只基线平均收缩期应力>115达因/平方厘米的狗中有18只出现功能障碍,而8只静息应力≤115达因/平方厘米的狗中有6只维持正常功能。

结论

我们得出结论,该犬模型模拟了人类中观察到的异质性肥厚反应。在最终出现功能障碍的组中,尽管基线时壁应力高60%,但心脏质量较小,这表明两组心肌生长的调节设定点不同。

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