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β受体阻滞剂可改善舒张性心力衰竭高血压大鼠的生存率、左心室功能和心肌重塑。

Beta-blocker improves survival, left ventricular function, and myocardial remodeling in hypertensive rats with diastolic heart failure.

作者信息

Kobayashi Masayuki, Machida Noboru, Mitsuishi Megumi, Yamane Yoshihisa

机构信息

Department of Veterinary Surgery, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo 183-8509, Japan.

出版信息

Am J Hypertens. 2004 Dec;17(12 Pt 1):1112-9. doi: 10.1016/j.amjhyper.2004.07.007.

Abstract

BACKGROUND

Chronic beta-blocker therapy improves survival and left ventricular (LV) systolic function in patients with congestive heart failure. However, its efficacy in diastolic heart failure (DHF) with preserved normal LV systolic function remains uncertain.

METHODS

Dahl salt-sensitive hypertensive rats fed a high-salt diet from 7 weeks of age were randomized to groups that were either not treated (DHF; n = 20) or treated with metoprolol (MP) from 7 weeks of age (DHF+7wkMP; n = 22) or from 17 weeks of age (DHF+17wkMP; n = 8). Both LV function and remodeling were evaluated by serial echocardiography, followed by hemodynamic and pathologic studies.

RESULTS

Hypertension and pressure-overload LV hypertrophy were established by 17 weeks of age in DHF rats. At about 20 weeks of age DHF rats experienced overt heart failure, which was accompanied not by a decrease in LV fractional shortening but by diastolic filling abnormalities. The LV concentric hypertrophy was strikingly attenuated in DHF+7wkMP rats but not in DHF+17wkMP rats. However, LV myocardial fibrosis and the further progression of diastolic dysfunction were prevented in both MP-treated groups. Survival at 21 weeks of age was significantly improved in DHF+7wkMP (86%) and DHF+17wkMP (75%) rats compared with DHF rats (25%).

CONCLUSIONS

In this study, MP prevented not only the development of LV hypertrophy but also the progression of diastolic dysfunction, and improved survival in rats with DHF. The preventive effect of MP on myocardial fibrosis is suggested as one of the mechanisms contributing to halt the progression of diastolic dysfunction, a finding that may lead to clinical benefits in regard to DHF caused by hypertension.

摘要

背景

慢性β受体阻滞剂治疗可改善充血性心力衰竭患者的生存率和左心室(LV)收缩功能。然而,其在左心室收缩功能正常的舒张性心力衰竭(DHF)中的疗效仍不确定。

方法

7周龄开始喂高盐饮食的 Dahl 盐敏感高血压大鼠被随机分为未治疗组(DHF;n = 20)或从7周龄开始用美托洛尔(MP)治疗组(DHF + 7wkMP;n = 22)或从17周龄开始用美托洛尔治疗组(DHF + 17wkMP;n = 8)。通过连续超声心动图评估左心室功能和重塑,随后进行血流动力学和病理学研究。

结果

DHF大鼠在17周龄时出现高血压和压力超负荷性左心室肥厚。在约20周龄时,DHF大鼠出现明显心力衰竭,其并非伴有左心室缩短分数降低,而是伴有舒张期充盈异常。DHF + 7wkMP大鼠的左心室向心性肥厚明显减轻,而DHF + 17wkMP大鼠则未减轻。然而,两个MP治疗组均预防了左心室心肌纤维化和舒张功能障碍的进一步进展。与DHF大鼠(25%)相比,DHF + 7wkMP(86%)和DHF + 17wkMP(75%)大鼠在21周龄时的生存率显著提高。

结论

在本研究中,MP不仅预防了左心室肥厚的发展,还预防了舒张功能障碍的进展,并提高了DHF大鼠的生存率。MP对心肌纤维化的预防作用被认为是阻止舒张功能障碍进展的机制之一,这一发现可能对高血压引起的DHF具有临床益处。

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