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Wistar大鼠左心室对压力超负荷的早期反应。

Early responses of the left ventricle to pressure overload in Wistar rats.

作者信息

Roussel Elise, Gaudreau Martin, Plante Eric, Drolet Marie-Claude, Breault Catherine, Couet Jacques, Arsenault Marie

机构信息

Groupe de Recherche en Valvulopathies, Centre de Recherche Hôpital Laval, Institut de cardiologie de Québec, Université Laval, Québec, Canada.

出版信息

Life Sci. 2008 Jan 30;82(5-6):265-72. doi: 10.1016/j.lfs.2007.11.008. Epub 2007 Nov 29.

DOI:10.1016/j.lfs.2007.11.008
PMID:18155733
Abstract

The early events leading to the establishment of left ventricular hypertrophy associated to pressure overload (PO) are not well characterized. To explore these early events, aortic banding (AB) was performed in rats to induce left ventricle (LV) PO. Animals were sacrificed after 24, 48 h or 14 days. An echocardiogram was performed before the procedure and at sacrifice. LVs were preserved for the evaluation of fibrosis, angiotensin II (AT) receptors expression and stress-related MAP kinases (ERK 1/2, JNK and p38) pathways. We observed that concentric LV hypertrophy was established after only 14 days. Collagen I and fibronectin gene expressions were decreased the first 2 days after AB induction whereas AT receptors mRNA levels were sharply increased. ERK 1/2 and JNK activities in LV homogenates were decreased 24 h after AB but came back to normal after 14 days. p38 activity however was stable during the period studied. We also evaluated the presence of two phosphorylated transcription factors related to JNK signaling pathway (ATF-2 and c-Jun) in cardiomyocyte nuclei. The proportion of LV cell nuclei positive for these two activated transcription factors was significantly reduced in AB rats compared to sham. These results suggest that the early response of the LV to acute PO is to attenuate the expression of some pro-fibrotic and pro-hypertrophic signaling pathways and possibly AT signaling by decreasing ERK 1/2 and JNK relative activities.

摘要

导致与压力超负荷(PO)相关的左心室肥厚形成的早期事件尚未得到充分表征。为了探究这些早期事件,对大鼠进行主动脉缩窄(AB)以诱导左心室(LV)压力超负荷。在24、48小时或14天后处死动物。在手术前和处死时进行超声心动图检查。保留左心室用于评估纤维化、血管紧张素II(AT)受体表达以及与应激相关的丝裂原活化蛋白激酶(ERK 1/2、JNK和p38)信号通路。我们观察到仅在14天后就形成了向心性左心室肥厚。AB诱导后的头2天,I型胶原和纤连蛋白基因表达降低,而AT受体mRNA水平急剧增加。AB后24小时,左心室匀浆中的ERK 1/2和JNK活性降低,但14天后恢复正常。然而,在研究期间p38活性保持稳定。我们还评估了心肌细胞核中与JNK信号通路相关的两种磷酸化转录因子(ATF-2和c-Jun)的存在情况。与假手术组相比,AB大鼠中这两种活化转录因子阳性的左心室细胞核比例显著降低。这些结果表明,左心室对急性压力超负荷的早期反应是通过降低ERK 1/2和JNK的相对活性来减弱一些促纤维化和促肥厚信号通路以及可能的AT信号的表达。

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