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首页> 外文期刊>Experimental Biology and Medicine: Journal of the Society for Experimental Biology and Medicine >The effects of debanding on the lung expression of ET-1, eNOS, and cGMP in rats with left ventricular pressure overload.
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The effects of debanding on the lung expression of ET-1, eNOS, and cGMP in rats with left ventricular pressure overload.

机译:解缠对左心室压力超负荷大鼠肺中ET-1,eNOS和cGMP表达的影响。

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摘要

Pulmonary hypertension (PH) usually develops secondary to left ventricular (LV) dysfunction; therefore, it is also called retrograde PH. To investigate our hypothesis that PH is at least partially reversible, as in some congenital heart diseases, in a rat model we investigated whether release of constriction could attenuate pulmonary vascular remodeling and change the expression of endothelin (ET)-1 and endothelial nitric oxide synthase (eNOS). We used rats with LV dysfunction produced by an ascending aortic banding. In this study, there were four groups enrolled: 4-weeks banded (AOB(1-28); n = 7), 7-weeks banded (AOB(1-49); n = 7), debanded groups (AOB(1-28)/DeB(29-49); n = 7), and rats receiving a sham operation (n = 7). Subsequently, there was significant attenuation of medial hypertrophy in pulmonary arterioles and reversal of PH in the AOB(1-28)/DeB(29-49) group (sham, 19 +/- 1.3 mm Hg; AOB(1-28), 31 +/- 2.7 mm Hg; AOB(1-49), 32 +/- 2.7 mm Hg; and AOB(1-28)/DeB(29-49), 20 +/- 1.3 mm Hg). PreproET-1 mRNA and eNOS mRNA were measured by competitive reverse transcriptase (RT) polymerase chain reaction (PCR), and eNOS was measured by Western blotting. Compared with the banded groups, debanding significantly decreased pulmonary preproET-1 mRNA, pulmonary ET-1 (sham, 210 +/- 12 pg/g protein; AOB(1-28), 242 +/- 12 pg/g protein; AOB(1-49), 370 +/- 49 pg/g protein; and AOB(1-28)/DeB(29-49), 206 +/- 1.9 pg/g protein), and plasma ET-1 levels (sham, 10.1 +/- 1.5 pg/ml; AOB(1-28), 13.4 +/- 2.0 pg/ml; AOB(1-49), 15.4 +/- 2.0 pg/ml; and AOB(1-28)/DeB(29-49), 10.3 +/- 0.9 pg/ml protein). Debanding could not, however, alter pulmonary eNOS, eNOS mRNA, or cGMP. These findings suggest that pulmonary vascular remodeling, increased pulmonary arterial pressure, and upregulation of ET-1 gene expression are all reversible. We infer that it is the upregulated gene expression of ET-1, not eNOS, that is closely related to the development of the PH secondary to 4 weeks of aortic banding.
机译:肺动脉高压(PH)通常继发于左心室(LV)功能障碍;因此,它也称为逆行PH。为了研究我们的假设,即在某些先天性心脏病中,PH至少是部分可逆的,我们在大鼠模型中研究了收缩的释放是否可以减弱肺血管重构并改变内皮素(ET)-1和内皮一氧化氮合酶的表达(eNOS)。我们使用由升主动脉束带产生的左室功能不全的大鼠。在这项研究中,分为四组:4周组(AOB(1-28); n = 7),7周组(AOB(1-49); n = 7),解散组(AOB(1 -28)/ DeB(29-49); n = 7),接受假手术的大鼠(n = 7)。随后,AOB(1-28)/ DeB(29-49)组的肺小动脉内侧肥大明显减弱,PH值逆转(假手术,19 +/- 1.3 mm Hg; AOB(1-28), 31 +/- 2.7毫米汞柱; AOB(1-49),32 +/- 2.7毫米汞柱; AOB(1-28)/ DeB(29-49),20 +/- 1.3毫米汞柱)。通过竞争性逆转录酶(RT)聚合酶链反应(PCR)测量PreproET-1 mRNA和eNOS mRNA,并通过Western印迹法测量eNOS。与带状组相比,解带显着降低了肺preproET-1 mRNA,肺ET-1(假,210 +/- 12 pg / g蛋白; AOB(1-28),242 +/- 12 pg / g蛋白; AOB (1-49),370 +/- 49 pg / g蛋白;和AOB(1-28)/ DeB(29-49),206 +/- 1.9 pg / g蛋白)和血浆ET-1水平(假) ,10.1 +/- 1.5 pg / ml; AOB(1-28),13.4 +/- 2.0 pg / ml; AOB(1-49),15.4 +/- 2.0 pg / ml;和AOB(1-28)/ DeB(29-49),10.3 +/- 0.9 pg / ml蛋白质)。解散不能改变肺eNOS,eNOS mRNA或cGMP。这些发现表明,肺血管重构,肺动脉压升高和ET-1基因表达上调都是可逆的。我们推断,是ET-1而不是eNOS的基因表达上调,与主动脉束带4周继发的PH的发展密切相关。

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