Dent Melissa R, Aroutiounova Nina, Dhalla N S, Tappia P S
Institute of Cardiovascular Sciences, St. Boniface Hospital Research Centre, Department of Physiology, Faculty of Medicine, University of Manitoba Winnipeg, Canada.
J Cell Mol Med. 2006 Apr-Jun;10(2):470-9. doi: 10.1111/j.1582-4934.2006.tb00412.x.
Because the left ventricular (LV) hypertrophy due to volume overload induced by arteriovenous (AV) shunt was associated with an increase in phospholipase C (PLC) isozyme mRNA levels, PLC is considered to be involved in the development of cardiac hypertrophy. Since the renin-angiotensin system (RAS) is activated in cardiac hypertrophy, the role of RAS in the stimulation of PLC isozyme gene expression in hypertrophied heart was investigated by inducing AV shunt in Sprague-Dawley rats. The animals were treated with or without losartan (20 mg/kg, daily) for 3 days as well as 1, 2 and 4 weeks, and atria, right ventricle (RV) and LV were used for analysis. The increased muscle mass as well as the mRNA levels for PLC beta1 and beta3 in atria and RV, unlike PLC beta3 gene expression in LV, at 3 days of AVshunt were attenuated by losartan. The increased gene expression for PLC beta1 at 2 weeks in atria, at 1 and 4 weeks in RV, and at 2 and 4 weeks in LV was also depressed by losartan treatment. Likewise, the elevated mRNA levels for PLC beta3 in RV at 1 week and in LVat 4 weeks of cardiac hypertrophy were decreased by losartan. On the other hand, the increased levels of mRNA for PLC gamma1 in RV and LV at 2 and 4 weeks of inducing hypertrophy, unlike in atria at 4 weeks were not attenuated by losartan treatment. While the increased mRNA level for PLC delta1 in LV was reduced by losartan, gene expression for PLC delta1 was unaltered in atria and decreased in RV at 3 days of inducing AV shunt. These results suggest that changes in PLC isozyme gene expression were chamber specific and time-dependent upon inducing cardiac hypertrophy due to AV shunt. Furthermore, partial attenuation of the increased gene expression for some of the PLC isozymes and no effect of losartan on others indicate that both RAS dependent and independent mechanisms may be involved in hypertrophied hearts due to volume overload.
由于动静脉(AV)分流引起的容量超负荷导致的左心室(LV)肥厚与磷脂酶C(PLC)同工酶mRNA水平升高有关,因此认为PLC参与了心脏肥大的发展。由于肾素-血管紧张素系统(RAS)在心脏肥大中被激活,通过在Sprague-Dawley大鼠中诱导AV分流来研究RAS在肥大心脏中刺激PLC同工酶基因表达的作用。动物接受或不接受氯沙坦(20mg/kg,每日)治疗3天以及1、2和4周,取心房、右心室(RV)和左心室进行分析。与左心室中PLCβ3基因表达不同,氯沙坦可减轻AV分流3天时心房和右心室中增加的肌肉质量以及PLCβ1和β3的mRNA水平。氯沙坦治疗还可抑制心房中2周、右心室中1周和4周以及左心室中2周和4周时PLCβ1基因表达的增加。同样,氯沙坦可降低心脏肥大1周时右心室和4周时左心室中PLCβ3升高的mRNA水平。另一方面,诱导肥大2周和4周时右心室和左心室中PLCγ1 mRNA水平的增加,与4周时心房中的情况不同,不受氯沙坦治疗的影响。虽然氯沙坦可降低左心室中PLCδ1增加的mRNA水平,但在诱导AV分流3天时,心房中PLCδ1的基因表达未改变,右心室中则降低。这些结果表明,PLC同工酶基因表达的变化具有腔室特异性,并且在由于AV分流导致心脏肥大时具有时间依赖性。此外,一些PLC同工酶基因表达增加的部分减弱以及氯沙坦对其他同工酶无作用表明,RAS依赖性和非依赖性机制可能都参与了由于容量超负荷导致的肥大心脏。