Immediate response of myocardium to pressure overload includes transient regulation of genes associated with mitochondrial bioenergetics and calcium availability

被引:2
作者
Deckmann, Ana Carolina [1 ,2 ]
Theizen, Thais Holz [2 ]
Medrano, Francisco Javier [1 ]
Franchini, Kleber Gomes [2 ]
Guimaraes Pereira, Goncalo Amarante [1 ]
机构
[1] Univ Estadual Campinas, Inst Biol, Dept Genet & Evolucao, BR-13083970 Campinas, SP, Brazil
[2] Univ Estadual Campinas, Escola Med, Dept Med Interna, BR-13083970 Campinas, SP, Brazil
关键词
pressure overload; myocardial hypertrophy; gene expression; SERCA2; ADULT-MOUSE HEART; CARDIAC-HYPERTROPHY; EXPRESSION; FAILURE; MICE;
D O I
10.1590/S1415-47572010005000004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ventricular hypertrophy is one of the major myocardial responses to pressure overload (PO). Most studies on early myocardial response focus on the days or even weeks after induction of hypertrophic stimuli. Since mechano-transduction pathways are immediately activated in hearts undergoing increased work load, it is reasonable to infer that the myocardial gene program may be regulated in the first few hours. In the present study, we monitored the expression of some genes previously described in the context of myocardial hypertrophic growth by using the Northern blot technique, to estimate the mRNA content of selected genes in rat myocardium for the periods 1, 3, 6, 12 and 48 h after PO stimuli. Results revealed an immediate switch in the expression of genes encoding alpha and beta isoforms of myosin heavy chain, and up-regulation of the cardiac isoform of alpha actin. We also detected transitory gene regulation as the increase in mitochondrial cytochrome c oxidase 1 gene expression, parallel to down-regulation of genes encoding sarco(endo) plasmic reticulum Ca(+2) ATPase and sodium-calcium exchanger. Taken together, these results indicate that initial myocardial responses to increased work load include alterations in the contractile properties of sarcomeres and transitory adjustment of mitochondrial bioenergetics and calcium availability.
引用
收藏
页码:12 / U19
页数:6
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