Key result
Heart failure induced by monocrotaline in rats selectively down-regulated MyoD gene expression and decreased MHC IIa/IIx protein isoforms in the diaphragm.
Why the study?
Does heart failure alter myogenic regulatory factor expression in the diaphragm muscle of rats?
Does heart failure alter myogenic regulatory factor expression in the diaphragm muscle of rats?
In a rat model of heart failure, MyoD is selectively down-regulated in the diaphragm, which may contribute to diaphragm myopathy.
Answers are grounded in this paper and cite their sources.
MyoD down-regulation may contribute to diaphragm myopathy in HF models; leaves open translation to humans and therapeutic targets.
Diaphragm myopathy has been described in patients with heart failure (HF), with alterations in myosin heavy chains (MHC) expression. The pathways that regulate MHC expression during HF have not been described, and myogenic regulatory factors (MRFs) may be involved. The purpose of this investigation was to determine MRF mRNA expression levels in the diaphragm. Diaphragm muscle from both HF and control Wistar rats was studied when overt HF had developed, 22 days after monocrotaline administration. MyoD, myogenin and MRF4 gene expression were determined by RT-PCR and MHC isoforms by polyacrylamide gel electrophoresis. Heart failure animals presented decreased MHC IIa/IIx protein isoform and MyoD gene expression, without altering MHC I, IIb, myogenin and MRF4. Our results show that in HF, MyoD is selectively down-regulated, which might be associated with alterations in MHC IIa/IIx content. These changes are likely to contribute to the diaphragm myopathy caused by HF.
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Lopes et al. (2008) studied Heart failure. Monocrotaline administration (Heart failure induction) vs. Control Wistar rats was evaluated on MRF mRNA expression levels (MyoD, myogenin, MRF4) and MHC isoforms in the diaphragm. Heart failure induced by monocrotaline in rats selectively down-regulated MyoD gene expression and decreased MHC IIa/IIx protein isoforms in the diaphragm.
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