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Heart failure decreases passive tension generation of rat diaphragm fibers.

Abstract：

BACKGROUND:Diaphragm dysfunction is well-known to limit quality of life and prognosis of patients with heart failure (HF), but its underlying mechanisms are not well understood. In an animal model for HF we recently showed that impaired diaphragm contractility arises at the single fiber level and is associated with sarcomeric injuries. For optimal muscle function and sarcomeric stability passive elastic structures, like titin, are indispensable. The current study aimed to investigate if impaired passive elasticity contributes to diaphragm dysfunction in rats with heart failure. METHODS:Skinned muscle fibers were isolated from the diaphragm and soleus of rats with chronic HF, induced by left coronary artery ligation and of sham-operated rats. Passive tension-length relationships were determined by applying segmental extension tests. Immunofluorescence was performed on muscle cryosections using antibodies (T12) against a titin epitope near the Z-line. Titin content was determined by SDS-agarose-gel electrophoresis. Titin's mobility on gel was studied to detect changes in titin size. RESULTS:Passive tension generation upon stretch was significantly reduced (>35%) in HF diaphragm fibers compared to sham. Immunostaining intensities against titin were reduced in diaphragm cryosections of HF rats compared to sham. Soleus fibers from HF and sham rats did not display differences, neither in passive tension nor in immunostaining. No differences in titin's size were detected in HF and sham diaphragm. Titin content, however, was significantly reduced ( approximately 25%) in HF diaphragm. DISCUSSION:We conclude that in the diaphragm of HF rats, passive elasticity is impaired, mainly resulting from titin loss.

journal_name

Int J Cardiol

journal_title

International journal of cardiology

authors

van Hees HW,Ottenheijm CA,Granzier HL,Dekhuijzen PN,Heunks LM

doi

10.1016/j.ijcard.2008.12.042

subject

Has Abstract

pub_date

2010-06-11 00:00:00

pages

275-83

issue

3

eissn

0167-5273

issn

1874-1754

pii

S0167-5273(08)01421-6

journal_volume

141

pub_type

杂志文章

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