Regression of pressure overload-induced left ventricular hypertrophy in mice.

Abstract

As a prelude to investigating the mechanism of regression of pressure overload-induced left ventricular (LV) hypertrophy (LVH), we studied the time course for the development and subsequent regression of LVH as well as accompanying alterations in cardiac function, histology, and gene expression. Mice were subjected to aortic banding for 4 or 8 wk to establish LVH, and regression was initiated by release of aortic banding for 6 wk. Progressive increase in LV mass and gradual chamber dilatation and dysfunction occurred after aortic banding. LVH was also associated with myocyte enlargement, interstitial fibrosis, and enhanced expression of atrial natriuretic peptide, collagen I, collagen III, and matrix metalloproteinase-2 but suppressed expression of alpha-myosin heavy chain and sarcoplasmic reticulum Ca(2+)-ATPase. Aortic debanding completely or partially reversed LVH, chamber dilatation and dysfunction, myocyte size, interstitial fibrosis, and gene expression pattern, each with a distinct time course. The extent of LVH regression was dependent on the duration of pressure overload, evidenced by the fact that restoration of LV structure and function was complete in animals subjected to 4 wk of aortic banding but incomplete in animals subjected to 8 wk of aortic banding. In conclusion, LVH regression comprises a variety of morphological, functional, and genetic components that show distinct time courses. A longer period of pressure overload is associated with a slower rate of LVH regression.

• Authors: Xiao-Ming Gao, Helen Kiriazis, Xiao-Lei Moore, Xin-Heng Feng, Karen Sheppard, Anthony Dart, Xiao-Jun Du
• Journal: American journal of physiology. Heart and circulatory physiology (Am J Physiol Heart Circ Physiol) Vol. 288 Issue 6 Pg. H2702-7 (Jun 2005) ISSN: 0363-6135 [Print] United States
• PMID: 15665058 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA Primers
• Atrial Natriuretic Factor
• Collagen
• Matrix Metalloproteinases
• Sarcoplasmic Reticulum Calcium-Transporting ATPases
• Calcium-Transporting ATPases

Topics

• Animals
• Atrial Natriuretic Factor (genetics)
• Calcium-Transporting ATPases (genetics)
• Collagen (genetics)
• DNA Primers
• Disease Models, Animal
• Echocardiography
• Female
• Hypertrophy, Left Ventricular (diagnostic imaging, etiology, physiopathology)
• Male
• Matrix Metalloproteinases (genetics)
• Mice
• Mice, Inbred C57BL
• Pressure
• Reverse Transcriptase Polymerase Chain Reaction
• Sarcoplasmic Reticulum Calcium-Transporting ATPases
• Ventricular Pressure (physiology)
• Ventricular Remodeling (physiology)