Salt loading exacerbates diastolic dysfunction and cardiac remodeling in young female Ren2 rats

AT Whaley-Connell, J Habibi, A Aroor, L Ma… - Metabolism, 2013 - Elsevier
AT Whaley-Connell, J Habibi, A Aroor, L Ma, MR Hayden, CM Ferrario, VG DeMarco
Metabolism, 2013Elsevier
Objective Recent data would suggest pre-menopausal insulin resistant women are more
prone to diastolic dysfunction than men, yet it is unclear why. We and others have reported
that transgenic (mRen2) 27 (Ren2) rats overexpressing the murine renin transgene are
insulin resistant due to oxidative stress in insulin sensitive tissues. As increased salt intake
promotes inflammation and oxidative stress, we hypothesized that excess dietary salt would
promote diastolic dysfunction in transgenic females under conditions of excess tissue Ang II …
Objective
Recent data would suggest pre-menopausal insulin resistant women are more prone to diastolic dysfunction than men, yet it is unclear why. We and others have reported that transgenic (mRen2)27 (Ren2) rats overexpressing the murine renin transgene are insulin resistant due to oxidative stress in insulin sensitive tissues. As increased salt intake promotes inflammation and oxidative stress, we hypothesized that excess dietary salt would promote diastolic dysfunction in transgenic females under conditions of excess tissue Ang II and circulating aldosterone levels.
Materials/methods
For this purpose we evaluated cardiac function in young female Ren2 rats or age-matched Sprague–Dawley (SD) littermates exposed to a high (4%) salt or normal rat chow intake for three weeks.
Results
Compared to SD littermates, at 10 weeks of age, female Ren2 rats fed normal chow showed elevations in left ventricular (LV) systolic pressures, LV and cardiomyocyte hypertrophy, and displayed reductions in LV initial filling rate accompanied by increases in 3-nitrotyrosine content as a marker of oxidant stress. Following 3 weeks of a salt diet, female Ren2 rats exhibited no further changes in LV systolic pressure, insulin resistance, or markers of hypertrophy but exaggerated increases in type 1 collagen, 3-nitrotryosine content, and diastolic dysfunction. These findings occurred in parallel with ultrastructural findings of pericapillary fibrosis, increased LV remodeling, and mitochondrial biogenesis.
Conclusion
These data suggest that a diet high in salt in hypertensive female Ren2 rats promotes greater oxidative stress, maladaptive LV remodeling, fibrosis, and associated diastolic dysfunction without further changes in LV systolic pressure or hypertrophy.
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