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Am J Physiol Regul Integr Comp Physiol (December 2, 2004). doi:10.1152/ajpregu.00556.2004
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Submitted on August 16, 2004
Accepted on November 22, 2004

Effects of cortisol on cardiac myocytes and on expression of cardiac genes in fetal sheep

E R Lumbers1*, A C Boyce1, G Joulianos1, V Kumarasamy1, E Barner2, J L Segar2, and J H Burrell1

1 Department of Physiology and Pharmacology, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia
2 Department of Pediatrics, University of Iowa, Iowa City, Iowa, USA

* To whom correspondence should be addressed. E-mail: e.lumbers{at}unsw.edu.au.

In 17 fetal sheep aged 129 days, the effects of large dose infusions of cortisol (72.1 mg.day-1 for 2-3 days) on proliferation, binucleation and hypertrophy of cardiac myocytes, cardiac expression of angiotensinogen, angiotensin receptor subtypes 1 and 2, Glut-1, glucocorticoid and mineralocorticoid receptors, proteins of the mitogen activated kinase (MAPK) pathways and calcineurin were studied. Cortisol levels were 8.7 ± 2.3 nM (SE) in 8 control and 1028 ± 189 nM in 9 treated fetuses (P<0.001). Cortisol had no effect on myocyte binucleation. Left ventricular free wall (LVFW) uni- and binucleated myocytes were larger in cortisol treated fetuses (P<0.001, P<0.05). Cortisol treated fetuses had higher right ventricular (RVFW) and LVFW angiotensinogen (Aogen) mRNA levels (treated: 2.30 ± 0.37, n=8, 2.05 ± 0.45, n=7 vs control: 0.94 ± 0.12, n=8 and 0.67 ± 0.09, n=7, P<0.02). Levels of the glucose transporter Glut-1 mRNA were lower in the LVFW of treated fetuses (0.83 ± 0.23 vs 1.47 ± 0.30 in control, P<0.05 n=7,8). The higher the cortisol level, the greater the Aogen mRNA level (RVFW, r=0.61, P<0.01, n=16; LVFW, r=0.83, P<0.0003, n=14). There were no other changes in mRNA levels nor in levels of extracellular kinase, JNK, p38, their phosphorylated forms and calcineurin. Thus high levels of cortisol such as occur after birth do not affect fetal cardiac myocyte binucleation or number but are associated with higher levels of ventricular Aogen mRNA, lower levels of Glut-1 mRNA, and hypertrophy of left ventricular free wall myocytes. These effects could impact on postnatal cardiac development.




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