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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 

Estrogen and salt sensitivity in the female mRen(2).Lewis rat.

The present study determined whether early loss of estrogen influences salt-sensitive changes in blood pressure, renal injury, and cardiac hypertrophy as well as the effects on the circulating renin-angiotensin-aldosterone system (RAAS) in the hypertensive female mRen(2).Lewis strain. Ovariectomy (OVX) of heterozygous mRen(2).Lewis rats on a normal salt (NS) diet (0.5% sodium) increased systolic blood pressure from 137 +/- 3 to 177 +/- 5 mmHg (P < 0.01) by 15 wk but did not show any changes in cardiac-to-body weight index (CI), proteinuria, or creatinine clearance. Maintenance with a high-sodium (HS) diet (4%) increased blood pressure (203 +/- 4 mmHg, P < 0.01), proteinuria (3.5 +/- 0.3 vs. 6.4 +/- 0.7 mg/day, P < 0.05), and CI (4.0 +/- 0.1 vs. 5.2 +/- 0.1 mg/kg, P < 0.01) but decreased creatinine clearance (0.89 +/- 0.15 vs. 0.54 +/- 0.06 ml/min, P < 0.05). OVX exacerbated the effects of salt on the degree of hypertension (230 +/- 5 mmHg), CI (5.6 +/- 0.2 mg/kg), and proteinuria (13 +/- 3.0 mg/day). OVX increased the urinary excretion of aldosterone approximately twofold in animals on the NS diet (3.8 +/- 0.5 vs. 6.6 +/- 0.5 ng.mg creatinine(-1).day(-1), P < 0.05) and HS diet (1.4 +/- 0.2 vs. 4.5 +/- 1.0 ng.mg creatinine(-1).day(-1), P < 0.05). Circulating renin, angiotensin-converting enzyme, and angiotensin II were also significantly increased in the OVX group fed a HS diet. These results reveal that the protective effects of estrogen apart from the increase in blood pressure were only manifested in the setting of a chronic HS diet and suggest that the underlying sodium status may have an important influence on the overall effect of reduced estrogen.[1]

References

  1. Estrogen and salt sensitivity in the female mRen(2).Lewis rat. Chappell, M.C., Yamaleyeva, L.M., Westwood, B.M. Am. J. Physiol. Regul. Integr. Comp. Physiol. (2006) [Pubmed]
 
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