Ovariectomy is protective against renal injury in the high-salt-fed older mRen2. Lewis rat

Am J Physiol Heart Circ Physiol. 2007 Oct;293(4):H2064-71. doi: 10.1152/ajpheart.00427.2007. Epub 2007 Jul 13.

Abstract

Studies in experimental animals and younger women suggest a protective role for estrogen; however, clinical trials may not substantiate this effect in older females. Therefore, the present study assessed the outcome of ovariectomy in older mRen2. Lewis rats subjected to a high-salt diet for 4 wk. Intact or ovariectomized (OVX, 15 wk of age) mRen2. Lewis rats were aged to 60 wk and then placed on a high-salt (HS, 8% sodium chloride) diet for 4 wk. Systolic blood pressures were similar between groups [OVX 169 +/- 6 vs. Intact 182 +/- 7 mmHg; P = 0.22] after the 4-wk diet; however, proteinuria [OVX 0.8 +/- 0.2 vs. Intact 11.5 +/- 2.6 mg/mg creatinine; P < 0.002, n = 6], renal interstitial fibrosis, glomerular sclerosis, and tubular casts were lower in OVX vs. Intact rats. Kidney injury molecule-1 mRNA, a marker of tubular damage, was 53% lower in the OVX HS group. Independent from blood pressure, OVX HS rats exhibited significantly lower cardiac (24%) and renal (32%) hypertrophy as well as lower C-reactive protein (28%). Circulating insulin-like growth factor-I (IGF-I) levels were not different between the Intact and OVX groups; however, renal cortical IGF-I mRNA and protein were attenuated in OVX rats [P < 0.05, n = 6]. We conclude that ovariectomy in the older female mRen2. Lewis rat conveys protection against salt-dependent increase in renal injury.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / metabolism
  • Angiotensin I / metabolism
  • Angiotensin II / metabolism
  • Animals
  • Animals, Congenic
  • Blood Pressure*
  • C-Reactive Protein / metabolism
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Disease Models, Animal
  • Female
  • Fibrosis
  • Hypertension / complications*
  • Hypertension / etiology
  • Hypertension / genetics
  • Hypertension / metabolism
  • Hypertension / physiopathology
  • Hypertrophy
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Kidney / metabolism*
  • Kidney / pathology
  • Kidney / physiopathology
  • Kidney Diseases / etiology
  • Kidney Diseases / metabolism
  • Kidney Diseases / physiopathology
  • Kidney Diseases / prevention & control*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Ovariectomy*
  • Peptide Fragments / metabolism
  • Proteinuria / etiology
  • Proteinuria / metabolism
  • Proteinuria / physiopathology
  • Proteinuria / prevention & control
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Lew
  • Renin / genetics
  • Renin / metabolism*
  • Renin-Angiotensin System
  • Sodium Chloride, Dietary

Substances

  • Cell Adhesion Molecules
  • Havcr1protein, rat
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • NPHS2 protein
  • Peptide Fragments
  • RNA, Messenger
  • Ren2 protein, mouse
  • Sodium Chloride, Dietary
  • nephrin
  • Angiotensin II
  • Insulin-Like Growth Factor I
  • C-Reactive Protein
  • Angiotensin I
  • Renin
  • angiotensin I (1-7)