Angiotensin-converting enzyme inhibition prevents glomerular-tubule disconnection and atrophy in passive Heymann nephritis, an effect not observed with a calcium antagonist

Am J Pathol. 2001 Nov;159(5):1743-50. doi: 10.1016/s0002-9440(10)63021-0.


In proteinuric nephropathies tubular atrophy leads to glomerular-tubule disconnection through an unknown mechanism. Here we studied whether proteinuria promoted glomerular-tubule disconnection in individual nephrons and whether this phenomenon was prevented by an angiotensin-converting enzyme (ACE) inhibitor. Passive Heymann nephritis (PHN) and control rats were studied at 4 and 8 months. Two additional groups of PHN rats received lisinopril (40 mg/L) or a calcium channel blocker (lacidipine, 3 mg/kg) from day 7 after surgery to 8 months. At sacrifice, kidneys were serially sectioned to identify glomerular- tubule abnormalities in individual nephrons and changes in interstitial volume. In PHN rats, the time-dependent increase in proteinuria was paralleled by tubular atrophy leading to glomerular-tubule disconnection and interstitial volume enlargement. Marked apoptosis was invariably found in atrophic tubules in contrast to the absent or very mild terminal dUTP nick-end labeling staining in tubules normally connected to glomeruli in PHN animals. Treatment with an ACE inhibitor prevented hypertension, proteinuria, the formation of atrophic tubuli, glomerular-tubule disconnection and limited the fractional interstitial volume expansion. Although lacidipine limited hypertension, it did not reduce proteinuria or prevent tubular atrophy and disconnection. Multivariate analysis showed that the appearance of atubular glomeruli and the increase in interstitial volume were better predicted by proteinuria than blood pressure. This study suggests that ACE inhibitors effectively prevent glomerular-tubule disconnection possibly by their ability of reducing proteinuria, which in turn favors proximal tubular cell apoptosis. Agents that only reduced hypertension but not proteinuria do not affect tubular behavior.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin-Converting Enzyme Inhibitors / pharmacology*
  • Animals
  • Apoptosis
  • Atrophy
  • Calcium Channel Blockers / pharmacology*
  • Dihydropyridines / pharmacology*
  • Glomerulonephritis / pathology*
  • Glomerulonephritis / physiopathology
  • Glomerulonephritis / urine
  • Kidney / drug effects
  • Kidney / physiopathology
  • Kidney Glomerulus / drug effects
  • Kidney Glomerulus / pathology*
  • Kidney Tubules / drug effects
  • Kidney Tubules / pathology*
  • Kidney Tubules / physiopathology
  • Lisinopril / pharmacology*
  • Male
  • Proteinuria / urine
  • Rats
  • Rats, Sprague-Dawley
  • Reference Values


  • Angiotensin-Converting Enzyme Inhibitors
  • Calcium Channel Blockers
  • Dihydropyridines
  • lacidipine
  • Lisinopril