Effects of rhGH and rhIGF-1 on renal growth and morphology

Kidney Int. 1993 Dec;44(6):1251-8. doi: 10.1038/ki.1993.376.

Abstract

It is known that in rodents recombinant human growth hormone (rhGH) and recombinant human insulin-like growth factor (rhIGF-1) increase renal mass. It is uncertain, however, whether renal mass increases in proportion to body growth, or whether renal growth is stimulated selectively. In 120 to 150 g female Sprague-Dawley rats, we measured the effects of rhGH and rhIGF-1 and their combination by the following parameters: kidney weight/body weight ratio, DNA/protein ratio, mRNA of GH receptor and of IGF-1, mitosis index and PCNA (by immunohistology), zonal architecture and glomerular diameter by micromorphometry. Both rhGH and rhIGF-1 dose-dependently increased renal weight and body weight over vehicle treated controls. With rhGH, liver dry weight/body weight ratio increased, but kidney dry weight/body weight ratio remained unchanged (0.99 +/- 0.06 x 10(-3) vs. 1.02 +/- 0.07 in vehicle controls). In contrast, a significant increase of kidney dry weight/body weight ratio was seen in rats treated with rhIGF-1 (1.3 +/- 0.21 x 10(-3). Addition of high doses of rhGH to high doses of rhIGF-1 caused no further increase of the ratio despite a significant further increase of body weight. rhGH increased the abundance of renal GH receptor mRNA (0.46 +/- 0.32 amol/microgram DNA vs. 0.08 +/- 0.07 in controls) and of IGF-1 mRNA (1.35 +/- 0.5 pg/micrograms DNA vs. 0.35 +/- 0.17), whereas no change was seen with IGF-1 treatment. rhGH and rhIGF-1 increased kidney DNA/protein ratio, mitoses and PCNA expression in various renal structures.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA / metabolism
  • Dose-Response Relationship, Drug
  • Drug Combinations
  • Female
  • Growth Hormone / pharmacology*
  • Insulin-Like Growth Factor I / pharmacology*
  • Kidney / drug effects*
  • Kidney / growth & development*
  • Kidney / metabolism
  • Liver / metabolism
  • Mitosis
  • Nuclear Proteins / metabolism
  • Proliferating Cell Nuclear Antigen
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Somatomedin / genetics
  • Receptors, Somatotropin / genetics
  • Recombinant Proteins
  • Time Factors

Substances

  • Drug Combinations
  • Nuclear Proteins
  • Proliferating Cell Nuclear Antigen
  • RNA, Messenger
  • Receptors, Somatomedin
  • Receptors, Somatotropin
  • Recombinant Proteins
  • Insulin-Like Growth Factor I
  • Growth Hormone
  • DNA