Histochemical characteristics of soleus muscle in angiotensin-converting enzyme gene knockout mice

Hypertens Res. 2005 Aug;28(8):681-8. doi: 10.1291/hypres.28.681.

Abstract

We examined the histochemical characteristics of soleus muscle in the angiotensin-converting enzyme (ACE) gene (Ace in mice, ACE in humans) knockout mice. Serial sections of soleus muscle of wild-type (Ace+/+, n=20) and heterozygous mutant (Ace+/-, n=24) mice were stained for myosin adenosine triphosphatase activity to identify different muscle fiber types. Capillaries were visualized by amylase-periodic acid-Schiff staining. ACE activity in the serum and gastrocnemius muscle was higher in male mice than in female mice. Female and male Ace+/- mice had markedly lower ACE activity in the serum and the gastrocnemius muscle than did female and male Ace+/+ mice, respectively. In both male and female mice, the composition of fiber types (type I and IIa) did not differ significantly between Ace+/+ and Ace+/- mice. There was no significant gender difference in capillary density. Ace+/- mice had significantly more capillaries around type IIa fibers (5.44 +/- 0.18 vs. 5.01 +/- 0.13, p<0.05) than Ace+/+ mice. The differences in the number of capillaries around type I fibers and in the number of capillaries around per fiber (capillary:fiber ratio) between Ace+/- and Ace+/+ mice were not significant (p<0.1). There was no significant difference in the mean cross-sectional area occupied by one capillary and the number of capillaries per fiber area between Ace+/+ and Ace+/- mice. In conclusion, knockout of the Ace gene in mice increased capillary density, as expressed by the mean number of capillaries around type IIa fibers. This finding suggests a possible mechanism for the cardioprotective effects of ACE inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin-Converting Enzyme Inhibitors / pharmacology
  • Animals
  • Capillaries / cytology
  • Cardiovascular Physiological Phenomena / drug effects
  • Cardiovascular System / drug effects
  • Female
  • Gene Expression
  • Heterozygote
  • Histocytochemistry
  • Male
  • Mice
  • Mice, Knockout
  • Muscle Fibers, Fast-Twitch / cytology
  • Muscle Fibers, Fast-Twitch / enzymology
  • Muscle Fibers, Slow-Twitch / cytology
  • Muscle Fibers, Slow-Twitch / enzymology
  • Muscle, Skeletal / blood supply*
  • Muscle, Skeletal / cytology*
  • Muscle, Skeletal / enzymology
  • Mutation
  • Peptidyl-Dipeptidase A / analysis*
  • Peptidyl-Dipeptidase A / blood
  • Peptidyl-Dipeptidase A / genetics*

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Peptidyl-Dipeptidase A