Astemizole reduces blood-retinal barrier leakage in experimental diabetes.
Journal
  Journal of diabetes and its complications.
Citation
  J Diabetes Complications. 6(4):230-5
Publication date
  1992 Oct-Dec
Authors
  Hollis TM
Sill HW
Butler C
Campos MJ
Gardner TW
Investigators
  Thomas W. Gardner
MeSH headings
  Astemizole
Capillary Permeability
Diabetes Mellitus, Experimental
Diabetic Retinopathy
Retinal Vessels
MeSH qualifiers
  pharmacology
drug effects
physiopathology
prevention & control
Abstract
  We examined the potential of astemizole, a histamine H1-receptor antagonist that does not cross the blood-brain barrier, to reverse blood-retinal barrier leakage to albumin in streptozotocin diabetic rats. Four groups of nondiabetic and four groups of diabetic rats received vehicle or astemizole at dosages of 5, 10, or 20 mg/kg body weight for days 22-28 of a 28-day holding period. There were no significant differences in nondiabetic plasma-vitreous albumin ratios between animals receiving vehicle or any of the three astemizole dosages. Only diabetic rats receiving vehicle showed a significant (p < 0.05) 100% increase in the plasma-vitreous albumin ratio over their nondiabetic counterparts. Diabetic rats receiving either 5, 10, or 20 mg/kg astemizole exhibited total normalization of vitreous albumin accumulation, despite persistence of diabetes. These data indicate that astemizole, an H1-receptor antagonist that does not cross the blood-retinal barrier, is effective in reversing blood-retinal barrier leakage of albumin in experimental diabetes.
Medline ID
  93129793