Prevention by L-arginine and polyamines of delayed development and embryotoxicity caused by chemically-induced diabetes in rats

Reprod Toxicol. 1999 Nov-Dec;13(6):501-9. doi: 10.1016/s0890-6238(99)00039-8.

Abstract

Diabetes mellitus induction with alloxan at a dose of 110 mg/kg i.p. in rats on Day 4 of pregnancy causes delayed development and resorptions as signs of embryotoxicity. In the present study, the administration of human NPH insulin at doses of 1 to 5 U/d to rats or 1.0 mL of 10 mM L-arginine for 8 d, starting the day following diabetes induction, prevented embryotoxicity and delayed development. Similar results were obtained when the polyamines putrescine, spermidine, or spermine were administered at doses of 1.0 mL of a 10 microM solution to each rat daily. However, even though L-arginine and polyamines prevented adverse effects of severe diabetes on the conceptus, and caused normalization of glucose, beta-hydroxybutyrate levels remained elevated. These results support the hypothesis that the mechanisms of normal and altered development could be mediated by the action of polyamines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine / therapeutic use*
  • Biogenic Polyamines / therapeutic use*
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / blood
  • Diabetes Mellitus, Experimental / drug therapy*
  • Female
  • Fetal Growth Retardation / prevention & control*
  • Fetal Resorption / prevention & control*
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Insulin / pharmacology
  • Male
  • Pregnancy
  • Pregnancy in Diabetics / blood
  • Pregnancy in Diabetics / drug therapy*
  • Putrescine / therapeutic use
  • Rats
  • Rats, Sprague-Dawley
  • Spermidine / therapeutic use
  • Spermine / therapeutic use

Substances

  • Biogenic Polyamines
  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin
  • Spermine
  • Arginine
  • Spermidine
  • Putrescine