Fructose-1,6-bisphosphate after hypoxic ischemic injury is protective to the neonatal rat brain

Brain Res. 1996 Nov 25;741(1-2):294-9. doi: 10.1016/s0006-8993(96)00984-5.

Abstract

Fructose-1,6-bisphosphate (FBP) has been shown to attenuate central nervous system injury in adult animals. We evaluated whether FBP given after an ischemic-hypoxic insult is protective to the developing brain in a neonatal rat model of hypoxia-ischemia. Postnatal day 7 rat pups were subjected to focal ischemia followed by global hypoxia and then administered either FBP or saline intraperitoneally. A dose of 500 mg/kg or greater of FBP significantly reduced the amount of injury such that 55% of FBP- vs. 17% of saline-treated rats had no injury; 6% of FBP- and 47% of saline-treated rats had severe damage (P = 0.004). There was less infarcted brain in FBP-treated rats (12 +/- 11% vs. 37 +/- 32%; P = 0.005); and fewer FBP-treated rats had > 30% ipsilateral cortical injury (12% of FBP- vs. 50% of saline-treated rats; P = 0.002). FBP lowered serum calcium levels during the first 24 h after the insult without significant changes in ionized calcium or osmolarity. These results indicate that FBP treatment administered systemically after hypoxia-ischemia reduces CNS injury in neonatal rats.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Animals, Newborn / physiology*
  • Blood Chemical Analysis
  • Brain Chemistry / drug effects
  • Brain Chemistry / physiology
  • Brain Ischemia / drug therapy
  • Brain Ischemia / pathology*
  • Calcium / metabolism
  • Cerebral Infarction / pathology
  • Fructosediphosphates / therapeutic use*
  • Hypoxia, Brain / drug therapy
  • Hypoxia, Brain / pathology*
  • Neuroprotective Agents / therapeutic use*
  • Phosphorus / metabolism
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Fructosediphosphates
  • Neuroprotective Agents
  • Phosphorus
  • fructose-1,6-diphosphate
  • Calcium