A novel nonpsychotropic cannabinoid, HU-211, in the treatment of experimental pneumococcal meningitis

J Infect Dis. 1996 Mar;173(3):735-8. doi: 10.1093/infdis/173.3.735.

Abstract

Typical features of pneumococcal meningitis have been demonstrated in rats inoculated with Streptococcus pneumoniae. HU-211, a novel noncompetitive N-methyl-D-aspartate antagonist recently demonstrated to inhibit tumor necrosis factor-alpha production under various conditions, improves recovery in some experimental models of brain injury. The present study tested the efficacy of HU-211 in combination with antimicrobial therapy in reducing brain damage in experimental pneumococcal meningitis. S. pneumoniae-infected rats were treated with saline alone, ceftriaxone alone, or with combination of ceftriaxone and HU-211 18 h after inoculation of the bacteria. Brain edema and blood-brain barrier impairment 48 h after infection were significantly (P<.05) reduced suggest that HU-211 when given concomitantly with antibiotics attenuates brain damage in the rat model of pneumococcal meningitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood-Brain Barrier / drug effects
  • Brain Edema / prevention & control
  • Ceftriaxone / administration & dosage
  • Disease Models, Animal
  • Dronabinol / administration & dosage
  • Dronabinol / analogs & derivatives*
  • Dronabinol / therapeutic use
  • Drug Therapy, Combination
  • Male
  • Meningitis, Pneumococcal / drug therapy*
  • Meningitis, Pneumococcal / pathology
  • Meningitis, Pneumococcal / physiopathology
  • Neuroprotective Agents / administration & dosage
  • Neuroprotective Agents / therapeutic use*
  • Rats
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Neuroprotective Agents
  • Tumor Necrosis Factor-alpha
  • Ceftriaxone
  • Dronabinol
  • HU 211