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

Roman Bass, Dan Engelhard, Victoria Trembovler, Esther Shohami*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

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-α 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 a 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 in rats treated with ceftriaxone-HU-211 compared with rats in other treatment groups. The results suggest that HU-211 when given concomitantly with antibiotics attenuates brain damage in the rat model of pneumococcal meningitis.

Original languageEnglish
Pages (from-to)735-738
Number of pages4
JournalJournal of Infectious Diseases
Volume173
Issue number3
DOIs
StatePublished - 1996

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