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PMID: 1488091 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The use of azathioprine to ameliorate post-treatment encephalopathy associated with African trypanosomiasis.

Neuropathology and applied neurobiology ·Vol. 18 ·No. 6 ·1992-12-00 ·Pages 619-25

Hunter CA, Jennings FW, Kennedy PG, Murray M

Abstract

The treatment of human African sleeping sickness is complicated by a post-treatment meningoencephalitis that may be fatal. Using a mouse model this study assesses the use of the non-steroidal anti-inflammatory drug, azathioprine, in the management of this post-treatment reaction. Female NIH mice treated with the trypanocidal compound diminazene aceturate (40 mg/kg), 28 days after infection, developed a similar post-treatment reaction to that seen in humans. Administration of azathioprine (100 mg/kg) for 5 days before and 5 days after trypanocidal chemotherapy abrogated the pathology in the central nervous system although this returned approximately 15 days after cessation of azathioprine. Activated astrocytes associated with the later stages of the infection did not appear to be affected by the use of azathioprine.

MeSH Terms
Animals Azathioprine/therapeutic use Brain Diseases/chemically induced,drug therapy,pathology Diminazene/adverse effects,analogs & derivatives,therapeutic use Disease Models, Animal Female Mice Mice, Inbred Strains Trypanocidal Agents/adverse effects,therapeutic use Trypanosomiasis, African/drug therapy
Chemicals
Trypanocidal Agents diminazene aceturate Azathioprine Diminazene
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hunter C A
Department of Veterinary Medicine, University of Glasgow, Scotland.
Jennings F W
Kennedy P G
Murray M
Article Info
Journal
Neuropathology and applied neurobiology
Abbr.
Neuropathol Appl Neurobiol
ISSN
0305-1846
Published
1992-12-00
Pages
619-25
Language
English
Region
England
NLM ID
7609829
Subset
IM
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