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PMID: 10773035 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Naloxone protects rat dopaminergic neurons against inflammatory damage through inhibition of microglia activation and superoxide generation.

The Journal of pharmacology and experimental therapeutics ·Vol. 293 ·No. 2 ·2000-05-00 ·Pages 607-17

Liu B, Du L, Hong JS

Abstract

Degeneration of dopaminergicrgic neurons in the substantia nigra of the brain is a hallmark of Parkinson's disease and inflammation and oxidative stress are closely associated with the pathogenesis of degenerative neurological disorders. Treatment of rat mesencephalic mixed neuron-glia cultures with lipopolysaccharide (LPS)-activated microglia, resident immune cells of the brain, to release proinflammatory and neurotoxic factors tumor necrosis factor-alpha, interleukin-1beta, nitric oxide, and superoxide and subsequently caused damage to midbrain neurons, including dopaminergic neurons. The LPS-induced degeneration of the midbrain neurons was significantly reduced by cotreatment with naloxone, an opioid receptor antagonist. This study focused on understanding the mechanism of action for the protective effect of naloxone on dopaminergic neurons because of relevance to Parkinson's disease. Both naloxone and its opioid receptor inactive stereoisomer (+)-naloxone protected the dopaminergic neurons with equal potency. Naloxone inhibited LPS-induced activation of microglia and release of proinflammatory factors, and inhibition of microglia generation of superoxide free radical best correlated with the neuroprotective effect of naloxone isomers. To further delineate the site of action, naloxone was found to partially inhibit the binding of [(3)H]LPS to cell membranes, whereas it failed to prevent damage to dopaminergic neurons by peroxynitrite, a product of nitric oxide and superoxide. These results suggest that naloxone at least in part interferes with the binding of LPS to cell membranes to inhibit microglia activation and protect dopaminergic neurons as well as other neurons in the midbrain cultures from inflammatory damage.

MeSH Terms
Animals Cells, Cultured Dopamine/physiology Immunohistochemistry Inflammation/pathology Interleukin-1/metabolism Lipopolysaccharides/pharmacology Mesencephalon/cytology,drug effects,metabolism Microglia/drug effects,enzymology,metabolism Mitogen-Activated Protein Kinase 3 Mitogen-Activated Protein Kinases/metabolism Naloxone/pharmacology Narcotic Antagonists/pharmacology Neurons/drug effects,enzymology,pathology Nitrates/pharmacology Nitrites/metabolism Oxidants/pharmacology Rats Rats, Inbred F344 Stereoisomerism Substantia Nigra/cytology,drug effects,enzymology Superoxides/metabolism Tumor Necrosis Factor-alpha/metabolism Tyrosine 3-Monooxygenase/metabolism
Chemicals
Interleukin-1 Lipopolysaccharides Narcotic Antagonists Nitrates Nitrites Oxidants Tumor Necrosis Factor-alpha Superoxides peroxynitric acid Naloxone Tyrosine 3-Monooxygenase Mitogen-Activated Protein Kinase 3 Mitogen-Activated Protein Kinases Dopamine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Liu B
Neuropharmacology Section, Laboratory of Pharmacology and Chemistry, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA. liu@niehs.nih.gov
Du L
Hong J S
Article Info
Journal
The Journal of pharmacology and experimental therapeutics
Abbr.
J Pharmacol Exp Ther
ISSN
0022-3565
Published
2000-05-00
Pages
607-17
Language
English
Region
United States
NLM ID
0376362
Subset
IM
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