Abstract
Proinflammatory cytokines are supposed to be involved in the pathophysiology of neuronal damage following excitotoxic lesions. We examined the effect of rolipram, a TNF-alpha-inhibitor, on excitotoxic neuronal damage. Quinolinic acid (240 nmol in 1 microl) was injected stereotactically into the striatum of male Wistar rats. Four groups of QA rats were treated i.p. with solvent, MK-801 (4 mg/kg) or rolipram (0.3 mg/kg) which was started either 6 or 24 h after QA injection and continued with daily applications for 14 days. QA injection induced neuronal damage which affected 93% of the striatal area. MK-801 reduced this damage to 12% of the striatal area. Treatment with rolipram when started at 6 h after QA injection resulted in neuronal damage amounting to 60%; the result after starting at 24 h was not different from solvent (91%). The present results demonstrate that rolipram reduces neuronal damage induced by intrastriatal QA application.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Animals
-
Antidepressive Agents / pharmacology*
-
Cell Count
-
Dizocilpine Maleate / pharmacology
-
Drug Interactions / physiology
-
Excitatory Amino Acid Antagonists / pharmacokinetics
-
Immunohistochemistry
-
Male
-
Neostriatum / drug effects*
-
Neostriatum / pathology
-
Neostriatum / physiopathology
-
Nerve Degeneration / chemically induced*
-
Nerve Degeneration / pathology
-
Nerve Degeneration / physiopathology
-
Neurons / drug effects*
-
Neurons / metabolism
-
Neurons / pathology
-
Neuroprotective Agents / pharmacology
-
Neurotoxins / antagonists & inhibitors*
-
Quinolinic Acid / pharmacology
-
Rats
-
Rats, Wistar
-
Rolipram / pharmacology*
-
Tumor Necrosis Factor-alpha / antagonists & inhibitors*
-
Tumor Necrosis Factor-alpha / metabolism
Substances
-
Antidepressive Agents
-
Excitatory Amino Acid Antagonists
-
Neuroprotective Agents
-
Neurotoxins
-
Tumor Necrosis Factor-alpha
-
Dizocilpine Maleate
-
Quinolinic Acid
-
Rolipram