期刊
BRAIN RESEARCH
卷 1538, 期 -, 页码 159-171出版社
ELSEVIER
DOI: 10.1016/j.brainres.2013.09.037
关键词
In vivo microdialysis; MPTP; Pargyline; Dopamine; Energy metabolism; Glucose; Lactate; Pyruvate
资金
- Regione Sardegna Legge Regionale
The neurotoxin MPTP is known to induce dopamine release and depletion of ATP in the striatum of rats. Therefore, we studied the changes induced by MPTP and pargyline protection both on striatal dopamine release and on extracellular energy metabolites in freely moving rats, using dual asymmetric-flow microdialysis. A dual microdialysis probe was inserted in the right striatum of rats. MPTP (25 mg/kg, 15 mg/kg, 10 mg/kg) was intraperitoneally administered for three consecutive days. MAO-B inhibitor pargyline (15 mg/kg) was systemically administered before neurotoxin administration. The first MPTP dose induced an increase in dialysate dopamine and a decrease of DOPAC levels in striatal dialysate. After the first neurotoxin administration, increases in striatal glucose, lactate, pyruvate, lactate/pyruvate (LIP) and lactate/glucose (L/G) ratios were observed. Subsequent MPTP administrations showed a progressive reduction of dopamine, glucose and pyruvate levels with a concomitant further increase in lactate levels and L/P and L/G ratios. At day 1, pargyline pre-treatment attenuated the MPTP-induced changes in all studied analytes. Starting from day 2, pargyline prevented the depletion of dopamine, glucose and pyruvate while reduced the increase of lactate, LIP ratio and L/G ratio. These in vivo results suggest a pargyline neuroprotection role against the MPTP-induced energetic impairment consequent to mitochondrial damage. This neuroprotective effect was confirmed by TH immunostaining of the substantia nigra. (C) 2013 Elsevier B.V. All rights reserved.
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