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HERO ID
1686249
Reference Type
Journal Article
Title
Neuroprotective effects of tacrolimus (FK506) in a model of ischemic coritcal cell cultures: Role of glutamate uptake and FK506 binding protein 12 kDa
Author(s)
Labrande, C; Velly, L; Canolle, B; Guillet, B; Masmejean, F; Nieoullon, A; Pisano, P
Year
2006
Is Peer Reviewed?
1
Journal
Neuroscience
ISSN:
0306-4522
EISSN:
1873-7544
Volume
137
Issue
1
Page Numbers
231-239
PMID
16289353
DOI
10.1016/j.neuroscience.2005.08.080
Web of Science Id
WOS:000234761200024
Abstract
Background: The mechanisms underlying the neuroprotective effects of the immunosuppressant tacrolimus, observed in vivo, remain unclear. Here we quantify these effects in vitro, and evaluate the potential involvement of the glutamate and/or immunophilin FK506 binding protein 12 kDa in tacrolimus-induced neuroprotection.
Methods: Primary cultures of neurons and astrocytes from rat cerebral cortex were subjected to transient oxygen., glucose deprivation. Neuronal injury was evaluated by cell counting after immunostaining experiments, lactate dehydrogenase release and 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide reduction. The involvement of the immunophilin FK506 binding protein 12 kDa was explored using an anti-FK506 binding protein 12 kDa antibody, (3-3-pyridyl)-1-propyl(2 s)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-pyrrolidine carboxylate and rapamycin. Extracellular glutamate and glutamate uptake were respectively measured by high performance liquid chromatography and L-[H-3]glutamate incorporation.
Results: When added during either oxygen-glucose deprivation or reoxygenation, FK506 (50-500 pM) offered signifficant neuro protection. During oxygen-glucose deprivation, it was able to reverse the oxygen-glucose deprivation-induced increase in extracellular glutamate and decrease in glutamate uptake and this effect was reversed in the presence of threo3-methyl glutamate, a specific inhibitor of glutamate transporter-1. Blocking FK506 binding protein 12 kDa inhibited the neuroprotection induced by tacrolimus added during either oxygen-glucose deprivation or reoxygenation. Tacrolimus-induced neuroprotection was also reversed in the presence of rapamycin, an immunosuppressant FK506 binding protein 12 kDa ligand devoid of neuroprotective properties and (3-3pyridyl)-1-propyl(2 s)-1-(3,3-dimethyl-1,2-dioxopentyl)-2-pyrrolidine carboxylate, a non-immunosuppressant ligand of FK506 binding protein 12 kDa, exerteing neuroprotective effects.
Conclusion: The beneficial effects of tacrolimus during in vitro ischemia/reperfusion seem to indicate the restoration of a glutamate transporter-1-mediated activity and could be mediated by a FK506 binding protein 12 kDa pathway. (c) 2005 Published by Elsevier Ltd on behalf of IBRO.
Keywords
immunosuppressive drugs; neuroprotection; oxygen-glucose deprivation; immunophilins
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