Neuroprotective mechanism of modafinil on Parkinson disease induced by 1-methyl-4-phenyl-1,2,3,6-tet

来源 :Acta Pharmacologica Sinica | 被引量 : 0次 | 上传用户:hxg0215
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AIM: To observe the neuroprotective mechanism of modafinil on Parkinson disease (PD) models induced by 1- methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP). METHODS: The model of PD was induced by intraperi- toneally injecting MPTP into C57BL/6J mice for 4 d. Modafinil ( ip, 50 or 100 mg·kg ·d-1 ) was administered at 30 -1 min following MPTP for 4 d and for another 10 d continuously. The contents of dopamine (DA), noradrenaline (NA), 5-hydroxytryptamine (5-HT), γ-aminobutyric acid (GABA) , glutamine (Glu) in the striatum, and the con- tents of GABA, Glu, malondialdehyde (MDA), and glutathione (GSH) in the substantia nigra (SN) of model mice were determined. RESULTS: Modafinil (50 and 100 mg/kg) prevented against the decrease of the contents of DA, 5-HT, and NA in the striatum and GSH, GABA in the SN induced by MPTP, but reduced the increase of MDA in the SN and GABA in the striatum induced by MPTP. Modafinil preferentially inhibited striatal GABA release, but it did not change the increase of nigrostriatal Glu release induced by MPTP. CONCLUSION: The anti-oxidation and the modulation of nigrostriatal GABA and striatal NA and 5-HT release contributed to the neuroprotective effects of modafinil on PD induced by MPTP. AIM: To observe the neuroprotective mechanism of modafinil on Parkinson disease (PD) models induced by 1-methyl-4-phenyl- 1, 2,3,6- tetrahydropyridine (MPTP). METHODS: The model of PD was induced by intraperi- The contents of dopamine (50 mg / kg · d-1) were administered 30 min to MPTP into C57BL / 6J mice for 4 d. (DA), noradrenaline (NA), 5-hydroxytryptamine (5-HT), γ-aminobutyric acid (GABA), glutamine (Glu) in the striatum, and the con tents of GABA, Glu, malondialdehyde RESULTS: Modafinil (50 and 100 mg / kg) prevented against the decrease of the contents of DA, 5-HT, and NA in the striatum and GSH, GABA in the SN induced by MPTP, but reduced the increase of MDA in the SN and GABA in the striatum induced by MPTP. Modafinil preferentially inhibited striatal GABA release, but it did not change th CONCLUSION: The anti-oxidation and the modulation of nigrostriatal GABA and striatal NA and 5-HT release contributed to the neuroprotective effects of modafinil on PD induced by MPTP.
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