Literature DB >> 8949944

Treatment of mice with methamphetamine produces cell loss in the substantia nigra.

P K Sonsalla1, N D Jochnowitz, G D Zeevalk, J A Oostveen, E D Hall.   

Abstract

Studies were conducted to determine if treatment of mice with methamphetamine (METH) would produce a loss of dopaminergic cells in the substantia nigra. The number of TH+/Nissl-stained was significantly decreased in both Swiss-Webster (S-W) and C57bl mice (approx. cell loss of 40% and 45%, respectively) 5-8 days after treatment with METH. In these same mice there was a corresponding decrease in neostriatal dopamine (DA) content (90% and 92%, respectively). In parallel studies, treatment with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) produced similar neuropathological effects. The finding that nigral cell loss occurs after METH treatment indicates that the METH-treated mouse may be a very relevant model of Parkinson's disease (PD).

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Year:  1996        PMID: 8949944     DOI: 10.1016/0006-8993(96)00995-x

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  49 in total

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Review 7.  Nucleus accumbens invulnerability to methamphetamine neurotoxicity.

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8.  Ginsenoside Re rescues methamphetamine-induced oxidative damage, mitochondrial dysfunction, microglial activation, and dopaminergic degeneration by inhibiting the protein kinase Cδ gene.

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Review 9.  Mitochondrial dysfunction in mouse models of Parkinson's disease revealed by transcriptomics and proteomics.

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10.  Chronic stress enhances methamphetamine-induced extracellular glutamate and excitotoxicity in the rat striatum.

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