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^ abVidaluc JL (1996). "MPTP as a Molecular Paradigm for Neurodegeneration. A Review of its Connections with Relevant Molecules". Current Medicinal Chemistry. Bentham Science Publishers. pp. 117–138. Retrieved 28 September 2024. Selective neurotransmitter depletion was observed with the MPTP analog 1-methyl-4-(2'-aminophenyl)-1-(2'-NH2-MPTP) leading to marked reductions (60-70%) in levels of 5-HT, 5-HIAA and NA in frontal cortex and hippocampus while not affecting striatal DA. In contrast, 1-methyl-4-(2'- methylphenyl)-1,2,3,6-tetrahydropyridine (2'-Me-MPTP) minimally affected 5-HT, 5-HIAA and NA, while markedly reducing (90%) striatal DA content [128].
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^Murphy DL, Lerner A, Rudnick G, Lesch KP (April 2004). "Serotonin transporter: gene, genetic disorders, and pharmacogenetics". Molecular Interventions. 4 (2): 109–123. doi:10.1124/mi.4.2.8. PMID15087484. SERT has some ability to transport other endogenous amines such as dopamine, and also is a drug transporter for agents that include fenfluramine, nonfenfluramine, substituted amphetamines (i.e., MDMA, and parachloroamphetamine), methcathinone, and the serotonin (but not dopamine) neurotoxin amino-MPTP [1-methyl-4-(2′-aminophenyl)-1,2,3,6-tetrahydropyridine], which enters neurons via SERT to induce persistent (months-long) reductions of serotonin accompanied by neurodegenerative changes (11–14).
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