Bnormal substantia nigra morphology in the stimulant group. There are a

Bnormal substantia nigra morphology in the stimulant group. There are a number of lines of evidence to support this view. In particular, methamphetamine exposure has been directly linked with changes in the substantia nigra. Adult vervet monkeys treated with 2 doses of methamphetamine (2 mg/kg) exhibit a 1? fold increase in the intensity of iron staining in the substantia nigra at 1-month post-drug administration and a 2.5 fold increase in iron staining intensity at 1.5 yrs post-drug administration [37]. Additionally, pre-synaptic dopaminergic dysfunction (i.e. reduced [18F]-dopa activity) is present in vervet monkey striatum 24 weeks after a 10-day period of amphetamine administration (4?8 mg/ kg/day) [57] and pre-synaptic dopaminergic dysfunction is also present in the striatum of healthy young adult humans with substantia nigra hyperechogenicity [31,58]. In cocaine dependent 23727046 individuals, order K162 increased activation of microglia is present in the substantia nigra at post-mortem [59] and increased activation of microglia is associated with substantia nigra hyperechogenicity in healthy adults [33]. Finally, amphetamine, methamphetamine, and cocaine damage dopaminergic nerve terminals and chronic use of amphetamines is associated with long-lasting dopaminergic dysfunction [3,10]. Concurrent use of stimulants and tobacco, hallucinogens, and inhalants could also have contributed to the abnormal substantia nigra morphology. In the stimulant group, there was a positive correlation between the area of substantia nigra echogenicity and lifetime use of hallucinogens and a trend for a positive correlation with lifetime use of tobacco and inhalants. The most commonly used hallucinogens were LSD and `magic’ mushrooms (likely Psilocybe species). The psychoactive compound in LSD and Psilocybe exhibits a chemical structure that resembles serotonin. These drugs are considered to have a low level of toxicity but Psilocybe can be mistaken for other varieties that have poisonous, and sometimes lethal, effects. In regards to tobacco, cigarettes contain chemicals that are monoamine oxidase inhibitors [60]. Concurrent use of tobacco and amphetamines may facilitate the effect of amphetamines on nerve terminals by impairing degradation of monoamine neurotransmitters. Use of cannabis and opiates is unlikely to have had a strong effect given that illicit opiate use was minimal in the current cohort and substantia nigra morphology was normal in cannabis users.Stimulant Drugs and Substantia Nigra MorphologyFigure 1. Single subject data MedChemExpress BTZ-043 showing echomorphology of the mesencephalic brainstem. A) Images from 1 control subject, 1 cannabis subject, and 1 stimulant subject. The substantia nigra ipsilateral to the probe (the side at which the planimetric measurement is done) is encircled with a dotted line. B) Schematic drawing of the mesencephalic brainstem. * aqueduct. Raphe, echogenicity of midline structures. doi:10.1371/journal.pone.0056438.gThe results of the current study cause one to speculate about the potential association between chemical exposure and substantia nigra hyperechogenicity. One study that supports a link between chemical exposure and substantia nigra echogencity involved administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineFigure 2. Group data showing the area of substantia nigra echogenicity. Data represent the largest area across the right and left side. Data for the control, stimulant, and cannabis groups are shown. The boundary of each box i.Bnormal substantia nigra morphology in the stimulant group. There are a number of lines of evidence to support this view. In particular, methamphetamine exposure has been directly linked with changes in the substantia nigra. Adult vervet monkeys treated with 2 doses of methamphetamine (2 mg/kg) exhibit a 1? fold increase in the intensity of iron staining in the substantia nigra at 1-month post-drug administration and a 2.5 fold increase in iron staining intensity at 1.5 yrs post-drug administration [37]. Additionally, pre-synaptic dopaminergic dysfunction (i.e. reduced [18F]-dopa activity) is present in vervet monkey striatum 24 weeks after a 10-day period of amphetamine administration (4?8 mg/ kg/day) [57] and pre-synaptic dopaminergic dysfunction is also present in the striatum of healthy young adult humans with substantia nigra hyperechogenicity [31,58]. In cocaine dependent 23727046 individuals, increased activation of microglia is present in the substantia nigra at post-mortem [59] and increased activation of microglia is associated with substantia nigra hyperechogenicity in healthy adults [33]. Finally, amphetamine, methamphetamine, and cocaine damage dopaminergic nerve terminals and chronic use of amphetamines is associated with long-lasting dopaminergic dysfunction [3,10]. Concurrent use of stimulants and tobacco, hallucinogens, and inhalants could also have contributed to the abnormal substantia nigra morphology. In the stimulant group, there was a positive correlation between the area of substantia nigra echogenicity and lifetime use of hallucinogens and a trend for a positive correlation with lifetime use of tobacco and inhalants. The most commonly used hallucinogens were LSD and `magic’ mushrooms (likely Psilocybe species). The psychoactive compound in LSD and Psilocybe exhibits a chemical structure that resembles serotonin. These drugs are considered to have a low level of toxicity but Psilocybe can be mistaken for other varieties that have poisonous, and sometimes lethal, effects. In regards to tobacco, cigarettes contain chemicals that are monoamine oxidase inhibitors [60]. Concurrent use of tobacco and amphetamines may facilitate the effect of amphetamines on nerve terminals by impairing degradation of monoamine neurotransmitters. Use of cannabis and opiates is unlikely to have had a strong effect given that illicit opiate use was minimal in the current cohort and substantia nigra morphology was normal in cannabis users.Stimulant Drugs and Substantia Nigra MorphologyFigure 1. Single subject data showing echomorphology of the mesencephalic brainstem. A) Images from 1 control subject, 1 cannabis subject, and 1 stimulant subject. The substantia nigra ipsilateral to the probe (the side at which the planimetric measurement is done) is encircled with a dotted line. B) Schematic drawing of the mesencephalic brainstem. * aqueduct. Raphe, echogenicity of midline structures. doi:10.1371/journal.pone.0056438.gThe results of the current study cause one to speculate about the potential association between chemical exposure and substantia nigra hyperechogenicity. One study that supports a link between chemical exposure and substantia nigra echogencity involved administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridineFigure 2. Group data showing the area of substantia nigra echogenicity. Data represent the largest area across the right and left side. Data for the control, stimulant, and cannabis groups are shown. The boundary of each box i.