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Functional Neuroimaging Using Ultrasonic Blood-brain Barrier Disruption and Manganese-enhanced MRI
Published on: July 12, 2012
Animal models of manganese's neurotoxicity
1Department of Psychology, Auburn University, AL 36849, USA. newlamc@mail.aubum.edu
Abstract:
Manganese's neurotoxicity continues to present a puzzling array of differences across individuals and across published reports in the profile of effects seen in humans and nonhuman species, but some of the sources of individual variability are becoming clear from studies of animals. The kinetics of manganese is a critical component of any assessment of risk associated with exposure. After inhalation, the uptake of manganese into and elimination from the central nervous system are slow and some manganese remains in the nervous system a year after inhalation. Comparison with other parenteral routes suggests that manganese depots in lung prolongs exposure even after environmental exposure has ended. Manganese's neurotoxicity is associated with its appearance in basal ganglia structures, especially the globus pallidus. Manganese also appears in the pituitary gland but the functional consequences of this are not well understood. Other critical components in characterizing manganese's neurotoxicity appear to be the behavioral endpoints used, the species studied, and the exposure rate. Over neurological signs and excitability are associated with high exposure rates and the appearance of manganese throughout basal ganglia and basal forebrain regions. More focused behavioral endpoints are required to detect the subtle signs associated with slow exposure rates low exposure levels, but when such designs are used the effect is unequivocal. At lower exposure levels, doses of 5 mg/kg and greater, deficits in a task in which a monkey executed a rowing type motion against a spring approximating its body weight were clearly related to manganese exposure while other traditional measures of response patterns under schedules of reinforcement remained intact. Excitability and other signs of emotionality have not been reported at low exposure rates. In rodents, manganese accumulation and alterations in the function or concentration of neurotransmitters have been reported. Investigations of behavioral effects in these species, which usually involved locomotor activity, have resulted in less consistent results. Manganese produces a constellation of neurotoxic signs whose appearance and detection are influenced by dose and exposure rate. Despite investigations of manganese's neurotoxicity in animals over a wide range of exposure levels, a NOAEL has not been identified.
Insights
Manganese neurotoxicity varies, influenced by exposure kinetics and dose. Animal studies reveal slow CNS uptake and prolonged exposure from lung depots, impacting basal ganglia and behavior.
Area of Science:
- Neuroscience
- Toxicology
- Environmental Health
Background:
- Manganese neurotoxicity exhibits significant individual variability in humans and animal models.
- Understanding manganese kinetics is crucial for assessing exposure risks.
- Manganese accumulation in the central nervous system, particularly basal ganglia, is linked to neurotoxic effects.
Purpose of the Study:
- To elucidate the factors contributing to variability in manganese neurotoxicity.
- To characterize the relationship between manganese exposure kinetics, dose, and behavioral outcomes.
- To identify sensitive behavioral endpoints for detecting subtle neurotoxic effects.
Main Methods:
- Animal studies investigating manganese uptake, distribution, and elimination in the central nervous system after inhalation.
- Behavioral assessments in nonhuman primates and rodents using varied exposure rates and doses.
- Analysis of neurochemical alterations and neurotransmitter function in response to manganese exposure.
Main Results:
- Slow manganese uptake and elimination from the central nervous system, with prolonged retention.
- Manganese depots in the lungs extend exposure duration even after cessation of environmental contact.
- High exposure rates correlate with widespread manganese in basal ganglia and forebrain, causing overt neurological signs and excitability.
- Low exposure rates reveal subtle deficits in specific motor tasks (e.g., rowing motion) in primates, while traditional measures remain unaffected.
- Rodent studies show manganese accumulation and altered neurotransmitter function, though behavioral results (locomotor activity) are inconsistent.
Conclusions:
- Manganese neurotoxicity is dose- and exposure rate-dependent, affecting specific behavioral endpoints.
- Subtle neurotoxic effects can be detected with sensitive behavioral assays at lower exposure levels.
- A definitive no observed adverse effect level (NOAEL) for manganese neurotoxicity has not yet been established.
- Further research is needed to fully understand the functional consequences of manganese accumulation in areas like the pituitary gland.

