Identifying neuronal targets and mechanisms of manganese-induced neuromotor disease
Ended Project Grant Awarded Last action
- Award ID
- F31ES036908
- Recipient
-
University Of Texas At Austin UEI V6AFQPN18437 Part of University Of Texas System
- Awarding agency
-
National Institute of Environmental Health Sciences
National Institutes of Health, Department of Health and Human Services
- Obligated
- $115,206
Award facts
- Assistance listing
- 93.113 Environmental Health
- Completion date
- Place of performance
- Austin, TX 78759, USA
Award details come from USAspending.gov.
Description
- Abstract
- Manganese (MN) is an essential micronutrient, but in excess, IT is neurotoxic. Humans who are over-exposed to MN environmentally or occupationally develop cognitive and motor deficits. Under conditions of over-exposure, MN builds up in the basal ganglia of the brain, which primarily contains dopaminergic or gabaergic neurons. However, the exact neural targets and mechanisms of MN toxicity are poorly understood. A question that remains unanswered is whether MN targets dopaminergic or gabaergic neurons of the basal ganglia to induce motor disease. In the proposed work, we use the critical MN efflux transporter protein SLC30A10 as a tool to address this question. Homozygous loss-of-function mutations of SLC30A10 causes childhood dystonia and adult-onset parkinsonism. We previously showed that loss of SLC30A10 in the brain leads to elevated MN levels in the basal ganglia in early-life, lifelong motor deficits, and impaired evoked dopamine release. Previous studies also revealed that selective loss of SLC30A10 in dopaminergic neurons leads to motor deficits in early-life that persist into adulthood. These findings show that activity of SLC30A10 in dopaminergic neurons is required to protect against MN toxicity and suggest that MN targets dopaminergic neurons of the basal ganglia. To definitively identify the neuronal targets and mechanisms of MN toxicity, we will use dopaminergic- or gabaergic-specific SLC30A10 knockin mice. These mouse models allow US to selectively increase SLC30A10 expression in specific neurons and attenuate increased MN levels after exposure. In the proposed work, we will use behavioral and neurochemical approaches to test the hypothesis that dopaminergic neurons are the primary target of MN. Knockin and control mice will receive an oral MN treatment or vehicle treatment starting from birth, and we will perform behavioral assays at various timepoints from PND28-180. Proposed experiments also include metal analyses and assaying for changes in evoked dopamine and gaba release by in- vivo microdialysis. Results from early-life behavioral assays with the dopaminergic-specific SLC30A10 knockin strain have shown that knockin mice are protected from early-life MN-induced motor deficits after MN exposure, compared to control littermates that develop motor deficits. These novel findings corroborate the hypothesis that MN primarily targets dopaminergic neurons of the basal ganglia to induce motor disease. This proposed study will therefore provide valuable insight into the prevention of MN-induced disease and inform future studies towards developing treatments.
Transactions
| Action | Obligated | Date |
|---|---|---|
| Amendment | -$7,197 | |
| Amendment | $41,177 | |
| Amendment | $40,613 | |
| Amendment | $0 | |
| Amendment | $0 | |
| Amendment | $0 | |
| Original award | $40,613 |
Quick answers
Who received award F31ES036908?
F31ES036908 was awarded to University Of Texas At Austin by National Institute of Environmental Health Sciences (National Institutes of Health) on January 19, 2025.
How much is award F31ES036908 worth?
$115,206 has been obligated on F31ES036908.
On GovTribe
See this award's full record
- Every transaction and subaward
- The recipient's other awards and teaming partners
- Similar grant awards
- Ask GovTribe AI about this award