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Effects of Li(+) transport and Li(+) immobilization on Li(+)/Mg(2+) competition in cells: implications for bipolar
Brian T Layden1, Abde M Abukhdeir, Nicole Williams
1Department of Chemistry, Loyola University Chicago, 6525 N. Sheridan Rd., Chicago, IL 60626, USA.
Insights
Lithium (Li+) transport and competition with magnesium (Mg2+) vary by cell type. Neuroblastoma and lymphoblastoma cells show greater Li+ immobilization and Mg2+ increase than erythrocytes.
Area of Science:
- Biochemistry
- Cell Biology
- Pharmacology
Background:
- Lithium (Li+) is a key treatment for bipolar illness.
- Li+/Mg2+ competition is a proposed mechanism for Li+ therapy.
- Cell-specific properties may influence this competition.
Purpose of the Study:
- To investigate Li+ transport, immobilization, and Li+/Mg2+ competition.
- To determine if these processes are cell-specific.
- To elucidate the relationship between Li+ and intracellular Mg2+ dynamics.
Main Methods:
- Comparing Li+ accumulation, binding affinity, and immobilization in lymphoblastomas, neuroblastomas, and erythrocytes.
- Measuring intracellular free Mg2+ levels after Li+ loading.
- Analyzing Li+/Mg2+ competition across different cell types.
Main Results:
- Li+ accumulation was highest in lymphoblastomas, followed by neuroblastomas and erythrocytes.
- Li+ immobilization was greatest in neuroblastomas and least in erythrocytes.
- Neuroblastoma and lymphoblastoma cells showed significant increases in free intracellular Mg2+ after Li+ loading, unlike erythrocytes.
Conclusions:
- Li+ immobilization and transport are linked to intracellular Mg2+ levels.
- The extent of Li+/Mg2+ competition is cell-specific.
- These findings highlight cell-specific mechanisms in Li+ action.
Abstract:
Li(+)/Mg(2+) competition has been implicated in the therapeutic action of Li(+) treatment in bipolar illness. We hypothesized that this competition depended on cell-specific properties. To test this hypothesis, we determined the degree of Li(+) transport, immobilization, and Li(+)/Mg(2+) competition in lymphoblastomas, neuroblastomas, and erythrocytes. During a 50 mM/L Li(+)-loading incubation, Li(+) accumulation at 30 min (mmoles Li(+)/L cells) was the greatest in lymphoblastomas (11.1+/-0.3), followed by neuroblastomas (9.3+/-0.5), and then erythrocytes (4.0+/-0.5). Li(+) binding affinities to the plasma membrane in all three cell types were of the same order of magnitude; however, Li(+) immobilization in intact cells was greatest in neuroblastomas and least in erythrocytes. When cells were loaded for 30 min in a 50 mM/L Li(+)-containing medium, the percentage increase in free intracellular [Mg(2+)] in neuroblastoma and lymphoblastoma cells ( approximately 55 and approximately 52%, respectively) was similar, but erythrocytes did not exhibit any substantial increase ( approximately 6%). With the intracellular [Li(+)] at 15 mM/L, the free intracellular [Mg(2+)] increased by the greatest amount in neuroblastomas ( approximately 158%), followed by lymphoblastomas ( approximately 75%), and then erythrocytes ( approximately 50%). We conclude that Li(+) immobilization and transport are related to free intracellular [Mg(2+)] and to the extent of Li(+)/Mg(2+) competition in a cell-specific manner.
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