Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0240066 (
iron deficiency
)
7,156
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Neurological development and functioning are adversely affected by
iron deficiency
in early life. Iron-deficient rats are known to have elevations in extracellular DA and NE, suggesting alterations in reuptake of these monoamines. To explore possible mechanisms by which cellular iron concentrations may alter NE transporter functioning, we utilized
NET
expressing PC12 cells and iron-deficient rats to explore the relationship between
NET
protein and mRNA expression patterns and iron concentrations. Treatment of PC12 with the iron chelator, desferrioxamine mesylate (DFO, 50 microM for 24 h), significantly decreased [3H] NE uptake by more than 35% with no apparent change in Km. PC12 cells exposed to increasing concentrations of DFO (25-100 microM) exhibited a dose response decrease in [3H] NE uptake within 24 h (38-73% of control) that paralleled a decrease in cellular
NET
protein content. Inhibition of protein synthesis with cycloheximide resulted in
NET
disappearance rates from DFO-treated cells greatly exceeding the rate of loss from control cells. RT-PCR analysis revealed only a modest decrease in
NET
mRNA levels. Rat brain locus ceruleus and thalamus
NET
mRNA levels were also only modestly decreased (10-15%) despite a 40% reduction in regional brain iron. In contrast,
NET
proteins levels in thalamus and locus ceruleus were strongly affected by regional
iron deficiency
with high correlations with iron concentrations (r > 0.94 and r > 0.80 respectively). The present findings demonstrate that
NET
protein concentrations and functioning are dramatically reduced with
iron deficiency
; the modest effect on mRNA levels suggests a stronger influence on
NET
trafficking and degradation than on protein synthesis.
...
PMID:Cellular iron concentrations directly affect the expression levels of norepinephrine transporter in PC12 cells and rat brain tissue. 1665 Aug 37