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Changes in cortical protein markers of iron transport with gender, major depressive disorder and suicide

Version 2 2020-05-07, 08:50
Version 1 2018-12-04, 22:14
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posted on 2020-05-07, 08:50 authored by Brian Dean, Andrew Tsatsanis, Linh Q. Lam, Elizabeth Scarr, James A. Duce

Objectives: The objective of this study was to determine whether a breakdown in proteins regulating cortical iron homeostasis could be involved in the pathophysiology of mood disorders.

Methods: Levels of select proteins responsible for cortical iron transport were quantitated by Western blotting of Brodmann’s (BA) areas 6 and 10 from patients with major depressive disorder (n = 13), bipolar disorder (n = 12) and age/sex matched controls (n = 13).

Results: We found the inactive form of ceruloplasmin was lower in BA 6 from males compared to females. Levels of copper containing ceruloplasmin was lower in BA 6 from suicide completers whilst levels of amyloid precursor protein, TAU and transferrin were higher in BA 10 from those individuals. The level of prion protein was lower in BA 6 from subjects with major depressive disorder.

Conclusions: Our data suggests that perturbation in cortical iron transport proteins is not prevalent in mood disorders. By contrast, our data suggests changes in iron transport proteins in BA 6 and BA 10 are present after suicide completion. If these changes were present before death, they could have had a role in the genesis of the contemplation and completion of suicide.

Funding

This work was supported by the National Medical & Health Research Council [grant numbers 1025774, 566967, 1002240, 1025774, 1044542 & 1061587], the CRC for Mental Health, One in Five and the Andrew and Claire Heenan Ride for Ben as well as Operational Infrastructure Support from the Victorian State Government.

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    World Journal of Biological Psychiatry

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