Iron and n-3 fatty acid depletion, alone and in combination, during early development provoke neurochemical changes, anhedonia, anxiety and social dysfunction in rats.

Journal: Nutritional neuroscience

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Affiliated Institutions:  Center of Excellence for Nutrition, North-West University, Potchefstroom, South Africa. School of Pharmacy and Center of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.

Abstract summary 

Both iron and omega-3 (n-3) fatty acids (FA) play important roles in the development and functioning of the brain. We investigated the effects of n-3 FA and iron deficiencies, alone and in combination, during early development on behaviour and brain monoamines in rats. Using a 2-factorial design, female Wistar rats were randomly allocated to one of four diet groups: Control, n-3 FA deficient (n-3 FAD), iron deficient (ID), or n-3 FAD + ID. Females received these diets throughout mating, pregnancy and lactation. Offspring ( = 24/group; male:female = 1:1) continued on the same diet until post-natal day 42-45, and underwent a sucrose preference test (SPT), novel object recognition test, elevated plus maze (EPM) and social interaction test (SIT). ID offspring consumed less sucrose in the SPT and spent more time in closed arms and less time in open arms of the EPM than non-ID offspring. In female offspring only, ID and n-3 FAD reduced time approaching and together in the SIT, with an additive effect of ID and n-3 FAD for even less time approaching and spent together in the n-3 FAD + ID group compared to controls. ID offspring had higher striatal dopamine and norepinephrine and lower frontal cortex dopamine concentrations. N-3 FAD and ID affected frontal cortex serotonin concentrations in a sex-specific manner. Our results suggest that ID and n-3 FAD during early development provoke anhedonia, anxiety and social dysfunction in rats, with potential additive and attenuating effects when combined. These effects may in part be attributed to disturbances in brain neurochemistry and may be sex-specific.

Authors & Co-authors:  Kemp Erna T ET Zandberg Lizelle L Harvey Brian H BH Smuts Cornelius M CM Baumgartner Jeannine J

Study Outcome 

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Statistics
Citations : 
Authors :  5
Identifiers
Doi : 10.1080/1028415X.2023.2245615
SSN : 1476-8305
Study Population
Female,Females
Mesh Terms
Other Terms
Social behaviour;anxious behaviour;cognition;early development;iron deficiency;monoamines;n-3 fatty acid deficiency;psychiatric comorbidity
Study Design
Cross Sectional Study
Study Approach
Country of Study
Publication Country
England