Maternal protein restriction during gestation and lactation in the rat results in increased brain levels of kynurenine and kynurenic acid in their adult offspring

Early malnutrition is a risk factor for depression and schizophrenia. Since the offspring of malnourished dams exhibit increased brain levels of serotonin (5‐HT), a tryptophan‐derived neurotransmitter involved in the pathophysiology of these mental disorders, it is believed that the deleterious effe...

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Veröffentlicht in:Journal of neurochemistry 2017-01, Vol.140 (1), p.68-81
Hauptverfasser: Honório de Melo Martimiano, Paula, Sa Braga Oliveira, André, Ferchaud‐Roucher, Véronique, Croyal, Mikaël, Aguesse, Audrey, Grit, Isabelle, Ouguerram, Khadija, Lopes de Souza, Sandra, Kaeffer, Bertrand, Bolaños‐Jiménez, Francisco
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Sprache:eng
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Zusammenfassung:Early malnutrition is a risk factor for depression and schizophrenia. Since the offspring of malnourished dams exhibit increased brain levels of serotonin (5‐HT), a tryptophan‐derived neurotransmitter involved in the pathophysiology of these mental disorders, it is believed that the deleterious effects of early malnutrition on brain function are due in large part to altered serotoninergic neurotransmission resulting from impaired tryptophan (Trp) metabolism. However, tryptophan is also metabolized through the kynurenine (KYN) pathway yielding several neuroactive compounds including kynurenic (KA), quinolinic (QA) and xanthurenic (XA) acids. Nevertheless, the impact of perinatal malnutrition on brain kynurenine pathway metabolism has not been examined to date. Here, we used ultra‐performance liquid chromatography‐tandem mass spectrometry for the simultaneous quantification of tryptophan and a set of seven compounds spanning its metabolism through the serotonin and kynurenine pathways, in the brain of embryos and adult offspring of rat dams fed a protein‐restricted (PR) diet. Protein‐restricted embryos showed reduced brain levels of Trp, serotonin and KA, but not of KYN, XA, or QA. In contrast, PR adult rats exhibited enhanced levels of Trp in the brainstem and cortex along with increased concentrations of 5‐HT, kynurenine and XA. The levels of XA and KA were also increased in the hippocampus of adult PR rats. These results show that early protein deficiency induces selective and long‐lasting changes in brain kynurenine metabolism. Given the regulatory role of KYN pathway metabolites on brain development and function, these changes might contribute to the risk of developing psychiatric disorders induced by early malnutrition. Early malnutrition results in a high risk of developing psychiatric disorders in adulthood such as depression and schizophrenia. Here, we show that the adult offspring born to dams fed a low‐protein diet during pregnancy and lactation exhibit increased brain levels of kynurenine (KYN) and kynurenic acid (KA). Given that the concentration of these metabolites is also enhanced in the brain of schizophrenic patients, this result suggests that altered kynurenine pathway metabolism might be a key link between perinatal malnutrition and the development of schizophrenia later in life.
ISSN:0022-3042
1471-4159
DOI:10.1111/jnc.13874