Maternal Perinatal Undernutrition has Long-Term Consequences on Morphology, Function and Gene Expression of the Adrenal Medulla in the Adult Male Rat
Epidemiological studies suggest that maternal undernutrition sensitises to the development of chronic adult diseases, such as type 2 diabetes, hypertension and obesity. Although the physiological mechanisms involved in this ‘perinatal programming’ remain largely unknown, alterations of stress neuroe...
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Veröffentlicht in: | Journal of neuroendocrinology 2011-08, Vol.23 (8), p.711-724 |
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Sprache: | eng |
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Zusammenfassung: | Epidemiological studies suggest that maternal undernutrition sensitises to the development of chronic adult diseases, such as type 2 diabetes, hypertension and obesity. Although the physiological mechanisms involved in this ‘perinatal programming’ remain largely unknown, alterations of stress neuroendocrine systems such as the hypothalamic‐pituitary‐adrenal (HPA) and sympathoadrenal axes might play a crucial role. Despite recent reports showing that maternal perinatal undernutrition disturbs chromaffin cells organisation and activity in male rats at weaning, its long‐term effects on adrenal medulla in adult animals are unknown. Using a rat model of maternal perinatal 50% food restriction (FR50) from the second week of gestation until weaning, histochemistry approaches revealed alterations in noradrenergic chromaffin cells aggregation and in cholinergic innervation in the adrenal medulla of 8‐month‐old FR50 rats. Electron microscopy showed that chromaffin cell granules exhibited ultrastructural changes in FR50 rats. These morphological changes were associated with reduced circulating levels and excretion of catecholamines. By contrast, catecholamine plasma levels were significantly increased after a 16 or 72 h of fasting, indicating that the responsiveness of the sympathoadrenal system to food deprivation was accentuated in FR50 adult rats. Among 384 pituitary adenylate cyclase‐activating polypeptide‐sensitive genes, we identified 129 genes (33.6%) that were under expressed (ratio |
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ISSN: | 0953-8194 1365-2826 |
DOI: | 10.1111/j.1365-2826.2011.02159.x |