Prenatal stress inhibits neuronal maturation through downregulation of mineralocorticoid receptors

• Published in: The Journal of neuroscience Vol. 31; no. 32; pp. 11505 - 11514
• Main Authors: Tamura, Makoto, Sajo, Mari, Kakita, Akiyoshi, Matsuki, Norio, Koyama, Ryuta
• Format: Journal Article
• Language: English
• Published: United States Society for Neuroscience 10.08.2011
• Subjects: Animals; Animals, Newborn; Down-Regulation - physiology; Female; Mineralocorticoid Receptor Antagonists; Neural Inhibition - physiology; Neurogenesis - physiology; Neurons - cytology; Neurons - metabolism; Pregnancy; Pregnancy Complications - metabolism; Pregnancy Complications - psychology; Prenatal Exposure Delayed Effects - metabolism; Prenatal Exposure Delayed Effects - psychology; Rats; Rats, Wistar; Receptors, Mineralocorticoid - biosynthesis; Receptors, Mineralocorticoid - metabolism; Stress, Psychological - complications; Stress, Psychological - metabolism; Stress, Psychological - psychology
• ISSN: 0270-6474; 1529-2401
• DOI: 10.1523/jneurosci.3447-10.2011

Prenatal stress (PS) increases the risk of depressive disorders in adult offspring. The pathophysiology of depressive disorders has been linked to hippocampal dysfunction; however, whether and how PS attenuates the development and function of hippocampal networks remains unknown. Using a rat model of PS, in which pregnant mothers receive daily restraint stress during late gestation and their offspring exhibit depressive-like behavior later in life, we show that PS impairs the morphological and functional maturation of hippocampal granule cells in adult offspring via the downregulated expression of mineralocorticoid receptors. PS reduced the dendritic complexity and spine density of neonatal-generated granule cells, which persists into adulthood. These granule cells exhibited depressed synaptic responses to stimulation of the medial perforant path. We further revealed that the expression of mineralocorticoid receptors, which we found is necessary for proper dendritic maturation in this study, was significantly downregulated in granule cells after PS. These results suggest that PS-induced downregulation of mineralocorticoid receptors attenuates neuronal maturation, which results in dysfunction of neuronal network in adulthood.