Early emergence of altered 5-HT2A receptor-evoked behavior, neural activation and gene expression following maternal separation. Issue 65 (April 2018)

• Record Type: Journal Article
• Authors: Sood, Ankit; Pati, Sthitapranjya; Bhattacharya, Amrita; Chaudhari, Karina; Vaidya, Vidita A.
• Is Part Of: International journal of developmental neuroscience. Issue 65(2018:Apr.)
• Page Start: 21
• Page End: 28
• Publication Date: 2018-04
• Subjects: Serotonin -- Early stress -- mPFC -- Head twitch behavior -- c-Fos -- Immediate early gene; Developmental neurobiology -- Periodicals; Neurology -- Periodicals; Neurologie du développement -- Périodiques; Developmental neurobiology; Periodicals; 612.8
• DOI: 10.1016/j.ijdevneu.2017.10.005
• Languages: English
• ISSNs: 0736-5748

Abstract

Highlights: Postnatal pups with a history of maternal separation exhibit enhanced 5-HT2A receptor-mediated head-twitch behavior. Maternally separated pups exhibit reduced neural activation in the prefrontal cortex and lateral septum. A history of maternal separation alters the pattern of 5-HT2A receptor activation evoked immediate early gene expression in the prefrontal cortex. Abstract: The early stress of Maternal Separation (MS) contributes to the establishment of adult psychopathology. The serotonergic (5-HT) system is implicated during this temporal window in mediating the development of mood-related behaviors. MS is reported to evoke altered 5-HT2A receptor function in adulthood. However, the ontogeny of altered 5-HT2A receptor responsivity following MS remains unknown. Here, we examined 5-HT2A receptor agonist, DOI (1-(2, 5-dimethoxy-4-iodophenyl)-2-aminopropane) (2 mg/kg) evoked responses, namely stereotypical head-twitch behaviors in control and MS Sprague-Dawley rat pups at postnatal day 21 (P21). MS involved a separation of pups from the dam for 3 h daily from postnatal day 2–14. MS pups at P21 exhibited significantly enhanced head-twitch behaviors compared to controls. Using c-Fos cell counting we examined neural activation in control and MS pups following DOI treatment. MS pups exhibited altered DOI-evoked c-Fos expression within all mPFC subdivisions, but not in the hippocampus, lateral septum and hypothalamus, suggesting differential prefrontal neural activation upon 5-HT2A receptor stimulation following early stress. Gene profiling of 5-HT2A receptor-regulated immediate early genes (IEGs) indicated a decline in the expression of Fos, Fra1 and Egr1 mRNA under baseline conditions in the mPFC of MS pups. MS pups also showed an altered pattern in the regulation of several 5-HT2A receptor-regulated IEGs ( Fos, Fra1, Bdnf, Egr1, Egr3 ) following DOI treatment. Collectively, these results highlight an early emergence of altered 5-HT2A receptor-evoked behavioral responses and neural activation patterns in multiple brain regions in animals with a history of MS.