Hippocampal cell fate regulation by chronic cocaine during periods of adolescent vulnerability: Consequences of cocaine exposure during adolescence on behavioral despair in adulthood. (24th September 2015)

• Record Type: Journal Article
• Authors: García-Cabrerizo, R.; Keller, B.; García-Fuster, M.J.
• Is Part Of: Neuroscience. Volume 304(2015)
• Page Start: 302
• Page End: 315
• Publication Date: 2015-09-24
• Subjects: ANOVA analysis of variance -- BDNF brain-derived neurotrophic factor -- BrdU 5-bromo-2′-deoxyuridine -- BSA bovine serum albumin -- Cdk-5 cyclin-dependent kinase-5 -- DAB diaminobenzidine -- DG dentate gyrus -- DMI desipramine -- FADD Fas-associated protein with death domain -- FST forced swim test -- HC hippocampus -- IHC immunohistochemistry -- i.p. intraperitoneal -- mTOR mammalian target of rapamycin -- NF-κB nuclear factor-κB -- PARP-1 poly (ADP-ribose) polymerase 1 -- PBS phosphate-buffered saline -- PFA paraformaldehyde -- p-FADD phosphorylated Ser191 FADD -- PFC prefrontal cortex -- PND post-natal day -- PSD-95 post-synaptic density-95 -- SEM standard error of the mean -- WB Western blot; adolescence -- cocaine -- FADD -- hippocampus; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2015.07.040
• Languages: English
• ISSNs: 0306-4522

Abstract

Graphical abstract: Highlights: There is a vulnerable period during adolescence for cocaine effects in the rat brain. Chronic cocaine induces hippocampal neurotoxicity during early adolescence. Consequences of early cocaine exposure during adolescence in adulthood. Abstract: Given that adolescence represents a critical moment for shaping adult behavior and may predispose to disease vulnerability later in life, the aim of this study was to find a vulnerable period during adolescence in which hippocampal cell fate regulation was altered by cocaine exposure, and to evaluate the long-term consequences of a cocaine experience during adolescence in affecting hippocampal plasticity and behavioral despair in adulthood. Study I: Male rats were treated with cocaine (15 mg/kg, i.p.) or saline for 7 consecutive days during adolescence (early post-natal day (PND) 33–39, mid PND 40–46, late PND 47–53). Hippocampal plasticity (i.e., cell fate regulation, cell genesis) was evaluated 24 h after the last treatment dose during the course of adolescence (PND 40, PND 47, PND 54). Study II: The consequences of cocaine exposure during adolescence (PND 33–39 or PND 33–46; 7 or 14 days) were measured in adulthood at the behavioral (i.e., forced swim test, PND 62–63) and molecular (hippocampal cell markers, PND 64) levels. Chronic cocaine during early adolescence dysregulated FADD forms only in the hippocampus (HC), as compared to other brain regions, and during mid adolescence, impaired cell proliferation (Ki-67) and increased PARP-1 cleavage (a cell death maker) in the HC. Interestingly, chronic cocaine exposure during adolescence did not alter the time adult rats spent immobile in the forced swim test. These results suggest that this paradigm of chronic cocaine administration during adolescence did not contribute to the later manifestation of behavioral despair (i.e., one pro-depressive symptom) as measured by the forced swim test in adulthood.