Abstract

MicroRNA (miRNA) expression was measured within frontal cortex of male Holtzman rats subjected to repeated inescapable shocks at days 1 and 7, tested for learned helplessness (LH) at days 2 and 8, and sacrificed at day 15. We compared rats that did vs. did not exhibit LH, as well as rats that were placed in the apparatus and tested for avoidance but not given shocks (tested controls, TC). Non-learned helpless (NLH) rats showed a robust adaptive miRNA response to inescapable shock whereas LH rats showed a markedly blunted response. One set of 12 miRNAs showed particularly large, significant down-regulation in NLH rats relative to tested controls (mir-96, 141, 182, 183, 183*, 298, 200a, 200a*, 200b, 200b*, 200c, 429). These were encoded at a few shared polycistronic loci, suggesting that the down-regulation was coordinately controlled at the level of transcription. Most of these miRNAs are enriched in synaptic fractions. Moreover, almost all of these share 5'-seed motifs with other members of the same set, suggesting that they will hit similar or overlapping sets of target mRNAs. Finally, half of this set is predicted to hit Creb1 as a target. We also identified a core miRNA co-expression module consisting of 36 miRNAs that are highly correlated with each other across individuals of the LH group (but not in the NLH or TC groups). Thus, miRNAs participate in the alterations of gene expression networks that underlie the normal (NLH) as well as aberrant (LH) response to repeated shocks.

Highlights

  • Clinical studies have demonstrated that stress acts as a predisposing and precipitating factor in depression (Lloyd, 1980 ; Paykel, 1982)

  • Escape latencies were significantly higher (p

  • We have repeatedly demonstrated that the rats that were tested on day 8 and showed LH behaviour after second inescapable shock (IS), remained LH on day 14 (Dwivedi et al 2004b, 2005a, b)

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Summary

Introduction

Clinical studies have demonstrated that stress acts as a predisposing and precipitating factor in depression (Lloyd, 1980 ; Paykel, 1982). Parallel studies of the effects of uncontrollable stress have been performed in animals with results of proactive interference with the acquisition of escape/ avoidance responding (Seligman & Maier, 1967) This phenomenon, termed learned helplessness (LH), has been used extensively as an animal model of stressinduced behavioural depression (Greenwood & Fleshner, 2008 ; Hajszan et al 2009 ; Mironova & Rybnikova, 2008 ; Petty & Sherman, 1979 ; Sherman et al 1982). Behavioural changes after a single session persist only for a short period of time (24 h) whereas, by definition, depression persists much longer after negative life events To overcome this issue, we recently modified the LH model to include repeated-shock sessions, which greatly prolonged the duration of LH (Dwivedi et al 2004b, 2005a, b). In the present study, we used the repeated-shock model

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