Psychoneuroendocrinology
Volume 31, Issue 6 , Pages 769-780, July 2006

Prenatal stress alters Fos protein expression in hippocampus and locus coeruleus stress-related brain structures

  • Odile Viltart

      Affiliations

    • Laboratory of Perinatal Stress, JE2365, University of Lille 1, 59655 Villeneuve d'Ascq, France
    • O. Viltart and J. Mairesse contribute equally to the work presented here.
  • ,
  • Jérôme Mairesse

      Affiliations

    • Laboratory of Perinatal Stress, JE2365, University of Lille 1, 59655 Villeneuve d'Ascq, France
    • O. Viltart and J. Mairesse contribute equally to the work presented here.
  • ,
  • Muriel Darnaudéry

      Affiliations

    • Laboratory of Perinatal Stress, JE2365, University of Lille 1, 59655 Villeneuve d'Ascq, France
  • ,
  • Hélène Louvart

      Affiliations

    • Laboratory of Perinatal Stress, JE2365, University of Lille 1, 59655 Villeneuve d'Ascq, France
  • ,
  • Christel Vanbesien-Mailliot

      Affiliations

    • Laboratory of Perinatal Stress, JE2365, University of Lille 1, 59655 Villeneuve d'Ascq, France
  • ,
  • Assia Catalani

      Affiliations

    • Laboratory of Pharmacology, Dip Erspamer, University of Rome1 ‘La Sapienza’, 00185 Rome, Italy
  • ,
  • Stefania Maccari

      Affiliations

    • Laboratory of Perinatal Stress, JE2365, University of Lille 1, 59655 Villeneuve d'Ascq, France
    • Department of Experimental Medicine and Pathology, University Rome1 ‘La Sapienza’, Rome, Italy
    • Corresponding Author InformationCorresponding author. Address: Laboratory Neurophysiology/Perinatal Stress, Departement of Biology, University of Lille 1, Cite Scientifique, Batiment SN4.1, 59655 Villeneuve d'Ascq, France. Fax: +33 3 20 43 46 02.

Received 30 November 2005; received in revised form 18 February 2006; accepted 19 February 2006.

Summary 

Prenatal stress (PS) durably influences responses of rats from birth throughout life by inducing deficits of the hypothalamo–pituitary–adrenal (HPA) axis feedback. The neuronal mechanisms sustaining such alterations are still unknown. The purpose of the present study was to determine whether in PS and control rats, the exposure to a mild stressor differentially induces Fos protein in hippocampus and locus coeruleus, brain areas involved in the feedback control of the HPA axis. Moreover, Fos protein expression was also evaluated in the hypothalamic paraventricular nucleus (PVN) that reflect the magnitude of the hormonal response to stress. Basal plasma corticosterone levels were not different between the groups, while, PS rats exhibited higher number of Fos-immunoreactive neurons than controls, in the hippocampus and locus coeruleus in basal condition. A higher basal expression of a marker of GABAergic synapses, the vGAT, was also observed in the hypothalamus of PS rats. Fifteen minutes after the end of the exposure to the open arm of the elevated plus-maze (mild stress) a similar increased plasma corticosterone levels was observed in both groups in parallel with an increased number of Fos-immunoreactive neurons in the PVN. Return to basal plasma corticosterone values was delayed only in the PS rats. On the contrary, after stress, no changes in Fos-immunoreactivity were observed in the hippocampus and locus coeruleus of PS rats compared to basal condition. After stress, only PS rats presented an elevation of the number of activated catecholaminergic neurons in the locus coeruleus. In conclusion, these results suggest for the first time that PS alters the neuronal activation of hippocampus and locus coeruleus implicated in the feedback mechanism of the HPA axis. These data give anatomical substrates to sustain the HPA axis hyperactivity classically described in PS rats after stress exposure.

Keywords: Restraint maternal stress, HPA axis, Noradrenaline Hippocampus, Locus coeruleus, Paraventricular nucleus

Abbreviations: AP-1, transcription factor activator, AVP, arginin–vasopressin, CA3, amon horn 3, C, control, CRH, corticotropin-releasing hormone, DG, dentate gyrus, GR, glucocorticoid receptor, HPA axis, hypothalamo–pituitary–adrenal axis, MR, mineralocorticoid receptor, PaMP, PVN, medial parvocellular part, PaLM, PVN, lateral magnocellular part, PS, prenatal stress, PVN, paraventricular nucleus, vGAT, GABA vesicular transporter, vGlut1, vesicular glutamate transporter 1

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PII: S0306-4530(06)00034-5

doi:10.1016/j.psyneuen.2006.02.007

Psychoneuroendocrinology
Volume 31, Issue 6 , Pages 769-780, July 2006