PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Czasopismo

2006 | 65 | 4 |

Tytuł artykułu

The influence of acute and chronic open-field exposure on the hippocampal formation: an immunohistochemical study

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The hippocampus plays a role in new learning, memory and emotion and is a component of the neuroanatomical stress circuit. The structure is involved in terminating hypothalamic-pituitary-adrenocortical (HPA) axis responses to stress and attenuates stress responses by shutting off this axis. The immunoreactivity (-ir) of c-Fos, NGF and its receptor TrkA following acute and chronic open-field stress were studied in CA1-CA3 and the DG of the hippocampus. The material consisted of 21 male adult rats divided into three groups: nonstressed (control) animals and rats exposed to acute (15 min once) and chronic (15 min daily for 21 days) aversive stimulation (open-field exposure). The brains were stained with use of immunohistochemical methods for c-Fos, NGF or TrkA. In the animals exposed to acute open-field stress the number of c-Fos-, TrkAand NGF-ir cells was higher in all the structures studied than in the control animals. However they were differentiated only in c-Fos immunoreactivity. In the rats exposed to chronic open-field stress the number of c-Fos-ir cells in the structures of the hippocampal formation studied was smaller than in rats exposed to acute stress and was comparable to that in the control group. No differences were observed between the groups exposed to acute and chronic stress in the number of TrkA-ir cells in the structures under investigation. The number of NGF-ir neurons in CA1 and CA2 was lower after exposure to chronic than after exposure to acute stress but was still higher than that in the control group. Our findings indicate that neurons of CA1-CA3 and the DG are engaged in the stress response after acute as well as chronic open-field exposure. This is probably related to the important role of the hippocampus in processing new spatial information as well as in the habituation processes, although these appear to have different mechanisms.

Wydawca

-

Czasopismo

Rocznik

Tom

65

Numer

4

Opis fizyczny

p.343-351,fig.,ref.

Twórcy

  • Medical University of Gdansk, Debinki 1, 80-211 Gdansk, Poland
autor
autor
autor

Bibliografia

  • 1. Aggleton JP, Brown MW (2005) Contrasting hippocampal and perirhinal cortex function using immediate early gene imaging. Q J Exp Psychol B, 58: 218–233.
  • 2. Alfonso J, Frick LR, Silberman DM, Palumbo ML, Genaro AM, Frasch AC (2006) Regulation of hippocampal gene expression is conserved in two species subjected to different stressors and antidepressant treatments. Biol Psychiatry, 59: 244–251.
  • 3. Alleva E, Santucci D (2001) Psychosocial vs. “physical” stress situations in rodents and humans: role of neurotrophins. Physiol Behav. 73: 313–320.
  • 4. Aloe L, Alleva E, Fiore M (2002) Stress and nerve growth factor: findings in animal models and humans. Pharmacol Biochem Behav, 73: 159–166.
  • 5. Amaral DG, Witter MP (1995) Hippocampal formation. In: Paxinos G (ed.). The rat nervous system. 2nd ed. Academic Press, San Diego, pp. 443–494.
  • 6. Bartolomucci A, de Biurrun G, Czeh B, van Kampen M, Fuchs E (2002) Selective enhancement of spatial learning under chronic psychosocial stress. Eur J Neurosci, 15: 1863–1866.
  • 7. Branchi I, Francia N, Alleva E (2004) Epigenetic control of neurobehavioural plasticity: the role of neurotrophins. Behav Pharmacol, 15: 353–362.
  • 8. Bremner JD (1999) Does stress damage the brain? Biol Psychiatry, 45:797–805.
  • 9. Charney DS, Manji HK (2004) Life stress, genes, and depression: multiple pathways lead to increased risk and new opportunities for intervention. Sci STKE, 225: 5.
  • 10. Chowdhury GM, Fujioka T, Nakamura S (2000) Induction and adaptation of Fos expression in the rat brain by two types of acute restraint stress. Brain Res Bull, 52: 171–182.
  • 11. Cirulli F (2001) Role of environmental factors on brain development and nerve growth factor expression. Physiol Behav, 73: 321–330.
  • 12. Conti AM, Fischer SJ, Windebank AJ (1997) Inhibition of axonal growth from sensory neurons by excess nerve growth factor. Ann Neurol, 42: 838–846.
  • 13. De Kloet ER, Sutanto W, Rots N, van Haarst A, van den Berg D, Oitzl M, van Eekelen A, Voorhuis D (1991) Plasticity and function of brain corticosteroid receptors during aging. Acta Endocrinol (Copenh), 125 (suppl 1): 65–72.
  • 14. Del Bel EA, Silveira MC, Graeff FG, Garcia-Cairasco N, Guimaraes FS (1998) Differential expression of c-fos mRNA and Fos protein in the rat brain after restraint stress or pentylenetetrazol-induced seizures. Cell Mol Neurobiol, 18: 339–346.
  • 15. Diamond DM, Fleshner M, Ingersoll N, Rose GM (1996) Psychological stress impairs spatial working memory: relevance to electrophysiological studies of hippocampal function. Behav Neurosci, 110: 661–672.
  • 16. Emmert MH, Herman JP (1999) Differential forebrain c-fos mRNA induction by ether inhalation and novelty: evidence for distinctive stress pathways. Brain Res, 845: 60–67.
  • 17. Gatzinsky KP, Haugland RP, Thrasivoulou C, Orike N, Budi-Santoso AW, Cowen T (2001) p75 and TrkA receptors are both required for uptake of NGF in adult sympathetic neurons: use of a novel fluorescent NGF conjugate. Brain Res, 920: 226–238.
  • 18. Geddes JW, Bondada V, Keller JN (1994) Effects of intrahippocampal colchicine administration on the levels and localization of microtubule-associated proteins, tau and MAP2. Brain Res, 633: 1–8.
  • 19. Hadjiconstantinou M, McGuire L, Duchemin AM, Laskowski B, Kiecolt-Glaser J, Glaser R (2001) Changes in plasma nerve growth factor levels in older adults associated with chronic stress. J Neuroimmunol, 116: 102–106.
  • 20. Hamano T, Mutoh T, Tabira T, Araki W, Kuriyama M, Mihara T, Yano S, Yamamoto H (2005) Abnormal intracellular trafficking of high affinity nerve growth factor receptor, Trk, in stable transfectants expressing presenilin 1 protein. Brain Res Mol Brain Res, 137: 70–76.
  • 21. He J, Yamada K, Nabeshima T (2002) A role of Fos expression in the CA3 region of the hippocampus in spatial memory formation in rats. Neuropsychopharmacology, 26: 259–268.
  • 22. Hellweg R, von Richthofen S, Anders D, Baethge C, Ropke S, Hartung HD, Gericke CA (1998) The time course of nerve growth factor content in different neuropsychiatric diseases — a unifying hypothesis. J Neural Transm, 105: 871–903.
  • 23. Herman JP, Cullinan WE (1997) Neurocircuitry of stress: central control of the hypothalamo-pituitary-adrenocortical axis. Trends Neurosci, 20: 78–84.
  • 24. Herman JP, Figueiredo H, Mueller NK, Ulrich-Lai Y, Ostrander MM, Choi DC, Cullinan WE (2003) Central mechanisms of stress integration: hierarchical circuitry controlling hypothalamo-pituitary-adrenocortical responsiveness. Front Neuroendocrinol, 24: 151–180.
  • 25. Jenkins TA, Amin E, Pearce JM, Brown MW, Aggleton JP (2004) Novel spatial arrangements of familiar visual stimuli promote activity in the rat hippocampal formation but not the parahippocampal cortices: a c-fos expression study. Neuroscience, 124: 43–52.
  • 26. Kabbaj M, Akil H (2001) Individual differences in novelty-seeking behavior in rats: a c-fos study. Neuroscience, 106: 535–545.
  • 27. Knipper M, Leung LS, Zhao D, Rylett RJ (1994) Short-term modulation of glutamatergic synapses in adult rat hippocampus by NGF. Neuroreport, 5: 2433–2436.
  • 28. Kollack-Walker S, Don C, Watson SJ, Akil H (1999) Differential expression of c-fos mRNA within neurocircuits of male hamsters exposed to acute or chronic defeat. J Neuroendocrinol, 11: 547–559.
  • 29. Kordower JH, Chen EY, Sladek JR Jr, Mufson EJ (1994) trk-immunoreactivity in the monkey central nervous system: forebrain. J Comp Neurol, 349: 20–35.
  • 30. Lang UE, Jockers-Scherubl MC, Hellweg R (2004) State of the art of the neurotrophin hypothesis in psychiatric disorders: implications and limitations. J Neural Transm, 111: 387–411.
  • 31. LeDoux J (1995) Emotion: clues from the brain. Annu Rev Psychol, 46: 209–235.
  • 32. LeDoux JE (2000) Emotion circuits in the brain. Annu Rev Neurosci, 23: 155–184.
  • 33. Lee FS, Chao MV (2001) Activation of Trk neurotrophin receptors in the absence of neurotrophins. Proc Natl Acad Sci USA, 98: 3555–3560.
  • 34. Lee TH, Jang MH, Shin MC, Lim BV, Kim YP, Kim H, Choi HH, Lee KS, Kim EH, Kim CJ (2003) Dependence of rat hippocampal c-Fos expression on intensity and duration of exercise. Life Sci, 72: 1421–1436.
  • 35. Lee TH, Kato H, Chen ST, Kogure K, Itoyama Y (1998) Expression of nerve growth factor and trkA after transient focal cerebral ischemia in rats. Stroke, 29: 1687–1696.
  • 36. Lemaire V, Aurousseau C, Le Moal M, Abrous DN (1999) Behavioural trait of reactivity to novelty is related to hippocampal neurogenesis. Eur J Neurosci, 11: 4006–4014.
  • 37. Levi-Montalcini R, Skaper SD, Dal Toso R, Petrelli L, Leon A (1996) Nerve growth factor: from neurotrophin to neurokine. Trends Neurosci, 19: 514–520.
  • 38. Lisman JE (1999) Relating hippocampal circuitry to function: recall of memory sequences by reciprocal dentate-CA3 interactions. Neuron, 22: 233–242.
  • 39. McEwen BS (1994) Corticosteroids and hippocampal plasticity. Ann NY Acad Sci, 746: 134–142.
  • 40. McEwen BS (1999) Stress and hippocampal plasticity. Annu Rev Neurosci, 22: 105–122.
  • 41. McEwen BS, Magarinos AM (2001) Stress and hippocampal plasticity: implications for the pathophysiology of affective disorders. Hum Psychopharmacol, 16: S7–S19.
  • 42. McGaugh JL (2002) Memory consolidation and the amygdala: a systems perspective. Trends Neurosci, 25: 456.
  • 43. Melia KR, Ryabinin AE, Schroeder R, Bloom FE, Wilson MC (1994) Induction and habituation of immediate early gene expression in rat brain by acute and repeated restraint stress. J Neurosci, 14: 5929–5938.
  • 44. Nagahara AH, Handa RJ (1997) Age-related changes in c-fos mRNA induction after open-field exposure in the rat brain. Neurobiol Aging, 18: 45–55.
  • 45. Pace TW, Gaylord R, Topczewski F, Girotti M, Rubin B, Spencer RL (2005) Immediate-early gene induction in hippocampus and cortex as a result of novel experience is not directly related to the stressfulness of that experience. Eur J Neurosci, 22: 1679–1690.
  • 46. Park IK, Hou X, Lee KY, Park OS, Lee KY, Kim MY, Min TS, Lee GJ, Kim WS, Kim MK (2004) Distribution of trkA in cerebral cortex and diencephalon of the mongolian gerbil after birth. J Vet Sci, 5: 303–307.
  • 47. Pawlak R, Skrzypiec A, Sulkowski S, Buczko W (2002) Ethanol-induced neurotoxicity is counterbalanced by increased cell proliferation in mouse dentate gyrus. Neurosci Lett, 327: 83–86.
  • 48. Pereira PA, Cardoso A, Paula-Barbosa MM (2005) Nerve growth factor restores the expression of vasopressin and vasoactive intestinal polypeptide in the suprachiasmatic nucleus of aged rats. Brain Res, 1048: 123–130.
  • 49. Pham TM, Ickes B, Albeck D, Soderstrom S, Granholm AC, Mohammed AH (1999) Changes in brain nerve growth factor levels and nerve growth factor receptors in rats exposed to environmental enrichment for one year. Neuroscience, 94: 279–286.
  • 50. Pham TM, Soderstrom S, Winblad B, Mohammed AH (1999) Effects of environmental enrichment on cognitive function and hippocampal NGF in the non-handled rats. Behav Brain Res, 103: 63–70.
  • 51. Pikkarainen M, Rönkkö S, Savander V, Insausti R, Pitkänen A (1999) Projections from the lateral, basal, and accessory basal nuclei of the amygdala to the hippocampal formation in rat. J Comp Neurol, 403: 229–260.
  • 52. Prut L, Belzung C (2003) The open field as a paradigm to measure the effects of drugs on anxiety-like behaviors: a review. Eur J Pharmacol, 463: 3–33.
  • 53. Richter-Levin G (2004) The amygdala, the hippocampus, and emotional modulation of memory. Neuroscientist, 10: 31–39.
  • 54. Scaccianoce S, Lombardo K, Angelucci L (2000) Nerve growth factor brain concentration and stress: changes depend on type of stressor and age. Int J Dev Neurosci, 18: 469–479.
  • 55. Sobreviela T, Clary DO, Reichardt LF, Brandabur MM, Kordower JH, Mufson EJ (1994) TrkA-immunoreactive profiles in the central nervous system: colocalization with neurons containing p75 nerve growth factor receptor, choline acetyltransferase, and serotonin. J Comp Neurol, 350: 587–611.
  • 56. Sobreviela T, Jaffar S, Mufson EJ (1998) Tyrosine kinase A, galanin and nitric oxide synthase within basal forebrain neurons in the rat. Neuroscience, 87: 447–461.
  • 57. Sousa N, Lukoyanov NV, Madeira MD, Almeida OF, Paula-Barbosa MM (2000) Reorganization of the morphology of hippocampal neurites and synapses after stress-induced damage correlates with behavioral improvement. Neuroscience, 97: 253–266.
  • 58. Taglialatela G, Angelucci L, Scaccianoce S, Foreman PJ, Perez-Polo JR (1991) Nerve growth factor modulates the activation of the hypothalamo-pituitary-adrenocortical axis during the stress response. Endocrinology, 129: 2212–2218.
  • 59. Titze-de-Almeida R, Shida H, Guimaraes FS, Del Bel EA (1994) Stress-induced expression of the c-fos protooncogene in the hippocampal formation. Braz J Med Biol Res, 27: 1083–1088.
  • 60. Ueyama T, Kawai Y, Nemoto K, Sekimoto M, Tone S, Senba E (1997) Immobilization stress reduced the expression of neurotrophins and their receptors in the rat brain. Neurosci Res, 28: 103–110.
  • 61. von Richthofen S, Lang UE, Hellweg R (2003) Effects of different kinds of acute stress on nerve growth factor content in rat brain. Brain Res, 987: 207–213.
  • 62. Wirtshafter D (2005) Cholinergic involvement in the cortical and hippocampal Fos expression induced in the rat by placement in a novel environment. Brain Res, 1051: 57–65.
  • 63. Zheng H, Yang Q, Xu CT (2004) Effects of chronic stress and phenytoin on the long-term potentiation (LTP) in rat hippocampal CA1 region. Acta Biochim Biophys Sin (Shanghai), 36: 375–378.
  • 64. Zhu SW, Pham TM, Aberg E, Brene S, Winblad B, Mohammed AH, Baumans V (2006) Neurotrophin levels and behaviour in BALB/c mice: impact of intermittent exposure to individual housing and wheel running. Behav Brain Res, 167: 1–8.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-03fb99e2-edd6-4b2b-80de-a15615655f9d
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.