Dehydroepiandrosterone stimulates nerve growth factor and brain derived neurotrophic factor in cortical neurons

Advances in Pharmacological Sciences

Volumn 2013, Issue , 2013, Pages

  Rahmani, Anahita ^a   Shoae Hassani, Alireza ^a,b   Keyhanvar, Peyman ^c   Kheradmand, Danial ^d   Darbandi Azar, Amir ^c  

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84893721768     PISSN: 16876334     EISSN: 16876342     Source Type: Journal    
DOI: 10.1155/2013/506191     Document Type: Article

References (30)

1. Berkemeier L. R., Winslow J. W., Kaplan D. R., Nikolics K., Goeddel D. V., Rosenthal A., Neurotrophin-5: a novel neurotrophic factor that activates trk and trkB. Neuron 1991 7 5 857 866 2-s2.0-0026038850 10.1016/0896-6273(91)90287- A
2. Noureddini M., Verdi J., Mortazavi Tabatabaei S. A., Sharif S., Shoae-Hassani A., Human endometrial stem cell neurogenesis in response to NGF and bFGF. Cell Biology International 2012 36 961 966
3. Levi-Montalcini R., The nerve growth factor: thirty-five years later. The EMBO Journal 1987 6 5 1145 1154 2-s2.0-0013067786
4. Davies A. M., The role of neurotrophins in the developing nervous syste (Pubitemid 24325060)
5. Ahmed S., Reynolds B. A., Weiss S., BDNF enhances the differentiation but not the survival of CNS stem cell-derived neuronal precursors. The Journal of Neuroscience 1995 15 8 5765 5778 2-s2.0-0029165971
6. Compagnone N. A., Mellon S. H., Dehydroepiandrosterone: a potential signalling molecule for neocortical organization during development. Proceedings of the National Academy of Sciences of the United States of America 1998 95 8 4678 4683 2-s2.0-0032516063 10.1073/pnas.95.8.4678 (Pubitemid 28207973)
7. Shoae-Hassani A., Mortazavi-Tabatabaei S. A., Sharif S., Rezaei-Khaligh H., Verdi J., DHEA provides a microenvironment for endometrial stem cells neurogenesis. Medical Hypotheses 2011 76 6 843 846 2-s2.0-79955733511 10.1016/j.mehy.2011.02.033
8. Kimonides V. G., Khatibi N. H., Svendsen C. N., Sofroniew M. V., Herbert J., Dehydroepiandrosterone (DHEA) and DHEA-sulfate (DHEAS) protect hippocampal neurons against excitatory amino acid-induced neurotoxicity. Proceedings of the National Academy of Sciences of the United States of America 1998 95 4 1852 1857 2-s2.0-0032539540 10.1073/pnas.95.4.1852 (Pubitemid 28103483)
9. Bastianetto S., Ramassamy C., Poirier J., Quirion R., Dehydroepiandrosterone (DHEA) protects hippocampal cells from oxidative stress-induced damage. Molecular Brain Research 1999 66 1-2 35 41 2-s2.0-0033586349 10.1016/S0169-328X(99)00002-9 (Pubitemid 29148331)
10. Kimonides V. G., Spillantini M. G., Sofroniew M. V., Fawcett J. W., Herbert J., Dehydroepiandrosterone antagonizes the neurotoxic effects of corticosterone and translocation of stress-activated protein kinase 3 in hippocampal primary cultures. Neuroscience 1999 89 2 429 436 2-s2.0-0033103126 10.1016/S0306-4522(98)00347-9 (Pubitemid 29044326)
11. Chopp M., Li Y., Treatment of neural injury with marrow stromal cells. The Lancet Neurology 2002 1 2 92 100 2-s2.0-0013278301 10.1016/S1474-4422(02) 00040-6 (Pubitemid 37163494)
12. Durand M., Aguerre S., Fernandez F., Edno L., Combourieu I., Mormède P., Chaouloff F., Strain-dependent neurochemical and neuroendocrine effects of desipramine, but not fluoxetine or imipramine, in Spontaneously Hypertensive and Wistar-Kyoto rats. Neuropharmacology 2000 39 12 2464 2477 2-s2.0-0033884271 10.1016/S0028-3908(00)00088-5 (Pubitemid 30642790)
13. Tejani-Butt S., Kluczynski J., Paré W. P., Strain-dependent modification of behavior following antidepressant treatment. Progress in Neuro-Psychopharmacology and Biological Psychiatry 2003 27 1 7 14 2-s2.0-0037305603 10.1016/S0278-5846(02)00308-1 (Pubitemid 36126641)
14. Will C. C., Aird F., Redei E. E., Selectively bred Wistar-Kyoto rats: an animal model of depression and hyper-responsiveness to antidepressants. Molecular Psychiatry 2003 8 11 925 932 2-s2.0-0242469018 10.1038/sj.mp.4001345 (Pubitemid 37421699)
15. Malkesman O., Asaf T., Shbiro L., Goldstein A., Maayan R., Weizman A., Kinor N., Okun E., Sredni B., Yadid G., Weller A., Monoamines, BDNF, dehydroepiandrosterone, DHEA-Sulfate, and childhood depression: an animal model study. Advances in Pharmacological Sciences 2009 2009 11 2-s2.0-70449709180 10.1155/2009/405107 405107
16. Pechnick R. N., Zonis S., Wawrowsky K., Pourmorady J., Chesnokova V., p21Cip1 restricts neuronal proliferation in the subgranular zone of the dentate gyrus of the hippocampus. Proceedings of the National Academy of Sciences of the United States of America 2008 105 4 1358 1363 2-s2.0-39549096892 10.1073/pnas.0711030105 (Pubitemid 351397058)
17. Maayan R., Morad O., Dorfman P., Overstreet D. H., Weizman A., Yadid G., The involvement of dehydroepiandrosterone (DHEA) and its sulfate ester (DHEAS) in blocking the therapeutic effect of electroconvulsive shocks in an animal model of depression. European Neuropsychopharmacology 2005 15 3 253 262 2-s2.0-16844385304 10.1016/j.euroneuro.2004.10.005 (Pubitemid 40487727)
18. Barde Y. A., Edgar D., Thoenen H., Purification of a new neurotrophic factor from mammalian brain. The EMBO Journal 1982 1 5 549 553 2-s2.0-0020338405
19. Rahmani A., Kheradmand D., Keyhanvar P., Shoae-Hassani A., Darbandi-Azar A., Neurogenesis and increase in differentiated neural cell survival via phosphorylation of Akt1 after fluoxetine treatment of stem cells. BioMed Research International 2013 2013 9 582526 10.1155/2013/582526
20. Karishma K. K., Herbert J., Dehydroepiandrosterone (DHEA) stimulates neurogenesis in the hippocampus of the rat, promotes survival of newly formed neurons and prevents corticosterone-induced suppression. European Journal of Neuroscience 2002 16 3 445 453 2-s2.0-0036460078 10.1046/j.1460-9568.2002.02099. x (Pubitemid 35471862)
21. Suzuki M., Wright L. S., Marwah P., Lardy H. A., Svendsen C. N., Mitotic neurogenic effects of dehydroepiandrosterone (DHEA) on human neural stem cell cultures derived the fetal cortex. Proceedings of the National Academy of Sciences of the United States of America 2004 101 9 3202 3207 2-s2.0-1542297733 10.1073/pnas.0307325101 (Pubitemid 38327758)
22. Shoae-Hassani A., Sharif S., Verdi J., The neurosteroid dehydroepiandrosterone could improve somatic cell reprogramming. Cell Biology International 2011 35 10 1037 1041 2-s2.0-80054983103 10.1042/CBI20100927
23. Åberg M. A. I., Åberg N. D., Hedbäcker H., Oscarsson J., Eriksson P. S., Peripheral infusion of IGF-I selectively induces neurogenesis in the adult rat hippocampus. The Journal of Neuroscience 2000 20 8 2896 2903 2-s2.0-0034656167 (Pubitemid 30220315)
24. Morales A. J., Nolan J. J., Nelson J. C., Yen S. S. C., Effects of replacement dose of dehydroepiandrosterone in men and women of advancing age. Journal of Clinical Endocrinology and Metabolism 1994 78 1360 1367 (Pubitemid 24181005)
25. Charalampopoulos I., Alexaki V., Tsatsanis C., Minas V., Dermitzaki E., Lasaridis I., Vardouli L., Stournaras C., Margioris A. N., Castanas E., Gravanis A., Neurosteroids as endogenous inhibitors of neuronal cell apoptosis in aging. Annals of the New York Academy of Sciences 2006 1088 139 152 2-s2.0-34447570373 10.1196/annals.1366.003 (Pubitemid 47092025)
26. Korte M., Kang H., Bonhoeffer T., Schuman E., A role for BDNF in the late-phase of hippocampal long-term potentiation. Neuropharmacology 1998 37 4-5 553 559 2-s2.0-0031748674 10.1016/S0028-3908(98)00035-5 (Pubitemid 28306944)
27. Lindholm D., Castren E., Berzaghi M., Blochl A., Thoenen H., Activity-dependent and hormonal regulation of neurotrophin mRNA levels in the brain: implications for neuronal plasticity. Journal of Neurobiology 1994 25 11 1362 1372 2-s2.0-0027970123 10.1002/neu.480251105 (Pubitemid 24325062)
28. Gubba E. M., Fawcett J. W., Herbert J., The effects of corticosterone and dehydroepiandrosterone on neurotrophic factor mRNA expression in primary hippocampal and astrocyte cultures. Molecular Brain Research 2004 127 1-2 48 59 2-s2.0-4043096873 10.1016/j.molbrainres.2004.05.004 (Pubitemid 39078591)
29. Lazaridis I., Charalampopoulos I., Alexaki V., Avlonitis N., Pediaditakis I., Efstathopoulos P., Calogeropoulou T., Castanas E., Gravanis A., Neurosteroid dehydroepiandrosterone interacts with nerve growth factor (NGF) receptors, preventing neuronal apoptosis. PLoS Biology 2011 9 4 2-s2.0-79955514139 10.1371/journal.pbio.1001051 e1001051
30. Pham T. M., Ickes B., Albeck D., Söderström S., Granholm A.-C., Mohammed A. H., Changes in brain nerve growth factor levels and nerve growth factor receptors in rats exposed to environmental enrichment for one year. Neuroscience 1999 94 1 279 286 2-s2.0-0032862062 10.1016/S0306-4522(99)00316-4 (Pubitemid 29457618)