Stress-induced changes in brain-derived neurotrophic factor expression are attenuated in aged Fischer 344/N rats

Stress and glucocorticoids affect the expression of brain-derived neurotrophic factor and neurotrophin-3 mRNAs in the hippocampus

Smith, M., Makino, S., Květňanský, R., & Post, R. M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01768.1995 · Cited by 1,429 · see citing works

Stress induces atrophy of apical dendrites of hippocampal CA3 pyramidal neurons

Watanabe, Y., Gould, E., & McEwen, B. S. (1992) · Brain Research · doi:10.1016/0006-8993(92)91597-8 · Cited by 1,212 · see citing works

BDNF mRNA is decreased in the hippocampus of individuals with Alzheimer's disease

Phillips, H. S., Hains, J. M., Armanini, M., Laramee, G. R., Johnson, S. A., & Winslow, J. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90273-3 · Cited by 921 · see citing works

Repeated stress causes reversible impairments of spatial memory performance.

Luine, V., Villegas, M., Martinez, C., & McEwen, B. (1994) · Brain Research · doi:10.1016/0006-8993(94)91778-7 · Cited by 813 · see citing works

Untitled work

(1992) · Cited by 777 · see citing works

Molecular cloning and neurotrophic activities of a protein with structural similarities to nerve growth factor: developmental and topographical expression in the brain.

Ernfors, P., Ibáñez, C. F., Ebendal, T., Olson, L., & Persson, H. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.14.5454 · Cited by 700 · see citing works

Enduring effects of chronic corticosterone treatment on spatial learning, synaptic plasticity, and hippocampal neuropathology in young and mid-aged rats

Bodnoff, S., Humphreys, A., Lehman, J., Diamond, D. M., Rose, G., & Meaney, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00061.1995 · Cited by 522 · see citing works

Brain Aging Correlates: Retardation by Hormonal-Pharmacological Treatments

Landfield, P. W., Baskin, R. K., & Pitler, T. (1981) · Science · doi:10.1126/science.6270791 · Cited by 522 · see citing works

Adrenal and Urinary Catecholamines in Rats During Adaptation to Repeated Immobilization Stress

Květňanský, R., & MIKULAJ, L. (1970) · Endocrinology · doi:10.1210/endo-87-4-738 · Cited by 513 · see citing works

Human and rat brain-derived neurotrophic factor and neurotrophin-3: Gene structures, distributions, and chromosomal localizations

Maisonpierre, P. C., Beau, M. M. L., Espinosa, R., Ip, N. Y., Belluscio, L., de la Monte, S. M., Squinto, S. P., Furth, M. E., & Yancopoulos, G. D. (1991) · Genomics · doi:10.1016/0888-7543(91)90436-i · Cited by 511 · see citing works

Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus

Shors, T. J., Seib, T. B., Levine, S., & Thompson, R. F. (1989) · Science · doi:10.1126/science.2704997 · Cited by 458 · see citing works

Increased expression of brain-derived neurotrophic factor mRNA in rat hippocampus is associated with improved spatial memory and enriched environment

Falkenberg, T., Mohammed, A. K., Henriksson, B. G., Persson, H., Winblad, B. G., & Lindefors, N. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90494-r · Cited by 388 · see citing works

Potentiated Necrosis of Cultured Cortical Neurons by Neurotrophins

Koh, J., Gwag, B. J., Lobner, D., & Choi, D. W. (1995) · Science · doi:10.1126/science.7725105 · Cited by 365 · see citing works

Rat β‐nerve growth factor sequence and site of synthesis in the adult hippocampus

Whittemore, S. R., Friedman, P. L., Larhammar, D., Persson, H., Gonzalez-Carvajal, M., & Holets, V. R. (1988) · Journal of Neuroscience Research · doi:10.1002/jnr.490200402 · Cited by 308 · see citing works

Chronic stress-induced acceleration of electrophysiologic and morphometric biomarkers of hippocampal aging

Kerr, D. S., Campbell, L., Applegate, M. D., Brodish, A., & Landfield, P. W. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-05-01316.1991 · Cited by 257 · see citing works

Decreased level of nerve growth factor (NGF) and its messenger RNA in the aged rat brain

Lärkfors, L., Ebendal, T., Whittemore, S. R., Persson, H., Hoffer, B. J., & Olson, L. (1987) · Molecular Brain Research · doi:10.1016/0169-328x(87)90044-1 · Cited by 245 · see citing works

Intraventricular administration of BDNF increases neuropeptide expression in newborn rat brain

Nawa, H., Pelleymounter, M., & Carnahan, J. F. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03751.1994 · Cited by 235 · see citing works

Stress increases brain-derived neurotropic factor messenger ribonucleic acid in the hypothalamus and pituitary

Smith, M. A., Makino, S., Kim, S. Y., & Květňanský, R. (1995) · Endocrinology · doi:10.1210/endo.136.9.7649080 · Cited by 226 · see citing works

Neurotrophin-3 prevents the death of adult central noradrenergic neurons in vivo

Arenas, E., & Persson, H. (1994) · Nature · doi:10.1038/367368a0 · Cited by 209 · see citing works

Environmental influences on the central nervous system and their implications for the aging rat

Mohammed, A. H. S., Henriksson, B. G., Söderström, S., Ebendal, T., Olsson, T., & Seckl, J. R. (1993) · Behavioural Brain Research · doi:10.1016/0166-4328(93)90134-c · Cited by 204 · see citing works

Nerve growth factor levels and choline acetyltransferase activity in the brain of aged rats with spatial memory impairments

Hellweg, R., Fischer, W., Hock, C., Gage, F. H., Björklund, A., & Thoenen, H. (1990) · Brain Research · doi:10.1016/0006-8993(90)90348-f · Cited by 135 · see citing works

Mechanisms of neuronal death in brain aging and alzheimer's disease: Role of endocrine‐mediated calcium dyshomeostasis

Landfield, P. W., Thibault, O., Mazzanti, M. L., Porter, N. M., & Kerr, D. S. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230914 · Cited by 118 · see citing works

Stress and antidepressants differentially regulate neurotrophin 3 mRNA expression in the locus coeruleus.

Smith, M. A., Makino, S., Altemus, M., Michelson, D., Hong, S. K., Květňanský, R., & Post, R. M. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8788 · Cited by 110 · see citing works

BDNF and trkB mRNA expression in the hippocampal formation of aging rats

Lapchak, P. A., Araujo, D. M., Beck, K. D., Finch, C. E., Johnson, S. A., & Hefti, F. F. (1993) · Neurobiology of Aging · doi:10.1016/0197-4580(93)90087-r · Cited by 105 · see citing works

Hippocampal nerve growth factor levels are related to spatial learning ability in aged rats

Henriksson, B. G., Söderström, S., Gower, A. J., Ebendal, T., Winblad, B. G., & Mohammed, A. H. (1992) · Behavioural Brain Research · doi:10.1016/s0166-4328(05)80134-2 · Cited by 91 · see citing works

Neuron numbers in locus coeruleus do not change with age in fisher 344 rat

Goldman, G., & Coleman, P. D. (1981) · Neurobiology of Aging · doi:10.1016/0197-4580(81)90056-7 · Cited by 87 · see citing works

Male Fischer 344/N rats show a progressive central impairment of the hypothalamic-pituitary-adrenal axis with advancing age

Cizza, G., Calogero, A. E., Brady, L. S., Bagdy, G., Bergamini, E., Blackman, M. R., Chrousos, G. P., & Gold, P. W. (1994) · Endocrinology · doi:10.1210/endo.134.4.8137722 · Cited by 86 · see citing works

Lesion-induced sprouting of commissural/associational axons and induction of GAP-43 mRNA in hilar and CA3 pyramidal neurons in the hippocampus are diminished in aged rats

Schauwecker, P. E., Cheng, H., Serquinia, R., Mori, N., & McNeill, T. H. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-02462.1995 · Cited by 80 · see citing works

Energy metabolism in disorders of the nervous system.

Blass, J. P., Sheu, R., & Cedarbaum, J. M. (1988) · PubMed · Cited by 65 · see citing works

Hippocampal NGF levels are not reduced in the aged Fischer 344 rat

Crutcher, K. A., & Weingartner, J. A. (1991) · Neurobiology of Aging · doi:10.1016/0197-4580(91)90072-r · Cited by 64 · see citing works

Impaired up-regulation of type II corticosteroid receptors in hippocampus of aged rats

Eldridge, J. C., Fleenor‐Heyser, D. G., Kerr, D. S., & Landfield, P. W. (1989) · Brain Research · doi:10.1016/0006-8993(89)91505-9 · Cited by 63 · see citing works

Molecular cloning and regional distribution of rat brain cyclophilin

Lad, R. P., Smith, M. A., & Hilt, D. C. (1991) · Molecular Brain Research · doi:10.1016/0169-328x(91)90007-k · Cited by 57 · see citing works

Plasticity of Substance P in Mature and Aged Sympathetic Neurons in Culture

Adler, J. E., & Black, I. B. (1984) · Science · doi:10.1126/science.6206570 · Cited by 55 · see citing works

Apparent age-related resistance of type II hippocampal corticosteroid receptors to down-regulation during chronic escape training

Eldridge, J. C., Brodish, A., Kute, T., & Landfield, P. W. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-09-03237.1989 · Cited by 53 · see citing works

Decreased stress responsivity of central and peripheral catecholaminergic systems in aged 344/N Fischer rats.

Cizza, G., Pacák, K., Květňanský, R., Palkovits, M., Goldstein, D. S., Brady, L. S., Fukuhara, K., Bergamini, E., Kopin, I. J., & Blackman, M. R. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117771 · Cited by 49 · see citing works

Increased NGF-like activity in young but not aged rat hippocampus after septal lesions

Scott, S. A., Shi, L., Weingartner, J. A., & Crutcher, K. A. (1994) · Neurobiology of Aging · doi:10.1016/0197-4580(94)90029-9 · Cited by 49 · see citing works

Nerve growth factor and p75NGFR factor receptor mRNA change in rodent CNS following stress activation of the hypothalamo‐pituitary‐adrenocortical axis

Foreman, P. J., Taglialatela, G., Angelucci, L., Turner, C. P., & Perez-Polo, J. R. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490360103 · Cited by 41 · see citing works

Age- and sex-related differences in the nerve growth factor distribution in the rat brain

Nishizuka, M., Katoh‐Semba, R., ETO, K., Arai, Y., Iizuka, R., & Kato, K. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90045-l · Cited by 39 · see citing works

Central hypothyroidism is associated with advanced age in male Fischer 344/N rats: in vivo and in vitro studies

Cizza, G., Brady, L. S., Calogero, A. E., Bagdy, G., Lynn, A. B., Kling, M. A., Blackman, M. R., Chrousos, G. P., & Gold, P. W. (1992) · Endocrinology · doi:10.1210/endo.131.6.1446609 · Cited by 30 · see citing works

Physiology and neurobiology of stress and adaptation: central role of the brain

McEwen, B. S. (2007) · Physiological Reviews · doi:10.1152/physrev.00041.2006 · Cited by 4,981 · see citing works

Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators

McEwen, B. S. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.071 · Cited by 1,864 · see citing works

Central role of the brain in stress and adaptation: Links to socioeconomic status, health, and disease

McEwen, B. S., & Gianaros, P. J. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05331.x · Cited by 1,715 · see citing works

Protective and damaging effects of stress mediators: central role of the brain

McEwen, B. S. (2006) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2006.8.4/bmcewen · Cited by 1,220 · see citing works

BDNF and Activity-Dependent Synaptic Modulation: Figure 1.

Lu, B. (2003) · Learning & Memory · doi:10.1101/lm.54603 · Cited by 945 · see citing works

Psychobiological allostasis: resistance, resilience and vulnerability

Karatsoreos, I. N., & McEwen, B. S. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.10.005 · Cited by 458 · see citing works

Aging, plasticity and environmental enrichment: Structural changes and neurotransmitter dynamics in several areas of the brain

Mora, F., Segovia, G., & Arco, A. D. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.03.011 · Cited by 401 · see citing works

Stress, sex, and neural adaptation to a changing environment: mechanisms of neuronal remodeling

McEwen, B. S. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05568.x · Cited by 335 · see citing works

Voluntary exercise protects against stress-induced decreases in brain-derived neurotrophic factor protein expression

Adlard, P. A., & Cotman, C. W. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.12.039 · Cited by 265 · see citing works

Cutting Edge: Clonally Restricted Production of the Neurotrophins Brain-Derived Neurotrophic Factor and Neurotrophin-3 mRNA by Human Immune Cells and Th1/Th2-Polarized Expression of Their Receptors

Besser, M. J., & Wank, R. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.11.6303 · Cited by 214 · see citing works

Acute social defeat reduces neurotrophin expression in brain cortical and subcortical areas in mice

Pizarro, J. M., Lumley, L. A., Medina, W., Robison, C. L., Chang, W. E., Alagappan, A., Bah, M. J., Dawood, M. Y., Shah, J. D., Mark, B., et al. (2004) · Brain Research · doi:10.1016/j.brainres.2004.06.085 · Cited by 196 · see citing works

Electroconvulsive Therapy (ECT) increases serum Brain Derived Neurotrophic Factor (BDNF) in drug resistant depressed patients

Bocchio‐Chiavetto, L., Zanardini, R., Bortolomasi, M., Abate, M., Segala, M., Giacopuzzi, M., Riva, M. A., Marchina, E., Pasqualetti, P., Pérez, J., et al. (2006) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2006.04.010 · Cited by 180 · see citing works

The ever‐changing brain: Cellular and molecular mechanisms for the effects of stressful experiences

McEwen, B. S. (2012) · Developmental Neurobiology · doi:10.1002/dneu.20968 · Cited by 165 · see citing works

The NGF saga: From animal models of psychosocial stress to stress-related psychopathology

Cirulli, F., & Alleva, E. (2009) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2009.05.002 · Cited by 160 · see citing works

Protective and damaging effects of stress mediators: central role of the brain

McEwen, B. S. (2000) · Progress in brain research · doi:10.1016/s0079-6123(08)62128-7 · Cited by 158 · see citing works

Mood Stabilizers Target Cellular Plasticity and Resilience Cascades: Implications for the Development of Novel Therapeutics

Bachmann, R. F., Schloesser, R. J., Gould, T. D., & Manji, H. K. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:2:173 · Cited by 149 · see citing works

Sex, Stress, and Mood Disorders: At the Intersection of Adrenal and Gonadal Hormones

Fernández‐Guasti, A., Fiedler, J. L., Herrera, L., & Handa, R. (2012) · Hormone and Metabolic Research · doi:10.1055/s-0032-1312592 · Cited by 143 · see citing works

Aging in the rat hippocampus is associated with widespread reductions in the number of glutamate decarboxylase‐67 positive interneurons but not interneuron degeneration

Stanley, D. P., & Shetty, A. K. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02318.x · Cited by 141 · see citing works

Identification and localization of neurohypophysial peptides in the brain of a caecilian amphibian, Typhlonectes natans (amphibia: Gymnophiona)

Hilscher-Conklin, C., Conlon, J. M., & Boyd, S. K. (1998) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19980504)394:2 · Cited by 25 · see citing works

Desipramine treatment reduces the long-term behavioural and neurochemical sequelae of early-life maternal separation

MacQueen, G. M., Ramakrishnan, K., Ratnasingan, R., Chen, B., & Young, L. T. (2003) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145703003729 · Cited by 96 · see citing works

3xTgAD mice exhibit altered behavior and elevated Aβ after chronic mild social stress

Rothman, S. M., Herdener, N. D., Camandola, S., Texel, S. J., Mughal, M. R., Cong, W., Martin, B., & Mattson, M. P. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.07.005 · Cited by 95 · see citing works

Aging and infection reduce expression of specific brain-derived neurotrophic factor mRNAs in hippocampus

Chapman, T. R., Barrientos, R. M., Ahrendsen, J. T., Hoover, J. M., Maier, S. F., & Patterson, S. L. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.07.015 · Cited by 84 · see citing works

Resilience and vulnerability: a neurobiological perspective

Karatsoreos, I. N., & McEwen, B. S. (2013) · F1000Prime Reports · doi:10.12703/p5-13 · Cited by 84 · see citing works

Spatial memory deficits in middle‐aged mice correlate with lower exploratory activity and a subordinate status: role of hippocampal neurotrophins

Francia, N., Cirulli, F., Chiarotti, F., Antonelli, A., Aloe, L., & Alleva, E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04585.x · Cited by 77 · see citing works

Stress and ageing interactions: A paradox in the context of shared etiological and physiopathological processes

Pardon, M. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.02.007 · Cited by 72 · see citing works

Leptin regulates exon-specific transcription of the Bdnf gene via epigenetic modifications mediated by an AKT/p300 HAT cascade

Li, C., Meng, F., Lei, Y., Liu, J., Liu, J., Zhang, J., Liu, F., Liu, C., Guo, M., & Lu, X. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00922-0 · Cited by 62 · see citing works

Social threat and novel cage stress-induced sustained extracellular-regulated kinase1/2 (ERK1/2) phosphorylation but differential modulation of brain-derived neurotrophic factor (BDNF) expression in the hippocampus of NMRI mice

Pardon, M., Roberts, R. E., Marsden, C. A., Bianchi, M., Latif, M. L., Duxon, M. S., & Kendall, D. A. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.01.033 · Cited by 60 · see citing works

Agonistic encounters in aged male mouse potentiate the expression of endogenous brain NGF and BDNF: possible implication for brain progenitor cells' activation

Fiore, M., Amendola, T., Triaca, V., Tirassa, P., Alleva, E., & Aloe, L. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02573.x · Cited by 55 · see citing works

Effects of different timing of stress on corticosterone, BDNF and memory in male rats

Radahmadi, M., Alaei, H., Sharifi, M. R., & Hosseini, N. (2014) · Physiology & Behavior · doi:10.1016/j.physbeh.2014.12.004 · Cited by 54 · see citing works

Blood–Brain and Spinal Cord Barriers in Stress

SHARMA, H. S. (2004) · Elsevier eBooks · doi:10.1016/b978-012639011-7/50019-x · Cited by 54 · see citing works

Neuronal expression of arylalkylamine N-acetyltransferase (AANAT) mRNA in the rat brain

Uz, T., Qu, T., Sugaya, K., & Manev, H. (2002) · Neuroscience Research · doi:10.1016/s0168-0102(02)00011-1 · Cited by 53 · see citing works

Brain-derived neurotrophic factor modulates angiotensin signaling in the hypothalamus to increase blood pressure in rats

Erdös, B., Backes, I. M., McCowan, M. L., Hayward, L. F., & Scheuer, D. A. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00776.2014 · Cited by 48 · see citing works

Neural Stem Cell Therapy in the Aging Brain: Pitfalls and Possibilities

Limke, T. L., & Rao, M. S. (2003) · Stem Cells and Development · doi:10.1089/15258160360732641 · Cited by 44 · see citing works

Resistance of the dentate gyrus to induced apoptosis during ageing is associated with increases in transforming growth factor-β1 messenger RNA

Bye, N., Zieba, M., Wreford, N. G., & Nichols, N. R. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00236-6 · Cited by 39 · see citing works

Mild stress facilitates learning and exercise improves retention in aged mice

Adlard, P. A., Engesser‐Cesar, C., & Cotman, C. W. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.10.001 · Cited by 37 · see citing works

Environmental enrichment alters dentate granule cell morphology in oldest‐old rat

Darmopil, S., Petanjek, Z., Mohammed, A. H. S., & Bogdanović, N. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00560.x · Cited by 28 · see citing works

Comparison of Glucocorticoid Receptor and Ionized Calcium-Binding Adapter Molecule 1 Immunoreactivity in the Adult and Aged Gerbil Hippocampus Following Repeated Restraint Stress

Park, J. H., Yoo, K., Lee, C. H., Kim, I. H., Shin, B. N., Choi, J. H., Park, J. H., Hwang, I. K., & Won, M. (2011) · Neurochemical Research · doi:10.1007/s11064-011-0444-z · Cited by 21 · see citing works

BDNF acting in the hypothalamus induces acute pressor responses under permissive control of angiotensin II

Schaich, C. L., Wellman, T. L., Koi, B., & Erdös, B. (2016) · Autonomic Neuroscience · doi:10.1016/j.autneu.2016.02.011 · Cited by 22 · see citing works

Extinction-induced “despair” in aged and adult rats: Links to neurotrophins in frontal cortex and hippocampus

Topic, B., Huston, J. P., Náměstková, K., Zhu, S., Mohammed, A. H. S., & Schulz, D. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.06.011 · Cited by 22 · see citing works

Daily Intermittent Normobaric Hypoxia Over 2 Weeks Reduces BDNF Plasma Levels in Young Adults – A Randomized Controlled Feasibility Study

Becke, A., Müller, P., Dordevic, M., Leßmann, V., Brigadski, T., & Müller, N. G. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01337 · Cited by 21 · see citing works

Neurocalcin-immunoreactive cells in the rat hippocampus are GABAergic interneurons

Martinez-Guijarro, F. J., Briñón, J. G., Blasco-Ib��ez, J. M., Okazaki, K., Hidaka, H., & Alonso, J. R. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:1 · Cited by 11 · see citing works

Inhibition of BDNF signaling in the paraventricular nucleus of the hypothalamus lowers acute stress-induced pressor responses

Schaich, C. L., Wellman, T. L., Einwag, Z., Dutko, R. A., & Erdös, B. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00459.2017 · Cited by 16 · see citing works

Carob (Ceratonia siliqua L.) Prevents Short-Term Memory Deficit Induced by Chronic Stress in Rats

Alzoubi, K. H., Alibbini, S., Khabour, O. F., El‐Elimat, T., Alzubi, M. A., & Alali, F. Q. (2018) · Journal of Molecular Neuroscience · doi:10.1007/s12031-018-1161-8 · Cited by 15 · see citing works

Prior neonatal isolation reduces induction of NGF mRNA and decreases GDNF mRNA in the hippocampus of juvenile and adult rodents subjected to immobilization stress

Kawano, K.-I., Morinobu, S., Sawada, T., Tsuji, S., Erabi, K., Fuchikami, M., Kozuru, T., Yamawaki, S., Hisaoka, K., & Takebayashi, M. (2008) · Synapse · doi:10.1002/syn.20487 · Cited by 11 · see citing works

Repeated Exposure to Sublethal Doses of the Organophosphorus Compound VX Activates BDNF Expression in Mouse Brain

Pizarro, J. M., Chang, W. E., Bah, M. J., Wright, L. K. M., Saviolakis, G. A., Alagappan, A., Robison, C. L., Shah, J., Meyerhoff, J. L., Cerasoli, D. M., et al. (2012) · Toxicological Sciences · doi:10.1093/toxsci/kfr353 · Cited by 12 · see citing works

Lithium attenuates stress-induced impairment of long-term potentiation induction

Lim, K. Y., Yang, J.-J., Lee, D. S., Noh, J. S., Jung, M. W., & Chung, Y.-K. (2005) · Neuroreport · doi:10.1097/01.wnr.0000179078.54906.52 · Cited by 11 · see citing works

Glucocorticoids and the Aging Brain: Cause or Consequence?

Lucassen, P. J., & de Kloet, E. R. (2001) · Elsevier eBooks · doi:10.1016/b978-012351830-9/50064-0 · Cited by 10 · see citing works

Exposure to mild stress and brain derived neurotrophin factor (BDNF) immunoreactivity in the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei: Comparison between aged and adult rats

Badowska‐Szalewska, E., Ludkiewicz, B., Krawczyk, R., & Moryś, J. (2016) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2016.08.007 · Cited by 9 · see citing works

The Effect of Preventive, Therapeutic and Protective Exercises on Hippocampal memory Mediators in Stressed Rats

Radahmadi, M., Hosseini, N., Alaei, H., & Sharifi, M. R. (2016) · Malaysian Journal of Medical Sciences · doi:10.21315/mjms2016.23.5.4 · Cited by 9 · see citing works

Comparison of the influence of two models of mild stress on hippocampal brain‑derived neurotrophin factor (BDNF) immunoreactivity in old age rats

Badowska‐Szalewska, E., Ludkiewicz, B., Krawczyk, R., Melka, N., & Moryś, J. (2017) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2017-037 · Cited by 9 · see citing works

Role of brain-derived neurotrophic factor in shaping the behavioural response to environmental stressors

Badowska‐Szalewska, E., Lietzau, G., Moryś, J., & Kowiański, P. (2021) · Folia Morphologica · doi:10.5603/fm.a2021.0079 · Cited by 8 · see citing works

Augmentation of morphine-conditioned place preference by food restriction is associated with alterations in the oxytocin/oxytocin receptor in rat models

Mousavi, A., Askari, N., & Mahdavi, M. R. V. (2019) · The American Journal of Drug and Alcohol Abuse · doi:10.1080/00952990.2019.1648483 · Cited by 8 · see citing works

Semen Cuscutae flavonoids activated the cAMP-PKA-CREB-BDNF pathway and exerted an antidepressant effect in mice

Shao, Q., Li, Y., Jin, L., Zhou, S., Fu, X., Liu, T., Luo, G., Du, S., & Chen, C. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1491900 · Cited by 6 · see citing works

Evaluation of the Effects of Developmental Trauma on Neurotransmitter Systems Using Functional Molecular Imaging

Lee, N., Oh, S. J., Park, J., Nam, K. R., Kang, K.-J., Lee, K.-C., Lee, Y., Choi, J.-S., Seok, J., & Choi, J.-Y. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052522 · Cited by 5 · see citing works

Chronic Pain, Impulsivity, and Risk for Opioid Misuse

Ramesh, D., & Evans, H. (2018) · Topics in Pain Management · doi:10.1097/01.tpm.0000541408.17994.3f · Cited by 5 · see citing works

Estrogens and Depression in Women

Rubinow, D. R., Roca, C. A., & Schmidt, P. J. (2007) · Elsevier eBooks · doi:10.1016/b978-012369443-0/50030-2 · Cited by 4 · see citing works

The role of neurotrophic factors in the stress response

Riva, M. A. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80035-5 · Cited by 3 · see citing works

Overactive bladder phenotype induced by chronic activation of hypothalamic neuroendocrine stress pathways in rats with no extrinsic behavioral stress applied

Husain, J., Bakhareva, A., Pace, A. L. D., Noterman, M. F., Herrera, G. M., & Erdös, B. (2025) · Scientific Reports · doi:10.1038/s41598-025-32428-6 · Cited by 2 · see citing works

Chronobiology of Mood Disorders

Iasevoli, F., Avvisati, L., Gilardi, V., Latte, G., Prinzivalli, E., Berardis, D. D., Valchera, A., Fornaro, M., Tomasetti, C., & de Bartolomeis, A. (2016) · Springer eBooks · doi:10.1007/978-81-322-2803-5_20 · Cited by 1 · see citing works

Voluntary Wheel Running Alters Brain-Derived Neurotrophic Factor Levels in the Hippocampus of Senescence Accelerated Mice

Janke, K. L. (2009) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1 · see citing works

The Effects Of Hypothalamic Brain-Derived Neurotrophic Factor On Catecholaminergic Regulation Of Cardiovascular Function.

Cruickshank, N. C. (2017) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont) · Cited by 1 · see citing works

Sex-Dependent Effects of Chronic Microdrive Implantation on Acquisition of Trace Eyeblink Conditioning

Rapp, A. P., Hark, T. J., Power, J., Savas, J. N., Oh, M. M., & Disterhoft, J. F. (2022) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2022.107649 · Cited by 1 · see citing works

Trophins as Mediators of Astrocyte Effects in the Aging and Regenerating Brain

Lackland, J., & Dreyfus, C. F. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-105-3_11 · Cited by 1 · see citing works

Developmental Mechanisms in Aging and Age-Related Diseases of the Nervous System

Mattson, M. P., & Limke, T. L. (2006) · Kluwer Academic Publishers-Plenum Publishers eBooks · doi:10.1007/0-387-28117-7_13

MOLECULAR MECHANISMS OF AGING IN THE PERIPHERAL NOCICEPTIVE SYSTEM

Wang, S. (2007) · D-Scholarship@Pitt (University of Pittsburgh)

An extension of unpredictable chronic stress on brain-derived neurotrophic factor expression in different aged rats hippocampus

Zhou, L., & Peng, F. (2020) · Chinese Medical Journal · doi:10.1097/cm9.0000000000000961

Effects of unpredictable chronic stress on behavior and brain-derived neurotrophic factor expression in CA3 subfield and dentate gyrus of the hippocampus in different aged rats.

Li, Y., Ji, Y.-J., Jiang, H., Liu, D.-X., Zhang, Q., Fan, S.-J., & Pan, F. (2009) · PubMed · Cited by 28 · see citing works

Effects of Stress on Neurotrophic Factor Expression in the Rat Brain

SMITH, M. A., Makino, S., Květňanský, R., & Post, R. M. (1995) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1995.tb44684.x · Cited by 255 · see citing works

Acute Stress and Chronic Stress Change Brain-Derived Neurotrophic Factor (BDNF) and Tyrosine Kinase-Coupled Receptor (TrkB) Expression in Both Young and Aged Rat Hippocampus

Shi, S.-S., Shao, S.-H., Yuan, B.-P., Pan, F., & Li, Z.-L. (2010) · Yonsei Medical Journal · doi:10.3349/ymj.2010.51.5.661 · Cited by 139 · see citing works

Aging Effects on the BDNF mRNA and TrkB mRNA Expression of the Hippocampus in Different Durations of Stress

Shao, S.-H. (2010) · The Chinese Journal of Physiology · doi:10.4077/cjp.2010.amk056 · Cited by 15 · see citing works