Effects of chronic exercise and treatment with the antipsychotic drug olanzapine on hippocampal volume in adult female rats.
Abstract
Numerous studies have reported that the hippocampus in schizophrenia patients is reduced in volume compared to the normal population. Antipsychotic medications have had mixed benefits in maintaining hippocampal volume or reversing volume loss. Recent evidence indicates that routine aerobic exercise represents a promising intervention for reversing hippocampal loss and cognitive deficits. In the present study, we measured the effects of chronic treatment with olanzapine and daily exercise on the hippocampal volumes of rats. Adult female rats were treated during the week with either olanzapine (10mg/kg) or vehicle for 9 consecutive weeks. Subgroups of animals were provided access to exercise running wheels for 1 or 3h per day during the same period, or were sedentary. Metabolic indices, including glucose tolerance, were measured on a weekly basis. At the conclusion of the study, brains were perfused and hippocampal sections were Nissl stained. Total hippocampal volume was measured using the Cavalieri estimator. Treatment with olanzapine caused a significant decrease in hippocampal volume in sedentary rats. However, exercise was able to reverse most of this volume loss. The hippocampal sub-regions of the dentate gyrus and CA1 were most strongly affected by olanzapine and exercise. Of interest, there was a strong and highly significant negative correlation between glucose intolerance and hippocampal volume, whereby greater glucose intolerance was associated with a smaller hippocampal volume. These findings indicate that exercise may have beneficial effects on the hippocampus when antipsychotic medication can contribute to changes in volume.
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Recent animal studies have demonstrated that AE was able to reverse most of the damage caused to hippocampal volume and hippocampal synaptic connectivity caused by antipsychotic medication.
“For example, recent animal studies have demonstrated that AE was able to reverse most of damage caused to hippocampal volume and hippocampal synaptic connectivity caused by antipsychotic medication (Barr et al., 2013; Ramos-Miguel et al., 2015).”
From Aerobic Exercise as a Tool to Improve Hippocampal Plasticity and Function in Humans: Practical Implications for Mental Health Treatment (2016) · cites this paper as Barr et al., 2013
Cites
The rat brain in stereotaxic coordinates
Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959 · see citing works
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works
The efficiency of systematic sampling in stereology and its prediction *
Gundersen, H., & Jensen, E. B. V. (1987) · Journal of Microscopy · doi:10.1111/j.1365-2818.1987.tb02837.x · Cited by 3,586 · see citing works
The efficiency of systematic sampling in stereology—reconsidered
GUNDERSEN, H. J. G., JENSEN, E. B. V., KIÊU, K., & NIELSEN, J. (1999) · Journal of Microscopy · doi:10.1046/j.1365-2818.1999.00457.x · Cited by 1,317 · see citing works
Hippocampal Plasticity in Response to Exercise in Schizophrenia
Pajonk, F.-G., Wobrock, T., Gruber, O., Scherk, H., Berner, D., Kaizl, I., Kierer, A., Müller, S., Oest, M., Meyer, T., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.193 · Cited by 592 · see citing works
The Hippocampal Formation in Schizophrenia
Tamminga, C. A., Stan, A. D., & Wagner, A. D. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09081187 · Cited by 583 · see citing works
Hippocampal damage and memory impairments as possible early brain complications of type 2 diabetes
Gold, S. M., Dziobek, I., Sweat, V., Tirsi, A., Rogers, K., Bruehl, H., Tsui, W., Richardson, S., Javier, E., & Convit, A. (2007) · Diabetologia · doi:10.1007/s00125-007-0602-7 · Cited by 489 · see citing works
Cell loss in the hippocampus of schizophrenics
Falkai, P., & Bogerts, B. (1986) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf00380943 · Cited by 487 · see citing works
Dorph‐Petersen, K., Pierri, J. N., Perel, J. M., Sun, Z., Sampson, A. R., & Lewis, D. A. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300710 · Cited by 438 · see citing works
Kodama, M., Fujioka, T., & Duman, R. S. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.07.008 · Cited by 387 · see citing works
Schobel, S., Lewandowski, N. M., Corcoran, C. M., Moore, H. M., Brown, T. R., Malaspina, D., & Small, S. A. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.115 · Cited by 364 · see citing works
Eack, S. M., Hogarty, G. E., Cho, R. Y., Prasad, K. M. R., Greenwald, D. P., Hogarty, S. S., & Keshavan, M. S. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.63 · Cited by 360 · see citing works
Hippocampal Volume Reduction in First-Episode and Chronic Schizophrenia: A Review and Meta-Analysis
Adriano, F., Caltagirone, C., & Spalletta, G. (2012) · The Neuroscientist · doi:10.1177/1073858410395147 · Cited by 285 · see citing works
Davey, K. J., O’Mahony, S. M., Schellekens, H., O’Sullivan, O., Bienenstock, J., Cotter, P. D., Dinan, T. G., & Cryan, J. F. (2012) · Psychopharmacology · doi:10.1007/s00213-011-2555-2 · Cited by 275 · see citing works
Regional specificity of hippocampal volume reductions in first-episode schizophrenia
Narr, K. L., Thompson, P. M., Szeszko, P. R., Robinson, D. G., Jang, S., Woods, R. P., Kim, S. H., Hayashi, K. M., Asunction, D., Toga, A. W., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.011 · Cited by 262 · see citing works
Bekinschtein, P., Oomen, C. A., Saksida, L. M., & Bussey, T. J. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.07.002 · Cited by 256 · see citing works
Fuss, J., Ben Abdallah, N. M. ‐., Vogt, M. A., Touma, C., Pacifici, P. G., Palme, R., Witzemann, V., Hellweg, R., & Gass, P. (2010) · Hippocampus · doi:10.1002/hipo.20634 · Cited by 240 · see citing works
Snyder, J. S., Radik, R., Wojtowicz, J. M., & Cameron, H. A. (2008) · Hippocampus · doi:10.1002/hipo.20525 · Cited by 224 · see citing works
Hippocampal Pathology in Schizophrenia
Heckers, S., & Konradi, C. L. (2010) · Current topics in behavioral neurosciences · doi:10.1007/7854_2010_43 · Cited by 208 · see citing works
Links between cognitive impairment in insulin resistance: An explanatory model
Convit, A. J. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.09.018 · Cited by 198 · see citing works
Vernon, A. C., Natesan, S., Modo, M., & Kapur, S. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.11.010 · Cited by 173 · see citing works
Adult neurogenesis in mammals – a theme with many variations
Bonfanti, L., & Peretto, P. M. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07832.x · Cited by 173 · see citing works
Higher normal fasting plasma glucose is associated with hippocampal atrophy
Cherbuin, N., Sachdev, P. S., & Anstey, K. J. (2012) · Neurology · doi:10.1212/wnl.0b013e31826846de · Cited by 170 · see citing works
Cardiovascular side-effects of antipsychotic drugs: The role of the autonomic nervous system
Leung, J. Y. T., Barr, A. M., Procyshyn, R. M., Honer, W. G., & Pang, C. C. Y. (2012) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2012.04.003 · Cited by 163 · see citing works
Self-citationEffects of Antipsychotic Drugs on Neurogenesis in the Forebrain of the Adult Rat
Wang, H.-D., Dunnavant, F. D., Jarman, T., & Deutch, A. Y. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300449 · Cited by 162 · see citing works
The effects of running and of inhibiting adult neurogenesis on learning and memory in rats.
Wojtowicz, J. M., Askew, M. L., & Winocur, G. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06128.x · Cited by 158 · see citing works
Stereological Approaches to Identifying Neuropathology in Psychosis
Dorph‐Petersen, K., & Lewis, D. A. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.04.030 · Cited by 151 · see citing works
Scheewe, T. W., van Haren, N. E. M., Sarkisyan, G., Schnack, H. G., Brouwer, R. M., de Glint, M., Hulshoff Pol, H. E., Backx, F. J. G., Kahn, R. S., & Cahn, W. (2013) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2012.08.008 · Cited by 148 · see citing works
Bechara, R. G., & Kelly, A. M. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.02.018 · Cited by 132 · see citing works
Henseler, I., Falkai, P., & Gruber, O. (2009) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2009.09.003 · Cited by 126 · see citing works
Hippocampal Complexin Proteins and Cognitive Dysfunction in Schizophrenia
Sawada, K., Barr, A. M., Nakamura, M., Arima, K., Young, C. E., Dwork, A. J., Falkai, P., Phillips, A. G., & Honer, W. G. (2005) · Archives of General Psychiatry · doi:10.1001/archpsyc.62.3.263 · Cited by 115 · see citing works
Biedermann, S. V., Fuß, J., Zheng, L., Sartorius, A., Falfán-Melgoza, C., Demirakça, T., Gass, P., Ende, G., & Weber‐Fahr, W. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.04.010 · Cited by 111 · see citing works
Preclinical models of antipsychotic drug-induced metabolic side effects
Boyda, H. N., Tse, L., Procyshyn, R. M., Honer, W. G., & Barr, A. M. (2010) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2010.07.002 · Cited by 104 · see citing works
Hippocampal CA1 deformity is related to symptom severity and antipsychotic dosage in schizophrenia
Zierhut, K. C., Graßmann, R., Kaufmann, J., Steiner, J. H., Bogerts, B., & Schiltz, K. (2013) · Brain · doi:10.1093/brain/aws335 · Cited by 95 · see citing works
Hui, J., Zhang, Z., Liu, S., Xi, G., Zhang, X.-R., Teng, G., Chan, K. C., Wu, E. X., Nie, B., Shan, B., et al. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.10.014 · Cited by 91 · see citing works
Toulopoulou, T., Grech, A., Morris, R. G., Schulze, K., McDonald, C., Chapple, B., Rabe‐Hesketh, S., & Murray, R. M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.06.026 · Cited by 87 · see citing works
Ebdrup, B. H., Skimminge, A., Rasmussen, H., Aggernæs, B., Oranje, B., Lublin, H., Baaré, W. F. C., & Glenthoj, B. Y. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000817 · Cited by 85 · see citing works
Boyda, H. N., Tse, L., Procyshyn, R. M., Wong, D., Wu, T. K. Y., Pang, C. C. Y., & Barr, A. M. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.04.024 · Cited by 69 · see citing works
Digital Atlas of Anatomical Subdivisions and Boundaries of the Rat Hippocampal Region
Kjønigsen, L. J., Leergaard, T. B., Witter, M. P., & Bjaalie, J. G. (2011) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2011.00002 · Cited by 68 · see citing works
Type 2 diabetes affects hippocampus volume differentially in men and women
Hempel, R., Onopa, R., & Convit, A. J. (2011) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.1230 · Cited by 60 · see citing works
Heterozygous reeler mice exhibit alterations in sensorimotor gating but not presynaptic proteins
Barr, A. M., Fish, K. N., Markou, A., & Honer, W. G. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06233.x · Cited by 60 · see citing works
Hippocampal Volume Change in Schizophrenia
Koolschijn, P. C. M. P., van Haren, N. E. M., Cahn, W., Schnack, H. G., Janssen, J., Klumpers, F., Pol, H. E. H., & Kahn, R. S. (2010) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.08m04574yel · Cited by 58 · see citing works
Barr, A. M., Young, C. E., Sawada, K., Trimble, W. S., Phillips, A. G., & Honer, W. G. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03457.x · Cited by 57 · see citing works
Hippocampal volume in subjects at high risk of psychosis: A longitudinal MRI study
Walter, A., Studerus, E., Smieskova, R., Küster, P., Aston, J., Lang, U. E., Radue, E. W., Riecher‐Rössler, A., & Borgwardt, S. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.10.013 · Cited by 56 · see citing works
Barakauskas, V., Beasley, C. L., Barr, A. M., Ypsilanti, A. R., Li, H., Thornton, A. E., Wong, H., Rosokilja, G., Mann, J. J., Mancevski, B., et al. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.228 · Cited by 55 · see citing works
Boyda, H. N., Procyshyn, R. M., Tse, L., Hawkes, E., Chen, J., Pang, C. C. Y., Honer, W. G., & Barr, A. M. (2012) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.110140 · Cited by 55 · see citing works
Boyda, H. N., Ramos‐Miguel, A., Procyshyn, R. M., Töpfer, E. T., Lant, N., Choy, H. H.-T., Wong, R., LI, L. C., Pang, C. C. Y., Honer, W. G., et al. (2013) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713000795 · Cited by 52 · see citing works
Intermittent treatment with olanzapine causes sensitization of the metabolic side-effects in rats
Boyda, H. N., Procyshyn, R. M., Tse, L., Wong, D. W., Pang, C. C. Y., Honer, W. G., & Barr, A. M. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.02.019 · Cited by 48 · see citing works
Sensitivity of the female rat to olanzapine-induced weight gain—Far from the clinic?
Weston–Green, K., Huang, X., & Deng, C. (2009) · Schizophrenia Research · doi:10.1016/j.schres.2009.09.034 · Cited by 45 · see citing works
Hippocampal volume reduction and autobiographical memory deficits in chronic schizophrenia
Herold, C. J., Lässer, M. M., Schmid, L. A., Seidl, U., Kong, L., Fellhauer, I., Thomann, P. A., Essig, M., & Schröder, J. (2013) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2012.04.002 · Cited by 41 · see citing works
Boyda, H. N., Procyshyn, R. M., Pang, C. C. Y., Hawkes, E., Wong, D., Jin, C. H., Honer, W. G., & Barr, A. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053459 · Cited by 39 · see citing works
Panenka, W. J., Khorram, B., Barr, A. M., Smith, G. N., Lang, D. J., Kopala, L. C., Vandorpe, R. A., & Honer, W. G. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.05.002 · Cited by 38 · see citing works
Green, W., Patil, P. G., Marsden, C. A., Bennett, G. W., & Wigmore, P. M. (2006) · Brain Research · doi:10.1016/j.brainres.2005.11.047 · Cited by 38 · see citing works
Barr, A. M., Young, C. E., Phillips, A. G., & Honer, W. G. (2005) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145705006000 · Cited by 31 · see citing works
Landers, M. R., Kinney, J. W., Allen, D. N., & van Breukelen, F. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.002 · Cited by 28 · see citing works
Tomassoni, D., Bellagamba, G., Postacchini, D., Venarucci, D., & Amenta, F. (2004) · Clinical and Experimental Hypertension · doi:10.1081/ceh-120034136 · Cited by 20 · see citing works
Antipsychotic polypharmacy increases metabolic dysregulation in female rats.
Boyda, H. N., Procyshyn, R. M., Tse, L., Xu, J., Jin, C. H., Wong, D., Pang, C. C. Y., Honer, W. G., & Barr, A. M. (2013) · Experimental and Clinical Psychopharmacology · doi:10.1037/a0031228 · Cited by 18 · see citing works
Characterization of the neurogenesis quiescent zone in the rodent brain: Effects of age and exercise
Gil‐Mohapel, J., Simpson, J. M., Titterness, A. K., & Christie, B. R. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07132.x · Cited by 13 · see citing works
Létourneau, G., Bentaleb, L. A., Stip, B., Luck, D., & Stip, É. (2011) · Schizophrenia Research and Treatment · doi:10.1155/2011/862350 · Cited by 5 · see citing works
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Kandola, A., Hendrikse, J., Lucassen, P. J., & Yücel, M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00373 · Cited by 155 · see citing works
“For example, recent animal studies have demonstrated that AE was able to reverse most of damage caused to hippocampal volume and hippocampal synaptic connectivity caused by antipsychotic medication (Barr et al., 2013; Ramos-Miguel et al., 2015).”
Hippocampal volume and cell number in depression, schizophrenia, and suicide subjects
Chen, F., Bertelsen, A., Holm, I. E., Nyengaard, J. R., Rosenberg, R., & Dorph‐Petersen, K. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146546 · Cited by 84 · see citing works
Rief, W., Barsky, A. J., Bingel, U., Doering, B. K., Schwarting, R., Wöhr, M., & Schweiger, U. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.11.008 · Cited by 67 · see citing works
Papiol, S., Popovic, D., Keeser, D., Hasan, A., Schneider-Axmann, T., Degenhardt, F., Rossner, M. J., Bickeböller, H., Schmitt, A., Falkai, P., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.131 · Cited by 62 · see citing works
Hippocampal volume and vasculature before and after exercise in treatment-resistant schizophrenia
Woodward, M. L., Gicas, K. M., Warburton, D. E. R., White, R. F., Rauscher, A., Leonova, O., Su, W., Smith, G. N., Thornton, A. E., Vertinsky, A. T., et al. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.06.054 · Cited by 48 · see citing works
Ramos‐Miguel, A., Hercher, C., Beasley, C. L., Barr, A. M., Bayer, T. A., Falkai, P., Leurgans, S. E., Schneider, J. A., Bennett, D. A., & Honer, W. G. (2015) · Molecular Neurodegeneration · doi:10.1186/s13024-015-0061-4 · Cited by 46 · see citing works
Babic, I., Gorak, A., Engel, M., Sellers, D., Else, P. L., Osborne, A. L., Pai, N. B., Huang, X., Nealon, J. R., & Weston–Green, K. (2018) · Journal of Psychopharmacology · doi:10.1177/0269881118756061 · Cited by 44 · see citing works
Meng, L., Li, K., Li, W., Xiao, Y., Lui, S., Sweeney, J. A., & Gong, Q. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.08.021 · Cited by 44 · see citing works
Lack of Social Support Raises Stress Vulnerability in Rats with a History of Ancestral Stress
Faraji, J., Soltanpour, N., Lotfi, H., Moeeini, R., Moharreri, A., Roudaki, S., Hosseini, S. A., Olson, D. M., Abdollahi, A. A., Soltanpour, N., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05440-8 · Cited by 37 · see citing works
Rhindress, K., Robinson, D. G., Gallego, J. A., Wellington, R. L., Malhotra, A. K., & Szeszko, P. R. (2017) · Psychological Medicine · doi:10.1017/s0033291717000137 · Cited by 29 · see citing works
Brain insulin action: Implications for the treatment of schizophrenia
Agarwal, S. M., Kowalchuk, C., Castellani, L. N., Costa-Dookhan, K. A., Caravaggio, F., Asgariroozbehani, R., Chintoh, A. F., Graff‐Guerrero, A., & Hahn, M. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.05.032 · Cited by 28 · see citing works
Differential Effects of Acute Treatment With Antipsychotic Drugs on Peripheral Catecholamines
Boyda, H. N., Ho, A. A., Tse, L., Procyshyn, R. M., Yuen, J. W. Y., Kim, D. D., Honer, W. G., & Barr, A. M. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.617428 · Cited by 22 · see citing works
Wu, C., Yuen, J. W. Y., Boyda, H. N., Procyshyn, R. M., Wang, C. K., Asiri, Y. I., Pang, C. C. Y., Honer, W. G., & Barr, A. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107116 · Cited by 21 · see citing works
Fredrikson, D. H., Boyda, H. N., Tse, L., Whitney, Z., Pattison, M. A., Ott, F. J., Hansen, L., & Barr, A. M. (2014) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2014.00105 · Cited by 19 · see citing works
Ramos-Miguel, A., Honer, W. G., Boyda, H. N., Sawada, K., Beasley, C. L., Procyshyn, R. M., & Barr, A. M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.06.022 · Cited by 18 · see citing works
Halene, T. B., Kozlenkov, A., Jiang, Y., Mitchell, A. C., Javidfar, B., Dincer, A., Park, R., Wiseman, J., Croxson, P. L., Giannaris, E. L., et al. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2015.12.016 · Cited by 18 · see citing works
Interaction of clozapine with metformin in a schizophrenia rat model
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Crum, W. R., Danckaers, F., Huysmans, T., Côtel, M.-C., Natesan, S., Modo, M., Sijbers, J., Williams, S., Kapur, S., & Vernon, A. C. (2016) · Psychological Medicine · doi:10.1017/s0033291716001768 · Cited by 15 · see citing works
Lang, X., Wang, D., Chen, D., Xiu, M., Zhou, H., Wang, L., Cao, B., & Zhang, X. (2022) · Neurotherapeutics · doi:10.1007/s13311-021-01174-8 · Cited by 13 · see citing works
Faraji, J., Lotfi, H., Moharrerie, A., Jafari, S. Y., Soltanpour, N., Tamannaiee, R., Marjani, K., Roudaki, S., Naseri, F., Moeeini, R., et al. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab395 · Cited by 12 · see citing works
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Tréhout, M., & Dollfus, S. (2018) · L Encéphale · doi:10.1016/j.encep.2018.05.005 · Cited by 12 · see citing works
Xia, M., Wang, Y., Su, W., Tang, Y., Zhang, T., Cui, H., Wei, Y., Tang, X., Xu, L., Hu, H., et al. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110780 · Cited by 5 · see citing works
Xue, Y.-Q., Li, J., Yan, L., Lu, L., & Liao, F. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.06.023 · Cited by 4 · see citing works
Woodward, M. L., Ker, A. H., Barr, A. M., Beasley, C. L., Hercher, C., Boyda, H. N., Procyshyn, R. M., Honer, W. G., & Lang, D. J. (2019) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2019.172834 · Cited by 1 · see citing works
- Authors
- Barr, A. M., Wu, C. H., Wong, C., Hercher, C., Töpfer, E., Boyda, H. N., Procyshyn, R. M., Honer, W. G., & Beasley, C. L.
- Affiliations
- University of British Columbia (CA)
- Corresponding author
- Barr, A.M.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 255
- Pages
- 147-157
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2058786486
- Cited by
- 26
- References
- 59
- Citations by year
- 2023: 1 · 2022: 1 · 2021: 3 · 2020: 1 · 2019: 3 · 2018: 4 · 2017: 3 · 2016: 4 · 2015: 4 · 2014: 2
- FWCI
- 2.36
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Pfizer
- Sunovion
- H. Lundbeck A/S
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- olanzapine, exercise training, hippocampal volume, antipsychotic adverse effects, schizophrenia, impaired glucose tolerance, aerobic exercise, dentate gyrus, CA1, female rats, running wheel
- MeSH terms
- Olanzapine, Aging, Animals, Benzodiazepines, Female, Hippocampus, Physical Conditioning, Animal, Antipsychotic Agents, Rats, Sprague-Dawley, Rats
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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