18
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Long‐term stability and characteristics of behavioral, biochemical, and molecular markers of three different rodent models for depression

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Objective

          The present study was designed to explore the long‐term differences between three mouse models for depression.

          Method

          In the present study, the unpredictable chronic mild stress (UCMS) model, the glucocorticoid/corticosterone model, and the olfactory bulbectomy model were compared at two, three, and five weeks after model induction. Behavioral testing performed included forced‐swimming, tail suspension, open‐field and elevated plus‐maze tests. In addition, 5‐hydroxytryptamine (5‐HT) and dopamine levels, and mRNA and protein expressions related to 5‐HT synthesis, transport, and signaling were analyzed in the hippocampus of tested animals.

          Results

          Our results revealed that each model demonstrated a specific profile of markers, whereas the stability of them differed over testing time.

          Conclusions

          Each model provided a unique set of advantages that can be considered depending on the context and aims of each study. Among the three models, the UCMS model was mostly stable and appeared to the best model for testing long‐term depression‐like state.

          Abstract

          There were varied degrees of change from behavior to molecular levels in the three models of depressive mice throughout the length of the modeling time. This includes an evaluation of the time period to be investigated when testing new antidepressants.

          Related collections

          Most cited references48

          • Record: found
          • Abstract: found
          • Article: not found

          Animal models of neuropsychiatric disorders.

          Modeling of human neuropsychiatric disorders in animals is extremely challenging given the subjective nature of many symptoms, the lack of biomarkers and objective diagnostic tests, and the early state of the relevant neurobiology and genetics. Nonetheless, progress in understanding pathophysiology and in treatment development would benefit greatly from improved animal models. Here we review the current state of animal models of mental illness, with a focus on schizophrenia, depression and bipolar disorder. We argue for areas of focus that might increase the likelihood of creating more useful models, at least for some disorders, and for explicit guidelines when animal models are reported.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Neurobiology of Depression

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The use of a plus-maze to measure anxiety in the mouse.

              R Lister (1987)
              To investigate whether an elevated plus-maze consisting of two open and two closed arms could be used as a model of anxiety in the mouse, NIH Swiss mice were tested in the apparatus immediately after a holeboard test. Factor analysis of data from undrugged animals tested in the holeboard and plus-maze yielded three orthogonal factors interpreted as assessing anxiety, directed exploration and locomotion. Anxiolytic drugs (chlordiazepoxide, sodium pentobarbital and ethanol) increased the proportion of time spent on the open arms, and anxiogenic drugs (FG 7142, caffeine and picrotoxin) reduced this measure. Amphetamine and imipramine failed to alter the indices of anxiety. The anxiolytic effect of chlordiazepoxide was reduced in mice that had previously experienced the plus-maze in an undrugged state. Testing animals in the holeboard immediately before the plus-maze test significantly elevated both the percentage of time spent on the open arms and the total number of arm entries, but did not affect the behavioral response to chlordiazepoxide. The plus-maze appears to be a useful test with which to investigate both anxiolytic and anxiogenic agents.
                Bookmark

                Author and article information

                Contributors
                Fei_H@hotmail.com
                xiaojunwu320@126.com
                Journal
                Brain Behav
                Brain Behav
                10.1002/(ISSN)2157-9032
                BRB3
                Brain and Behavior
                John Wiley and Sons Inc. (Hoboken )
                2162-3279
                22 December 2019
                February 2020
                : 10
                : 2 ( doiID: 10.1002/brb3.v10.2 )
                : e01508
                Affiliations
                [ 1 ] Shanghai Key Laboratory of Compound Chinese Medicines the Ministry of Education (MOE) Key Laboratory for Standardization of Chinese Medicines Shanghai R&D Center for Standardization of Chinese Medicines Institute of Chinese Materia Medica Shanghai University of Traditional Chinese Medicine Shanghai China
                [ 2 ] Center for Counseling and Development Department of Student Affairs Shanghai University of Traditional Chinese Medicine Shanghai China
                [ 3 ] Department of Psychiatry Laboratory of Molecular Psychiatry University of Münster Münster Germany
                Author notes
                [*] [* ] Correspondence

                Xiaojun Wu; Fei Huang, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Pudong District, Shanghai 201203, China.

                Emails: xiaojunwu320@ 123456126.com ; Fei_H@ 123456hotmail.com

                Author information
                https://orcid.org/0000-0001-6554-5341
                Article
                BRB31508
                10.1002/brb3.1508
                7010584
                31867894
                a51a79c2-b77f-4b82-b089-1a968a264a2e
                © 2019 The Authors. Brain and Behavior published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 August 2019
                : 22 October 2019
                : 27 November 2019
                Page count
                Figures: 7, Tables: 4, Pages: 12, Words: 7841
                Funding
                Funded by: National Natural Science Foundation of China , open-funder-registry 10.13039/501100011002;
                Award ID: 81703734
                Funded by: Shanghai Sailing Program
                Award ID: 17YF1417700
                Funded by: Program from Shanghai Municipal Commission of Health and Family Planning
                Award ID: 20184Y0177
                Funded by: Natural Science Foundation of Shanghai , open-funder-registry 10.13039/100007219;
                Award ID: 17ZR1430200
                Funded by: Shanghai Key Laboratory of Psychotic Disorders
                Award ID: 16‐K03
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                February 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.5 mode:remove_FC converted:10.02.2020

                Neurosciences
                5‐ht,corticosterone,depression model,glucocorticoid,olfactory bulbectomy,ucms
                Neurosciences
                5‐ht, corticosterone, depression model, glucocorticoid, olfactory bulbectomy, ucms

                Comments

                Comment on this article