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      Tricyclic antidepressants and selective serotonin reuptake inhibitors but not anticonvulsants ameliorate pain, anxiety, and depression symptoms in an animal model of central post-stroke pain

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          Abstract

          Background

          Central post-stroke pain (CPSP) is a type of neuropathic pain caused by dysfunction in the spinothalamocortical pathway. However, no animal studies have examined comorbid anxiety and depression symptoms. Whether the typical pharmacological treatments for CPSP, which include antidepressants, selective serotonin reuptake inhibitors (SSRIs), and anticonvulsants, can treat comorbid anxiety and depression symptoms in addition to pain remains unclear? The present study ablated the ventrobasal complex of the thalamus (VBC) to cause various CPSP symptoms. The effects of the tricyclic antidepressants amitriptyline and imipramine, the SSRI fluoxetine, and the anticonvulsant carbamazepine on pain, anxiety, and depression were examined.

          Results

          The results showed that VBC lesions induced sensitivity to thermal pain, measured using a hot water bath; mechanical pain, assessed by von Frey test; anxiety behavior, determined by the open-field test, elevated plus-maze test, and zero-maze test; and depression behavior, assessed by the forced swim test. No effect on motor activity in the open-field test was observed. Amitriptyline reduced thermal and mechanical pain sensitivity and anxiety but not depression. Imipramine suppressed thermal and mechanical pain sensitivity, anxiety, and depression. Fluoxetine blocked mechanical but not thermal pain sensitivity, anxiety, and depression. However, carbamazepine did not affect pain, anxiety, or depression.

          Conclusion

          In summary, antidepressants and SSRIs but not anticonvulsants can effectively ameliorate pain and comorbid anxiety and depression in CPSP. The present findings, including discrepancies in the effects observed following treatment with anticonvulsants, antidepressants, and SSRIs in this CPSP animal model, can be applied in the clinical setting to guide the pharmacological treatment of CPSP symptoms.

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          Most cited references46

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          Depression: a new animal model sensitive to antidepressant treatments.

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            The use of the elevated plus maze as an assay of anxiety-related behavior in rodents.

            The elevated plus maze is a widely used behavioral assay for rodents and it has been validated to assess the anti-anxiety effects of pharmacological agents and steroid hormones, and to define brain regions and mechanisms underlying anxiety-related behavior. Briefly, rats or mice are placed at the junction of the four arms of the maze, facing an open arm, and entries/duration in each arm are recorded by a video-tracking system and observer simultaneously for 5 min. Other ethological parameters (i.e., rears, head dips and stretched-attend postures) can also be observed. An increase in open arm activity (duration and/or entries) reflects anti-anxiety behavior. In our laboratory, rats or mice are exposed to the plus maze on one occasion; thus, results can be obtained in 5 min per rodent.
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              Post Stroke Pain: Identification, Assessment, and Therapy

              Background: Pain is a common complication after stroke and is associated with the presence of depression, cognitive dysfunction, and impaired quality of life. It remains underdiagnosed and undertreated, despite evidence that effective treatment of pain may improve function and quality of life. Summary: We provide an overview of the means for clinical assessment and risk factors for the development of post-stroke pain, then review the newest available literature regarding the commonest post-stroke pain syndromes, including central post-stroke pain, complex regional pain syndrome, musculoskeletal pain including shoulder subluxation, spasticity-related pain, and post-stroke headache, as well as the available epidemiology and current treatment options. Key Messages: In the best interests of optimizing quality of life and function after stroke, clinicians should be aware of pain as a common complication after stroke, identify those patients at highest risk, directly inquire as to the presence and characteristics of pain, and should be aware of the options for treatment for the various pain syndromes.
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                Author and article information

                Journal
                Mol Pain
                Mol Pain
                spmpx
                MPX
                Molecular Pain
                SAGE Publications (Sage CA: Los Angeles, CA )
                1744-8069
                2021
                14 December 2021
                : 17
                : 17448069211063351
                Affiliations
                [1 ]universityInstitute of Biomedical Sciences; , Taipei, Taiwan
                [2 ]Department of Psychology, Ringgold 56854, universityFo Guang University; , Yilan County 26247, Taiwan
                [3 ]Department of Biotechnology and Animal Science, universityNational Ilan University; , Yilan City, Yilan County 260, Taiwan
                Author notes
                [*]Andrew Chih Wei Huang, Department of Psychology, Fo Guang University, No. 160, Linwei Road, Jiaosi Shiang, Yilan County 26247, Taiwan. Email: chweihuang@ 123456mail.fgu.edu.tw
                Author information
                https://orcid.org/0000-0001-5619-2281
                https://orcid.org/0000-0001-9794-7302
                Article
                10.1177_17448069211063351
                10.1177/17448069211063351
                8679055
                34903115
                228575dc-c8c7-4cd5-b78c-f75d3ed75800
                © The Author(s) 2021

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 24 August 2021
                : 29 October 2021
                : 10 November 2021
                Funding
                Funded by: Ministry of Science and Technology, Taiwan, FundRef https://doi.org/10.13039/501100004663;
                Award ID: MOST 110-2410-H-431-004
                Award ID: MOST-109-2320-B-001-010
                Categories
                Research Article
                Custom metadata
                January-December 2021
                ts10

                Molecular medicine
                central post-stroke pain,pain,anxiety,depression,tricyclic antidepressants,anticonvulsants,selective serotonin reuptake inhibitor,pharmacological treatments,rats

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