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      Automated home-cage for the evaluation of innate non-reflexive pain behaviors in a mouse model of inflammatory pain

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          Abstract

          The failure to develop analgesic drugs is attributed not only to the complex and diverse pathophysiology of pain in humans but also to the poor experimental design and poor preclinical assessment of pain. Although considerable efforts have been devoted to overcoming the relevant problems, many features of the behavioral pain assessment remain to be characterized. For example, a decreased locomotor activity as a common presentation of pain-like behavior has yet to be described. Studies on mice experimentally induced with carrageenan have provided opportunities to explore pain-related behaviors in automated home-cage monitoring. Through this approach, the locomotor activities of mice with carrageenan-induced inflammatory pain can be precisely and objectively captured. Here, we found that the mobile behaviors of mice reduced, and their immobility increased, indicating that carrageenan induction in mice caused a significant decrease in locomotor activity. These non-reflexive pain behaviors were strongly correlated with the reflexive pain behaviors measured via von Frey and plantar tests. Furthermore, the pharmacological intervention using indomethacin improved the locomotor activity of mice with carrageenan-induced pain. Thus, the analysis of the locomotor activity in automated home-cage monitoring is useful for studying the behavioral analgesia and the pharmacological screening of analgesic drugs. The combined evaluation of reflexive and non-reflexive pain behaviors enhances the translational utility of preclinical pain research in rodents.

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          Clinical development success rates for investigational drugs.

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            Men and mice: Relating their ages

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              Stress-induced analgesia.

              For over 30 years, scientists have been investigating the phenomenon of pain suppression upon exposure to unconditioned or conditioned stressful stimuli, commonly known as stress-induced analgesia. These studies have revealed that individual sensitivity to stress-induced analgesia can vary greatly and that this sensitivity is coupled to many different phenotypes including the degree of opioid sensitivity and startle response. Furthermore, stress-induced analgesia is influenced by age, gender, and prior experience to stressful, painful, or other environmental stimuli. Stress-induced analgesia is mediated by activation of the descending inhibitory pain pathway. Pharmacological and neurochemical studies have demonstrated involvement of a large number of neurotransmitters and neuropeptides. In particular, there are key roles for the endogenous opioid, monoamine, cannabinoid, gamma-aminobutyric acid and glutamate systems. The study of stress-induced analgesia has enhanced our understanding of the fundamental physiology of pain and stress and can be a useful approach for uncovering new therapeutic targets for the treatment of pain and stress-related disorders.
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                Author and article information

                Contributors
                pasarapa.c@chula.ac.th
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                10 June 2021
                10 June 2021
                2021
                : 11
                : 12240
                Affiliations
                [1 ]GRID grid.7922.e, ISNI 0000 0001 0244 7875, Pharmaceutical Sciences and Technology Program, Faculty of Pharmaceutical Sciences, , Chulalongkorn University, ; Bangkok, 10330 Thailand
                [2 ]GRID grid.7922.e, ISNI 0000 0001 0244 7875, Research Affairs, Faculty of Pharmaceutical Sciences, , Chulalongkorn University, ; Bangkok, 10330 Thailand
                [3 ]GRID grid.7922.e, ISNI 0000 0001 0244 7875, Department of Food and Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, , Chulalongkorn University, ; Bangkok, 10330 Thailand
                [4 ]GRID grid.7922.e, ISNI 0000 0001 0244 7875, Natural Products for Ageing and Chronic Diseases Research Unit, , Chulalongkorn University, ; Bangkok, 10330 Thailand
                [5 ]GRID grid.7922.e, ISNI 0000 0001 0244 7875, Department of Pharmacology and Physiology, Faculty of Pharmaceutical Sciences, , Chulalongkorn University, ; Bangkok, 10330 Thailand
                Article
                91444
                10.1038/s41598-021-91444-4
                8192791
                34112846
                1fae2996-1d8f-470b-b3b1-7fe4faa71bbd
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 20 February 2021
                : 24 May 2021
                Funding
                Funded by: Chulalongkorn University
                Funded by: FundRef http://dx.doi.org/10.13039/501100004704, National Research Council of Thailand;
                Award ID: IRN FY2020 507/2563
                Award Recipient :
                Funded by: Thailand Science Research and Innovation (TSRI) Fund
                Award ID: CU_FRB640001_01_33_3
                Award Recipient :
                Categories
                Article
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                © The Author(s) 2021

                Uncategorized
                experimental models of disease,preclinical research
                Uncategorized
                experimental models of disease, preclinical research

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