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      The Walker 256 Breast Cancer Cell- Induced Bone Pain Model in Rats

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          Abstract

          The majority of patients with terminal breast cancer show signs of bone metastasis, the most common cause of pain in cancer. Clinically available drug treatment options for the relief of cancer-associated bone pain are limited due to either inadequate pain relief and/or dose-limiting side-effects. One of the major hurdles in understanding the mechanism by which breast cancer causes pain after metastasis to the bones is the lack of suitable preclinical models. Until the late twentieth century, all animal models of cancer induced bone pain involved systemic injection of cancer cells into animals, which caused severe deterioration of animal health due to widespread metastasis. In this mini-review we have discussed details of a recently developed and highly efficient preclinical model of breast cancer induced bone pain: Walker 256 cancer cell- induced bone pain in rats. The model involves direct localized injection of cancer cells into a single tibia in rats, which avoids widespread metastasis of cancer cells and hence animals maintain good health throughout the experimental period. This model closely mimics the human pathophysiology of breast cancer induced bone pain and has great potential to aid in the process of drug discovery for treating this intractable pain condition.

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          Most cited references185

          • Record: found
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          Different immune cells mediate mechanical pain hypersensitivity in male and female mice.

          A large and rapidly increasing body of evidence indicates that microglia-to-neuron signaling is essential for chronic pain hypersensitivity. Using multiple approaches, we found that microglia are not required for mechanical pain hypersensitivity in female mice; female mice achieved similar levels of pain hypersensitivity using adaptive immune cells, likely T lymphocytes. This sexual dimorphism suggests that male mice cannot be used as proxies for females in pain research.
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            Olfactory exposure to males, including men, causes stress and related analgesia in rodents.

            We found that exposure of mice and rats to male but not female experimenters produces pain inhibition. Male-related stimuli induced a robust physiological stress response that results in stress-induced analgesia. This effect could be replicated with T-shirts worn by men, bedding material from gonadally intact and unfamiliar male mammals, and presentation of compounds secreted from the human axilla. Experimenter sex can thus affect apparent baseline responses in behavioral testing.
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              Molecular mechanisms of opioid receptor-dependent signaling and behavior.

              Opioid receptors have been targeted for the treatment of pain and related disorders for thousands of years and remain the most widely used analgesics in the clinic. Mu (μ), kappa (κ), and delta (δ) opioid receptors represent the originally classified receptor subtypes, with opioid receptor like-1 (ORL1) being the least characterized. All four receptors are G-protein coupled and activate inhibitory G proteins. These receptors form homo- and heterodimeric complexes and signal to kinase cascades and scaffold a variety of proteins.The authors discuss classic mechanisms and developments in understanding opioid tolerance and opioid receptor signaling and highlight advances in opioid molecular pharmacology, behavioral pharmacology, and human genetics. The authors put into context how opioid receptor signaling leads to the modulation of behavior with the potential for therapeutic intervention. Finally, the authors conclude there is a continued need for more translational work on opioid receptors in vivo.
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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                31 August 2016
                2016
                : 7
                : 286
                Affiliations
                [1] 1School of Biomedical Sciences, The University of Queensland Brisbane, QLD, Australia
                [2] 2Centre for Integrated Preclinical Drug Development, The University of Queensland Brisbane, QLD, Australia
                [3] 3Institute for Molecular Bioscience, The University of Queensland Brisbane, QLD, Australia
                [4] 4School of Pharmacy, The University of Queensland Brisbane, QLD, Australia
                Author notes

                Edited by: Ajay Sharma, Chapman University, USA

                Reviewed by: Guilherme Lucas, University of São Paulo, Brazil; Dan Cacsire Castillo-Tong, Medical University of Vienna, Austria; Roberto Jose Fajardo, University of Texas Health Science Center at San Antonio, USA

                *Correspondence: Maree T. Smith maree.smith@ 123456uq.edu.au

                This article was submitted to Experimental Pharmacology and Drug Discovery, a section of the journal Frontiers in Pharmacology

                Article
                10.3389/fphar.2016.00286
                5005431
                f2ab216e-1f09-4fe4-ba07-eef9d96fc509
                Copyright © 2016 Shenoy, Kuo, Vetter and Smith.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 June 2016
                : 18 August 2016
                Page count
                Figures: 0, Tables: 2, Equations: 0, References: 216, Pages: 13, Words: 12366
                Categories
                Pharmacology
                Mini Review

                Pharmacology & Pharmaceutical medicine
                breast cancer,metastasis,bone pain,walker 256 cell,rat model

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