Assessment of the anti-allodynic efficacy of a glycine transporter 2 inhibitor relative to pregabalin and duloxetine in
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SHORT COMMUNICATION
Assessment of the anti‑allodynic efficacy of a glycine transporter 2 inhibitor relative to pregabalin and duloxetine in a rat model of prostate cancer‑induced bone pain Mohammad Zafar Imam1 · Andy Kuo1 · Janet R. Nicholson2 · Laura Corradini2 · Maree T. Smith1 Received: 30 April 2020 / Revised: 16 July 2020 / Accepted: 18 July 2020 © Maj Institute of Pharmacology Polish Academy of Sciences 2020
Abstract Background The pathobiology of prostate cancer-induced bone pain (PCIBP) is underpinned by both inflammatory and neuropathic components. Here, we used a rat model of PCIBP to assess the analgesic efficacy of a glycine transporter 2 (GlyT2) inhibitor (N-(6-((1,3-dihydroxypropan-2-yl)amino)-2-(dimethylamino)pyridin-3-yl)-3,5-dimethoxy-4-(4-(trifluoromethyl) phenoxy) benzamide) relative to two clinically available adjuvant drugs that are recommended for the relief of neuropathic pain, viz, pregabalin and duloxetine. Methods PCIBP was induced in male Wistar Han rats following intra-tibial injection (ITI) of rat prostate cancer (AT3B) cells into the left tibia. Sham-rats received an ITI of heat-killed AT3B cells. PCIBP rats with fully developed mechanical allodynia in the ipsilateral hindpaws as assessed using von Frey filaments, received single oral (p.o.) bolus doses of the GlyT2 inhibitor (3–30 mg/kg), pregabalin (3–100 mg/kg), duloxetine (3–100 mg/kg), or vehicle. Baseline paw withdrawal thresholds (PWTs) were determined in the ipsilateral (injured side) and contralateral hindpaws immediately prior to dosing and at scheduled times for 3 h post dosing in individual animals. Results Single oral bolus doses of the GlyT2 inhibitor (3–30 mg/kg) evoked partial pain relief at the doses tested in the ipsilateral hindpaws of PCIBP rats without any discernible behavioural side effects. By contrast, single oral bolus doses of pregabalin at 10–100 mg/kg evoked dose-dependent and complete alleviation of mechanical allodynia. By comparison, single oral bolus doses of duloxetine at doses up to 100 mg/kg lacked efficacy. Conclusion Oral administration of this GlyT2 inhibitor evoked partial pain relief in PCIBP rats and did not evoke central nervous system side effects in contrast to GlyT2 inhibitors reported by others. Keywords Pregabalin · Duloxetine · Glycine transporter 2 inhibitor · Cancer-induced bone pain
Introduction
Mohammad Zafar Imam and Andy Kuo Co-first authors. Electronic supplementary material The online version of this article (https://doi.org/10.1007/s43440-020-00145-8) contains supplementary material, which is available to authorized users. * Maree T. Smith [email protected] 1
Centre for Integrated Preclinical Drug Development, School of Biomedical Sciences, Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia
Boehringer Ingelheim Pharma GmbH and Co. KG, Biberach, Germany
2
Prostate cancer-induced bone pain (PCIBP) may develop secondary to the formation of skeletal metastases and its pathobiology is underpinned by both inflammatory and neurop
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