A Thermal Place Preference Test for Discovery of Neuropathic Pain Drugs

被引:2
作者
Caporoso, Joel [5 ]
Moses, Mark [5 ]
Koper, Kerryann [5 ]
Tillman, Tommy S. [5 ]
Jiang, Lingling [5 ]
Brandon, Nicole [5 ]
Chen, Qiang [5 ]
Tang, Pei [1 ,2 ]
Xu, Yan [3 ,4 ]
机构
[1] Univ Pittsburgh, Dept Anesthesiol & Perioperat Med, Dept Computat & Syst Biol, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Anesthesiol & Perioperat Med, Dept Pharmacol & Chem Biol, Dept Struct Biol, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Dept Phys & Astron, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Dept Anesthesiol & Perioperat Med, Pittsburgh, PA 15260 USA
关键词
pain; neuropathic pain; cold allodynia; thermal place preference test; chronic constriction injury; drug discovery; CHRONIC CONSTRICTION; RAT; MODEL; ALLODYNIA; DIAZEPAM; BEHAVIOR; MORPHINE; NERVE; HEAT;
D O I
10.1021/acschemneuro.0c00013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Developing potent non-opioid pain medications is an integral part of the battle to conquer both chronic pain and the current opioid crisis. Although most screening approaches use in vitro surrogate targets, in vivo screening of analgesic candidates is a necessary preclinical step in drug discovery. Here, we report the design of a new automated behavioral testing apparatus based on the principle of a thermal place preference test (TPPT). This new design can detect, quantify, and differentiate behavioral responses to cold stimuli between sham and chronic constriction injury (CCI) rodents with up to 12 animals tested simultaneously. At an optimized temperature pair of 12.5 degrees C vs 30.0 degrees C (+/- 0.5 degrees C), the TPPT design has captured the antinociceptive effects of morphine and pregabalin on CCI rats in individual 10 min tests. Moreover, it can differentiate analgesic effects by morphine or pregabalin from anxiolytic effects by diazepam. The results, along with the relatively low cost to construct the apparatus and moderately high throughput, make our TPPT design applicable for behavioral studies of chronic pain in rodents and for high-throughput in vivo screening of the next generation of pain medications.
引用
收藏
页码:1006 / 1012
页数:7
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