亚有效剂量GABA激动剂对大鼠吗啡耐受减弱的影响:行为学和电生理研究

H. Manaheji, S. Mehrabadi
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引用次数: 2

摘要

gaba能药物能改变吗啡的镇痛作用。宽动态范围(WDR)神经元在疼痛传递中起重要作用,并可能改变吗啡耐受行为。本研究记录吗啡耐受大鼠和GABA激动剂治疗大鼠的WDR神经元行为,以阐明吗啡和GABA激动剂对WDR行为改变的影响。将大鼠分为4组:1;控制,2。吗啡耐受性(MT);MT+ muscimol, 4- MT+巴氯芬。大鼠腹腔注射硫酸吗啡10 mg/kg,连续8天诱导吗啡耐受。治疗组分别于吗啡注射前第1、3、5、8天注射GABA激动剂。采用福尔马林试验证实吗啡耐受。采用细胞外单单元记录法记录脊髓WDR神经元。结果表明,长期给药吗啡不能减轻福尔马林疼痛,但GABA激动剂能改善吗啡的镇痛效果。
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Effect of sub-effective dose of GABA agonists on attenuation of morphine tolerance in rats: Behavioral and electrophysiological studies
GABAergic drugs can change analgesic effect of morphine. Wide dynamic range (WDR) neurons play an important role in pain transmission and may change behaviors in morphine tolerance. In this study WDR neuron behaviors in morphine tolerant rats and rats treated with GABA agonists, were recorded to elucidate the effect of morphine and GABA agonists on WDR behavioral changes. Rats were divided to 4 groups: 1. Control, 2. Morphine tolerance (MT), 3. MT+ muscimol, 4- MT+ baclofen. To induce morphine tolerance in rats, they received morphine sulfate 10 mg/kg intraperitoneally for 8 days. In treatment group, GABA agonists were injected on days 1, 3, 5 and 8 before injection of morphine. To confirm morphine tolerance induced, formalin test was used. Extracellular single unit recording was used to record spinal WDR neurons. Results showed that chronic administration of morphine failed to attenuate formalin pain but GABA agonists improved analgesic effect of morphine.
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