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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Nociceptive behavior induced by mustard oil injection into the temporomandibular joint is blocked by a peripheral non-opioid analgesic and a central opioid analgesic.
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Nociceptive behavior induced by mustard oil injection into the temporomandibular joint is blocked by a peripheral non-opioid analgesic and a central opioid analgesic.

机译:芥子油注入颞下颌关节引起的伤害感受行为被周围的非阿片类镇痛药和中枢的阿片类镇痛药阻断。

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The aim of this study was to improve the mustard oil (MO) induced temporomandibular joint (TMJ) nociception model and to investigate the potential analgesic activity of systemic dipyrone and tramadol on the nociceptive behavioral responses induced by injection of low concentrations of the MO into the rat TMJ region. TMJ injection of 2.5% MO produced a significant nociceptive behavior expressed by head flinching and orofacial rubbing. This activity was related to the MO injection since mineral oil (vehicle) did not elicit response. Local application of the lidocaine N-ethyl bromide quaternary salt, QX-314 (2%) and systemic administration of morphine (4 mg/kg) significantly reduced the MO-induced nociceptive responses, validating the nociceptive character of the behaviors. The pretreatment with systemic dipyrone (19, 57 or 95 mg/kg) as well as tramadol (5, 7.5 or 10 mg/kg) was effective in decreasing the nociceptive behavioral responses induced by the injection of MO into the rat TMJ. In conclusion, TMJ injection of low concentrations of MO in rats produces well defined and quantifiable nociceptive behaviors constituting a reliable behavioral model for studying TMJ pain mechanisms and testing analgesic drugs. The results also suggest that dipyrone and tramadol could be effective analgesic options in the management of TMJ pain.
机译:这项研究的目的是改善芥子油(MO)引起的颞下颌关节(TMJ)伤害感受模型,并研究全身性双嘧啶和曲马多对通过向其注射低浓度的MO引起的伤害行为反应的潜在镇痛活性。大鼠TMJ区。 TMJ注射2.5%MO会产生显着的伤害行为,表现为头部退缩和口颊摩擦。由于矿物油(车辆)未引起反应,因此该活性与MO注射有关。利多卡因N-乙基溴化季铵盐QX-314(2%)的局部应用和吗啡(4 mg / kg)的全身给药显着降低了MO诱导的伤害感受,从而验证了行为的伤害感受特性。全身性双嘧啶(19、57或95 mg / kg)和曲马多(5、7.5或10 mg / kg)的预处理有效降低了将MO注射入大鼠TMJ中诱导的伤害行为反应。总之,在大鼠中低浓度MO的TMJ注射产生定义明确且可量化的伤害性行为,构成研究TMJ疼痛机制和测试镇痛药的可靠行为模型。结果还表明,双嘧达隆和曲马多可能是治疗TMJ疼痛的有效止痛药。

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