首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >A differential modulation of allodynia, hyperalgesia and nociception by neuropeptide FF in the periaqueductal gray of neuropathic rats: interactions with morphine and naloxone.
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A differential modulation of allodynia, hyperalgesia and nociception by neuropeptide FF in the periaqueductal gray of neuropathic rats: interactions with morphine and naloxone.

机译:神经肽FF在神经病变大鼠的导水管周围灰色中对异常性疼痛,痛觉过敏和伤害感受的差异调节:与吗啡和纳洛酮的相互作用。

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摘要

The effect of neuropeptide FF in the periaqueductal gray on pain behaviour was studied in rats with a chronic neuropathy induced by unilateral ligation of two spinal nerves. Neuropeptide FF produced in a non-monotonic fashion a significant attenuation of tactile allodynia. The antiallodynic effect was not significantly modulated by naloxone administered systemically or intracerebrally. The dose of neuropeptide FF producing a significant antiallodynic effect was not antinociceptive in a test of mechanical or thermal nociception. The thermal antinociceptive effect induced by morphine administered in the periaqueductal gray was significantly attenuated by neuropeptide FF, whereas that induced by systemically administered morphine was not. The interaction of neuropeptide FF with intracerebrally or systemically administered morphine in a test of tactile allodynia was not significant. The results indicate that neuropeptide FF in the periaqueductal gray may produce a selective attenuation of tactile allodynia in neuropathic rats. This antiallodynic effect is at least partly independent of naloxone-sensitive opioid receptors. Furthermore, neuropeptide FF in the periaqueductal gray attenuates antinociception induced by intracerebrally but not systemically administered morphine.
机译:在单侧结扎两条脊神经引起的慢性神经病变大鼠中,研究了导水管周围灰色神经肽FF对疼痛行为的影响。以非单调方式产生的神经肽FF明显减轻了触觉异常性疼痛。全身或脑内施用纳洛酮对抗痛觉过敏作用没有明显的调节作用。在机械或热伤害感受测试中,产生显着抗痛觉过敏作用的神经肽FF剂量不是抗伤害感受的。神经肽FF显着减弱了在导水周灰色中给予吗啡引起的热镇痛作用,而全身性给予吗啡则没有引起热镇痛作用。在触觉性异常性疼痛测试中,神经肽FF与脑内或全身施用的吗啡的相互作用不显着。结果表明,导水管周围灰色的神经肽FF可能会选择性减轻神经性大鼠的触觉异常性疼痛。这种抗痛觉过敏作用至少部分独立于纳洛酮敏感的阿片受体。此外,导水管周围灰色中的神经肽FF减弱了脑内但未全身施用吗啡引起的镇痛作用。

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