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伊达唑胺可阻断去甲肾上腺素的作用,但不能阻断猫蓝斑和柯利克-福斯核电刺激引起的脊髓抑制。

Idazoxan blocks the action of noradrenaline but not spinal inhibition from electrical stimulation of the locus coeruleus and nucleus Kolliker-Fuse of the cat.

作者信息

Zhao Z Q, Duggan A W

机构信息

Department of Pharmacology, John Curtin School of Medical Research, Australian National University, Canberra.

出版信息

Neuroscience. 1988 Jun;25(3):997-1005. doi: 10.1016/0306-4522(88)90052-8.

Abstract

The effects of idazoxan, a specific alpha 2-adrenoceptor antagonist, on spinal inhibition by administration of noradrenaline and from electrical stimulation of the dorsolateral pons were studied in 26 cats anaesthetized with sodium pentobarbitone. The excitation of dorsal horn neurons of the spinal cord by noxious heating of the skin or by impulses in unmyelinated primary afferent fibres was markedly reduced when noradrenaline was administered microelectrophoretically in the substantia gelatinosa or near cell bodies. Electrical stimulation of the region of the locus coeruleus selectively inhibited spinal nociceptive transmission when dorsal horn neurons were excited by noxious and non-noxious stimuli. In contrast to stimulation of the locus coeruleus, stimulation of the nucleus Kolliker-Fuse produced non-selective inhibition of both nociceptive and non-nociceptive responses of dorsal horn neurons of the spinal cord. Microelectrophoretic ejection of idazoxan reduced or abolished noradrenaline-induced inhibition with 19 of 20 neurons. This antagonist did not alter inhibition from stimulation of the locus coeruleus and the nucleus Kolliker-Fuse, regardless of whether it was administered microelectrophoretically (11 neurons), systemically (3 neurons) or topically (4 neurons). The results suggest that alpha 2-adrenoceptors do not mediate inhibition of spinal nociceptive transmission from electrical stimulation of the locus coeruleus and the nucleus Kolliker-Fuse. Other possibilities for the failure of idazoxan to modify inhibition from such stimulation are discussed.

摘要

在26只戊巴比妥钠麻醉的猫身上,研究了特异性α₂ - 肾上腺素能受体拮抗剂咪唑克生对注射去甲肾上腺素及电刺激脑桥背外侧所致脊髓抑制的影响。当在脊髓胶状质或细胞体附近微量电泳注射去甲肾上腺素时,皮肤有害热刺激或无髓鞘初级传入纤维冲动引起的脊髓背角神经元兴奋明显减弱。当背角神经元受到有害和无害刺激而兴奋时,电刺激蓝斑区域可选择性抑制脊髓伤害性传入。与刺激蓝斑不同,刺激科利克 - 福斯核可对脊髓背角神经元的伤害性和非伤害性反应产生非选择性抑制。20个神经元中有19个,咪唑克生的微量电泳喷射可减少或消除去甲肾上腺素诱导的抑制。无论微量电泳注射(11个神经元)、全身给药(3个神经元)还是局部给药(4个神经元),这种拮抗剂均不改变刺激蓝斑和科利克 - 福斯核所产生的抑制。结果表明,α₂ - 肾上腺素能受体并不介导电刺激蓝斑和科利克 - 福斯核所致脊髓伤害性传入的抑制。文中还讨论了咪唑克生未能改变此类刺激所致抑制的其他可能原因。

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