Hill R G, Pepper C M
Eur J Pharmacol. 1978 Jan 15;47(2):223-5. doi: 10.1016/0014-2999(78)90393-x.
The activity of single thalamic nociceptive neurones was recorded extracellularly. BW 180C, (D-ala2,D-leu5-enkephalin) applied locally, by iontophoresis (10--40 nA) or systemically by i.v. injection (1.5--6 mg/kg) markedly depressed the evoked excitation of these neurones following peripheral noxious stimulation. This effect could be antagonised by naloxone. Enhanced enzymic stability did not appear to prolong the duration of action of BW 180C iontrophoretically applied to these neurones.
采用细胞外记录法记录单个丘脑伤害性神经元的活动。通过离子导入法(10 - 40纳安)局部应用BW 180C(D-丙氨酸2,D-亮氨酸5-脑啡肽),或通过静脉注射(1.5 - 6毫克/千克)全身应用,均可显著抑制这些神经元在周围伤害性刺激后诱发的兴奋。这种效应可被纳洛酮拮抗。增强的酶稳定性似乎并未延长离子导入法应用于这些神经元时BW 180C的作用持续时间。