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使用快速循环伏安法对大鼠脑片内源性去甲肾上腺素释放进行实时监测。2.终纹床核腹侧部α2 自身受体的操作特性。

Real-time monitoring of endogenous noradrenaline release in rat brain slices using fast cyclic voltammetry. 2. Operational characteristics of the alpha 2 autoreceptor in the bed nucleus of stria terminalis, pars ventralis.

作者信息

Palij P, Stamford J A

机构信息

Anaesthetics Unit, London Hospital Medical College, Royal London Hospital, Whitechapel, UK.

出版信息

Brain Res. 1993 Apr 2;607(1-2):134-40. doi: 10.1016/0006-8993(93)91498-h.

Abstract

Fast cyclic voltammetry (FCV) at carbon fibre microelectrodes was used to monitor stimulated noradrenaline (NA) efflux in slices of the ventral part of the rat bed nucleus of stria terminalis (BSTV) superfused with artificial cerebrospinal fluid at 32 degrees C. NA efflux was evoked by local electrical stimulation (trains of 10-50 pulses, 0.2 ms duration, 10 mA constant current at 10-500 Hz). The effects of four alpha 2 antagonists (yohimbine, rauwolscine, prazosin and WB 4101) and three alpha 2 agonists (clonidine, oxymetazoline and UK 14304) were examined. All drugs (1 microM) were added via the superfusate. Yohimbine and rauwolscine increased NA efflux on the lower but not the higher frequency trains: maximum increases (on 20 Hz, 50 pulse stimulation) were to 392 +/- 63% (yohimbine) and 243 +/- 7% (rauwolscine). There was a threshold train duration for demonstration of autoreceptor antagonism of 500-1000 ms. Prazosin and WB 4101 did not increase NA efflux but caused a modest decrease at the higher (100-500 Hz) frequencies. The effects of the alpha 2 agonists were also affected by stimulus train duration. Longer trains reduced agonist (clonidine) effects. When tested on pseudo-one pulse (POP) stimulations (less than 100 ms duration), the alpha 2 agonists decreased NA efflux. UK 14304 reduced NA efflux on 20 pulse/200 Hz stimulation to a greater degree (86 +/- 7%) than the partial agonists clonidine (39 +/- 3%) or oxymetazoline (40 +/- 8%). The present results demonstrate that alpha 2 autoreceptors are a major mechanism in the control of NA efflux in the BSTV.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在32摄氏度下,使用碳纤维微电极上的快速循环伏安法(FCV)监测灌注人工脑脊液的大鼠终纹床核腹侧部(BSTV)切片中刺激诱发的去甲肾上腺素(NA)流出。通过局部电刺激(10 - 50个脉冲序列,持续时间0.2毫秒,10 - 500赫兹时10毫安恒定电流)诱发NA流出。研究了四种α2拮抗剂(育亨宾、萝芙素、哌唑嗪和WB 4101)和三种α2激动剂(可乐定、羟甲唑啉和UK 14304)的作用。所有药物(1微摩尔)通过灌流液添加。育亨宾和萝芙素在较低频率刺激序列时增加NA流出,但在较高频率时无此作用:最大增加量(在20赫兹、50个脉冲刺激时)分别为392±63%(育亨宾)和243±7%(萝芙素)。存在一个500 - 1000毫秒的刺激序列持续时间阈值,用于证明自身受体拮抗作用。哌唑嗪和WB 4101不会增加NA流出,但在较高(100 - 500赫兹)频率时会导致适度下降。α2激动剂的作用也受刺激序列持续时间影响。较长的刺激序列会降低激动剂(可乐定)的作用。当在伪单脉冲(POP)刺激(持续时间小于100毫秒)上进行测试时,α2激动剂会降低NA流出。UK 14304在20脉冲/200赫兹刺激时比部分激动剂可乐定(39±3%)或羟甲唑啉(40±8%)更显著地降低NA流出(86±7%)。目前的结果表明,α2自身受体是控制BSTV中NA流出的主要机制。(摘要截短于250字)

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