首页> 外文期刊>Analytical chemistry >In Vitro Continuous Amperometry with a Diamond Microelectrode Coupled with Video Microscopy for Simultaneously Monitoring Endogenous Norepinephrine and Its Effect on the Contractile Response of a Rat Mesenteric Artery
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In Vitro Continuous Amperometry with a Diamond Microelectrode Coupled with Video Microscopy for Simultaneously Monitoring Endogenous Norepinephrine and Its Effect on the Contractile Response of a Rat Mesenteric Artery

机译:体外连续安培法与金刚石微电极结合视频显微镜同时监测内源性去甲肾上腺素及其对大鼠肠系膜动脉收缩反应的影响

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Continuous amperometry with a diamond microelectrode and video microscopy were used to record (in vitro) endogenous norepinephrine release simultaneously with the evoked contractile response of a mesenteric artery from a healthy Sprague Dawley rat. Norepinephrine (NE) is a vasoconstricting neurotransmitter released from sympathetic nerves that innervate the smooth muscle cell layers surrounding arteries and veins. Using these two techniques along with several drugs, the NE released at sympathetic neuroeffector junctions nearby the microelectrode was measured as an oxidation current. Key to the amperometric measurement was the use of a diamond microelectrode because of the response sensitivity, reproducibility, and stability it provided. NE release was elicited by electrical stimulation at frequencies between 1 and 60 Hz, with a maximum response seen at 20 Hz. Confirmation that the oxidation current was, in fact, associated with endogenous NE came from the results of several drugs. Tetrodotoxin (TTX, 0.3 (mu)M), a voltage-dependent sodium channel antagonist that blocks nerve conduction, abolished both the oxidation current and the arterial constriction. The (alpha)_(2)-adrenergic autoreceptor antagonist, yohimbine (1.0 (mu)M), caused an increase in the oxidation current and the corresponding constriction. The addition of cocaine (10 (mu)M), an antagonist that inhibits neuronal NE reuptake, caused both the oxidation current and the contractile response to increase. These results, combined with the fact that the hydrodynamic voltammetric E_(1/2) for endogenous NE was identical to that for a standard solution, confirmed that the oxidation current was due to NE and that this compound caused, at least in part, the contractile response. The results demonstrate that continuous amperometric monitoring of NE with a diamond microelectrode and video imaging of vascular tone allow real time local measurement of the temporal relationship between nerve-stimulated NE release and arterial constriction.
机译:用钻石微电极和视频显微镜进行的连续安培法记录(体外)内源性去甲肾上腺素的释放,同时记录健康Sprague Dawley大鼠的肠系膜动脉的收缩反应。去甲肾上腺素(NE)是从交感神经释放的血管收缩性神经递质,可支配动脉和静脉周围的平滑肌细胞层。使用这两种技术以及几种药物,在微电极附近的交感神经效应连接处释放的NE被测量为氧化电流。安培测量的关键是使用金刚石微电极,因为它具有响应灵敏度,可重复性和稳定性。在1至60 Hz的频率下通过电刺激引起NE释放,最大响应出现在20 Hz。氧化电流实际上与内源性NE有关的证实来自几种药物的结果。河豚毒素(TTX,0.3μM)是一种电压依赖性钠通道拮抗剂,可阻断神经传导,从而消除了氧化电流和动脉收缩。 α_(2)-肾上腺素能自受体拮抗剂育亨宾(1.0μM)引起氧化电流增加和相应的收缩。可卡因(10μM)的添加(一种抑制神经元NE再摄取的拮抗剂)导致氧化电流和收缩反应均增加。这些结果,加上内源性NE的流体动力学伏安E_(1/2)与标准溶液相同,证实了氧化电流是由NE引起的,并且该化合物至少部分地引起了氧化。收缩反应。结果表明,使用钻石微电极对NE进行连续的安培监测以及血管紧张度的视频成像可以实时局部测量神经刺激的NE释放与动脉收缩之间的时间关系。

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