Hirst G D S, Bywater R A R, Teramoto N, Edwards F R
Division of Neuroscience, John Curtin School of Medical Research, Australian National University, Canberra, ACT, Australia.
J Physiol. 2004 Aug 1;558(Pt 3):841-55. doi: 10.1113/jphysiol.2004.065052. Epub 2004 Jun 11.
Intracellular recordings were made from either sheets or isolated bundles of the circular muscle layer of guinea-pig proximal colon and the responses evoked by stimulating inhibitory nerve fibres were analysed. Inhibitory junction potentials (IJPs), evoked by single stimuli, had two components which could be separated on their pharmacological and temporal characteristics and their voltage sensitivities. The initial component, which was abolished by apamin and reduced in amplitude by pyridoxalphosphate-6-azophenyl-2',4'-disulphonic acid (PPADS), had a brief time course: its amplitude was changed when the external concentration of potassium ions (K+) was changed. The second component of the IJP had a slower onset than the first component, was abolished by l-nitroarginine (NOLA) and oxadiazolo quinoxalin-1-one (ODQ), an inhibitor of soluble guanylate cyclase: its amplitude was little affected by changing K+ and was increased when the membrane potential of the circular layer was hyperpolarized. The observations suggest that the initial component of the IJP results from the release of ATP which triggers an increase in membrane conductance to K+ and that the second component results from the release of nitric oxide which suppresses a background inward current.
采用细胞内记录法,从豚鼠近端结肠环行肌层的薄片或分离束状组织进行记录,并分析刺激抑制性神经纤维所诱发的反应。由单个刺激诱发的抑制性接头电位(IJPs)有两个成分,可根据其药理学和时间特性以及电压敏感性进行分离。初始成分可被蜂毒明肽消除,且其幅度可被磷酸吡哆醛 -6-偶氮苯 -2',4'-二磺酸(PPADS)降低,其时程短暂:当细胞外钾离子浓度(K⁺)改变时,其幅度也会改变。IJP的第二个成分比第一个成分起始更慢,可被L - 硝基精氨酸(NOLA)和氧化二氮喹喔啉 -1-酮(ODQ,一种可溶性鸟苷酸环化酶抑制剂)消除:其幅度受K⁺变化影响较小,且当环行层膜电位超极化时其幅度增加。这些观察结果表明,IJP的初始成分是由ATP释放引起的,ATP触发了膜对K⁺的电导增加,而第二个成分是由一氧化氮释放引起的,一氧化氮抑制了背景内向电流。