Cai Ying, Tang He, Jiang Fan, Dong Zhaojun
Institute of Toxicology, College of Preventive Medicine, Third Military Medical University, Chongqing, China.
J Neurogastroenterol Motil. 2017 Jan 30;23(1):117-123. doi: 10.5056/jnm16012.
BACKGROUND/AIMS: Myenteric plexus interstitial cells of Cajal (ICC-MY) are involved in the generation of gut pacemaker activity and neuronal communication. We performed patch clamp on ICC-MY in situ to observe the changes of pacemaker activity in response to neural modulations.
A fresh longitudinal muscle with myenteric plexus (LMMP) from mouse jejunum was prepared. ICC-MY and ganglion neurons embedded in the layer of longitudinal muscles were targeted by patch clamping in whole-cell configuration in a model of current or voltage clamp. Neurogenic modulators were applied to evaluate their effects on ICC pacemaker activity.
In situ ICC-MY showed spontaneous and rhythmical voltage oscillations with a frequency of 27.2 ± 3.9 cycles/min, amplitude of 32.6 ± 6.3 mV, and resting membrane potential of -62.2 ± 2.8 mV. In situ neurons showed electrically evocable action potential in single or multiple spikes. Pacemaker activity was modulated by neuronal activators through receiving a neuronal input. Application of tetrodotoxin depolarized pacemaker potentials in a dose dependent manner, and decreased the amplitude at tetrodotoxin 0.3 μM for about 40 ± 10%; capsaicin (1 μM) ameliorated ICC-MY K⁺ current for about 49 ± 14.8%; and, nitric oxide hyperpolarized pacemaker potential and decreased the amplitude and frequency.
The in situ preparation patch clamp study further demonstrates that the pacemaker activity is an intrinsic property of ICC. The neurogenic activators change and shape pacemaker potential and activity in situ. LMMP preparation in situ patch clamp provides an ideal platform to study the functional innervation of the ICC and the enteric neural system, thereby, for evaluating the neural regulation of pacemaker activity, especially in disorder models.
背景/目的:肌间神经丛的Cajal间质细胞(ICC-MY)参与肠道起搏活动的产生和神经元通讯。我们对原位ICC-MY进行膜片钳实验,以观察其起搏活动在神经调节下的变化。
制备小鼠空肠含肌间神经丛的新鲜纵行肌(LMMP)。在电流或电压钳模式下,采用全细胞记录模式对纵行肌层中的ICC-MY和神经节神经元进行膜片钳记录。应用神经源性调节剂评估其对ICC起搏活动的影响。
原位ICC-MY表现出自发性、节律性电压振荡,频率为27.2±3.9次/分钟,振幅为32.6±6.3 mV,静息膜电位为-62.2±2.8 mV。原位神经元表现出电诱发的单个或多个峰动作电位。起搏活动通过接收神经元输入受到神经元激活剂的调节。应用河豚毒素使起搏电位呈剂量依赖性去极化,在0.3 μM河豚毒素时振幅降低约40±10%;辣椒素(1 μM)使ICC-MY钾电流改善约49±14.8%;一氧化氮使起搏电位超极化并降低振幅和频率。
原位膜片钳研究进一步证明起搏活动是ICC的内在特性。神经源性激活剂可改变并塑造原位起搏电位和活动。原位LMMP制备的膜片钳为研究ICC和肠神经系统的功能神经支配提供了理想平台,从而用于评估起搏活动的神经调节,尤其是在疾病模型中。