Pei X, Volgushev M, Vidyasagar T R, Creutzfeldt O D
Dept. of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, Göttingen-Nikolausberg, Germany.
Neuroreport. 1991 Aug;2(8):485-8. doi: 10.1097/00001756-199108000-00019.
Long and stable recordings of post-synaptic, action and membrane potentials from visual cortical neurons in-vivo, are possible with the patch-clamp technique. These are comparable to the whole-cell configuration, but with an incomplete seal. EPSPs and IPSPs of normal time course and up to several mV can be recorded. DC potentials ranged from - 30 to - 60 mV and input resistances from 50 to 150 M omega. Injected currents have the same effect as if applied intracellularly. Membrane conductance after electrical stimulation of the lateral geniculate nucleus is increased during the first 20 ms, but decreases from 60 to about 130 ms, during return of the membrane potential to its resting level. The recording method is compared to other intracellular recording techniques in-vivo and in-vitro.
采用膜片钳技术可以在体内对视觉皮层神经元的突触后电位、动作电位和膜电位进行长时间稳定的记录。这些记录与全细胞配置相当,但封接并不完全。可以记录到正常时程且幅度高达数毫伏的兴奋性突触后电位(EPSP)和抑制性突触后电位(IPSP)。直流电位范围为 -30至 -60毫伏,输入电阻为50至150兆欧。注入电流的效果与细胞内施加时相同。在外侧膝状体核受到电刺激后,膜电导在最初20毫秒内增加,但在膜电位恢复到静息水平的过程中,从60毫秒到约130毫秒会降低。将该记录方法与体内和体外的其他细胞内记录技术进行了比较。