School of Biomedical Sciences and Pharmacy, Faculty of Health and Hunter Medical Research Institute, The University of Newcastle, Callaghan, NSW 2308, Australia.
J Neurosci Methods. 2011 Sep 15;200(2):113-20. doi: 10.1016/j.jneumeth.2011.06.017. Epub 2011 Jun 24.
In spinal cord injury (SCI) research, axon regeneration across spinal lesions is most often assessed using anatomical methods. It would be extremely advantageous, however, to examine the functional synaptic connectivity of regenerating fibres, using high-resolution electrophysiological methods. We have therefore developed a mouse horizontal spinal cord slice preparation that permits detailed analysis of evoked dorsal column (DCol) synaptic inputs on spinal neurons, using whole-cell patch clamp electrophysiology. This preparation allows us to characterise postsynaptic currents and potentials in response to electrical stimulation of DCol fibres, along with the intrinsic properties of spinal neurons. In addition, we demonstrate that low magnification calcium imaging can be used effectively to survey the spread of excitation from DCol stimulation in horizontal slices. This preparation is a potentially valuable tool for SCI research where confirmation of regenerated, functional synapses across a spinal lesion is critical.
在脊髓损伤 (SCI) 研究中,通常使用解剖学方法评估脊髓损伤部位的轴突再生。然而,如果能够使用高分辨率电生理学方法来检测再生纤维的功能性突触连接,那将是非常有利的。因此,我们开发了一种小鼠水平脊髓切片制备方法,该方法允许使用全细胞膜片钳电生理学技术对脊髓神经元上诱发性背柱 (DCol) 突触输入进行详细分析。该制备方法使我们能够描述对 DCol 纤维电刺激的突触后电流和电位,以及脊髓神经元的固有特性。此外,我们证明低倍钙成像可以有效地用于调查水平切片中 DCol 刺激引起的兴奋的传播。该制备方法是 SCI 研究中的一种有潜力的工具,在 SCI 研究中,确认脊髓损伤部位的再生功能性突触至关重要。