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通过轴突追踪技术鉴定的自主神经和传入神经元亚群的膜片钳记录。

Patch-clamp recordings from subpopulations of autonomic and afferent neurons identified by axonal tracing techniques.

作者信息

Yoshimura N, White G, Weight F F, de Groat W C

机构信息

Department of Pharmacology, School of Medicine, University of Pittsburgh, PA 15261.

出版信息

J Auton Nerv Syst. 1994 Sep;49(1):85-92. doi: 10.1016/0165-1838(94)90024-8.

Abstract

This study determined whether axonal tracing methods can be used in combination with patch-clamp techniques to examine the electrical properties of identified populations of autonomic and afferent neurons in the adult rat. Fluorescent dyes (Fast Blue, FB and Fluoro-Gold, FG) were injected into the wall of the urinary bladder or colon and into various somatic structures to label postganglionic neurons in the major pelvic ganglia (MPG) as well as visceral and somatic afferent neurons in the lumbosacral dorsal root ganglia (DRG) and trigeminal ganglia (TG). One to 3 weeks after dye injection, neurons were isolated from ganglia by enzymatic dissociation. Following dissociation, single neurons labelled with FB were identified in the three types of ganglion preparations; however FG was only identified consistently in TG neurons. FB was retained in neurons during short-term culture (1-5 days). Following 10 to 20 s exposure to UV light which was required for identification of the cells, whole-cell patch-clamp recordings revealed that the electrophysiological properties of FB-labelled cells did not differ from those of unlabelled cells. However, a more prolonged exposure (1-5 min) of the neurons to UV light produced irreversible damage to the cells which was evident as changes in the action potential, sodium current and resting membrane potential. These results indicate that patch-clamp recording in combination with axonal tracing is a useful approach for studying the electrical properties of identified populations of autonomic and afferent neurons.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究确定了轴突示踪方法是否可与膜片钳技术联合使用,以检测成年大鼠中已识别的自主神经元和传入神经元群体的电特性。将荧光染料(快蓝,FB和荧光金,FG)注入膀胱壁或结肠壁以及各种躯体结构中,以标记主要盆神经节(MPG)中的节后神经元以及腰骶背根神经节(DRG)和三叉神经节(TG)中的内脏和躯体传入神经元。染料注射后1至3周,通过酶解从神经节中分离出神经元。解离后,在三种神经节制剂中均鉴定出用FB标记的单个神经元;然而,FG仅在TG神经元中持续被识别。FB在短期培养(1-5天)期间保留在神经元中。在暴露于用于识别细胞所需的紫外光10至20秒后,全细胞膜片钳记录显示,FB标记细胞的电生理特性与未标记细胞的电生理特性没有差异。然而,神经元更长时间(1-5分钟)暴露于紫外光会对细胞产生不可逆的损伤,这在动作电位、钠电流和静息膜电位的变化中很明显。这些结果表明,膜片钳记录与轴突示踪相结合是研究已识别的自主神经元和传入神经元群体电特性的一种有用方法。(摘要截断于250字)

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