Aplysia Ganglia Preparation for Electrophysiological and Molecular Analyses of Single Neurons

被引:6
作者
Akhmedov, Komol [1 ]
Kadakkuzha, Beena M. [1 ]
Puthanveettil, Sathyanarayanan V. [1 ]
机构
[1] Scripps Res Inst, Dept Neurosci, La Jolla, CA 92037 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2014年 / 83期
关键词
Neurobiology; Issue; 83; intracellular recording; identified neuron; neural circuitry; gene expression; action potential; CREB; Aplysia californica; genomics; GILL-WITHDRAWAL REFLEX; RELATING CELLULAR EVENTS; TRITONIA SWIM CPG; LONG-TERM-MEMORY; SENSORY NEURONS; FEEDING-BEHAVIOR; COMMAND NEURONS; BUCCAL NEURONS; POND SNAIL; MECHANISMS;
D O I
10.3791/51075
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A major challenge in neurobiology is to understand the molecular underpinnings of neural circuitry that govern a specific behavior. Once the specific molecular mechanisms are identified, new therapeutic strategies can be developed to treat abnormalities in specific behaviors caused by degenerative diseases or aging of the nervous system. The marine snail Aplysia californica is well suited for the investigations of cellular and molecular basis of behavior because neural circuitry underlying a specific behavior could be easily determined and the individual components of the circuitry could be easily manipulated. These advantages of Aplysia have led to several fundamental discoveries of neurobiology of learning and memory. Here we describe a preparation of the Aplysia nervous system for the electrophysiological and molecular analyses of individual neurons. Briefly, ganglion dissected from the nervous system is exposed to protease to remove the ganglion sheath such that neurons are exposed but retain neuronal activity as in the intact animal. This preparation is used to carry out electrophysiological measurements of single or multiple neurons. Importantly, following the recording using a simple methodology, the neurons could be isolated directly from the ganglia for gene expression analysis. These protocols were used to carry out simultaneous electrophysiological recordings from L7 and R15 neurons, study their response to acetylcholine and quantitating expression of CREB1 gene in isolated single L7, L11, R15, and R2 neurons of Aplysia.
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页数:9
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