В этом видео показано, как применять проводимости в дофаминергических нейронов, записанные в целом конфигурации клетки в срезах мозга крыс. Эта техника называется динамическим зажимом.
Neuroscientists study the function of the brain by investigating how neurons in the brain communicate. Many investigators look at changes in the electrical activity of one or more neurons in response to an experimentally-controlled input. The electrical activity of neurons can be recorded in isolated brain slices using patch clamp techniques with glass micropipettes. Traditionally, experimenters can mimic neuronal input by direct injection of current through the pipette, electrical stimulation of the other cells or remaining axonal connections in the slice, or pharmacological manipulation by receptors located on the neuronal membrane of the recorded cell.
Direct current injection has the advantages of passing a predetermined current waveform with high temporal precision at the site of the recording (usually the soma). However, it does not change the resistance of the neuronal membrane as no ion channels are physically opened. Current injection usually employs rectangular pulses and thus does not model the kinetics of ion channels. Finally, current injection cannot mimic the chemical changes in the cell that occurs with the opening of ion channels.
Receptors can be physically activated by electrical or pharmacological stimulation. The experimenter has good temporal precision of receptor activation with electrical stimulation of the slice. However, there is limited spatial precision of receptor activation and the exact nature of what is activated upon stimulation is unknown. This latter problem can be partially alleviated by specific pharmacological agents. Unfortunately, the time course of activation of pharmacological agents is typically slow and the spatial precision of inputs onto the recorded cell is unknown.
The dynamic clamp technique allows an experimenter to change the current passed directly into the cell based on real-time feedback of the membrane potential of the cell (Robinson and Kawai 1993, Sharp et al., 1993a,b; for review, see Prinz et al. 2004). This allows an experimenter to mimic the electrical changes that occur at the site of the recording in response to activation of a receptor. Real-time changes in applied current are determined by a mathematical equation implemented in hardware.
We have recently used the dynamic clamp technique to investigate the generation of bursts of action potentials by phasic activation of NMDA receptors in dopaminergic neurons of the substantia nigra pars compacta (Deister et al., 2009; Lobb et al., 2010). In this video, we demonstrate the procedures needed to apply a NMDA receptor conductance into a dopaminergic neuron.
Динамический метод зажима продемонстрировали здесь улучшает традиционную технику постоянного тока инъекции, позволяя экспериментатором, чтобы имитировать электрических эффектов активации рецептора. В этом видео, мы показали, что можно добавить эффекты активации NMDA-рецепторов к спонтанной активности дофаминергических нейронов, то есть взрыв потенциалов действия вызываются.
Благодаря гибкости аппаратной / программной реализации, различные расширения могут быть использованы. Знак вводится ток может быть включен с отрицательного на положительный, что составляет сценарий, при котором эффекты активированного рецептора удаляется из нейрона. Модель нейронов, представить в виде серии дифференциальных уравнений, также может быть решена численно и позволяет экспериментатору для исследования малых сетей.
The authors have nothing to disclose.
Эта работа была поддержана MH084494 (CJL), а MH079276 и NS060658 (CAP).
Material Name | Type | Company | Catalogue Number | Comment |
---|---|---|---|---|
K-gluconate anhydrous | Reagent | Sigma-Aldrich | ||
HEPES | Reagent | Fisher Scientific | ||
CaCl2 X 2H2O | Reagent | Fisher Scientific | ||
Ethylene glycol-bis(B-aminoethyl ether)-N,N,N’,N’-tetraacetic acid | Reagent | EGTA; Sigma-Aldrich | ||
MgATP | Reagent | MP Biomedicals | ||
NaGTP | Reagent | MP Biomedicals | ||
MgCl2 | Reagent | Sigma-Aldrich | ||
NaHCO3 | Reagent | Sigma-Aldrich | ||
KCl | Reagent | Fisher Scientific | ||
NaH2PO4, Anhydrous | Reagent | Fisher Scientific | ||
Glucose | Reagent | Acros Organics | ||
NaCl | Reagent | Fisher Scientific | ||
CholCl | Reagent | Sigma-Aldrich | ||
Sodium Pyruvate | Reagent | Fisher Scientific | ||
Ascorbic Acid | Reagent | Acros Organics | ||
Glutathione | Reagent | Sigma-Aldrich | ||
Olympus BX51WI Microscope (with 40x objective) | Microscope | Olympus | ||
2 A/D converters | Equipment | e.g. Heka Instruments Inc. ITC-18, National Instruments BNC-2090A | ||
Multiclamp 700B with CV-7B headstage | Equipment | Molecular Devices | ||
P-97 Flaming/Brown Micropipette Puller | Equipment | Sutter Instrument Company | ||
Microfil syringe needles | Equipment | World Precision Instruments | ||
Micromanipulator | Equipment | Siskiyou, Inc. | ||
Monitor | Equipment | Triview |