Lecture 1: In Vitro Electrophysiology Of The NS Flashcards

1
Q

Why are electrophysiology rigs not usually on the top floor of a building?

A

Tops of buildings move in the wind, this throws the calibration off.

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2
Q

Why are hippocampal slices often used for electrophysiology?

A

The hippocampus has very clearly laid out cells and it is easier to get your bearings than in other brain areas.

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3
Q

Why is it important to measure the fibre volley in relation to the EPSP?

A

To ensure that plasticity is actually occurring, not just a change in stimulus.

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4
Q

Why is sodium chloride often put into the recording electrode? Why must precautions be taken with it?

A

It conducts really well. Must ensure it doesn’t leak out though as it can interfere with or kill the neuronal slice.

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5
Q

Where does a sharp electrode record from?

A

The inside of the cell.

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6
Q

For a cell-attached recording, why is positive pressure applied to the pipette whilst setting it up?

A

Positive pressure stops gunk entering pipette, the pipette can measure resistance, when resistance increases due to contact with the membrane, positive pressure released causing a slight suction so that the membrane is sucked into the pipette, enabling the pipette to clamp on.

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7
Q

In inside out recording, what happens when you retract the patch clamp slightly and expose it to air?

A

This causes the membrane to break and the desired membrane piece to stay in the clamp, often including an ion channel for study.

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8
Q

For whole cell recording, what causes the hole in the membrane within the pipette clamp?

A

Strong pulse of suction from within the pipette that makes a hole in the clamped part of membrane.

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9
Q

Is potential quoted as outside vs inside or inside vs outside?

A

Inside vs outside

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10
Q

Are extracellular or intracellular voltages recorded in microvolts or millivolts?

A

Extracellular - microvolts

Intracellular - millivolts

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