Sucrose gap
Sucrose gap is a technique used in neurophysiology to study the electrical properties of excitable cells such as neurons and muscle cells. This technique involves replacing a portion of the extracellular fluid surrounding the cell with a solution of sucrose, which is a non-conducting substance. This creates a "gap" in the electrical conductivity around the cell, allowing researchers to measure changes in the cell's membrane potential.
History[edit | edit source]
The sucrose gap technique was first developed in the 1960s as a way to study the electrical properties of excitable cells. It has since been used in a wide range of research studies, including investigations into the mechanisms of action potentials, the properties of ion channels, and the effects of various drugs on cellular excitability.
Technique[edit | edit source]
In a typical sucrose gap experiment, a cell or tissue sample is placed in a chamber filled with an electrolyte solution. A portion of this solution is then replaced with a solution of sucrose, creating a "gap" in the electrical conductivity around the cell. Electrodes are placed on either side of the sucrose gap, allowing researchers to measure changes in the cell's membrane potential.
The sucrose gap technique has several advantages over other methods of studying cellular excitability. For example, it allows for the direct measurement of membrane potential changes, rather than relying on indirect methods such as voltage clamp or patch clamp techniques. It also allows for the study of cells in their natural, intact state, rather than requiring them to be broken apart or otherwise manipulated.
Applications[edit | edit source]
The sucrose gap technique has been used in a wide range of research studies. For example, it has been used to investigate the mechanisms of action potentials, the properties of ion channels, and the effects of various drugs on cellular excitability. It has also been used to study the electrical properties of various types of cells, including neurons, muscle cells, and cardiac cells.
See also[edit | edit source]
References[edit | edit source]
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