2-deoxyglucose method

This is an experimental demo page. A more comprehensive demonstration of the usefulness of the 2-deoxyglucose method will be installed in due time.

Principle of the method: Radioactive 2-deoxyglucose is taken up by active neurons via the glucose transporter, yet not metabolized. Radioactivity accumulates in active cells. Specimen are freeze dried, sectioned and activity is subsequently recorded by autoradiography. Neuronal activity depends on previous stimulus conditions, see example below:


Unilateral stimulation of tethered flies in two small neighbouring windows with moving stimuli.

overview, click for magnification

Note that radioactivity has accumulated on the stimulated side only. Boxed area is enlarged and analysed below.


click for magnification

The two neighbouring visual fields stimulated are clearly reflected in the retinotopic arrays of the optic lobe labelled by 2-deoxyglucose. The boxed area has been used to produce the activity profile shown as insert. Note that layers 1, 5 and 9,10 of the medulla are strongly movement sensitive. Compare 2-deoxyglucose staining pattern with Golgi-shapes of L1- and Mi1-neurons (links will be established).


Data from Bernhard Bausenwein

Literature

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