Nicholas P. Franks, FRCA, FMedSci.

Professor of Biophysics and Anaesthetics,
Head of Division of Cell and Molecular Biology,
Head of Biophysics Section,
Blackett Laboratory,
Imperial College London
SW7 2AZ, U.K.
Tel: 020-7594-7629 Fax: 020-7589-0191

My publications

Other group members

Research Opportunities

UG/PG Teaching

My Research Interests

Neuronal pathways of sleep and anaesthesia

sleep spindles in the neocortex

The sleeping brain is similar, in many ways, to the brain following anaesthetic-induced loss of consciousness, and we are following the hypothesis that the same neuronal pathways may be involved. In this work we are hoping to identify which neuronal pathways and brain regions are responsible. The figure shows anaesthetic-induced spindles in the EEG just prior to loss of consciousness, which closely resemble the sleep spindles that occur during the early stages of natural sleep.

Two-pore-domain potassium channels in general anaesthesia

Halothane induced theta oscillations

For many years our group has been interested in the possible role that anaesthetic-activated potassium channels play in general anaesthesia. These channels are members of the two-pore-domain potassium channel family which are believed to regulate baseline neuronal excitability. Some members of this family are activated by inhalational anaesthetics. The figure shows a neuronal oscillation at theta frequencies (about 6 Hz) that is triggered by an anaesthetic (halothane) and is dependent upon one of these potassium channels (TASK-3). .

Mechanisms of xenon anaesthesia and neuroprotection

The inert gas xenon is an effective general anaesthetic and may prove to be clinically useful as a neuroprotectant. We have identified both two-pore-domain potassium channels (such as TREK-1) and NMDA receptors as possible molecular targets and we are exploring the molecular and cellular mechanisms that underlie xenon's actions. The figure illustrates xenon atoms within the glycine binding site on the NMDA receptor, the site we believe is responsible, at least in part, for xenon's neuroprotection.

The use of photolabels to identify anaesthetic binding sites

A long-term project in the group has been the synthesis and use of photolabelled general anaesthetics. The aim here is to synthesise analogues of general anaesthetics that maintain their normal pharmacology, but carry photoactivatable groups which react irreversibly to the molecular targets following irradiation. The figure shows the positions of two binding sites for etomidate on the plasma protein human serum albumin, which were identified using the analogue, acyl azide etomidate.

Related links
Anaesthetics and Neuronal Excitability | Biophysics Section | Department of Life Sciences | Imperial College London

November 2009