It is proposed to investigate, on a molecular scale, whether nerve block by general anesthetics is a consequence of a multi-mechanistic mode of anesthetic action. Single sodium channels from the central nervous system will be used to infer the extent of any simultaneous involvement of several, and different anesthetic interactions: hydrogen bonding, bilayer thickness and surface tension, interfacial potentials and membrane fluidity, etc. Sodium channels from canine forebrain synaptosomes will be incorporated into lipid bilayer membranes following procedures first described by Krueger et al. (1983). Currents through individual sodium channels will be examined in the presence of general anesthetic agents with systematically varied molecular structure. The composition and the physico-chemical properties of lipid bilayer membranes will be varied, such that it should be possible to estimate the extent to which the membrane environment, and particularly the anesthetic modified bilayer, can influence sodium channel function. Halogenated ethers and alcohol derivatives will be examined in order to establish whether the ability of an anesthetic molecule to form hydrogen bonds plays an important role in the spectrum of anesthetic interactions. Anesthetic responses of the central nervous system sodium channels will be compared with those of previously studied sodium channels from the peripheral nervous system. The comparisons will establish the extent to which the extensive data base regarding anesthetic actions on peripheral sodium channels is applicable to CNS sodium channels. It should thus become possible to determine whether different sodium channels vary in their anesthetic responses. Information will likewise be gained on the influence of an anesthetic-modified membrane environment on sodium channel function. The proposed studies will consequently address the question of the relative importance of direct interactions between membrane proteins and anesthetics as opposed to indirect interactions mediated via the lipid bilayer environment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS022602-03
Application #
3405208
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1985-09-09
Project End
1989-03-31
Budget Start
1987-09-01
Budget End
1989-03-31
Support Year
3
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
Schools of Medicine
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Frenkel, C; Wartenberg, H C; Duch, D S et al. (1998) Steady-state properties of sodium channels from healthy and tumorous human brain. Brain Res Mol Brain Res 59:22-34
Urban, B W (1994) [Mechanisms of action of narcotics on various levels of the central nervous system] Klin Anasthesiol Intensivther 46:277-92
Frenkel, C; Duch, D S; Urban, B W (1993) Effects of i.v. anaesthetics on human brain sodium channels. Br J Anaesth 71:15-24
Urban, B W (1993) Differential effects of gaseous and volatile anaesthetics on sodium and potassium channels. Br J Anaesth 71:25-38
Frenkel, C; Urban, B W (1992) [The molecular action profile of intravenous anesthetics] Anasthesiol Intensivmed Notfallmed Schmerzther 27:101-8
Frenkel, C; Urban, B W (1992) Molecular actions of racemic ketamine on human CNS sodium channels. Br J Anaesth 69:292-7
Urban, B W; Frenkel, C; Duch, D S et al. (1991) Molecular models of anesthetic action on sodium channels, including those from human brain. Ann N Y Acad Sci 625:327-43
Frenkel, C; Urban, B W (1991) Human brain sodium channels as one of the molecular target sites for the new intravenous anaesthetic propofol (2,6-diisopropylphenol). Eur J Pharmacol 208:75-9
Recio-Pinto, E; Thornhill, W B; Duch, D S et al. (1990) Neuraminidase treatment modifies the function of electroplax sodium channels in planar lipid bilayers. Neuron 5:675-84
Levinson, S R; Thornhill, W B; Duch, D S et al. (1990) The role of nonprotein domains in the function and synthesis of voltage-gated sodium channels. Ion Channels 2:33-64

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