Theories of general anaesthetic action


A general anaesthetic is a drug that brings about a reversible loss of consciousness. These drugs are generally administered by an anaesthetist/anesthesiologist in order to induce or maintain general anaesthesia to facilitate surgery.
General anaesthetics have been widely used in surgery since 1842 when Crawford Long for the first time administered diethyl ether to a patient and performed a painless operation. It has long been believed that general anaesthetics exert their effects by modulating the activity of membrane proteins in the neuronal membrane. However, the exact location and mechanism of this action are still largely unknown although much research has been done in this area. There are a number of theories, both outdated and modern, that attempt to explain anaesthetic action.
The concept of specific interactions between receptors and drugs first introduced by Paul Ehrlich states that drugs act only when they are bound to their targets. However, this concept does not seem to apply in the case of general anaesthetics because:
All these common features of general anaesthetics made it hard for early researchers to believe that general anaesthetics act in a specific manner and their action on neuronal membrane was thought to be global rather than through specific sites.

Lipid solubility-anaesthetic potency correlation (the Meyer-Overton correlation)

The nonspecific mechanism of general anaesthetic action was first proposed by Von Bibra and Harless in 1847.
They suggested that general anaesthetics may act by dissolving in the fatty fraction of brain cells and removing fatty constituents from them, thus changing activity of brain cells and inducing anaesthesia. In 1899 Hans Horst Meyer published the first experimental evidence of the fact that anaesthetic potency is related to lipid solubility in his article entitled "Zur Theorie der Alkoholnarkose". Two years later a similar theory was published independently by Overton.
Meyer compared the potency of many agents, defined as the reciprocal of the molar concentration required to induce anaesthesia in tadpoles, with their olive oil/water partition coefficient. He found a nearly linear relationship between potency and the partition coefficient for many types of anaesthetic molecules such as alcohols, aldehydes, ketones, ethers, and esters.
The anaesthetic concentration required to induce anaesthesia in 50% of a population of animals was independent of the means by which the anaesthetic was delivered, i.e., the gas or aqueous phase.
Meyer and Overton had discovered the striking correlation between the physical properties of general anaesthetic molecules and their potency: the greater the lipid solubility of the compound in olive oil the greater is its anaesthetic potency. This correlation is true for a wide range of anaesthetics with lipid solubilities ranging over 4-5 orders of magnitude if olive oil is used as the oil phase. However, this correlation can be improved considerably in terms of both the quality of the correlation and the increased range of anaesthetics if bulk octanol or a fully hydrated fluid lipid bilayer is used as the “oil” phase. It was noted also that volatile anaesthetics are additive in their effects.

Outdated lipid hypotheses of general anaesthetic action

From the correlation between lipid solubility and anaesthetic potency, both Meyer and Overton had surmised a unitary mechanism of general anaesthesia. They assumed that solubilization of lipophilic general anaesthetic in lipid bilayer of the neuron causes its malfunction and anaesthetic effect when critical concentration of anaesthetic is reached. Later in 1973 Miller and Smith suggested the critical volume hypothesis also called lipid bilayer expansion hypothesis.
They assumed that bulky and hydrophobic anaesthetic molecules accumulate inside the hydrophobic regions of neuronal lipid membrane causing its distortion and expansion due to volume displacement. Accumulation of critical amounts of anaesthetic causes membrane thickening sufficient to reversibly alter function of membrane ion channels thus providing anaesthetic effect. Actual chemical structure of the anaesthetic agent per se is not important, but its molecular volume plays the major role: the more space within membrane is occupied by anaesthetic - the greater is the anaesthetic effect.
Based on this theory, in 1954 Mullins suggested that the Meyer-Overton correlation with potency can be improved if molecular volumes of anaesthetic molecules are taken into account. This theory existed for over 60 years and was supported by experimental fact that increases in atmospheric pressure reverse anaesthetic effect.
Then other theories of anaesthetic action emerged mostly ‘physicochemical’ theories that took into account the diverse chemical nature of general anaesthetics and suggested that anaesthetic effect is exerted through some perturbation of the lipid bilayer. Several types of bilayer perturbations were proposed to cause anaesthetic effect :
According to the lateral phase separation theory anaesthetics exert their action by fluidizing nerve membranes to a point when phase separations in the critical lipid regions disappear. This anaesthetic-induced fluidization makes membranes less able to facilitate the conformational changes in proteins that may be the basis for such membrane events as ion gating, synaptic transmitter release, and transmitter binding to receptors.
All these outdated lipid theories generally suffer from four weaknesses :
Therefore, the correlation between lipid solubility and potency of general anaesthetics is a necessary but not sufficient condition for inferring a lipid target site. General anaesthetics could equally well be binding to hydrophobic target sites on proteins in the brain. The main reason that more polar general anaesthetics are less potent is that they have to cross the blood–brain barrier to exert their effect on neurons in the brain.

Objections to the outdated lipid hypotheses

1. Stereoisomers of an anaesthetic drug

Stereoisomers that represent mirror images of each other are termed enantiomers or optical isomers - and S-.
Physicochemical effects of enantiomers are always identical in an achiral environment. However, in vivo enantiomers of many general anaesthetics can differ greatly in their anaesthetic potency despite the similar oil/gas partition coefficients. For example, the R- isomer of etomidate is 10 times more potent anaesthetic than its S- isomer. This means that optical isomers partition identically into lipid, but have differential effects on ion channels and synaptic transmission. This objection provides a compelling evidence that the primary target for anaesthetics is not the achiral lipid bilayer itself but rather stereoselective binding sites on membrane proteins that provide a chiral environment for specific anaesthetic-protein docking interactions.

2. Nonimmobilizers

All general anaesthetics induce immobilization through depression of spinal cord functions, whereas their amnesic actions are exerted within the brain. According to the Meyer-Overton correlation the anaesthetic potency of the drug is directly proportional to its lipid solubility, however, there are many compounds that do not satisfy this rule. These drugs are strikingly similar to potent general anaesthetics and are predicted to be potent anaesthetics based on their lipid solubility, but they exert only one constituent of the anaesthetic action and do not suppress movement as all anaesthetics do. These drugs are referred to as nonimmobilizers. The existence of nonimmobilizers suggests that anaesthetics induce different components of anaesthetic effect by affecting different molecular targets and not just the one target as it was believed earlier. Good example of non-immobilizers are halogenated alkanes that are very hydrophobic, but fail to suppress movement in response to noxious stimulation at appropriate concentrations. See also: flurothyl.

3. Temperature increases do not have anaesthetic effect

Experimental studies have shown that general anaesthetics including ethanol are potent fluidizers of natural and artificial membranes. However, changes in membrane density and fluidity in the presence of clinical concentrations of general anaesthetics are so small that relatively small increases in temperature can mimic them without causing anaesthesia. The change in body temperature of approximately 1 °C is within the physiological range and clearly it is not sufficient to induce loss of consciousness per se. Thus membranes are fluidized only by large quantities of anaesthetics, but there are no changes in membrane fluidity when concentrations of anaesthetics are small and restricted to pharmacologically relevant.

4. Effect vanishes beyond a certain chain length

According to the Meyer-Overton correlation, in a homologous series of any general anaesthetic, increasing the chain length increases the lipid solubility, and thereby should produce a corresponding increase in anaesthetic potency. However, beyond a certain chain length the anaesthetic effect disappears. For the n-alcohols, this cutoff occurs at a carbon chain length of about 13 and for the n-alkanes at a chain length of between 6 and 10, depending on the species.
If general anaesthetics disrupt ion channels by partitioning into and perturbing the lipid bilayer, then one would expect that their solubility in lipid bilayers would also display the cutoff effect. However, partitioning of alcohols into lipid bilayers does not display a cutoff for long-chain alcohols from n-decanol to n-pentadecanol. A plot of chain length vs. the logarithm of the lipid bilayer/buffer partition coefficient K is linear, with the addition of each methylene group causing a change in the Gibbs free energy of -3.63 kJ/mol.
The cutoff effect was first interpreted as evidence that anaesthetics exert their effect not by acting globally on membrane lipids but rather by binding directly to hydrophobic pockets of well-defined volumes in proteins. As the alkyl chain grows, the anaesthetic fills more of the hydrophobic pocket and binds with greater affinity. When the molecule is too large to be entirely accommodated by the hydrophobic pocket, the binding affinity no longer increases with increasing chain length. Thus the volume of the n-alkanol chain at the cutoff length provides an estimate of the binding site volume. This objection provided the basis for protein hypothesis of anaesthetic effect.
However, cutoff effect can still be explained in the frame of lipid hypothesis. In short-chain alkanols segments of the chain are rather rigid and very close to hydroxyl group tethered to aqueous interfacial region. Consequently, these segments efficiently redistribute lateral stresses from the bilayer interior toward the interface. In long-chain alkanols hydrocarbon chain segments are located further from hydroxyl group and are more flexible than in short-chain alkanols. Efficiency of pressure redistribution decreases as the length of hydrocarbon chain increases until anaesthetic potency is lost at some point. It was proposed that polyalkanols will have anaesthetic effect similar to short-chain 1-alkanols if the chain length between two neighbouring hydroxyl groups is smaller than the cutoff. This idea was supported by the experimental evidence because polyhydroxyalkanes 1,6,11,16-hexadecanetetraol and 2,7,12,17-octadecanetetraol exhibited significant anaesthetic potency as was originally proposed.

Modern lipid hypothesis

The modern version of lipid hypothesis states that anaesthetic effect happens if solubilization of general anaesthetic in the bilayer causes a redistribution of membrane lateral pressures.
Each bilayer membrane has a distinct profile of how lateral pressures are distributed within it. Most membrane proteins are sensitive to changes in this lateral pressure distribution profile. These lateral stresses are rather large and vary with depth within the membrane. According to the modern lipid hypothesis a change in the membrane lateral pressure profile shifts the conformational equilibrium of certain membrane proteins known to be affected by clinical concentrations of anaesthetics such as ligand-gated ion channels. This mechanism is also nonspecific because the potency of the anaesthetic is determined not by its actual chemical structure, but by the positional and orientational distribution of its segments and bonds within the bilayer. However, it is still not obvious what the exact molecular mechanism is.
In 1997, Cantor suggested a detailed mechanism of general anesthesia based on lattice statistical thermodynamics. It was proposed that incorporation of amphiphilic and other interfacially active solutes into the bilayer increases the lateral pressure selectively near the aqueous interfaces, which is compensated by a decrease in lateral pressure toward the centre of the bilayer. Calculations showed that general anaesthesia likely involves inhibition of the opening of the ion channel in a postsynaptic ligand-gated membrane protein by the following mechanism:
Thus, according to the modern lipid hypothesis anaesthetics do not act directly on their membrane protein targets, but rather perturb specialized lipid matrices at the protein-lipid interface, which act as mediators. This is a new kind of transduction mechanism, different from the usual key-lock interaction of ligand and receptor, where the anaesthetic affects the function of membrane proteins by binding to the specific site on the protein. Thus, some membrane proteins are proposed to be sensitive to their lipid environment.
A slightly different detailed molecular mechanism of how bilayer perturbation can influence the ion-channel was proposed in the same year. Oleamide is an endogenous anaesthetic found in vivo and it is known to potentiate sleep and lower the temperature of the body by closing the gap junction channel connexion. The detailed mechanism is shown on the picture: the well-ordered lipid/cholesterol ring that exists around connexon becomes disordered on treatment with anaesthetic, promoting a closure of connexon ion channel. This decreases brain activity and induces lethargy and anaesthetic effect.
Recently super resolution imaging showed direct experimental evidence that volatile anesthetic disrupt the ordered lipid domains as predicted. In the same study, a related mechanism emerged where the anesthetics released the enzyme phospholipase D from lipid domains and the enzyme bound to and activated TREK-1 channel by the production of phosphatidic acid. These results showed experimentally that the membrane is a physiologically relevant target of general anesthetics.

Membrane protein hypothesis of general anaesthetic action

In the early 1980s, Franks and Lieb demonstrated that the Meyer-Overton correlation can be reproduced using a soluble protein. They found that two classes of proteins are inactivated by clinical doses of anaesthetic in the total absence of lipids. These are luciferases, which are used by bioluminescent animals and bacteria to produce light, and cytochrome P450, which is a group of heme proteins that hydroxylate a diverse group of compounds, including fatty acids, steroids, and xenobiotics such as phenobarbital. Remarkably, inhibition of these proteins by general anaesthetics was directly correlated with their anaesthetic potencies. Luciferase inhibition also exhibits a long-chain alcohol cutoff, which is related to the size of the anaesthetic-binding pocket.
These observations were important because they demonstrated that general anaesthetics may also interact with hydrophobic protein sites of certain proteins, rather than affect membrane proteins indirectly through nonspecific interactions with lipid bilayer as mediator.
It was shown that anaesthetics alter the functions of many cytoplasmic signalling proteins, including protein kinase C, however, the proteins considered the most likely molecular targets of anaesthetics are ion channels. According to this theory general anaesthetics are much more selective than in the frame of lipid hypothesis and they bind directly only to small number of targets in CNS mostly ligand-gated ion channels in synapse and G-protein coupled receptors altering their ion flux. Particularly Cys-loop receptors are plausible targets for general anaesthetics that bind at the interface between the subunits. The Cys-loop receptor superfamily includes inhibitory receptors and excitatory receptors. General anaesthetics can inhibit the channel functions of excitatory receptors or potentiate functions of inhibitory receptors, respectively. Although protein targets for anaesthetics have been partly identified the exact nature of general anaesthetic-protein interactions still remains a mystery.
It was initially hypothesized that general anaesthetic binds to its target ion channel by a key-lock mechanism and changes its structure dramatically from open to closed conformation or vice versa. However, there is a significant amount of evidence against direct key-lock interaction of membrane proteins with general anaesthetics
Various studies have shown that low affinity drugs including inhaled general anaesthetics do not usually interact with their target proteins via specific lock-and-key binding mechanism because they do not change molecular structures of transmembrane receptors, ion channels and globular proteins. Based on these experimental facts and some computer simulations modern version of protein hypothesis was proposed. Proteins of four-α-helix bundle structural motif served as models of monomer of pentameric Cys-loop receptor because binding pockets of inhaled anaesthetics are believed to be within transmembrane four-α-helix bundles of Cys-loop receptors. Inhaled general anaesthetic does not change structure of membrane channel but changes its dynamics especially dynamics in the flexible loops that connect α-helices in a bundle and are exposed to the membrane-water interface. It is a well known fact that dynamics of protein in microsecond-millisecond timescale is often coupled with functions of the protein. Thus it was logical to propose that since inhaled general anaesthetics do not change protein structure they may exert their effect on proteins by modulating protein dynamics in a slow microsecond-millisecond timescale and/or by disrupting the modes of motion essential for function of this protein. Normal interactions between residues in protein regions at the water-lipid interface that play critical roles in protein functions and agonist binding may be disrupted by general anaesthetic. Interactions within the same loop or between different loops may be disrupted by anaesthetics and ultimately functions of Cys-loop receptors may be altered.

Microtubule quantum vibration theory of anesthetic action

Anesthetic gases bind within neuronal membrane proteins, but their effects upon them are inconsistent and paradoxical. In 2008 leading researchers concluded: “…two decades of focused investigation have not identified a ligand- or voltage-gated channel that alone is sufficient to mediate immobility….Furthermore, no combination…seems sufficient…”. But anesthetics also bind and alter functions of cytoplasmic proteins inside neurons, including cytoskeletal actin and tubulin in microtubules. Polymers of tubulin, microtubules direct neuronal growth, regulate synapses, and are theoretically proposed to encode memory and mediate consciousness.  At high concentrations the anesthetic gas halothane causes reversible depolymerization of microtubules. At ~1 MAC halothane, genomic, proteomic, optogenetic and clinical studies point to tubulin/microtubules as the functional site of anesthetic action.
What might anesthetics do to microtubules to cause loss of consciousness? A highly disputed theory put forth in the mid-1990s by Stuart Hameroff and Sir Roger Penrose suggests consciousness is based on quantum vibrations in tubulin/microtubules inside brain neurons. Computer modeling of tubulin’s atomic structure found that anesthetic gas molecules bind adjacent to amino acid aromatic rings of non-polar pi electron resonance clouds, and that collective quantum dipole oscillations among all 86 pi resonance rings in each tubulin showed a spectrum of quantum vibrations with a common mode peak at 613 terahertz. Simulated presence of each of 8 different anesthetic gases, and 2 Non-anesthetic/Non-immobilizer gases showed that all 8 anesthetics dampened tubulin terahertz oscillations proportional to their potency, and abolished the 613 terahertz peak. NAs did not dampen the terahertz spectrum, nor affect the 613 terahertz peak. NAs were found to have significantly higher polarizability than anesthetic gases, implying NA electron cloud dipoles ‘go along for the ride’ without dampening, whereas coupling by less polarizable anesthetics exerts sufficient ‘drag’ to dampen dipole oscillations. Orch OR suggests terahertz oscillations in tubulin are the small, fast end of a scale-invariant multi-level hierarchy which extends upward by resonant interference to slower frequencies seen in EEG, and that anesthetics prevent consciousness at its biological origin, terahertz oscillations in microtubules.
The ‘Microtubule quantum vibration theory’ of anesthetic action is controversial due to several critical flaws in the premise of Orch OR and falsification of data used in support of the theory. Despite these issues, proponents argue that it is consistent with many known criteria of the molecular action of anesthetic gases described above:
Meyer-Overton correlationStereoisomers with different potenciesNon anesthetics/Non immobilizers Temperature lipid bilayer disorderingSize cutoff effectPressure reversal
Membrane lipidsYesNoNoNoNoYes
Membrane proteinsNoYesNoYesYesYes
Microtubule quantum vibrationYesYesYesYesYesYes