Local Anesthetics

Local anesthesia can be defined as loss of sensation in a discrete region of the body caused by disruption of impulse generation or propagation. Local anesthesia can be produced by various chemical and physical means. However, in routine clinical practice, local anesthesia is produced by several compounds whose mechanism of action is similar, although they have different durations of action, and from which recovery is normally spontaneous, predictable, and complete.


Clinical use of local anesthetics began with cocaine in the 1880s. The topically applied local anesthetic benzocaine and the injectable drugs procaine, tetracaine, and chloroprocaine were subsequently developed as adaptations of cocaine’s structure as an amino ester ( Figs. 10.1 and 10.2 ).

Fig. 10.1

Local anesthetics have three portions: (1) lipophilic, (2) hydrophilic, and a connecting (3) hydrocarbon chain. This figure illustrates creative ways of altering this basic structure for desired pharmacologic characteristics (duration of action, cardiovascular).

Fig. 10.2

Chemical structures of ester (i.e., procaine, chloroprocaine, tetracaine, and cocaine) and amide (i.e., lidocaine, mepivacaine, bupivacaine, etidocaine, prilocaine, and ropivacaine) local anesthetics.

In 1948, lidocaine was introduced as the first member of a new class of local anesthetics, the amino amides. Advantages of the amino amides over the earlier amino esters included more stability and a reduced frequency of allergic reactions. Because of these favorable properties, lidocaine became the template for the development of a series of amino-amide anesthetics (see Fig. 10.2 ).

Along with lidocaine, most amino-amide local anesthetics are derived from the aromatic amine xylidine, including mepivacaine, bupivacaine, ropivacaine, and levobupivacaine. Ropivacaine and levobupivacaine share an additional distinctive characteristic: they are single enantiomers rather than racemic mixtures. They are products of a developmental strategy that takes advantage of the differential stereoselectivity of neuronal and cardiac sodium ion channels in an effort to reduce the potential for cardiac toxicity (see “ Adverse Effects ”). Almost all of the amides undergo biotransformation in the liver, whereas the esters undergo hydrolysis in plasma.

Nerve Conduction

Under normal or resting circumstances, the neural membrane is characterized by a negative potential of roughly –90 mV (the potential inside the nerve fiber is negative relative to the extracellular fluid). This negative potential is created by energy-dependent outward transport of sodium and inward transport of potassium ions, combined with greater membrane permeability to potassium ions relative to sodium ions. With excitation of the nerve, there is an increase in the membrane permeability to sodium ions, causing a decrease in the transmembrane potential. If a critical potential is reached (i.e., threshold potential), there is a rapid and self-sustaining influx of sodium ions resulting in a propagating wave of depolarization, the action potential, after which the resting membrane potential is reestablished.

Nerve fibers can be classified according to fiber diameter, presence (type A and B) or absence (type C) of myelin, and function ( Table 10.1 ). The nerve fiber diameter influences conduction velocity; a larger diameter correlates with more rapid nerve conduction. The presence of myelin also increases conduction velocity. This effect results from insulation of the axolemma from the surrounding media, forcing current to flow through periodic interruptions in the myelin sheath (i.e., nodes of Ranvier) ( Fig. 10.3 ).

Table 10.1

Classification of Nerve Fibers

Fiber Diameter (μm) Conduction Velocity (m/sec) Function
Type Subtype
A (myelinated) Alpha 12-20 80-120 Proprioception, large motor
Beta 5-15 35-80 Small motor, touch, pressure
Gamma 3-8 10-35 Muscle tone
Delta 2-5 5-25 Pain, temperature, touch
B (myelinated) 3 5-15 Preganglionic autonomic
C (unmyelinated) 0.3-1.5 0.5-2.5 Dull pain, temperature, touch

Fig. 10.3

Pattern of “local circuit currents” flowing during propagation of an impulse in a nonmyelinated C fiber’s axon (A) and a myelinated axon (B). During propagation of impulses, from left to right, current entering the axon at the initial rising phase of the impulse (large vertical arrows) passes through the axoplasm (local circuit current) and depolarizes the adjacent membrane. Plus and minus signs adjacent to the axon membrane indicate the polarization state of the axon membrane: negative inside at rest, positive inside during active depolarization under the action potential, and less negative in regions where local circuit currents flow. This ionic current passes relatively uniformly across the nonmyelinated axon, but in the myelinated axon it is restricted to entry at the nodes of Ranvier, several of which are simultaneously depolarized during a single action potential.

From Berde CB, Strichartz GR. Local anesthetics. In Miller RD, Cohen NH, Eriksson LI, et al, eds. Miller’s Anesthesia. 8th ed. Philadelphia: Saunders Elsevier; 2015.

Local Anesthetic Actions On Sodium Channels

Local anesthetics act on a wide range of molecular targets, but they exert their predominant desired clinical effects by blocking sodium ion flux through voltage-gated sodium channels. Voltage-gated sodium channels are complex transmembrane proteins comprising large alpha subunits and much smaller beta subunits ( Fig. 10.4 ).

Fig. 10.4

Structural features of the Na + channel that determine local anesthetic (LA) interactions. (A) Consensus arrangement of the single peptide of the Na + channel α-subunit in a plasma membrane. Four domains with homologous sequences (D-1 through D-4) each contain six α-helical segments that span the membrane (S1 to S6). Each domain folds within itself to form one cylindrical bundle of segments, and these bundles converge to form the functional channel’s quaternary structure (B). Activation gating leading to channel opening results from primary movement of the positively charged S4 segments in response to membrane depolarization (see panel C). Fast inactivation of the channel follows binding to the cytoplasmic end of the channel of part of the small loop that connects D-3 to D-4. Ions travel through an open channel along a pore defined at its narrowest dimension by the P region formed by partial membrane penetration of the four extracellular loops of protein connecting S5 and S6 in each domain. Intentional, directed mutations of different amino acids on the channel indicate residues that are involved in LA binding in the inner vestibule of the channel (X on S6 segments), at the interior regions of the ion-discriminating “selectivity filter (square on the P region), and also are known to influence stereoselectivity for phasic inhibition (circle, also on S6 segments). (C) Schematic cross section of the channel speculating on the manner in which S6 segments, forming a “gate,” may realign during activation to open the channel and allow entry and departure of a bupivacaine molecule by the “hydrophilic” pathway. The closed (inactivated) channel has a more intimate association with the LA molecule, whose favored pathway for dissociation is no longer between S6 segments (the former pore) but now, much more slowly, laterally between segments and then through the membrane, the “hydrophobic” pathway. Na + ions entering the pore will compete with the LA for a site in the channel, and H + ions, which pass very slowly through the pore, can enter and leave from the extracellular opening, thereby protonating and deprotonating a bound LA molecule and thus regulating its rate of dissociation from the channel.

From Berde CB, Strichartz GR. Local anesthetics. In Miller RD, Cohen NH, Eriksson LI, et al, eds. Miller’s Anesthesia. 8th ed. Philadelphia: Saunders Elsevier; 2015.

The alpha subunits have four homologous domains arranged in a square, each composed of six transmembrane helices, and the pore lies in the center of these four domains. Beta subunits modulate electrophysiologic properties of the channel and they also have prominent roles in channel localization, binding to adhesion molecules, and connection to intracellular cytoskeletons. There are nine major subtypes of sodium channel alpha subunits in mammalian tissues and four major subtypes of beta subunits.

Different sodium channel subtypes are expressed in different tissues, at diverse developmental stages, and in a range of disease states. Sodium channel subtypes are an active area of investigation around human diseases with spontaneous pain and pain insensitivity, as targets of new analgesics, and in other areas of medicine, including cardiology and neurology. Sodium channel subtypes will be discussed briefly again later in this chapter (see “ When Local Anesthesia Fails ” and “ Future Local Anesthetics ”).

From an electrophysiologic standpoint, local anesthetics block conduction of impulses by decreasing the rate of depolarization in response to excitation, preventing achievement of the threshold potential. They do not alter the resting transmembrane potential, and they have little effect on the threshold potential.

Sodium channels cycle between resting, open, and inactive conformations. During excitation, the sodium channel moves from a resting closed state to an open activated state, with an increase in the inward flux of sodium ions and consequent depolarization. The channel transitions to an inactive state and must undergo further conformational change back to a resting state before it can again open in response to a wave of depolarization.

According to the modulated receptor model, local anesthetics act not by physically “plugging the pore” of the channel but rather by an allosteric mechanism; that is, by changing the relative stability and kinetics of cycling of channels through resting, open, and inactive conformations. In so doing, the fraction of channels accessible to opening and conducting inward sodium currents in response to a wave of depolarization is reduced. This mechanism provides nerve blocks that are either a “use-dependent” or “frequency-dependent” type of block; that is, the block intensifies with more frequent rates of nerve firing.

pH, Net Charge, and Lipid Solubility

The predominant binding site for local anesthetics on sodium channels is near the cytoplasmic side of the plasma membrane. A major structural requirement for a molecule to be an effective local anesthetic is sufficient solubility and rapid diffusion in both hydrophilic environments (extracellular fluid, cytosol, and the headgroup region of membrane phospholipids) and in the hydrophobic environment of the lipid bilayers in plasma membranes.

The amino-amide and amino-ester local anesthetics in common clinical use achieve this aim of good solubility in both water and fat because they each contain a tertiary amine group that can rapidly convert between a protonated hydrochloride form (charged, hydrophilic) and an unprotonated base form (uncharged, hydrophobic). The charged, protonated form is the predominant active species at binding sites on sodium channels ( Fig. 10.5 ).

Fig. 10.5

During diffusion of local anesthetic across the nerve sheath and membrane to receptor sites within the inner vestibule of the sodium channel, only the uncharged base (LA) can penetrate the lipid membrane. After reaching the axoplasm, ionization occurs, and the charged cationic form (LAH + ) attaches to the receptor. Anesthetic may also reach the channel laterally (i.e., hydrophobic pathway).

From Covino BG, Scott DB, Lambert DH. Handbook of Spinal Anesthesia and Analgesia. Philadelphia: WB Saunders; 1994:7, used with permission.

The relative proportion of charged and uncharged local anesthetic molecules is a function of the dissociation constant of the drug and the environmental pH. Recalling the Henderson-Hasselbalch equation, the dissociation constant (Ka) can be expressed as follows:

<SPAN role=presentation tabIndex=0 id=MathJax-Element-1-Frame class=MathJax style="POSITION: relative" data-mathml='pKa=pH−log([base]/[conjugate acid])’>pKa=pHlog([base]/[conjugate acid])pKa=pH−log([base]/[conjugate acid])
pKa=pH−log([base]/[conjugate acid])

If the concentrations of the base and conjugate acid are equal, the latter component of the equation cancels (because log 1 = 0). Thus, the pKa provides a useful way to describe the propensity of a local anesthetic to exist in a charged or an uncharged state. The lower the pKa, the greater is the percent of un-ionized fraction at a given pH. In contrast, because the pKa values of the commonly used injectable anesthetics are between 7.6 and 8.9, less than one half of the molecules are un-ionized at physiologic pH ( Table 10.2 ). The base forms of local anesthetics are poorly soluble in water and less stable, so they are generally marketed as water-soluble hydrochloride salts at slightly acidic pH. Bicarbonate is sometimes added to local anesthetic solutions immediately before injection to increase the un-ionized fraction in an effort to hasten the onset of anesthesia. Other conditions that lower pH, such as tissue acidosis produced by infection, inflammation, or ischemia, may likewise have a negative impact on the onset and quality of local anesthesia.

Table 10.2

Comparative Pharmacology and Common Current Use of Local Anesthetics

Classification and Compounds pK a % Nonionized at pH 7.4 Potency a Max. Dose (mg) for Infiltration b Duration After Infiltration (min) Topical Local IV Periph Epi Spinal
Procaine 8.9 3 1 500 45-60 No Yes No Yes No Yes
Chloroprocaine 8.7 5 2 600 30-60 No Yes Yes Yes Yes Yes c
Tetracaine 8.5 7 8 Yes Yes d No No No Yes
Lidocaine 7.9 24 2 300 60-120 Yes Yes Yes Yes Yes Yes c
Mepivacaine 7.6 39 2 300 90-180 No Yes No Yes Yes Yes c
Prilocaine 7.9 24 2 400 60-120 Yes e Yes Yes Yes Yes Yes c
Bupivacaine, levobupivacaine 8.1 17 8 150 240-480 No Yes No Yes Yes Yes
Ropivacaine 8.1 17 6 200 240-480 No Yes No Yes Yes Yes

Epi, Epidural; IV, intravenous; Periph, peripheral.

a Relative potencies vary based on experimental model or route of administration.

b Dosage should take into account the site of injection, use of a vasoconstrictor, and patient-related factors.

c Use of procaine, lidocaine, mepivacaine, prilocaine, and chloroprocaine for spinal anesthesia is somewhat controversial; indications are evolving (see text).

d Used in combination with another local anesthetic to increase duration.

e Formulated with lidocaine as eutectic mixture.

Lipid solubility of a local anesthetic affects tissue penetration, time course of uptake, potency, and duration of action. Duration of the local anesthetic action also correlates with protein binding, which likely serves to retain anesthetic within the nerve.

Degrees of anesthetic potency may be altered by the in vitro or in vivo system in which these effects are determined. For example, tetracaine is approximately 20 times more potent than bupivacaine when assessed in isolated nerve, but these drugs are nearly equipotent when assessed in vivo. Even when assessed in vivo, comparisons among local anesthetics may vary based on the specific site of application (spinal versus peripheral block) because of secondary effects such as the inherent vasoactive properties of the anesthetic.

Differential Local Anesthetic Blockade

From a clinical viewpoint and from electrophysiologic measurements, local anesthesia is not an all-or-none phenomenon: patients experience gradations in the intensity of sensory and motor blockade that vary over time following local anesthetic injections. Clinically apparent “numbness” generally correlates with intraneural concentrations of local anesthetics but also reflects complex integration and processing of inputs in the spinal dorsal horn and at supraspinal sites in the somatosensory pathway. When compound action potentials are recorded in peripheral nerves exposed to local anesthetics in varying concentrations and lengths of nerve exposed, conduction blockade is facilitated either by increasing the concentration of local anesthetic or by increasing the length of nerve exposed to more dilute concentrations. At the limit of short lengths of nerve exposed to local anesthetic, conduction blockade requires exposure of at least three successive nodes of Ranvier to prevent the action potential from “skipping over” the region of local anesthetic exposure.

Historically, the term differential blockade in clinical textbooks referred to the observation that infusions of dilute concentrations of local anesthetic could produce analgesia and signs of autonomic blockade with relative sparing of motor strength. This clinical trend is not readily explained by the electrophysiologic observations of action potential blockade in large and small fibers perfused to steady state. The mechanisms underlying this divergence between clinical experience and experimental data are poorly understood, but they may be related to the anatomic and geographic arrangement of nerve fibers, variability in the longitudinal spread required for neural blockade, effects on other ion channels, and inherent impulse activity.

Spread of Local Anesthesia After Injection

When local anesthetics are deposited around a peripheral nerve, they must cross a series of diffusion barriers to access sodium channels in nerve axons ( Fig. 10.6 ). With large nerve trunks, they diffuse from the outer surface (mantle) toward the center (core) of the nerve along a concentration gradient ( Fig. 10.7 ). As a result, nerve fibers located in the mantle of the mixed nerve are blocked first. These mantle fibers are generally distributed to more proximal anatomic structures, whereas distal structures are innervated by fibers near the core. This anatomic arrangement accounts for the initial development of proximal anesthesia with subsequent distal involvement as local anesthetic diffuses to reach more central core nerve fibers. Skeletal muscle weakness may precede sensory blockade if the motor nerve fibers are more superficial. The sequence of onset and recovery from conduction blockade of sympathetic, sensory, and motor nerve fibers in a mixed peripheral nerve depends as much or more on the anatomic location of the nerve fibers within the mixed nerve as on their intrinsic sensitivity to local anesthetics.

Oct 21, 2019 | Posted by in ANESTHESIA | Comments Off on Local Anesthetics
Premium Wordpress Themes by UFO Themes