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Physiology · Excitation Conduction and Synaptic Transmission

Classification of nerve fibers

Fibrae nervosae

In physiology, nerve fibers are typically divided into groups based on how quickly they can transmit an electrical signal. This conduction velocity is not a random value, but is strictly determined by anatomical structure: the presence of an insulating myelin sheath and the overall diameter of the axon. The most widespread and practically significant classification was proposed by Joseph Erlanger and Herbert Gasser.

VelocityRanges from 1 m/s in the thinnest fibers to 100 m/s in the thickest ones.
MyelinPresent in groups A and B, completely absent in group C.
PainSharp pain is transmitted via Aδ fibers, whereas dull and diffuse pain is transmitted via C fibers.
Action potentialChanges its shape as it moves away from the site of nerve stimulation.
4 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Factors determining conduction velocity

The ability of a nerve to rapidly transmit excitation depends on two key structural features. First, it is the fiber diameter: the thicker the fiber, the faster the signal propagates along it. Second, the presence of a myelin sheath is critically important. Myelinated fibers conduct impulses significantly faster than unmyelinated ones.

It is interesting to observe the behavior of the compound action potential (AP) of an entire nerve. If we record the AP close to the stimulation site, it will have a simple sinusoidal shape. This is because excitation starts synchronously across all structures. However, as the signal propagates further away from the stimulation site, the shape of the action potential becomes complex and multi-peaked. The reason for this change is that the nerve comprises fiber groups with different conduction velocities. Signals travel along them at different speeds, causing the impulses to become "stretched" in time and disrupting the initial synchrony.

Group A: the fastest and thickest (myelinated)

According to the Erlanger-Gasser classification, group A includes exclusively myelinated fibers. They are subdivided into four subcategories, each performing a specific function:

  • Aα (alpha): Absolute record-holders in velocity (about 100 m/s) and thickness (diameter about 10 µm). Functionally, these are efferent somatic pathways running from the CNS to skeletal muscles, providing motor responses. They also form afferent pathways from muscle proprioceptors.
  • Aβ (beta): Perform an afferent function. Their main task is to collect information from touch receptors located in the skin and transmit these signals to the central nervous system.
  • Aγ (gamma): Efferent structures that extend to intrafusal fibers (the so-called muscle spindles). They play a crucial role in the continuous regulation of muscle tone.
  • Aδ (delta): Predominantly afferent somatic fibers. These are the fibers that transmit signals from cutaneous thermoreceptors and nociceptors. In clinical practice, they are notable for providing the primary epicritic pain component—the fast, sharp, and very clearly localized pain felt in the first second after an injury.
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Groups B and C: autonomic and slow

These fiber groups are closely related to the function of the autonomic nervous system (ANS) and are characterized by lower conduction velocities.

Group B is represented by thin yet myelinated fibers. In the human body, they function as preganglionic fibers of the autonomic nervous system, delivering impulses to autonomic ganglia.

Group C consists of the thinnest (about 1 µm) and slowest fibers (conduction velocity of only about 1 m/s). Their main distinguishing feature is that they are unmyelinated. In the autonomic nervous system, they function as postganglionic fibers. Additionally, type C fibers act as afferent pathways transmitting information from internal organs to the CNS. The clinical significance of this group is immense: they form the secondary protopathic pain component. This is the slow, dull, diffuse, exhausting, and heavily emotionally charged pain that replaces the sharp pain.

Briefly: answers to topical questions

What exact conduction velocity is typical for group B fibers?

The conduction velocity for group B fibers is indicated in sources as follows:

  • 3–20 m/s for preganglionic fibers of the autonomic nervous system (group B).
  • 3–18 m/s for thin myelinated type B fibers.
  • 15 m/s for thin myelinated type B fibers.
  • Up to 10 m/s for myelinated fibers of the depressor nerve, among which group B is listed.

What is the diameter of group B nerve fibers?

The diameter of group B nerve fibers is indicated in sources as follows:

  • 1–3.5 µm for thin myelinated type B fibers / preganglionic ANS fibers.
  • 2–4 µm for group B fibers within the depressor nerve of the aortic reflexogenic zone.
  • 3 µm for thin myelinated type B fibers.
How to memorize

The classification is easy to remember alphabetically: the closer the letter is to the beginning of the alphabet (A, B, C), the faster the fiber. Within group A, velocity decreases according to the Greek alphabet: alpha (fastest) -> beta -> gamma -> delta.

Class and exam questions

Why does the compound action potential of a nerve change its shape far from the stimulation site?

A nerve consists of various fiber groups. Because they differ in thickness and degree of myelination, excitation is conducted at varying speeds and arrives at a distant point asynchronously, making the potential waveform complex.

Which fibers are responsible for sharp pain, and which for dull pain?

Fast, sharp, and well-localized pain (epicritic) is transmitted via myelinated Aδ fibers. Slow, dull, and diffuse pain (protopathic) is transmitted via unmyelinated group C fibers.

What is the difference between group B and group C fibers in the autonomic nervous system?

Group B fibers are myelinated and are preganglionic (running to the autonomic ganglion). Group C fibers lack myelin and are postganglionic (running from the ganglion to the target organ).

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What else to study on this topic

  • Mechanism of saltatory conduction of excitation
  • Structure of the myelin sheath and nodes of Ranvier
  • Neurophysiology of proprioception (muscle spindles)
  • Differences between the somatic and autonomic nervous systems
  • Theories of pain perception (nociception)

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