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Physiology · Pain

Afferent pathways of pain sensitivity

Pain sensitivity is provided by a complex system of neural pathways through which signals from peripheral receptors reach the brain. The separation of the sensory stream at the level of the spinal cord and brainstem forms two functionally distinct ascending systems that determine the nature of our pain perception.

A-δ fibersThick myelinated fibers with a conduction velocity of 4 to 30 m/s.
C fibersThin unmyelinated fibers with an impulse transmission velocity of only 0.5–2 m/s.
RelayThe thalamus is the main distribution center for pain signals before the cortex.
$S_I$ cortexThe primary somatosensory cortex is responsible for precise localization of the stimulus.
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

Peripheral nociceptive fibers

The transmission of information from pain receptors to the central nervous system is carried out via sensory nerves. They contain two cardinally different types of afferent fibers, each responsible for its own component of the pain sensation:

  1. A-δ fibers (A-delta): These are relatively thick nerve fibers covered with a myelin sheath. The presence of myelin ensures a high conduction velocity of the nerve impulse — from 4 to 30 m/s. Primary, acute pain is transmitted via these pathways.
  2. C fibers: These are thin fibers lacking myelin insulation. Due to the absence of myelin, the signal transmission velocity along them is extremely low, ranging from 0.5 to 2 m/s. They are responsible for transmitting secondary, slower pain impulses.

Lemniscal system (fast pathway)

At the level of the spinal cord and brainstem, the unified afferent stream splits. The first major system is the lemniscal system (Lemniscal system). Its main function is the rapid conduction of impulses and providing discriminative sensitivity (the ability to clearly distinguish spatial details of a stimulus).

  • Anatomical composition: Includes posterior column projections and the spinocervical tract.
  • Pathway course: Afferent fibers pass through the medial lemniscus and reach specific thalamic nuclei (optic thalami), where relaying occurs in the ventrobasal complex.
  • Cortical projections: Axons of thalamocortical neurons project predominantly to the primary somatosensory cortex ($S_I$), partially to the secondary area ($S_{II}$), and the orbital cortex.

It is the lemniscal system that allows us to instantly and precisely determine the localization of a pain stimulus on the body surface.

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Extralemniscal system (slow pathway)

The second ascending pathway system is the extralemniscal system (Extralemniscal system). It runs parallel to the lemniscal system but has a diffuse organization and provides relatively slow signal conduction.

  • Anatomical composition: Includes the spinoreticular, spinotectal, and spinobulbothalamic tracts.
  • Relay features: Signals enter the non-specific thalamic nuclei — the mediobasal thalamus, which includes intralaminar nuclei.
  • Cortical projections: Pathways project diffusely, predominantly to the secondary somatosensory cortex ($S_{II}$) and other brain regions.

Functions of the extralemniscal system: It is responsible for the formation of protopathic pain — a generalized sensation without fine differentiation of the modality and localization of the stimulus (it is difficult to determine the exact location of the pain). This system integrates the pain stream, provides emotional coloring to sensations, forms the phenomenon of slow pain, and maintains the general level of arousal of the central nervous system (arousal).

Electrophysiological markers

The organization of the two systems is clearly demonstrated by recording evoked potentials in the cerebral cortex:

  • The lemniscal system generates a clear, high-amplitude evoked potential in the $S_I$ area. This indicates rapid, synchronous signal transmission with minimal dispersion.
  • The extralemniscal system elicits polyphasic, time-spread potentials in the $S_{II}$ area. This distinct response form directly reflects the multisynaptic nature of transmission: the signal is relayed multiple times and spreads diffusely before reaching cortical structures.

Briefly: answers to topical questions

What neurotransmitters are released by the endings of nociceptive afferent fibers in the spinal cord?

At the presynaptic level in the axon terminals of primary afferents in the dorsal horns of the spinal cord, pain neurotransmitters are released: substance P and glutamate. A decrease in their release, for example during N-type calcium channel blockade, disrupts signal transmission to interneurons.

What are the main differences between epicritic and protopathic pain?

The main differences lie in the speed of onset, the nature of the sensations, the ability for precise localization, and the presence of adaptation.

SignEpicritic painProtopathic pain
CharacterAcuteDull
AwarenessQuickly perceivedPerceived more slowly
LocalizationEasily and precisely localizedPoorly localized
AdaptationRapid adaptation is characteristicNot accompanied by the development of adaptation
DurationTransientPersists for a long time

In addition, epicritic pain is considered primary and is transmitted via fast A fibers, whereas protopathic is regarded as an evolutionarily older type of pain.

How to memorize

Lemniscal system — Localization (precise, fast). Extralemniscal — Emotions (diffuse, slow protopathic pain).

Class and exam questions

Which fibers conduct pain faster and why?

A-delta fibers conduct impulses significantly faster (4–30 m/s) due to the presence of a myelin sheath and a larger diameter. C-fibers lack myelin, so their conduction velocity is only 0.5–2 m/s.

Where do lemniscal pathways relay in the diencephalon?

Relaying of the lemniscal system occurs in specific nuclei of the thalamus, specifically in its ventrobasal complex.

Which system is responsible for protopathic pain?

The extralemniscal ascending system, which projects to the $S_{II}$ area, is responsible for the formation of protopathic (poorly localized, generalized) pain.

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What else to study on this topic

  • Anatomy and physiology of the medial lemniscus
  • Spinocervical tract: structural features
  • Mechanisms of formation of protopathic and epicritic pain
  • The role of intralaminar thalamic nuclei in nociception
  • Integrative function of the secondary somatosensory cortex ($S_{II}$)

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