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Peripheral nervous system: nerves and ganglia
Last updated: 24.02.2026
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The peripheral nervous system includes all neural structures outside the brain and spinal cord. Its purpose is to deliver information from receptors to the central nervous system and transmit commands to muscles, glands, and internal organs. [1]
From a practical standpoint, it's more convenient to think of the peripheral nervous system as divided into two major "branches." The first branch is responsible for conscious sensations and voluntary movements (the somatic part). The second branch regulates the functioning of internal organs "in automatic mode" (the autonomic part), including the sympathetic, parasympathetic, and enteric divisions. [2]
The peripheral nervous system consists of 12 pairs of cranial nerves and 31 pairs of spinal nerves, as well as nodes (ganglia) where the cell bodies of neurons are located, and nerve endings in tissues. The spinal nerves are mixed: they carry sensory, motor, and some autonomic impulses. [3]
The ganglia in this system are not "mere thickenings." Sensory ganglia (e.g., dorsal root ganglia) contain the cell bodies of primary sensory neurons, and autonomic ganglia are "switching stations" between neurons of the central nervous system and organs. [4]
Table 1. Main components of the peripheral nervous system
| Component | Examples | Leading role |
|---|---|---|
| Cranial nerves | 12 pairs | The connection of the brain with the structures of the head and neck, part of the autonomic functions |
| Spinal nerves | 31 pairs | Connection of the spinal cord with the trunk and limbs, mixed fibers |
| Sensory ganglia | Dorsal root ganglia | Transmission of pain, temperature, touch, and proprioception to the central nervous system |
| Autonomic ganglia | Sympathetic trunks, parasympathetic ganglia | Switching of autonomous pathways to organs |
| Nerve endings | Receptors and effector endings | Input (sensitivity) and output (movement, secretion) |
The information in the table summarizes the data on the structure of the somatic and autonomic parts of the peripheral nervous system. [5]
Peripheral nerve as an "organ": bundles, sheaths, nutrition and blood-nerve barrier
A peripheral nerve is not structured as a single cable, but as a set of bundles (fascicles) containing axons. This is important because injury or compression damages not only the "wire" but also its sheaths, vessels, and the microenvironment, which are crucial for recovery. [6]
Connective tissue sheaths provide a framework and protection. The endoneurium surrounds individual fibers, the perineurium "packs" the fibers into bundles and maintains intrafascicular pressure, and the epineurium covers the nerve externally and unites several bundles into a single trunk. [7]
A key modern focus is the barrier function. Tight junctions between perineurium cells and endoneurial capillaries form a blood-nerve barrier, which limits the penetration of molecules and cells from the blood into the endoneurium. This barrier protects axons but also influences the course of inflammatory and immune neuropathies and drug penetration. [8]
The nerve's blood supply is provided by the vasa nervorum, which branch from nearby arteries and are particularly abundant near joints. Their tortuosity is considered an adaptation to the nerve's movement during flexion and extension, but diabetes and other conditions can impair the microcirculation of these vessels, increasing the nerve's vulnerability. [9]
Table 2. Nerve sheaths and their functions
| Layer | What surrounds | Main functions |
|---|---|---|
| Epineurium | The entire nerve trunk and several bundles | Mechanical protection, "frame", vascular guide |
| Perineurium | A separate bundle of fibers | Tensile strength, pressure support, participation in the blood-nerve barrier |
| Endoneurium | A single nerve fiber | Support and microenvironment for axons and Schwann cells |
| Endoneurial capillaries | Inside the bundle | Together with the perineurium they participate in the barrier function |
The information in the table reflects the current description of the fascial membranes and the blood-nerve barrier. [10]
Nerve fibers: myelin, conduction velocity, afferent and efferent pathways
Peripheral nerves contain different types of fibers. Some fibers are covered with myelin, which is formed by Schwann cells, while others are unmyelinated. Myelin allows signals to be transmitted more quickly and efficiently, and damage to it alters the symptomatic presentation and conduction test results. [11]
A simplified rule applies: the thicker the fiber and the better its myelination, the higher the conduction velocity. Therefore, fast fibers are usually associated with proprioception and fine tactile sensitivity, while the slowest fibers often carry information about pain and temperature. [12]
Signals can also be described by direction. Afferent fibers carry information from receptors to the central nervous system, while efferent fibers conduct impulses to muscles and glands. Within the spinal nerves, these streams are "collected together," which is why many peripheral nerves are mixed. [13]
Differences in fiber types underlie neurophysiological methods. In demyelinating processes, conduction velocity initially decreases and latency increases, while in axonal lesions, response amplitude often decreases. This logic is widely used in the electrophysiological diagnosis of peripheral neuropathies. [14]
Table 3. Fiber types by myelin and conduction velocity
| Fiber type | Myelin | Typical function | Typical conduction velocity |
|---|---|---|---|
| Large myelinated | Eat | Proprioception, vibration, fine touch, rapid motor signals | Tens or more meters per second |
| Thin myelinated | Yes, the layer is thinner. | "Fast" pain, cold, some skin sensitivity | Units and tens of meters per second |
| Unmyelinated | No | "Slow" pain, warmth, part of the autonomic influences | Fractions and units of meters per second |
| Preganglionic autonomic | Eat | Signal from the central nervous system to the autonomic ganglion | Units and tens of meters per second |
| Postganglionic autonomic | Usually no | Signal from the autonomic ganglion to the organ | Fractions and units of meters per second |
The information in the table is consistent with modern descriptions of myelin and the physiology of impulse conduction in the peripheral nervous system. [15]
Ganglia and the autonomic nervous system: sensory ganglia, sympathetic, parasympathetic and enteric divisions
Sensory ganglia are located near the spinal cord (dorsal root ganglia) or cranial nerves. They contain the cell bodies of primary sensory neurons, which receive signals from peripheral receptors and transmit them to the central nervous system. This is of particular importance for pain: dorsal root ganglia are involved in the development of chronic pain and are considered a therapeutic target in certain approaches. [16]
The autonomic nervous system controls involuntary functions: heart rate, vascular tone, respiration, digestion, and other processes. Its classic architecture consists of two neurons per organ: a preganglionic neuron extends from the central nervous system to the ganglion, and a postganglionic neuron extends from the ganglion to the organ. [17]
The sympathetic division typically mobilizes resources during stress, increasing the body's readiness for exertion, while the parasympathetic division primarily maintains a "recovery and digestion" mode. This functional opposition simplifies the picture, but it helps to understand why an imbalance of autonomic influences manifests itself, for example, in changes in heart rate, sweating, and intestinal motility. [18]
The enteric division of the autonomic nervous system is organized as a network of neurons in the wall of the gastrointestinal tract and is capable of coordinating a significant portion of digestive functions locally. It is closely linked to sympathetic and parasympathetic influences, so autonomic disorders often manifest as gastrointestinal symptoms. [19]
Table 4. Types of ganglia of the peripheral nervous system
| Ganglion type | Where is it located? | What neurons does it contain? | What does it do? |
|---|---|---|---|
| Dorsal root ganglion | In the intervertebral foramen | Cell bodies of primary sensory neurons | Transmission of pain, temperature, touch, proprioception |
| Sensory ganglia of the cranial nerves | At the brainstem and along the cranial nerves | Cell bodies of sensory neurons | Sensory signals from the head and neck |
| Sympathetic ganglia | Paravertebral and prevertebral | Postganglionic sympathetic neurons | Regulation of blood vessels, heart, sweat glands, etc. |
| Parasympathetic ganglia | Closer to the organ or in the organ | Postganglionic parasympathetic neurons | Regulation of "restorative" functions |
| Enteric ganglia | In the intestinal wall | Local area network neurons | Coordination of motility and secretion of the gastrointestinal tract |
The information in the table corresponds to modern descriptions of sensory ganglia and the autonomic nervous system. [20]
Table 5. Divisions of the autonomic nervous system: key differences
| Department | Common task | Where are the ganglia located? | Peculiarity of the path |
|---|---|---|---|
| Sympathetic | Rapid mobilization, stress response | Near the spine and in the abdominal cavity | Often a long postganglionic region |
| Parasympathetic | Recovery, digestion, resource conservation | Near an organ or inside an organ | Often a long preganglionic region |
| Enteral | Local regulation of the intestine | In the wall of the gastrointestinal tract | Capable of operating autonomously, but regulated externally |
The information in the table summarizes the anatomical and functional differences of the 3 divisions of the autonomic nervous system. [21]
Why it's important in the clinic: Nerve injury, regeneration, and examination
Peripheral nerves are vulnerable to trauma, compression, and metabolic stress. Clinically, injury classifications are widely used to help predict recovery: in mild cases, conduction is temporarily blocked; in more severe cases, the axon is damaged and Wallerian degeneration begins distally to the injury site. [22]
Regeneration in the peripheral nervous system is generally more feasible than in the central nervous system, but it depends on the integrity of the "guide tubes" of the sheaths and the response of Schwann cells. In Wallerian degeneration, Schwann cells switch to regeneration support mode and form structures that help axons re-grow toward their target. [23]
As a rough guideline, the rate of axon regrowth in the clinic is often given as about 1 mm per day under favorable conditions, but the actual rate and final outcome depend greatly on the distance to the muscle or skin, the degree of damage, age, concomitant diseases and the quality of surgical tactics in case of ruptures. [24]
Evaluation of suspected peripheral nervous system damage relies on a combination of clinical examination and neurophysiology. Nerve conduction velocity testing and electromyography help differentiate demyelinating from axonal processes, assess the severity and extent of damage, and monitor recovery. [25]
Table 6. Peripheral nerve injuries and expected recovery logic
| Type of damage | What suffers | Wallerian degeneration | Typical prognosis without surgery |
|---|---|---|---|
| Conductor block | Temporary dysfunction without axon rupture | Usually no | Often recovery is complete |
| Axon damage with intact sheaths | Axon, but the frame is preserved | Yes | Recovery is possible, but slower. |
| Complete rupture of the nerve | Axon and sheaths | Yes | Without surgical restoration, function usually does not return. |
The classification logic and relationship to Wallerian degeneration are described in current reviews of peripheral nerve injury.[26]
Table 7. Methods of examination of the peripheral nervous system
| Method | What does it show? | When it is especially useful |
|---|---|---|
| Neurological examination | Distribution of weakness, sensitivity, reflexes | The first step is to determine the site of the lesion |
| Nerve conduction velocity testing | Speed, latency, and response amplitudes | Demyelination versus axonopathy, focal compressions |
| Electromyography | Signs of denervation and reinnervation in muscles | Assessment of severity and duration, monitoring of recovery |
| Ultrasound examination of the nerve | Size, structure, compression, tumors of the membranes | Compression neuropathies, trauma, local changes |
| Magnetic resonance imaging as indicated | Deep structures, roots, plexuses | Lesions of plexuses, roots, space-occupying processes |
The diagnostic capabilities of electrophysiology and the principles of study planning are described in detail in modern guidelines. [27]

