Summary: LMU researchers report neural activity in the auditory system has a direct effect on myelination. Higher levels of neural activity resulted in the formation of thicker myelin sheaths and enhanced speed of signal transmission.
Source: LMU.
An LMU study reveals that sound-evoked activity of neurons in the auditory system of the mouse increases the thickness of their myelin sheaths – and enhances the speed of signal transmission – both during development and in the adult brain.
Nerve cells communicate by means of electrical impulses, which are transmitted along neural processes known as axons.
The speed of transmission depends on several factors, including the diameter of the axon and the thickness of the electrically insulating myelin sheaths that surround the axons.
As a rule, transmission speeds are positively correlated with the diameter and the thickness of the sheath. In mammals, the functional demands made on the auditory system require extremely precise and rapid neural processing of acoustic information, and it contains a strikingly high proportion of myelinated axons.
Using the mouse as an experimental model, LMU neurobiologist PD Dr. Conny Kopp-Scheinpflug and her research group have now demonstrated that the activity of nerve cells in the auditory system has a direct effect on myelinization – higher levels of activity correlate with the formation of thicker myelin sheaths. Their findings appear in the Journal of Neuroscience.
Specialized sensory neurons in the inner ear, called hair cells, are responsible for the detection of sounds, and this information is transmitted to the auditory cortex via several intermediate structures.
“The mouse is a particularly suitable model in which to study the development of the auditory system, because newborn mice are deaf and only begin to perceive acoustic signals at 12 days after birth. At this point, the level of activity of auditory neurons begins to increase,” Kopp-Scheinpflug explains.
She and her colleagues focused on the neuronal activity in the trapezoid body, a structure located in the brainstem that forms part of the pathway that eventually leads to the auditory cortex.
They were able to demonstrate that both the speed and frequency of signal transmission in the trapezoid body doubles as soon as the young mice begin to perceive sounds. Moreover, both the diameter of the axons and the thickness of their myelin sheaths progressively increased until they reached the values observed in the auditory system of the adult animal.
In addition, the team explored the developmental impact of reduced stimulation on the axons in the trapezoid body.
“To do so, we simply inserted earplugs in the ears of 10-day-old mice and left them in position for 10 more days. This intervention leads to a reversible hearing loss, i.e. rise in the hearing threshold of about 50 decibels“, says Kopp-Scheinpflug.
In these animals, the normal increase in axon diameter is mostly absent, and the myelin sheaths are also thinner. When the same experiment was carried out on adult mice, a decrease in the thickness of the myelin sheaths was also seen, although the diameter of the axons was not affected. Based on these results, the researchers conclude that neuronal activity itself plays an important role in the synthesis and maintenance of the myelin sheath, and that myelinated nerve cells therefore require a minimal level of sound-evoked stimulation.
“In order to understand the effects of reduced stimulation, we also developed a computer model based on our results. The model predicts that not only axonal conductivity, but also the capacity to transmit high-frequency action potentials should decline,” says Kopp-Scheinpflug.
“Such losses are particularly critical in the auditory system, because they reduce the temporal precision of signal transmission – and the quality of our perception of the acoustic environment is primarily dependent on rates of action potential generation and precise neural computation of their temporal sequences.”
Source: Luise Dirscherl – LMU
Image Source: NeuroscienceNews.com image is credited to J. Sinclair & C. Kopp-Scheinpflug, LMU.
Original Research: Abstract for “Sound-evoked activity influences myelination of brainstem axons in the trapezoid body” by James L. Sinclair, Matthew J. Fischl, Olga Alexandrova, Martin Heß, Benedikt Grothe, Christian Leibold and Conny Kopp-Scheinpflug in Journal of Neuroscience. Published online July 31 2017 doi:10.1523/JNEUROSCI.3728-16.2017
<http://neurosciencenews.com/brain-development-myelin-7224/>.
Abstract
Sound-evoked activity influences myelination of brainstem axons in the trapezoid body
Plasticity of myelination represents a mechanism to tune the flow of information by balancing functional requirements with metabolic and spatial constraints. The auditory system is heavily myelinated and operates at the upper limits of action potential generation frequency and speed observed in the mammalian CNS.
This study aimed to characterize the development of myelin within the trapezoid body, a central auditory fiber tract, and determine the influence sensory experience has on this process in mice of both sexes.
We find that in vitro conduction speed doubles following hearing onset and the ability to support high frequency firing increases concurrently. Also in this time, the diameter of trapezoid body axons and the thickness of myelin double, reaching mature-like thickness between 25-35 days of age. Earplugs were used to induce approximately 50dB elevation in auditory thresholds.
If introduced at hearing onset, trapezoid body fibers developed thinner axons and myelin than age-matched controls.
If plugged during adulthood, the thickest trapezoid body fibers also showed a decrease in myelin.
These data demonstrate the need for sensory activity in both development and maintenance of myelin and have important implications in the study of myelin plasticity and how this could relate to sensorineural hearing loss following peripheral impairment.
SIGNIFICANCE STATEMENT
The auditory system has many mechanisms to maximize the dynamic range of its afferent fibers, which operate at the physiological limit of action potential generation, precision and speed.
In this study we demonstrate for the first time that changes in peripheral activity modifies the thickness of myelin in sensory neurons, not only in development but also in mature animals.
The current study suggests that changes in CNS myelination occur as a downstream mechanism following peripheral deficit.
Given the required submillisecond temporal precision for binaural auditory processing, reduced myelination might augment sensorineural hearing impairment.
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