In A Noisy World, How Can
The Senses Project And Receive Information At The Same Time?
The answer to may be found
in the simple male crickets, which sing for hours at loud sound pressure
levels in order to attract females
April 1, 2003 (Bethesda, MD) – How do we hear
when some of us chatter all day? When we sing in the shower, why doesn’t
the active voice smother the rest of our body’s sensory systems? The answer
to these questions may be found in the simple male cricket (Gryllus
bimaculatus), which sing for hours at over 100 decibels sound pressure
levels (dB SPL) in order to attract females.
Background
The “songs” of crickets (except the one from Disney’s
famous character, “Jiminy Cricket, are generated by rhythmically
rubbing the fore wings together resulting in a form of sound
production called stridulation. As crickets’ ears are located on
the forelegs, they are fully exposed to the self-generated
sounds. Many animals reduce the responsiveness of their peripheral
auditory system during sound production, but crickets do
not. Despite this, behavioral experiments have shown that singing
crickets can respond to external sounds.
A modulation in the sensitivity to reafferent
(self-generated) stimulation by centrally generated neural signals has been
identified in a variety of sensory systems, e.g., visual,
electroreceptive, proprioceptive (perception at the subconscious level), and
mechanoreceptive. A reduction in the responsiveness of auditory
neurons in the brain has been recorded in humans and
other vertebrates during vocalization, but the nature and source of the
inhibition has never been characterized.
Crickets sing so loudly that reafferent sound could be
confused with external sound and/or desensitize the cricket’s own auditory
system. One solution to this problem could be to modulate the
biophysical sensitivity of the ear during sound production. However,
the tympanic membrane of the cricket remains fully responsive
during stridulation.
A New Study
Researchers have examined how their central
and simple auditory system copes with the intense reafferent
stimulation through desensitizing effect of loud sounds on the
responsiveness of ON1. Their research consisted of making intracellular
recordings of auditory afferents and an identified auditory interneuron
the Omega
1 neuron (ON1)
during
stridulation. The authors of “A Corollary Discharge Mechanism Modulates
Central Auditory Processing in Singing Crickets,” are
J.F.A. Poulet and B. Hedwig, from the
Department of Zoology, University of Cambridge, Cambridge, United
Kingdom. Their findings appear in the March 2003 edition of the Journal
of Neurophysiology, one of 14 publications published monthly by the
American Physiological Society.
Methodology
All experiments were performed on adult male G. bimaculatus
selected from a cricket colony maintained on a 12 hour light/12 hour
dark cycle. Prior to dissection they were chilled at 4°C for
30
min. They were then fixed in a standing position on a holder that
allowed free rotation of the animal. To allow for silent
stridulation, the left wing of the crickets was removed. When recording
false stridulation, the cricket was placed upside down in a
Plasticene well and its ventral cuticle was removed to expose the
abdominal and thoracic ganglia. The thoracic or thoracic and
abdominal nerves were cut, except for prothoracic nerve #5, which
contains the auditory afferents. Care was taken not to damage the
main ventral trachea. To deafen crickets, the forelegs were
removed just distal to the coxa. Other procedures performed include
pharmacological stimulation, acoustic stimulation, as well as recordings on
auditory neurons.
Results
During sonorous stridulation, the auditory
afferents and ON1 responded with bursts of spikes to the
crickets’ own song. When the crickets were stridulating silently,
after one wing had been removed, only a few spikes were recorded
in the afferents and ON1. Primary afferent depolarizations (PADs)
occurred in the terminals of the auditory afferents, and
inhibitory postsynaptic potentials (IPSPs) were apparent in ON1.
The PADs and IPSPs were composed of many summed, small-amplitude
potentials that occurred at a rate of about 230 Hz. The PADs and
the IPSPs started during the closing wing movement and peaked in
amplitude during the subsequent opening wing movement. As a
consequence, during silent stridulation, the ON1 response to acoustic
stimuli was maximally inhibited during wing opening. Inhibition
coincides with the time when ON1 would otherwise be most strongly
excited by self-generated sounds in a sonorously stridulating
cricket. The PADs and the IPSPs persisted in fictively stridulating
crickets whose ventral nerve cord had been isolated from muscles
and sense organs.
Conclusions
The findings demonstrate that the corollary
discharge inhibition during the chirps will prevent
desensitization in ON1 and allow the cricket to hear quieter,
subsequent sounds in the chirp intervals. In a group of
stridulating male G. bimaculatus, where individuals are spaced
apart by two meters on average, the ability to hear during singing
will be an advantage. It would allow males to defend their
territory from rival singing males, to maintain a fixed distance
from each other, and to hear noisy predators
This strongly suggests that the inhibition of
the auditory pathway is the result of a corollary discharge from
the stridulation motor network. Hyperpolarizing current injection into
ON1 while it was responding to a 100 dB SPL sound pulse mimicked the central
inhibition. This suppressed its spiking response to the acoustic
stimulus and maintained its response to subsequent, quieter
stimuli. The corollary discharge therefore prevents auditory
desensitization in stridulating crickets and allows the animals
to respond to external acoustic signals during the production of
calling song.
Source: March 2003 edition of the Journal of
Neurophysiology
-end-
The American Physiological
Society (APS) was founded in 1887 to foster basic and applied science, much
of it relating to human health. The Bethesda, MD-based Society has more than
10,000 members and publishes 3,800 articles in its 14 peer-reviewed journals
every year.
***
Editor’s Note: To set up
an interview with a member of the research team, please contact Donna Krupa
at 703.527.7357 (direct dial), 703.967.2751 (cell) or
djkrupa1@aol.com.