Hypothesis: The purpose of this study was to simulate an isolated direction
al preponderance (DP) on bithermal caloric testing by constructing a realis
tic neural network model. The simulation was designed to capture not only t
he characteristics of the nystagmus response to caloric stimulation but als
o the response to rotational stimulation in patients with an isolated calor
ic DP.
Background: The nature of an isolated DP-that is, a DP in the absence of a
significant spontaneous nystagmus or canal paresis-is outlined in the prece
ding article. In this article, the authors investigate the possible neural
basis for an isolated caloric DP using the mathematic modeling technique of
neural network simulation. Neural network models are typically abstract in
nature; however, in this case the network was based on the known structure
and function of the central vestibular system.
Methods: The neural network model was based on the known neuroanatomy and n
europhysiology of the horizontal vestibuloocular reflex pathway. A leftward
-rightward asymmetric modification of the dynamic responses of simulated me
dial vestibular nucleus type 1A neurons on one side, or of type 2 neurons o
n the other side, to peripheral input would generate an isolated caloric DP
.
Results: The values of DP and associated canal paresis produced by the netw
ork were within the same range as in the patient group. The network also pr
edicted that the rotational DP would be lower than the caloric DP: between
2.5% and 56.9% of the caloric DP value. The actual rotational DP value was
between 3% and 57% (average 31% of the corresponding caloric DP value.
Conclusions: An isolated caloric DP can be simulated by a neural network mo
del by modifying the activity of model units that represent medial vestibul
ar nucleus neurons. An asymmetric dynamic response by a gain-enhancement fu
nction of either type 1A neurons on one side or of type 2 neurons on the ot
her was sufficient to produce an isolated caloric DP. Excitatory gain enhan
cement of type 2 neurons produced a smaller rotational DP than a similar mo
dification of type 1 neurons. This result indicates a potential neural locu
s for the generation of an isolated DP in patients with vestibular disorder
s.