Modeling neuromuscular modulation in Aplysia.: III.: Interaction of central motor commands and peripheral modulatory state for optimal behavior

被引:27
作者
Brezina, V
Horn, CC
Weiss, KR
机构
[1] Mt Sinai Sch Med, Dept Physiol & Biophys, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Fishberg Res Ctr Neurobiol, New York, NY USA
[3] Monell Chem Senses Ctr, Philadelphia, PA 19104 USA
关键词
D O I
10.1152/jn.00475.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent work in computational neuroethology has emphasized that "the brain has a body": successful adaptive behavior is not simply commanded by the nervous system, but emerges from interactions of nervous system, body, and environment. Here we continue our study of these issues in the accessory radula closer (ARC) neuromuscular system of Aplysia. The ARC muscle participates in the animal's feeding behaviors, a set of cyclical, rhythmic behaviors driven by a central patient generator (CPG). Patterned firing of the ARC muscle's two motor neurons, B 15 and B 16, releases not only ACh to elicit the muscle's contractions but also peptide neuromodulators that then shape the contractions through a complex network of I actions on the muscle. These actions are dynamically complex: some are fast, but some are slow, so that they are temporally uncoupled from the motor neuron firing pattern in the current cycle. Under these circumstances, how can the nervous system, through just the narrow channel of the firm,, patterns of the motor neurons, control the contractions, movements, and behavior in the periphery? In two earlier papers, we developed a realistic mathematical model of the B15/B16-ARC neuromuscular system and its modulation. Here we use this model to study the functional performance of the system in a realistic behavioral task. We run the model with two kinds of inputs: a simple set of regular motor neuron firing patterns that allows us to examine the entire space of patterns. and the real firing patterns of B15 and B16 previously recorded in a 21/2-h-long meal of 749 cycles in an intact feeding animal. These real patterns are extremely irregular. Our main conclusions are the following. 1) The modulation in the periphery is necessary for superior functional performance. 2) The components of the modulatory network interact in nonlinear, context- and task-dependent combinations for best performance overall, although not necessarily in any particular cycle. 3) Both the fast and the slow dynamics of the modulatory state make important contributions. 4) The nervous system controls different components of the periphery to different degrees. To some extent the periphery operates semiautonomously. However. the structure of the peripheral modulatory network ensures robust performance under all circumstances, even with the irregular motor neuron firing patterns and even when the parameters of he functional task are randomly varied from cycle to cycle to simulate a variable feeding environment. In the variable environment, regular firing patterns. which are fine-tuned to one particular task, fail to provide robust performance. We propose that the CPG generates the irregular firing patterns, which nevertheless are guaranteed to give robust performance overall through the actions of the peripheral modulatory network, as part of a trial-and-error feeding strategy in a variable, uncertain environment.
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收藏
页码:1523 / 1556
页数:34
相关论文
共 90 条
[1]   CHEMOTAXIS IN BACTERIA [J].
ADLER, J .
ANNUAL REVIEW OF BIOCHEMISTRY, 1975, 44 :341-356
[2]   INTERCELLULAR COMMUNICATION IN THE BRAIN - WIRING VERSUS VOLUME TRANSMISSION [J].
AGNATI, LF ;
ZOLI, M ;
STROMBERG, I ;
FUXE, K .
NEUROSCIENCE, 1995, 69 (03) :711-726
[3]   Error and attack tolerance of complex networks [J].
Albert, R ;
Jeong, H ;
Barabási, AL .
NATURE, 2000, 406 (6794) :378-382
[4]   Robustness in bacterial chemotaxis [J].
Alon, U ;
Surette, MG ;
Barkai, N ;
Leibler, S .
NATURE, 1999, 397 (6715) :168-171
[5]  
[Anonymous], 1990, Intelligence as Adaptive Behavior: An Experiment in Computational Neuroethology
[6]   Robustness in simple biochemical networks [J].
Barkai, N ;
Leibler, S .
NATURE, 1997, 387 (6636) :913-917
[7]   A DYNAMICAL-SYSTEMS PERSPECTIVE ON AGENT ENVIRONMENT INTERACTION [J].
BEER, RD .
ARTIFICIAL INTELLIGENCE, 1995, 72 (1-2) :173-215
[8]   Evolution and analysis of model CPGs for walking: II. General principles and individual variability [J].
Beer, RD ;
Chiel, HJ ;
Gallagher, JC .
JOURNAL OF COMPUTATIONAL NEUROSCIENCE, 1999, 7 (02) :119-147
[9]   Flexibility at the edge of chaos: A clear example from foraging in ants [J].
Bonabeau, E .
ACTA BIOTHEORETICA, 1997, 45 (01) :29-50
[10]   Analyzing the functional consequences of transmitter complexity [J].
Brezina, V ;
Weiss, KR .
TRENDS IN NEUROSCIENCES, 1997, 20 (11) :538-543