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J Neurophysiol 95: 1982-1991, 2006. First published December 7, 2005; doi:10.1152/jn.00674.2005
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Spatiotemporal Activity Patterns During Respiratory Rhythmogenesis in the Rat Ventrolateral Medulla

Jonathan A. N. Fisher1, Vitaliy A. Marchenko2, Arjun G. Yodh1 and Robert F. Rogers2

1Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, Pennsylvania; and 2Department of Electrical and Computer Engineering, University of Delaware, Newark, Delaware

Submitted 28 June 2005; accepted in final form 2 December 2005

One of the most important brain rhythms is that which generates involuntary breathing movements. The lower brain stem contains neural circuitry for respiratory rhythm generation in mammals. To date, microsectioning and selective lesioning studies have revealed anatomical regions necessary for respiratory rhythmogenesis. Although respiratory neurons distributed within these regions can be identified by their firing patterns in different phases of the respiratory cycle, conventional electrophysiology techniques have limited the study of spatial organization within this network. Optical imaging techniques offer the potential for monitoring the spatiotemporal activity of large groups of neurons simultaneously. Using high-speed voltage-sensitive dye imaging and spatial correlation analysis in an arterially perfused in situ preparation of the juvenile rat, we determined the spatial distribution of respiratory neuronal activity in a region of the ventrolateral respiratory group containing the pre-Bötzinger complex (pBC) during spontaneous eupneic breathing. While distinctly pre- and postinspiratory-related responses were spatially localizable on length scales less than 100 µm, we found the studied area on whole exhibited a spatial mixture of phase-spanning and postinspiratory-related activity. Additionally, optical recordings revealed significant widespread hyperpolarization, suggesting inhibition in the same region during expiration. This finding is consistent with the hypothesis that inhibitory neurons play a crucial role in the inspiration-expiration phase transition in the pBC. To our knowledge this is the first optical imaging of a near fully intact in situ preparation that exhibits both eupneic respiratory activity and functional reflexes.


Address for reprint requests and other correspondence: J.A.N. Fisher, Dept. of Physics and Astronomy, Univ. of Pennsylvania, 209 S. 33rd St., Philadelphia, PA 19104 (E-mail: aafisher{at}physics.upenn.edu)




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