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Expression of hypoglossal long-term facilitation differs between substrains of Sprague-Dawley rat
Department of Comparative Biosciences, University of Wisconsin, Madison, Wisconsin 53706 Long-term facilitation (LTF) is a prolonged, serotonin-dependent augmentation of respiratory motor output following episodic hypoxia. Previous observations lead us to hypothesize that LTF is subject to genetic i...
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Published in: | Physiological genomics 2001-01, Vol.4 (3), p.175-181 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Department of Comparative Biosciences, University of Wisconsin, Madison, Wisconsin 53706
Long-term facilitation (LTF) is a prolonged, serotonin-dependent augmentation of respiratory motor output following episodic hypoxia. Previous observations lead us to hypothesize that LTF is subject to genetic influences and, as a result, differs between Sprague-Dawley (SD) rats from two vendors, Harlan (H) and Charles River Laboratories/Sasco (CRL/S). Using a blinded experimental design, we recorded integrated phrenic ( Phr) and hypoglossal neurograms in anesthetized, vagotomized, paralyzed, and ventilated rats. At 60 min following three 5-min hypoxic episodes (Pa O 2 = 40 ± 1 Torr; 5-min hyperoxic intervals), Phr was elevated from baseline in both SD substrains (i.e., LTF; P < 0.05). Conversely, hypoglossal LTF was present in CRL/S but not H rats ( P < 0.05 between substrains). Serotonin immunoreactivity within the hypoglossal nucleus was not different between H and CRL/S rats. We conclude that the expression of hypoglossal LTF differs between SD rat substrains, indicating a difference in their genetic predisposition to neural plasticity.
respiratory control; plasticity; genetics |
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ISSN: | 1094-8341 1531-2267 |
DOI: | 10.1152/physiolgenomics.2001.4.3.175 |