Document Detail


Ventilatory effects of substance P-saporin lesions in the nucleus tractus solitarii of chronically hypoxic rats.
MedLine Citation:
PMID:  21593425     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
During ventilatory acclimatization to hypoxia (VAH), time-dependent increases in ventilation lower Pco(2) levels, and this persists on return to normoxia. We hypothesized that plasticity in the caudal nucleus tractus solitarii (NTS) contributes to VAH, as the NTS receives the first synapse from the carotid body chemoreceptor afferents and also contains CO(2)-sensitive neurons. We lesioned cells in the caudal NTS containing the neurokinin-1 receptor by microinjecting the neurotoxin saporin conjugated to substance P and measured ventilatory responses in awake, unrestrained rats 18 days later. Lesions did not affect hypoxic or hypercapnic ventilatory responses in normoxic control rats, in contrast to published reports for similar lesions in other central chemosensitive areas. Also, lesions did not affect the hypercapnic ventilatory response in chronically hypoxic rats (inspired Po(2) = 90 Torr for 7 days). These results suggest functional differences between central chemoreceptor sites. However, lesions significantly increased ventilation in normoxia or acute hypoxia in chronically hypoxic rats. Hence, chronic hypoxia increases an inhibitory effect of neurokinin-1 receptor neurons in the NTS on ventilatory drive, indicating that these neurons contribute to plasticity during chronic hypoxia, although such plasticity does not explain VAH.
Authors:
Katherine A Wilkinson; Zhenxing Fu; Frank L Powell
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2011-05-18
Journal Detail:
Title:  American journal of physiology. Regulatory, integrative and comparative physiology     Volume:  301     ISSN:  1522-1490     ISO Abbreviation:  Am. J. Physiol. Regul. Integr. Comp. Physiol.     Publication Date:  2011 Aug 
Date Detail:
Created Date:  2011-08-03     Completed Date:  2011-10-18     Revised Date:  2013-06-28    
Medline Journal Info:
Nlm Unique ID:  100901230     Medline TA:  Am J Physiol Regul Integr Comp Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  R343-50     Citation Subset:  IM    
Affiliation:
Division of Physiology, Department of Medicine, University of California, San Diego, USA. kawilki@emory.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Anoxia / physiopathology*
Carbon Dioxide / metabolism,  pharmacology
Consciousness
Male
Neurons / drug effects,  physiology
Oxygen / metabolism,  pharmacology
Rats
Rats, Sprague-Dawley
Receptors, Neurokinin-1 / metabolism
Respiratory Physiological Processes / drug effects*
Ribosome Inactivating Proteins, Type 1 / toxicity*
Solitary Nucleus / cytology,  drug effects*
Substance P / toxicity*
Grant Support
ID/Acronym/Agency:
MO1-RR00827/RR/NCRR NIH HHS; R01 HL081823/HL/NHLBI NIH HHS; R01 HL081823/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Receptors, Neurokinin-1; 0/Ribosome Inactivating Proteins, Type 1; 124-38-9/Carbon Dioxide; 33507-63-0/Substance P; 7782-44-7/Oxygen; EC 3.2.2.22/saporin
Comments/Corrections

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