Experimental Physiology
	

Celebrating 100 years
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Experimental Physiology 91.1 pp 17-23
DOI: 10.1113/expphysiol.2005.031922
© The Physiological Society 2006
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
91/1/17    most recent
expphysiol.2005.031922v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Prabhakar, N. R
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Prabhakar, N. R
Related Collections
Right arrow Respiratory
Right arrow Hot Topic Reviews

Hot Topic Review

O2 sensing at the mammalian carotid body: why multiple O2 sensors and multiple transmitters?

Nanduri R Prabhakar1

1 Department of Physiology & Biophysics, School of Medicine, Case Western Reserve University, Cleveland, OH 440109, USA

Carotid bodies are the sensory organs for detecting systemic hypoxia and the ensuing reflexes prevent the development of tissue/cellular hypoxia. Although every mammalian cell responds to hypoxia, O2 sensing by the carotid body is unique in that it responds instantaneously (within seconds) to even a modest drop in arterial PO2. Sensing hypoxia in the carotid body requires an initial transduction step involving O2 sensor(s) and transmitter(s) for subsequent activation of the afferent nerve ending. This brief review focuses on: (a) whether the transduction involves ‘single’ or ‘multiple’ O2 sensors; (b) the identity of the excitatory transmitter(s) responsible for afferent nerve activation by hypoxia; and (c) whether inhibitory transmitters have any functional role. The currently proposed O2 sensors include various haem-containing proteins, and a variety of O2-sensitive K+ channels. It is proposed that the transduction involves an ensemble of, and interactions between, haem-containing proteins and O2-sensitive K+-channel proteins functioning as a ‘chemosome’; the former for conferring sensitivity to wide range of PO2 values and the latter for the rapidity of the response. Hypoxia releases both excitatory and inhibitory transmitters from the carotid body. ATP is emerging as an important excitatory transmitter for afferent nerve activation by hypoxia. Whereas the inhibitory messengers act in concert with excitatory transmitters like a ‘push–pull’ mechanism to prevent over excitation, conferring the ‘slowly adapting’ nature of the afferent nerve activation during prolonged hypoxia. Further studies are needed to test the interactions between putative O2 sensors and excitatory and inhibitory transmitters in the carotid body.

(Received 10 August 2005; accepted after revision 5 October 2005; first published online 20 October 2005)
Corresponding author N. R. Prabhakar: Department of Physiology & Biophysics, School of Medicine, Case Western Reserve University, 1090 Euclid Avenue, Cleveland, OH 44019, USA. Email: nrp{at}case.edu




This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
K. R. Olson
Hydrogen sulfide and oxygen sensing: implications in cardiorespiratory control
J. Exp. Biol., September 1, 2008; 211(17): 2727 - 2734.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
G. Montandon, A. Bairam, and R. Kinkead
Neonatal caffeine induces sex-specific developmental plasticity of the hypoxic respiratory chemoreflex in adult rats
Am J Physiol Regulatory Integrative Comp Physiol, September 1, 2008; 295(3): R922 - R934.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
M. G. Jonz and C. A. Nurse
New developments on gill innervation: insights from a model vertebrate
J. Exp. Biol., August 1, 2008; 211(15): 2371 - 2378.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
K. R. Olson, M. J. Healy, Z. Qin, N. Skovgaard, B. Vulesevic, D. W. Duff, N. L. Whitfield, G. Yang, R. Wang, and S. F. Perry
Hydrogen sulfide as an oxygen sensor in trout gill chemoreceptors
Am J Physiol Regulatory Integrative Comp Physiol, August 1, 2008; 295(2): R669 - R680.
[Abstract] [Full Text] [PDF]


Home page
Exp PhysiolHome page
D. J. Paterson
Celebrating 100 years of publishing discovery in physiology 1908 - 2008
Exp Physiol, January 1, 2008; 93(1): 1 - 15.
[Full Text] [PDF]


Home page
Circ. Res.Home page
Z.-Y. Tan, Y. Lu, C. A. Whiteis, C. J. Benson, M. W. Chapleau, and F. M. Abboud
Acid-Sensing Ion Channels Contribute to Transduction of Extracellular Acidosis in Rat Carotid Body Glomus Cells
Circ. Res., November 9, 2007; 101(10): 1009 - 1019.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
R. Varas, C. N. Wyatt, and K. J. Buckler
Modulation of TASK-like background potassium channels in rat arterial chemoreceptor cells by intracellular ATP and other nucleotides
J. Physiol., September 1, 2007; 583(2): 521 - 536.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
C. E. Cooper and C. Giulivi
Nitric oxide regulation of mitochondrial oxygen consumption II: molecular mechanism and tissue physiology
Am J Physiol Cell Physiol, June 1, 2007; 292(6): C1993 - C2003.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
G. Burnstock
Physiology and Pathophysiology of Purinergic Neurotransmission
Physiol Rev, April 1, 2007; 87(2): 659 - 797.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. N. Wyatt, K. J. Mustard, S. A. Pearson, M. L Dallas, L. Atkinson, P. Kumar, C. Peers, D. G. Hardie, and A. M. Evans
AMP-activated Protein Kinase Mediates Carotid Body Excitation by Hypoxia
J. Biol. Chem., March 16, 2007; 282(11): 8092 - 8098.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. A. Day and R. J. A. Wilson
Brainstem PCO2 modulates phrenic responses to specific carotid body hypoxia in an in situ dual perfused rat preparation
J. Physiol., February 1, 2007; 578(3): 843 - 857.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the The Physiological Society.