Oxygen sensing in the carotid body: ideas and models.

[1]  C. González,et al.  Effect of low O2 on glucose uptake in rabbit carotid body. , 1993, Journal of applied physiology.

[2]  D. Donnelly.  Electrochemical detection of catecholamine release from rat carotid body in vitro. , 1993, Journal of applied physiology.

[3]  G. Bokoch.  Biology of the Rap proteins, members of the ras superfamily of GTP-binding proteins. , 1993, The Biochemical journal.

[4]  H. Acker,et al.  The meaning of H2O2 generation in carotid body cells for PO2 chemoreception. , 1992, Journal of the autonomic nervous system.

[5]  J. López-Barneo,et al.  Potassium channel types in arterial chemoreceptor cells and their selective modulation by oxygen , 1992, The Journal of general physiology.

[6]  M. Duchen,et al.  Relative mitochondrial membrane potential and [Ca2+]i in type I cells isolated from the rabbit carotid body. , 1992, The Journal of physiology.

[7]  M. Duchen,et al.  Mitochondrial function in type I cells isolated from rabbit arterial chemoreceptors. , 1992, The Journal of physiology.

[8]  C. González,et al.  Time course of K+ current inhibition by low oxygen in chemoreceptor cells of adult rabbit carotid body Effects of carbon monoxide , 1992, FEBS letters.

[9]  R Iturriaga,et al.  Optical measurements of the dependence of chemoreception on oxygen pressure in the cat carotid body. , 1991, The American journal of physiology.

[10]  Stefan H. Heinemann,et al.  Regulation of fast inactivation of cloned mammalian IK(A) channels by cysteine oxidation , 1991, Nature.

[11]  K. Ikeda,et al.  Response of cytosolic calcium to anoxia and cyanide in cultured glomus cells of newborn rabbit carotid body , 1991, Brain Research.

[12]  J. Hancock,et al.  Inhibitors of NADPH oxidase as guides to its mechanism. , 1991, Biochemical Society transactions.

[13]  H. Acker,et al.  Involvement of an NAD(P)H oxidase as a pO2 sensor protein in the rat carotid body. , 1990, The Biochemical journal.

[14]  M. Wolin,et al.  Superoxide anion inhibits cGMP-associated bovine pulmonary arterial relaxation. , 1990, The American journal of physiology.

[15]  H. Acker,et al.  Indications to an NADPH oxidase as a possible pO2 sensor in the rat carotid body , 1989, FEBS letters.

[16]  M. Duchen,et al.  Measurements of intracellular Ca2+ in dissociated type I cells of the rabbit carotid body. , 1989, The Journal of physiology.

[17]  J. Hescheler,et al.  Ionic currents on type-I cells of the rabbit carotid body measured by voltage-clamp experiments and the effect of hypoxia , 1989, Brain Research.

[18]  J. López-Barneo,et al.  Low pO2 selectively inhibits K channel activity in chemoreceptor cells of the mammalian carotid body , 1989, The Journal of general physiology.

[19]  W. Rumsey,et al.  The oxygen dependence of mitochondrial oxidative phosphorylation measured by a new optical method for measuring oxygen concentration. , 1988, The Journal of biological chemistry.

[20]  B. Chance.  Early reduction of cytochrome c in hypoxia , 1988, FEBS letters.

[21]  M. Brand,et al.  CONTROL OF ELECTRON FLUX THROUGH THE RESPIRATORY CHAIN IN MITOCHONDRIA AND CELLS , 1987, Biological reviews of the Cambridge Philosophical Society.

[22]  D. Buerk,et al.  Cat carotid body oxygen metabolism and chemoreception described by a two-cytochrome model. , 1986, The American journal of physiology.

[23]  F. Pietruschka.  Calcium influx in cultured carotid body cells is stimulated by acetylcholine and hypoxia , 1985, Brain Research.

[24]  S. Lahiri,et al.  Carotid body O2 chemoreception and mitochondrial oxidative phosphorylation. , 1981, Journal of applied physiology: respiratory, environmental and exercise physiology.

[25]  R G DeLaney,et al.  Stimulus interaction in the responses of carotid body chemoreceptor single afferent fibers. , 1975, Respiration physiology.

[26]  L. Flohé,et al.  Oxidation in the NADP system and release of GSSG from hemoglobin‐free perfused rat liver during peroxidatic oxidation of glutathione by hydroperoxides , 1972, FEBS letters.

[27]  F. Jöbsis,et al.  Mitochondrial respiratory chain of carotid body and chemoreceptor response to changes in oxygen tension. , 1972, Journal of neurophysiology.