The DOI matches its Crossref record; 532 of the 532 references it cites were found in a registry or an index.
Peripheral Chemoreceptors: Function and Plasticity of the Carotid Body
Open accessAbstract
The discovery of the sensory nature of the carotid body dates back to the beginning of the 20th century. Following these seminal discoveries, research into carotid body mechanisms moved forward progressively through the 20th century, with many descriptions of the ultrastructure of the organ and stimulus‐response measurements at the level of the whole organ. The later part of 20th century witnessed the first descriptions of the cellular responses and electrophysiology of isolated and cultured type I and type II cells, and there now exist a number of testable hypotheses of chemotransduction. The goal of this article is to provide a comprehensive review of current concepts on sensory transduction and transmission of the hypoxic stimulus at the carotid body with an emphasis on integrating cellular mechanisms with the whole organ responses and highlighting the gaps or discrepancies in our knowledge. It is increasingly evident that in addition to hypoxia, the carotid body responds to a wide variety of blood‐borne stimuli, including reduced glucose and immune‐related cytokines and we therefore also consider the evidence for a polymodal function of the carotid body and its implications. It is clear that the sensory function of the carotid body exhibits considerable plasticity in response to the chronic perturbations in environmental O 2 that is associated with many physiological and pathological conditions. The mechanisms and consequences of carotid body plasticity in health and disease are discussed in the final sections of this article. © 2012 American Physiological Society.Compr Physiol 2:141‐219, 2012.
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Cites
Items 401–532 of 532
Nurse, C. A., & Vollmer, C. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8539 · Cited by 50
Carotid body chemoreceptors in dissociated cell culture
Nurse, C. A., & Fearon, I. M. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10199 · Cited by 50
The co-existence of biogenic amines and neuropeptides in the type I cells of the cat carotid body
Wang, Z.-Z., Stensaas, L. J., Dinger, B., et al. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90261-y · Cited by 49
He, L., Dinger, B., Sanders, K. A., Hoidal, J. R., Obeso, A., Stensaas, L. J., Fidone, S., & González, C. (2005) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00015.2005 · Cited by 49
Historical perspectives of cellular oxygen sensing and responses to hypoxia
Lahiri, S. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.4.1467 · Cited by 49
Expression of HIF-1α, VEGF and VEGF receptors in the carotid body of chronically hypoxic rat
Tipoe, G. L., & Fung, M. (2003) · Respiratory Physiology & Neurobiology · doi:10.1016/s1569-9048(03)00188-5 · Cited by 48
Robbins, P. A. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp017175 · Cited by 48
Lam, S. Y., Fung, M., & Leung, P. S. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00684.2003 · Cited by 48
Physiological chemoreceptor stimulation decreases enkephalin and substance P in the carotid body
Hanson, G. R., Jones, L., & Fidone, S. (1986) · Peptides · doi:10.1016/0196-9781(86)90093-8 · Cited by 48
Time-dependent modulation of carotid body afferent activity during and after intermittent hypoxia
Cummings, K. J., & Wilson, R. J. A. (2005) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00788.2004 · Cited by 47
AMP‐activated protein kinase and the regulation of Ca2+ signalling in O2‐sensing cells
Evans, A. M. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.108381 · Cited by 47
Effect of chronic hypoxia on cholinergic chemotransmission in rat carotid body
He, L., Dinger, B., & Fidone, S. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00714.2004 · Cited by 47
Chen, I. I., Rd, Y., & Jt, H. (1986) · PubMed · Cited by 47
Laidler, P., & Kay, J. M. (1978) · Journal of Neurocytology · doi:10.1007/bf01217917 · Cited by 46
Fan, J., Zhang, B., Shu, H., Zhang, X., Wang, X., Kuang, F., Liu, L., Peng, Z., Wu, R. J., Zhou, Z., et al. (2009) · Journal of Neuroscience Research · doi:10.1002/jnr.22107 · Cited by 46
Sensitivity of the carotid body to within-breath changes in arterial PCO2
Band, D. M., McClelland, M. E., Phillips, D. L., Saunders, K. B., & Wolff, C. B. (1978) · Journal of Applied Physiology · doi:10.1152/jappl.1978.45.5.768 · Cited by 45
Stulbarg, M. S., & Winn, W. R. (1989) · CHEST Journal · doi:10.1378/chest.95.5.1123 · Cited by 45
Zhang, M., & Nurse, C. A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02499-9 · Cited by 45
Morphological evidence for existence of IL‐6 receptor alpha in the glomus cells of rat carotid body
Wang, X., Zhang, X., Xu, Z., Li, X., Li, G., Ju, G., & Wang, B. (2006) · The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20310 · Cited by 45
Role of substance P in hypercapnic excitation of carotid chemoreceptors
Prabhakar, N. R., Mitra, J., & Cherniack, N. S. (1987) · Journal of Applied Physiology · doi:10.1152/jappl.1987.63.6.2418 · Cited by 45
Self-citationEffects of 2-deoxy-d-glucose on in vitro cat carotid body
Obeso, A., Almaraz, L., & González, C. (1986) · Brain Research · doi:10.1016/0006-8993(86)90806-1 · Cited by 44
Donnelly, D. F., Kim, I., Carle, C., et al. (2005) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01009.2004 · Cited by 44
Summers, B. A., Overholt, J. L., & Prabhakar, N. R. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1636 · Cited by 44
Self-citationHempleman, S. C. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.3.1880 · Cited by 44
Oxygen sensitive Kv channels in the carotid body
López‐López, J. R., & Pérez-García, M. T. (2007) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2007.01.022 · Cited by 43
Swelling‐ and cAMP‐Activated Cl− Currents in Isolated Rat Carotid Body Type I Cells
Carpenter, E. P., & Peers, C. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.497bg.x · Cited by 43
Lam, S., Tipoe, G. L., Liong, E. C., & Fung, M. (2008) · PubMed · doi:10.14670/hh-23.271 · Cited by 43
Valdés, V., Mosqueira, M., Rey, S., Río, R. D., & Iturriaga, R. (2003) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00494.2001 · Cited by 43
Chen, J., He, L., Liu, X., Dinger, B., Stensaas, L. J., & Fidone, S. (2007) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00419.2006 · Cited by 43
Further cholinergic aspects of carotid body chemotransduction of hypoxia in cats
Fitzgerald, R. S., Shirahata, M., & Ide, T. (1997) · Journal of Applied Physiology · doi:10.1152/jappl.1997.82.3.819 · Cited by 43
Ventilatory responses and carotid body function in adult rats perinatally exposed to hyperoxia
Prieto‐Lloret, J., Caceres, A. I., Obeso, A., Rocher, A., Rigual, R. J., Agapito, M. T., Bustamante, R., Castañeda, J., Pérez-García, M. T., López‐López, J. R., et al. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049445 · Cited by 42
Distribution of transient receptor potential channels in the rat carotid chemosensory pathway
Buniel, M. C. F., Schilling, W. P., & Kunze, D. L. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10798 · Cited by 42
Tafil‐Klawe, M., Ae, T., Raschke, F., Mayer, J., Jh, P., & von Wichert, W. (1991) · PubMed · Cited by 42
Alcayaga, J., Cerpa, V., Retamal, M. A., Arroyo, J., Iturriaga, R., & Zapata, P. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)00896-x · Cited by 41
Is ATP a suitable co-transmitter in carotid body arterial chemoreceptors?
Zapata, P. (2007) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2007.01.002 · Cited by 41
Biochemical studies on the release of catecholamines from the rat carotid body in vitro
Shaw, K., MONTAGUE, W., & Pallot, D. J. (1989) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/0167-4889(89)90125-0 · Cited by 41
Are oxygen dependent K+ channels essential for carotid body chemo-transduction?
Donnelly, D. F. (1997) · Respiration Physiology · doi:10.1016/s0034-5687(97)00085-6 · Cited by 41
Streller, T., Huckstorf, C., Pfeiffer, C., & Acker, H. (2002) · The FASEB Journal · doi:10.1096/fj.02-0166fje · Cited by 41
Arterial chemoreceptor‐like activity in the abdominal vagus of the rat.
Howe, A., Pack, R. J., & Wise, J. C. M. (1981) · The Journal of Physiology · doi:10.1113/jphysiol.1981.sp013951 · Cited by 40
Conde, S. V., Monteiro, E. C., Obeso, A., & González, C. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-90-481-2259-2_17 · Cited by 40
Macrophages: a major source of cytochrome b558 in the rat carotid body
Dvorakova, M. C., Höhler, B., Vollerthun, R., Fischbach, T., & Kummer, W. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02156-3 · Cited by 39
Teppema, L. J., Nieuwenhuijs, D. J. F., Sarton, E. Y., Romberg, R. R., Olievier, C. N., Ward, D. S., & Dahan, A. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.025999 · Cited by 39
Acute hypoxia elevates nitric oxide generation in rat carotid body in vitro
M.-L., F., J.-S., Y., & Fung, P. C. W. (2001) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240100610 · Cited by 39
Oxygen and life span: chronic hypoxia as a model for studying HIF-1α, VEGF and NOS during aging
Giulio, C. D., Bianchi, G., Cacchio, M., Artese, L., Rapino, C., Macrì, M. A., & Ilio, C. D. (2005) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2005.01.006 · Cited by 39
Obeso, A., Almaraz, L., & González, C. (1985) · Brain Research · doi:10.1016/0006-8993(85)90360-9 · Cited by 39
Peripheral chemoreflex in chronic heart failure: Friend and foe
Chugh, S. S., Chua, T. P., & Coats, A. J. S. (1996) · American Heart Journal · doi:10.1016/s0002-8703(96)90333-6 · Cited by 38
Cardiovascular Responses to Stress after Carotid Baroreceptor Denervation in Humans
Timmers, H. J. L. M., Wieling, W., Karemaker, J. M., & Lenders, J. W. M. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1296.063 · Cited by 38
Eyzaguirre, C., & Abudara, V. (1999) · Respiration Physiology · doi:10.1016/s0034-5687(99)00020-1 · Cited by 38
Nitric oxide synthase in autonomic innervation of the cat carotid body
Grimes, P. A., Anil, M., Stone, R. A., et al. (1995) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(95)00006-j · Cited by 38
Li, Y., Sun, S.-Y., Overholt, J. L., Prabhakar, N. R., Rozanski, G. J., Zucker, I. H., & Schultz, H. D. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.057422 · Cited by 38
Self-citationEndothelin Modulates Chemoreceptor Cell Function in Mammalian Carotid Body
He, L., Chen, J., Dinger, B., et al. (1996) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-5891-0_46 · Cited by 37
Roux, J., Brismar, H., Aperia, A. C., & Lagercrantz, H. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000163390.78239.ea · Cited by 37
Ye, J., Tipoe, G. L., Fung, P. C. W., & Fung, M. (2002) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-002-0785-1 · Cited by 37
Yamamoto, Y., König, P., Henrich, M., Dedio, J., & Kummer, W. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0178-4 · Cited by 37
Differential modulation by extracellular ATP of carotid chemosensory responses
Spergel, D. J., & Lahiri, S. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.74.6.3052 · Cited by 37
Effects on breathing of carotid body denervation in neonatal piglets
Lowry, T. F., Forster, H. V., Pan, L. G., Serra, A., Wenninger, J. M., Nash, R. W., Sheridan, D. C., & Franciosi, R. A. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.6.2128 · Cited by 37
Occurrence of Afferent Synaptic Complexes in the Carotid Body of the Mouse
Kobayashi, S., & UEHARA, M. (1970) · Archivum histologicum japonicum · doi:10.1679/aohc1950.32.193 · Cited by 37
Alveolar to arterial transmission of oxygen fluctuations due to respiration in anesthetized dogs
Yokota, H., & Kreuzer, F. (1973) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00592308 · Cited by 36
The distribution of thoracic glomus tissue (aortic bodies) in the rat
Easton, J., & Howe, A. (1983) · Cell and Tissue Research · doi:10.1007/bf00213792 · Cited by 36
Zhang, X., Wang, X., Xiong, L., Fan, J., Duan, X.-L., & Wang, B. (2007) · Histochemistry and Cell Biology · doi:10.1007/s00418-007-0346-y · Cited by 36
Hartness, M. E., Brazier, S. P., Peers, C., Bateson, A. N., Ashford, M. L. J., & Kemp, P. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m309463200 · Cited by 36
Chronic hypoxia activates a local angiotensin-generating system in rat carotid body
Lam, S. Y., & Leung, P. S. (2003) · Molecular and Cellular Endocrinology · doi:10.1016/s0303-7207(03)00087-x · Cited by 35
Postnatal development of carotid body glomus cell response to hypoxia
Wasicko, M. J., Breitwieser, G. E., Kim, I., et al. (2006) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2006.01.003 · Cited by 35
Autoradiographic localization of muscarinic receptors in rabbit carotid body
Dinger, B., Hirano, T., & Fidone, S. (1986) · Brain Research · doi:10.1016/0006-8993(86)91612-4 · Cited by 34
Chronic hypoxia upregulates connexin43 expression in rat carotid body and petrosal ganglion
Chen, J., He, L., Dinger, B., Stensaas, L. J., & Fidone, S. (2002) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00077.2001 · Cited by 34
Kumar, P., Nye, P. C. G., & Torrance, R. W. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp016933 · Cited by 33
Self-citationThe effect of low‐dose acetazolamide on the ventilatory CO2 response curve in the anaesthetized cat.
Wagenaar, M., Teppema, L. J., Berkenbosch, A., Olievier, C. N., & Folgering, H. T. M. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021587 · Cited by 33
Hypoxic Pulmonary Vasoconstriction – Invited Article
Evans, A. M., & Ward, J. P. T. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-90-481-2259-2_40 · Cited by 33
Localization and in vitro actions of atrial natriuretic peptide in the cat carotid body
Wang, Z.-Z., He, L., Stensaas, L. J., et al. (1991) · Journal of Applied Physiology · doi:10.1152/jappl.1991.70.2.942 · Cited by 33
Evidence for two types of nicotinic receptors in the cat carotid body chemoreceptor cells
Obeso, A., Gómez-Niño, Á., Almaraz, L., Dinger, B., Fidone, S., & González, C. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00185-6 · Cited by 32
Tachykinin antagonists in carotid body responses to hypoxia and subtance P in the rat
Cragg, P. A., Runold, M., Kou, Y. R., et al. (1994) · Respiration Physiology · doi:10.1016/0034-5687(94)90092-2 · Cited by 32
Carotid body chemoreceptor function: hypothesis based on a new circuit model.
Krammer, E. B. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.5.2507 · Cited by 32
EPAC signalling pathways are involved in low PO2 chemoreception in carotid body chemoreceptor cells
Rocher, A., Caceres, A. I., Almaraz, L., & González, C. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.172072 · Cited by 31
Peripheral and Central Chemoreceptor Control of Ventilation During Exercise in Humans
Ward, S. A. (1994) · Canadian Journal of Applied Physiology · doi:10.1139/h94-026 · Cited by 31
Kim, D.-K., Oh, E. K., Summers, B. A., Prabhakar, N. R., & Kumar, G. K. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03272-8 · Cited by 31
Self-citationAntioxidants reverse depression of the hypoxic ventilatory response by acetazolamide in man
Teppema, L. J., Bijl, H., Romberg, R. R., & Dahan, A. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2005.104174 · Cited by 31
Vicario, I., Obeso, A., Rocher, A., et al. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.1.c51 · Cited by 31
Acker, H., & L�bbers, D. W. (1977) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00591569 · Cited by 30
Caceres, A. I., Obeso, A., González, C., & Rocher, A. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04465.x · Cited by 30
Doyle, T. P., & Donnelly, D. F. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.6.2606 · Cited by 30
Oxygen tension measurements in carotid body of the cat
Whalen, W. J., Savoca, J., & Nair, P. (1973) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1973.225.4.986 · Cited by 30
Excitation of carotid body chemoreceptors by neuropeptide-Y
Potter, E. K., & McCloskey, D. I. (1987) · Respiration Physiology · doi:10.1016/0034-5687(87)90065-x · Cited by 29
MaxiK potassium channels in the function of chemoreceptor cells of the rat carotid body
Gómez-Niño, Á., Obeso, A., Baranda, J. A., et al. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00507.2008 · Cited by 29
Prabhakar, N. R., Cao, H., Lowe, J. A., III, et al. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.21.10041 · Cited by 29
Self-citationCat carotid body chemosensory discharge (in vitro) is insensitive to charybdotoxin
Osanai, S., Buerk, D. G., Mokashi, A., et al. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01313-3 · Cited by 29
Teppema, L. J., Dahan, A., & Olievier, C. N. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0221k.x · Cited by 27
A standing Na+ conductance in rat carotid body type I cells
Carpenter, E. P., & Peers, C. (2001) · Neuroreport · doi:10.1097/00001756-200105250-00025 · Cited by 27
Acute adaptation of carbohydrate metabolism to decreased arterial PO2
Zinker, B. A., Namdaran, K., Wilson, R., Lacy, D. B., & Wasserman, D. H. (1994) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1994.266.6.e921 · Cited by 27
Respiratory plasticity after perinatal hyperoxia is not prevented by antioxidant supplementation
Bavis, R. W., Wenninger, J. M., Miller, B. M., Dmitrieff, E. F., Olson, E. B., Mitchell, G. S., & Bisgard, G. E. (2007) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2007.10.013 · Cited by 26
Impaired ventilatory acclimatization to hypoxia in mice lacking the immediate early gene fos B
Malik, M. T., Peng, Y., Kline, D. D., Adhikary, G., & Prabhakar, N. R. (2004) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2004.08.009 · Cited by 24
Self-citationGeneral redox environment and carotid body chemoreceptor function
Agapito, M. T., Sanz‐Alfayate, G., Gómez-Niño, Á., González, C., & Obeso, A. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00542.2008 · Cited by 23
Do Carotid Chemoreceptors Inhibit the Hyperventilatory Response to Heavy Exercise?
Dempsey, J. A., & Smith, C. A. (1994) · Canadian Journal of Applied Physiology · doi:10.1139/h94-028 · Cited by 23
Does chronic hypoxia increase rat carotid body nitric oxide?
Giulio, C. D., Grilli, A., Lutiis, M. A. D., Natale, F. D., Sabatino, G., & Felaco, M. (1998) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/s1095-6433(98)00023-3 · Cited by 23
Montero, S., Mendoza, H., Valles, V., Lemus, M., Álvarez-Buylla, R., & de Álvarez-Buylla, E. R. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01414.2005 · Cited by 23
Overholt, J. L., & Prabhakar, N. R. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.1.225 · Cited by 23
Self-citationRoeggla, G., Roeggla, M., Wagner, A., & Laggner, A. N. (1995) · British Journal of Sports Medicine · doi:10.1136/bjsm.29.2.110 · Cited by 21
An important functional role of persistent Na+current in carotid body hypoxia transduction
Faustino, E. V. S., & Donnelly, D. F. (2006) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00090.2006 · Cited by 20
González‐Guerrero, P. R., Rigual, R. J., & González, C. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb13401.x · Cited by 20
Behavior of Junction Channels Between Rat Glomus Cells During Normoxia and Hypoxia
Abudara, V., Jiang, R. G., & Eyzaguirre, C. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.639 · Cited by 20
Kummer, W., & Yamamoto, Y. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10197 · Cited by 19
Effect of adenosine on chemosensory activity of the cat aortic body
Runold, M., Cherniack, N. S., & Prabhakar, N. R. (1990) · Respiration Physiology · doi:10.1016/0034-5687(90)90090-l · Cited by 19
Self-citationRotenone selectively occludes sensitivity to hypoxia in rat carotid body glomus cells
Ortega‐Sáenz, P., Pardal, R., Garcia-Fernandez, M., & López‐Barneo, J. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00789.x · Cited by 19
Interactions of chemostimuli at the single cell level: studies in a model system
Peers, C. (2003) · Experimental Physiology · doi:10.1113/expphysiol.2003.002657 · Cited by 18
Gauda, E. B., Bamford, O. S., & Northington, F. J. (1998) · Journal of the Autonomic Nervous System · doi:10.1016/s0165-1838(98)00141-6 · Cited by 18
Yu, G., Xu, L., Hadman, M., Hess, D. C., & Borlongan, C. V. (2004) · Brain Research · doi:10.1016/j.brainres.2004.04.055 · Cited by 18
Culture of arterial chemoreceptor cells from adult cats in defined medium
Shirahata, M., Schofield, B., Chin, B. Y., & Guilarte, T. R. (1994) · Brain Research · doi:10.1016/s0006-8993(09)90011-7 · Cited by 17
Transplantation of carotid body cells in the treatment of neurological disorders
Yu, G., Fournier, C. N., Hess, D. C., & Borlongan, C. V. (2005) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.011 · Cited by 17
Kusakabe, T., Kawakami, T., Tanabe, Y., et al. (1994) · Archivum histologicum japonicum · doi:10.1679/aohc.57.193 · Cited by 17
Prabhakar, N. R., Runold, M., Kumar, G. K., et al. (1989) · Peptides · doi:10.1016/0196-9781(89)90182-4 · Cited by 16
Self-citationEnzyme‐Linked Oxygen Sensing by Potassium Channels
Kemp, P. J., Telezhkin, V., Wilkinson, W. J., Mears, R., Hanmer, S. B., Gadeberg, H. C., Müller, C. T., Riccardi, D., & Brazier, S. P. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05025.x · Cited by 16
Kumar, G. K., Kou, Y. R., Overholt, J. L., et al. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.1.195 · Cited by 16
Increased blood osmolarity and its effect on respiration of dehydrating men
Senay, L. C. (1969) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00586966 · Cited by 15
Silveira, S. A., Lima, N. R. V., Haibara, A. S., & Coimbra, C. C. (2003) · Brain Research · doi:10.1016/j.brainres.2003.09.013 · Cited by 15
ATP causes glomus cell [Ca2+]c increase without corresponding increases in CSN activity
Mokashi, A., Li, J., Roy, A., et al. (2003) · Respiratory Physiology & Neurobiology · doi:10.1016/s1569-9048(03)00171-x · Cited by 14
Effects of osmotic changes on the chemoreceptor cell of rat carotid body
Molnár, Z., Petheö, G. L., Fülöp, C., & Spät, A. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2002.024125 · Cited by 14
RT-PCR and Pharmacological Analysis of L-and T-Type Calcium Channels in Rat Carotid Body
Caceres, A. I., González-Obeso, E., González, C., & Rocher, A. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-90-481-2259-2_12 · Cited by 13
Hayashida, Y., Kondo, H., & González, C. (2006) · Advances in experimental medicine and biology · doi:10.1007/0-387-31311-7 · Cited by 13
Bairam, A., Néji, H., Kinkead, R., & Marchal, F. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00227-9 · Cited by 13
Cadenas, J. L., Montero, S., Leal, C. A., Lemus, M., Buen, E. P., Alvarado, B. A., & de Álvarez-Buylla, E. R. (2010) · Nitric Oxide · doi:10.1016/j.niox.2010.02.003 · Cited by 13
Intracarotid Substance P infusion inhibits ventilation in the goat
Pizarro, J., Ryan, M. L., Hedrick, M. S., et al. (1995) · Respiration Physiology · doi:10.1016/0034-5687(95)00015-6 · Cited by 13
Chronic hypoxia modulates the function and expression of melatonin receptors in the rat carotid body
Tjong, Y.-W., Chen, Y., Liong, E. C., Tipoe, G. L., & Fung, M. (2005) · Journal of Pineal Research · doi:10.1111/j.1600-079x.2005.00286.x · Cited by 12
Central and Peripheral Chemosensitivity in Early Essential Hypertension in Man
Trzebski, A., Tafil, M., Zółtowski, M., et al. (1983) · Proceedings in life sciences · doi:10.1007/978-3-642-68657-3_26 · Cited by 11
Central Integration of Chemoreceptor Afferent Activity
Jordan, D. (1994) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-2572-1_8 · Cited by 11
Saiki, C., Seki, N., Furuya, H., & Matsumoto, S. (2005) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.2004.01375.x · Cited by 11
Carotid and aortic bodies in chronically anemic normotensive and spontaneously hypertensive rats
Habeck, J.-O., & Przybylski, J. (1989) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(89)90149-5 · Cited by 10
Teppema, L. J., Barts, P. W. J. A., & Evers, J. A. M. (1985) · Respiration Physiology · doi:10.1016/0034-5687(85)90073-8 · Cited by 10
Ortíz, F. C., Iturriaga, R., & Varas, R. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-90-481-2259-2_9 · Cited by 9
Donnelly, D. F. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.119263 · Cited by 9
Role of Substance P in Neutral Endopeptidase Modulation of Hypoxic Response of the Carotid Body
Kumara, G. K., Ru-Koub, Y., Overholtb, J. L., & Prabhakarb, N. R. (2002) · Advances in experimental medicine and biology · doi:10.1007/0-306-46825-5_70 · Cited by 9
Neuropeptide Processing Enzymes of the Carotid Body
Kumar, G. K. (1996) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-5891-0_48 · Cited by 5
Watanabe, T., Kumar, P., & Hanson, M. A. (1998) · Pediatric Research · doi:10.1203/00006450-199809000-00015 · Cited by 4
Self-citation
Cited by
Prabhakar, N. R., & Semenza, G. L. (2012) · Physiological Reviews · doi:10.1152/physrev.00030.2011 · Cited by 641
Pathophysiological mechanisms and therapeutic approaches in obstructive sleep apnea syndrome
Lv, R., Liu, X., Zhang, Y., Dong, N., Wang, X., He, Y., Yue, H., & Yin, Q. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01496-3 · Cited by 477
Functional Oxygen Sensitivity of Astrocytes
Angelova, P. R., Kasymov, V., Christie, I., Sheikhbahaei, S., Turovsky, E., Marina, N., Korsak, A., Zwicker, J., Teschemacher, A. G., Ackland, G. L., et al. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0045-15.2015 · Cited by 279
Drager, L. F., Polotsky, V. Y., O'Donnell, C. P., Cravo, S. L., Lorenzi-Filho, G., & Machado, B. H. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00094.2015 · Cited by 124
The “embreathment” illusion highlights the role of breathing in corporeal awareness
Monti, A., Porciello, G., Tieri, G., & Aglioti, S. M. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00617.2019 · Cited by 100
Metadata
- Authors
- Kumar, P., & Prabhakar, N. R.
- Venue
- Comprehensive Physiology
- Publisher
- Wiley
- Published
- 2012-01
- Volume
- 2
- Issue
- 1
- Pages
- 141-219
- ISSN
- 2040-4603 (ISSN-L)
- OpenAlex
- W1744173909
- Cited by
- 530
- References
- 532
- Type
- other
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.