Responses to hypoxia of petrosal ganglia in vitro

Brain Research

Volumn 845, Issue 1, 1999, Pages 28-34

  Alcayaga, Julio ^a   Varas, Rodrigo ^a   Arroyo, Jorge ^a   Iturriaga, Rodrigo ^b   Zapata, Patricio ^b  

^a UNIVERSITY OF CHILE   (Chile)

^b PONTIFICIA UNIVERSIDAD CATÓLICA DE CHILE   (Chile)

Author keywords

Arterial chemoreceptor; Carotid body; Cyanide; Hypoxia; Petrosal ganglion; Sensory ganglion

Indexed keywords

SODIUM CYANIDE;

ACTION POTENTIAL; ANIMAL TISSUE; ARTICLE; CAROTID BODY; CAROTID SINUS NERVE; CAT; CONTROLLED STUDY; GANGLION; GLOSSOPHARYNGEAL NERVE; HYPOXIA; IN VITRO STUDY; NONHUMAN; PRIORITY JOURNAL;

EID: 0032822426     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(99)01928-9     Document Type: Article

References (39)

1. Alcayaga J., Sanhueza Y., Zapata P. Thermal dependence of chemosensory activity in the carotid body superfused in vitro. Brain Res. 600:1993;103-111.
2. Alcayaga J., Iturriaga R., Varas R., Arroyo J., Zapata P. Selective activation of carotid nerve fibers by acetylcholine applied to the cat petrosal ganglion in vitro. Brain Res. 786:1998;47-54.
3. Alcayaga J., Varas R., Arroyo J., Iturriaga R., Zapata P. Dopamine modulates carotid nerve responses induced by acetylcholine on the cat petrosal ganglion in vitro. Brain Res. 831:1999;97-103.
4. S.V. Anichkov, M.L. Belen'kii, Pharmacology of the Carotid Body Chemoreceptors, Macmillan, New York, 1963, pp. 19-63, 176-192.
5. Belmonte C., Gallego R. Membrane properties of cat sensory neurones with chemoreceptor and baroreceptor endings. J. Physiol. (London). 342:1983;603-614.
6. Bisgard G.E., Forster H.V., Klein J.P. Recovery of peripheral chemoreceptor function after denervation in ponies. J. Appl. Physiol. 49:1980;964-970.
7. 3, and metabolic inhibitors. J. Gen. Physiol. 67:1976;91-112.
8. Borowitz J.L., Gunasekar P.G., Isom G.E. Hydrogen cyanide generation by μ-opiate receptor activation: possible neuromodulatory role of endogenous cyanide. Brain Res. 768:1997;294-300.
9. Bouverot P., Flandrois R., Puccinelli R., Dejours P. Étude du rôle des chémorécepteurs artériels dans la régulation de la respiration pulmonaire chez le chien éveillé Arch. Int. Pharmacodyn. Ther. 157:1965;253-271.
10. Buckler K.J., Vaughan-Jones R.D. Effects of hypoxia on membrane potential and intracellular calcium in rat neonatal carotid body type I cells. J. Physiol. (London). 476:1994;423-428.
11. Buckler K.J., Vaughan-Jones R.D. Effects of mitochondrial uncouplers on intracellular calcium, pH and membrane potential in rat carotid body type I cells. J. Physiol. (London). 513:1998;819-833.
12. Cárdenas H., Zapata P. Dual effects of dopamine upon chemosensory responses to cyanide. Neurosci. Lett. 18:1980;317-322.
13. Cummins T.R., Donnelly D.F., Haddad G.G. Effect of metabolic inhibition on the excitability of isolated hippocampal CA1 neurons: developmental aspects. J. Neurophysiol. 66:1991;1471-1482.
14. Donnelly D.F. Response to cyanide of two types of glomoid cells in mature rat carotid body. Brain Res. 630:1993;157-168.
15. Donnelly D.F. Modulation of glomus cell membrane currents of intact rat carotid body. J. Physiol. (London). 489:1995;677-688.
16. Donnelly D.F. Developmental changes in membrane properties of chemoreceptor afferent neurons of the rat petrosal ganglia. J. Neurophysiol. 82:1999;209-215.
17. 2 deprivation: in vitro intracellular studies. Am. J. Physiol. 262:1992;L549-L554.
18. Dubinsky J.M., Rothman S.M. Intracellular calcium concentrations during "chemical hypoxia" and excitotoxic neuronal injury. J. Neurosci. 11:1991;2545-2551.
19. Duchen M.R. Effects of metabolic inhibition on the membrane properties of isolated mouse primary sensory neurons. J. Physiol. (London). 424:1990;387-409.
20. Eugenín J., Larraín C., Zapata P. Correlative contribution of carotid and aortic afferences to the ventilatory chemosensory drive in steady-state normoxia and to the ventilatory chemoreflexes induced by transient hypoxia. Arch. Biol. Med. Exp. 22:1989;395-408.
21. Eyzaguirre C., Monti-Bloch L., Baron M., Hayashida Y., Woodbury J.W. Changes in glomus cell membrane properties in response to stimulants and depressants of carotid nerve discharge. Brain Res. 477:1989;265-279.
22. Gonzalez C., Almaraz L., Obeso A., Rigual R. Carotid body chemoreceptors: from natural stimuli to sensory discharges. Physiol. Rev. 74:1994;829-898.
23. 2 deprivation induces a major depolarization in brain stem neurons in the adult but not in the neonatal rat. J. Physiol. (London). 429:1990;411-428.
24. Hayashida Y., Koyano H., Eyzaguirre C. An intracellular study of chemosensory fibers and endings. J. Neurophysiol. 44:1980;1077-1088.
25. Inoue M., Fujishiro N., Imanaga I. Hypoxia and cyanide induce depolarization and catecholamine release in dispersed guinea-pig chromaffin cells. J. Physiol. (London). 507:1998;807-818.
26. Morales A., Ivorra I., Gallego R. Membrane properties of glossopharyngeal sensory neurons in the petrosal ganglion of the cat. Brain Res. 401:1987;340-346.
27. 2. J. Appl. Physiol. 50:1981;884-891.
28. Obeso A., Almaraz L., Gonzalez C. Effects of cyanide and uncouplers on chemoreceptor activity and ATP content of the cat carotid body. Brain Res. 481:1989;250-257.
29. Serani A., Zapata P. Relative contribution of carotid and aortic bodies to cyanide-induced ventilatory responses in the cat. Arch. Int. Pharmacodyn. Ther. 252:1981;284-297.
30. Serani A., Lavados M., Zapata P. Cardiovascular responses to hypoxia in the spontaneously breathing cat: reflexes originating from carotid and aortic bodies. Arch. Biol. Med. Exp. 16:1983;29-41.
31. Smith P.G., Mills E. Physiological and ultrastructural observations on regenerated carotid sinus nerves after removal of the carotid bodies in cats. Neuroscience. 4:1979;2009-2020.
32. St. John W.J. Respiratory neuron responses to hypercapnia and carotid chemoreceptor stimulation. J. Appl. Physiol. 51:1981;816-822.
33. Stea A., Nurse C.A. Whole-cell currents in two subpopulations of cultured rat petrosal neurons with different tetrodotoxin sensitivities. Neuroscience. 47:1992;727-736.
34. Sun M.-K., Reis D.J. Dopamine or transmitter release from rat carotid body may not be essential to hypoxic chemoreception. Am. J. Physiol. 267:1994;R1632-R1639.
35. + currents and depolarizes neonatal rat adrenal chromaffin cells. J. Physiol. (London). 512:1998;421-434.
36. Urbán L., Somjen G.G. Reversible effects of hypoxia on neurons in mouse dorsal root ganglia in vitro. Brain Res. 520:1990;36-42.
37. P. Willshaw, R.M. McAllen, Sinus nerve efferent activity originates outside the brain, in: C. Belmonte, D. Pallot, H. Acker, S. Fidone (Eds.), Arterial Chemoreceptors. Proceedings of the Sixth International Meeting, Leicester Univ. Press, UK, 1981, pp. 440-447.
38. Zapata P. Effects of dopamine on carotid chemo- and baroreceptors in vitro. J. Physiol. (London). 244:1975;235-251.
39. Zapata P., Stensaas L.J., Eyzaguirre C. Axon regeneration following a lesion of the carotid nerve: electrophysiological and ultrastructural observations. Brain Res. 113:1976;235-253.