Adenosine triphosphate-induced peripheral nerve discharges generated from the cat petrosal ganglion in vitro

被引:36
作者
Alcayaga, J [1 ]
Cerpa, V
Retamal, M
Arroyo, J
Iturriaga, R
Zapata, P
机构
[1] Univ Chile, Fac Ciencias, Dept Biol, Neurobiol Lab, Casilla 653, Santiago 1, Chile
[2] Catholic Univ Chile, Neurobiol Lab, Santiago 1, Chile
关键词
adenosine triphosphate; carotid nerve; glossopharyngeal branch; nucleotides; petrosal ganglion; sensory ganglia;
D O I
10.1016/S0304-3940(00)00896-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Since nucleotides have been postulated as transmitters between glomus cells and chemosensory nerve endings in the carotid body, we studied the effects of their application to the petrosal ganglion, where the perikarya of carotid (sinus) nerve are located. Cat petrosal ganglia were superfused in vitro, while electrical activities of their peripheral processes (carotid nerve and glossopharyngeal branch) were recorded simultaneously. Adenosine triphosphate (ATP) evoked dose-dependent bursts of impulses in carotid nerve, while those in glossopharyngeal branch were less intense and consistent, Adenosine monophosphate was less effective than ATP. ATP-induced carotid nerve responses presented no temporal desensitization and persisted after applying P-2Y receptor blocker Reactive Blue 2 to the ganglion. The results indicate that ATP has an excitatory effect on the perikarya of the population of petrosal ganglion neurons projecting peripherally through the carotid nerve. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:185 / 188
页数:4
相关论文
共 19 条
[1]   Selective activation of carotid nerve fibers by acetylcholine applied to the cat petrosal ganglion in vitro [J].
Alcayaga, J ;
Iturriaga, R ;
Varas, R ;
Arroyo, J ;
Zapata, P .
BRAIN RESEARCH, 1998, 786 (1-2) :47-54
[2]  
ANICHKOV SV, 1963, PHARM CAROTID BODY C, P176
[3]  
Bardoni R, 1997, J NEUROSCI, V17, P5297
[4]  
BEAN BP, 1990, J NEUROSCI, V10, P1
[5]  
DONTAS AS, 1955, J PHARMACOL EXP THER, V115, P46
[6]   Distribution of P2X3 receptors in the rat trigeminal ganglion after interior alveolar nerve injury [J].
Eriksson, J ;
Bongenhielm, U ;
Kidd, E ;
Matthews, T ;
Fried, K .
NEUROSCIENCE LETTERS, 1998, 254 (01) :37-40
[7]   PERSPECTIVES IN CAROTID-BODY RESEARCH [J].
EYZAGUIRRE, C ;
ZAPATA, P .
JOURNAL OF APPLIED PHYSIOLOGY, 1984, 57 (04) :931-957
[8]   Towards a revised nomenclature for P1 and P2 receptors [J].
Fredholm, BB ;
Abbracchio, MP ;
Burnstock, G ;
Dubyak, GR ;
Harden, TK ;
Jacobson, KA ;
Schwabe, U ;
Williams, M .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1997, 18 (03) :79-82
[9]   Characterization of cultured dorsal root ganglion neuron P2X receptors [J].
Grubb, BD ;
Evans, RJ .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (01) :149-154
[10]   IMPULSE ACTIVITY IN THE CAROTID SINUS NERVE FOLLOWING INTRA-CAROTID INJECTION OF POTASSIUM CHLORIDE, VERATRINE, SODIUM CITRATE, ADENOSINE-TRIPHOSPHATE AND ALPHA-DINITROPHENOL [J].
JARISCH, A ;
LANDGREN, S ;
NEIL, E ;
ZOTTERMAN, Y .
ACTA PHYSIOLOGICA SCANDINAVICA, 1952, 25 (2-3) :195-211