PHYSIOLOGICAL AND MORPHOLOGICAL PROPERTIES OF NEURONS IN SPHINCTER OF ODDI REGION OF THE GUINEA-PIG

被引:22
作者
WELLS, DG [1 ]
MAWE, GM [1 ]
机构
[1] UNIV VERMONT, COLL MED, DEPT ANAT & NEUROBIOL, BURLINGTON, VT 05405 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 265卷 / 02期
关键词
AUTONOMIC NERVOUS SYSTEM; ENTERIC NERVOUS SYSTEM; EXTRAHEPATIC BILIARY SYSTEM; CHOLEDOCHODUODENAL JUNCTION;
D O I
10.1152/ajpgi.1993.265.2.G258
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Intracellular recordings and dye injections were used to investigate neurons located in ganglia of the sphincter of Oddi (SO) region in guinea pigs. Four types of neurons were encountered based on physiological properties. The two most abundant types, tonic and phasic, had similar membrane characteristics and morphologies but yet could be differentiated by their spiking characteristics. Tonic cells spiked throughout a depolarizing current pulse and were sometimes spontaneously active. Phasic cells fired only a single action potential at the onset of a current pulse regardless of stimulus amplitude or duration. Both tonic and phasic cells had Dogiel type I morphologies. They typically had a single long process and several very short processes emanating from the soma. NADPH diaphorase activity was demonstrated in cells with similar morphologies, indicating that nitric oxide may be an intrinsic transmitter in some of these cells. Cells with a prolonged afterhyperpolarization (AH cells), similar to the type 1/AH cells of the gut, were rarely encountered. This finding was consistent with the observation that very few calbindin D-immunoreactive neurons exist in this region. Action potentials could not be generated in the fourth type of neuron, called nonspiking neurons, even though they did receive synaptic input. Most tonic and phasic cells received at least one nicotinic fast excitatory postsynaptic potential (EPSP). In addition, both slow EPSPs and inhibitory postsynaptic potentials were observed. Most AH cells received only slow excitatory synaptic input.
引用
收藏
页码:G258 / G269
页数:12
相关论文
共 44 条
[1]   PHARMACOLOGICAL CHARACTERIZATION OF EXCITATORY AND INHIBITORY CHOLECYSTOKININ RECEPTORS OF THE CAT GALLBLADDER AND SPHINCTER OF ODDI [J].
BEHAR, J ;
BIANCANI, P .
GASTROENTEROLOGY, 1987, 92 (03) :764-770
[2]   COLOCALIZATION OF NITRIC-OXIDE SYNTHASE AND NADPH-DIAPHORASE IN THE MYENTERIC PLEXUS OF THE RAT GUT [J].
BELAI, A ;
SCHMIDT, HHHW ;
HOYLE, CHV ;
HASSALL, CJS ;
SAFFREY, MJ ;
MOSS, J ;
FORSTERMANN, U ;
MURAD, F ;
BURNSTOCK, G .
NEUROSCIENCE LETTERS, 1992, 143 (1-2) :60-64
[3]   AN ELECTROPHYSIOLOGICAL COMPARISON OF SUBSTANCE P-IMMUNOREACTIVE NEURONS WITH OTHER NEURONS IN THE GUINEA-PIG SUBMUCOUS PLEXUS [J].
BORNSTEIN, JC ;
FURNESS, JB ;
COSTA, M .
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, 1989, 26 (02) :113-120
[4]   NITRIC-OXIDE SYNTHASE PROTEIN AND MESSENGER-RNA ARE DISCRETELY LOCALIZED IN NEURONAL POPULATIONS OF THE MAMMALIAN CNS TOGETHER WITH NADPH DIAPHORASE [J].
BREDT, DS ;
GLATT, CE ;
HWANG, PM ;
FOTUHI, M ;
DAWSON, TM ;
SNYDER, SH .
NEURON, 1991, 7 (04) :615-624
[5]   PEPTIDE IMMUNOREACTIVE NERVES AND CELLS OF THE GUINEA-PIG GALLBLADDER AND BILIARY PATHWAYS [J].
CAI, W ;
GU, J ;
HUANG, W ;
MCGREGOR, GP ;
GHATEI, MA ;
BLOOM, SR ;
POLAK, JM .
GUT, 1983, 24 (12) :1186-1193
[6]  
CAI WQ, 1983, J ANAT, V136, P97
[7]   STRUCTURE OF NEURONS AND GANGLIA OF THE GUINEA-PIG GALLBLADDER - LIGHT AND ELECTRON-MICROSCOPIC STUDIES [J].
CORNBROOKS, EB ;
POULIOT, WA ;
MAWE, GM .
JOURNAL OF COMPARATIVE NEUROLOGY, 1992, 317 (01) :31-44
[8]  
COSTA M, 1992, INT CONGR SER, V1008, P115
[9]   VIP ANTISERA INHIBIT THE RELAXATORY MOTOR-RESPONSES OF THE FELINE SPHINCTER OF ODDI AND GALLBLADDER INDUCED BY VIP OR VAGAL NERVE-STIMULATION [J].
DAHLSTRAND, C ;
THEODORSSON, E ;
DAHLSTROM, A ;
AHLMAN, H .
ACTA PHYSIOLOGICA SCANDINAVICA, 1989, 137 (03) :375-378
[10]   EVIDENCE FOR DUAL COMPONENTS IN THE NONADRENERGIC NONCHOLINERGIC RELAXATION IN THE RAT GASTRIC FUNDUS - ROLE OF ENDOGENOUS NITRIC-OXIDE AND VASOACTIVE INTESTINAL POLYPEPTIDE [J].
DAMATO, M ;
CURRO, D ;
MONTUSCHI, P .
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, 1992, 37 (03) :175-186