Chemosensitivity of rat medullary raphe neurones in primary tissue culture

被引:150
作者
Wang, WG
Pizzonia, JH
Richerson, GB
机构
[1] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06510 USA
[3] Vet Adm Med Ctr, W Haven, CT 06516 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1998年 / 511卷 / 02期
关键词
D O I
10.1111/j.1469-7793.1998.433bh.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. The medullary raphe, within the ventromedial medulla (VMM), contains putative central respiratory chemoreceptors. To study the mechanisms of chemosensitivity in the raphe, rat VMM neurones were maintained in primary dissociated tissue culture, and studied using perforated patch-clamp recordings. Baseline electrophysiological properties were similar to raphe neurones in brain slices and in vivo. 2. Neurones were exposed to changes in CO2 from 5% to 3 or 9% while maintaining a constant [NaHCO3]. Fifty-one per cent of neurones (n = 210) did not change their firing rate by more than 20% in response to hypercapnic acidosis. However, 22% of neurones responded to 9% CO2 with an increase in firing rate ('stimulated'), and 27% of neurones responded with a decrease in firing rate ('inhibited'). 3. Chemosensitivity has often been considered an all-or-none property. Instead, a method was developed to quantify the degree of chemosensitivity. Stimulated neurones had a mean increase in firing rate to 298 +/- 215% of control when pH decreased from 7.40 to 7.19. Inhibited neurones had a mean increase in firing rate to 232 +/- 265% of control when pH increased from 7.38 to 7.57. 4. Neurones were also exposed to isocapnic acidosis. All CO2-stimulated neurones tested (n = 15) were also stimulated by isocapnic acidosis, and all CO2-inhibited neurones tested (n = 19) were inhibited by isocapnic acidosis. Neurones with no response to hypercapnic acidosis also had no response to isocapnic acidosis (n = 12). Thus, the effects of CO2 on these neurones were mediated in part via changes in pH. 5. In stimulated neurones, acidosis induced a small increase in the after-hyperpolarization level of 1.38 +/- 1.15 mV per -0.2 pH units, which was dependent on the level of tonic depolarizing current injection, In voltage clamp mode at a holding potential near resting potential, there were small and inconsistent changes in whole-cell conductance and holding current in both stimulated and inhibited neurones. These results suggest that pH modulates a conductance in stimulated neurones that is activated during repetitive firing, with a reversal potential close to resting potential. 6. The two subtypes of chemosensitive VMM neurones could be distinguished by characteristics other than their response to acidosis. Stimulated neurones had a large multipolar soma, whereas inhibited neurones had a small fusiform soma. Stimulated neurones were more likely than inhibited neurones to fire with tale highly regular pattern typical of serotonergic raphe neurones in vivo. 7. Within the medullary raphe, chemosensitivity is a specialization of two distinct neuronal phenotypes. The response of these neurones to physiologically relevant changes in pH is of the magnitude that suggests that this chemosensitivity plays a functional role. Elucidating their mechanisms in vitro may help to define the cellular mechanisms of central chemo reception in vivo.
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页码:433 / 450
页数:18
相关论文
共 51 条
[1]   MODULATION OF A TRANSIENT OUTWARD CURRENT IN SEROTONERGIC NEURONS BY ALPHA-1-ADRENOCEPTORS [J].
AGHAJANIAN, GK .
NATURE, 1985, 315 (6019) :501-503
[2]  
[Anonymous], 1991, CULTURING NERVE CELL
[3]   Effects of serotonin on caudal raphe neurons: Inhibition of N- and P/Q-type calcium channels and the afterhyperpolarization [J].
Bayliss, DA ;
Li, YW ;
Talley, EM .
JOURNAL OF NEUROPHYSIOLOGY, 1997, 77 (03) :1362-1374
[4]   Evidence for central chemoreception in the midline raphe [J].
Bernard, DG ;
Li, AH ;
Nattie, EE .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (01) :108-115
[5]   EVIDENCE FOR DIFFERING ORIGINS OF THE SEROTONERGIC INNERVATION OF MAJOR CEREBRAL-ARTERIES AND SMALL PIAL VESSELS IN THE RAT [J].
BONVENTO, G ;
LACOMBE, P ;
MACKENZIE, ET ;
FAGE, D ;
BENAVIDES, J ;
ROUQUIER, L ;
SCATTON, B .
JOURNAL OF NEUROCHEMISTRY, 1991, 56 (02) :681-689
[6]   EFFECTS OF HYPERCAPNIA ON MEMBRANE-POTENTIAL AND INTRACELLULAR CALCIUM IN RAT CAROTID-BODY TYPE-I CELLS [J].
BUCKLER, KJ ;
VAUGHANJONES, RD .
JOURNAL OF PHYSIOLOGY-LONDON, 1994, 478 (01) :157-171
[7]   PACEMAKER POTENTIALS OF SEROTONERGIC DORSAL RAPHE NEURONS - CONTRIBUTION OF A LOW-THRESHOLD CA-2+ CONDUCTANCE [J].
BURLHIS, TM ;
AGHAJANIAN, GK .
SYNAPSE, 1987, 1 (06) :582-588
[8]   WIDESPREAD SITES OF BRAIN-STEM VENTILATORY CHEMORECEPTORS [J].
COATES, EL ;
LI, AH ;
NATTIE, EE .
JOURNAL OF APPLIED PHYSIOLOGY, 1993, 75 (01) :5-14
[9]  
Cunningham D.J.C., 1986, HDB PHYSL, P475, DOI DOI 10.1002/CPHY.CP030215
[10]   DISTRIBUTION AND COLOCALIZATION OF 5-HYDROXYTRYPTAMINE, THYROTROPIN-RELEASING-HORMONE AND SUBSTANCE-P IN THE CAT MEDULLA [J].
DEAN, C ;
MARSON, L ;
KAMPINE, JP .
NEUROSCIENCE, 1993, 57 (03) :811-822