Olivocerebellar climbing fibers in the granuloprival cerebellum: morphological study of individual axonal projections in the X-irradiated rat.

Elimination of cerebellar granule cells early during postnatal development produces abnormal neural organization that retains immature characteristics in the adult, including innervation of each Purkinje cell by multiple climbing fibers from the inferior olive. To elucidate mechanisms underlying development of the olivocerebellar projection, we studied light-microscopic morphology of single olivocerebellar axons labeled with biotinylated dextran amine in adult rats rendered agranular by a single postnatal X-irradiation. Each reconstructed olivocerebellar axon gave off approximately 12 climbing fibers, approximately twice as many as in normal rats. Terminal arborizations of climbing fibers made irregular tufts in most areas, whereas they were arranged vertically in a few mildly affected areas. Each climbing fiber terminal arborization innervated only part of the dendritic arbor of a Purkinje cell, and multiple climbing fibers innervated a single Purkinje cell. These climbing fibers originated either from the same olivocerebellar axon (pseudomultiple innervation) or from distinct axons (true multiple innervation). Abundant non-climbing fiber thin collaterals projected to all cortical layers. Although the longitudinal pattern of the zonal olivocerebellar projection was generally observed, lateral branching, including bilateral projections, was relatively frequent. These results suggest that the granule cell-parallel fiber system induces several important features of olivocerebellar projection: (1) organization of the climbing fiber terminal arborization tightly surrounding Purkinje cell dendrites, (2) elimination of pseudo- and true multiple innervations establishing one-to-one innervation, (3) retraction of non-climbing fiber thin collaterals from the molecular layer, and (4) probable refinement of the longitudinal projection domains by removing aberrant transverse branches.

The entire trajectories of single olivocerebellar axons in the cerebellar cortex and their contribution to Cerebellar compartmentalization.

The functional partitioning of the cerebellar cortex depends on the projection patterns of its afferent and efferent neurons. However, the entire morphology of individual projection neurons has been demonstrated in only a few classes of neurons in the vertebrate CNS. To investigate the contribution of the projection pattern of individual olivocerebellar axons to the cerebellar functional compartmentalization, we labeled individual olivocerebellar axons, which terminate in the cerebellar cortex as climbing fibers, with biotinylated dextran amine injected into the inferior olive in the rat, and completely reconstructed the entire trajectories of 34 olivocerebellar axons from serial sections of the cerebellum and medulla. Single axons had seven climbing fibers on average, which terminated at similar distances from the midline in a single or in multiple lobules. Cortical projection areas of adjacent olivary neurons were clustered as narrow but separate longitudinal segments and often innervated by collaterals of single neurons. Comparison of the cerebellar distribution of olivocerebellar axons arising from different sites within a single olivary subnucleus indicated that slightly distant neurons projected to complementary sets of such segments in a single longitudinal band. Several of these longitudinal bands formed a so-called parasagittal zone innervated by a subnucleus of the inferior olive. Single olivocerebellar axons projected rostrocaudally to segments within a single band but did not project mediolaterally to multiple bands. These results suggest fine substructural organization in the cerebellar compartmentalization that may represent functional units.

Activation and two modes of blockade by strontium of Ca2+-activated K+ channels in goldfish saccular hair cells.

Effects of internal Sr2+ on the activity of large-conductance Ca2+-activated K+ channels were studied in inside-out membrane patches from goldfish saccular hair cells. Sr2+ was approximately one-fourth as potent as Ca2+ in activating these channels. Although the Hill coefficient for Sr2+ was smaller than that for Ca2+, maximum open-state probability, voltage dependence, steady state gating kinetics, and time courses of activation and deactivation of the channel were very similar under the presence of equipotent concentrations of Ca2+ and Sr2+. This suggests that voltage-dependent activation is partially independent of the ligand. Internal Sr2+ at higher concentrations (>100 microM) produced fast and slow blockade both concentration and voltage dependently. The reduction in single-channel amplitude (fast blockade) could be fitted with a modified Woodhull equation that incorporated the Hill coefficient. The dissociation constant at 0 mV, the Hill coefficient, and zd (a product of the charge of the blocking ion and the fraction of the voltage difference at the binding site from the inside) in this equation were 58-209 mM, 0.69-0.75, 0.45-0.51, respectively (n = 4). Long shut events (slow blockade) produced by Sr2+ lasted approximately 10-200 ms and could be fitted with single-exponential curves (time constant, taul-s) in shut-time histograms. Durations of burst events, periods intercalated by long shut events, could also be fitted with single exponentials (time constant, taub). A significant decrease in taub and no large changes in taul-s were observed with increased Sr2+ concentration and voltage. These findings on slow blockade could be approximated by a model in which single Sr2+ ions bind to a blocking site within the channel pore beyond the energy barrier from the inside, as proposed for Ba2+ blockade. The dissociation constant at 0 mV and zd in the Woodhull equation for this model were 36-150 mM and 1-1.8, respectively (n = 3).

Morphology of single olivocerebellar axons labeled with biotinylated dextran amine in the rat.

The morphology of olivocerebellar (OC) axons originating from the inferior olive (IO) was investigated in the rat by reconstructing the entire trajectories of single axons that had been labeled with biotinylated dextran amine. Virtually all of the OC axons entered the cerebellum through the inferior cerebellar peduncle (ICP) contralateral to the IO, with a few exceptions. Although most OC projection was contralateral, a few axons projected bilaterally by crossing the midline within the cerebellum. Collaterals of OC axons could be classified into thick branches and thin collaterals. Thick branches of each OC axon (6.1 +/- 3.7/OC axon, mean +/- SD for n = 16 axons) terminated as climbing fibers (CFs) on single Purkinje cells (PCs) in a one-to-one relationship. Besides terminal arborization around PC thick dendrites, CFs had terminals that surrounded a PC soma, fine branchlets that extended transversely in the molecular layer, and thin retrograde collaterals that re-entered the PC and granular layers. Innervation of a single PC by two CFs originating from the same axon was seen, although infrequently. Concerning thin collaterals, about half of the OC axons had one or only a few collaterals terminating in the white matter of the ICP, most had 1 to 6 collaterals terminating in a single cerebellar nucleus, and all had 3 to 16 collaterals that terminated mainly in the granular layer, but occasionally in the cerebellar white matter and the PC layer. Some swellings of thin collaterals touched somata of presumed Golgi cells and PCs. No OC axons terminated solely in the ICP, cerebellar nucleus or granular layer without giving rise to CFs.

Projection patterns of single mossy fibers originating from the lateral reticular nucleus in the rat cerebellar cortex and nuclei.

Projection of neurons in the lateral reticular nucleus (LRN) to the cerebellar cortex (Cx) and the deep cerebellar nuclei (DCN) was studied in the rat by using the anterograde tracer biotinylated dextran amine (BDA). After injection of BDA into the LRN, labeled terminals were seen bilaterally in most cases in the vermis, intermediate zone, and hemisphere of the anterior lobe, and in various areas in the posterior lobe, except the flocculus, paraflocculus, and nodulus. Areas of dense terminal projection were often organized in multiple longitudinal zones. The entire axonal trajectory of single axons of labeled LRN neurons was reconstructed from serial sections. Stem axons entered the cerebellum through the inferior cerebellar peduncle (mostly ipsilateral), and ran transversely in the deep cerebellar white matter. They often entered the contralateral side across the midline. Along the way, primary collaterals were successively given off from the transversely running stem axons at almost right angles to the Cx and DCN, and individual primary collaterals had longitudinal arborizations that terminated as mossy fibers in multiple lobules of the Cx. These collaterals arising from single LRN axons terminated bilaterally or unilaterally in the vermis, intermediate area, and sometimes hemisphere, and in different cerebellar and vestibular nuclei simultaneously. The cortical terminals of single axons appeared to be distributed in multiple longitudinal zones that were arranged in a mediolateral direction. All of the LRN axons examined (n = 29) had axon collaterals to the DCN. All of the terminals observed in the DCN and vestibular nuclei belonged to axon collaterals of mossy fibers terminating in the Cx.

The entire trajectory of single climbing and mossy fibers in the cerebellar nuclei and cortex.

The present study has revealed that OC axons gave rise to a number of thin collaterals. Due to the abundance of these non-CF thin collaterals, it seems better to make a distinction between the terms CFs and OC axons, as was done in the present paper. The present findings on the innervation of PC dendrites by CFs are basically similar to those in previous reports (Ramón y Cajal, 1911; Palay and Chan-Palay, 1974). The number of swellings on a single CF in the present study (n = 250) is comparable to a previously measured value in the rat (n = 288; Rossi et al., 1993) and larger than a value in the frog (n = about 100 beads; Llinás et al., 1969). The average number of CFs per OC axon in this study was close to the number (n = about 7) inferred in the rat by counting the total number of IO neurons and PCs (Schild, 1970). Contact of interneurons by some swellings of CFs in the molecular layer was emphasized by Scheibel and Scheibel (1954) in their study with Golgi staining. Despite the contact of CF terminals on interneurons, the formation of a synaptic structure between them has been excluded in an electron-microscopic study (Hámori and Szentàothai, 1980). On the other hand, electrophysiological studies have demonstrated a weak excitatory effect of CFs on some interneurons (Eccles et al., 1966). Terminals in the granular layer were originated either from thin collaterals of OC axons or from retrograde collaterals of CF terminal arborizations. The former was the main source of swellings in the granular layer. The morphology of the thin collaterals in the present study was consistent with "globose varicosities connected by a fine thread" as described in Golgi preparations and electron micrograms (Chan-Palay and Palay, 1971). Swellings of thin collaterals (about 1.7% of the total number of swellings per OC axon) were most abundant in the upper portion of the granular layer just underneath the PC layer, in which Golgi cells are usually located. Furthermore, some of these swellings were observed to touch presumed Golgi cells in the present study, which is consistent with electron-microscopic findings on the innervation of somata of Golgi cells by thin collaterals (Hámori and Szentàothai, 1980; Chan-Palay and Palay, 1971). Inferior olive stimulation has been shown electrophysiologically to have a weak direct excitatory effect on Golgi cells (Eccles et al., 1966). Ninety-one percent of the OC axons examined had nuclear collaterals; since the possibility of insufficient staining could not be excluded, this percentage may be an underestimation. The ratio of swellings in the cerebellar nuclei versus those of CF terminal arborizations was about 0.036 in individual OC axons in the present study. However, since the volume of the cerebellar nuclei is much smaller than that of the cerebellar cortex, and significant convergence of input from OC axons to cerebellar nucleus neurons is present (Sugihara et al., 1996), cerebellar nucleus projection of OC fibers can still be functionally important. Some swellings seemed to make contact with the soma and the proximal portions of dendrites of large neurons in the present study, which is consistent with the steep rising phase of postsynaptic excitatory potentials in cerebellar nucleus neurons following IO stimulation (Kitai et al., 1977; Shinoda et al., 1987). Although intracellular potentials were presumably recorded only from large output neurons in the cerebellar nuclei, the present study suggested that small neurons were also innervated by OC axons. The present study revealed that virtually all reconstructed LRN axons projected not only to the Cx as mossy fibers, but also to the DCN including the VN by their axon collaterals. None of the LRN neurons specifically projected to the DCN without projecting to the Cx, namely all axon terminals of LRN neurons in the DCN and VN belonged to axon collaterals of mossy fibers projecting to the Cx. (ABSTRACT TRUNCATED)

Off-oscillation in hair cell membrane is correlated with the decremental response at the hair cell-afferent fibre synapse in the goldfish sacculus.

In this study, we examined the decremental response in the hair cell-afferent fibre synapse of goldfish. This decremental response is a transient reduction in sound-evoked EPSPs associated with a step reduction in sound intensity. To determine its presynaptic correlates, a patch clamp study was performed on oscillatory-type hair cells isolated from the sacculus of goldfish. Injection of depolarizing current produced a damped oscillation in the membrane potential of such cells. When the current intensity was reduced in steps, instead of simply being turned off, very marked dips were produced as off-oscillation in the hair cell membrane potential. These dips correlated with the decremental response in EPSPs.

Quickly flickering inwardly rectifying K channels in goldfish hair cell membrane.

The kinetics of the quickly flickering inwardly rectifying K channel were studied with the cell-attached patch clamp method in goldfish hair cells. The activity of the channel was very unique in repeating continuously open and closed events at an ultrafast rate. Moreover, open-close events of the channel showed a marked dependence on membrane potential; a shift toward hyperpolarized levels brought about an elongation of closed events resulting in a decrease in the open state probability, although no marked change was produced in open event duration itself. The unitary conductance of the channel was 109 pS as 123 mM KCl solution was used.

Morphology of axon collaterals of single climbing fibers in the deep cerebellar nuclei of the rat.

Projection of inferior olive (IO) neurons to the deep cerebellar nuclei (CN) was investigated in the rat by reconstructing single axons that were labeled with biotinylated dextran amine injected into the IO. All reconstructed terminal arborizations in the CN (n = 18) arose as collaterals from climbing fibers (CFs). One to six nuclear collaterals were given off from each of six CFs that were reconstructed along the nearly entire pathway backward from cortical terminal arborizations to the IO. Nuclear collaterals were much thinner (0.2-0.3 micron in diameter) than stem axons projecting to Purkinje cells (0.7-1.4 microns). The number of swellings per a single nuclear collateral ranged from 24 to 118 (n = 18). Terminal arborizations of nuclear collateral originating from a single CF spread for some hundreds of micrometers and occupied a localized portion within the CN.

Efferent innervation in the goldfish saccule examined by acetylcholinesterase histochemistry.

In contrast to the abundance of information available regarding the anatomy and physiology of afferents within the goldfish saccule, the efferent system of this auditory endorgan has been scarcely studied morphologically. In this study, acetylcholinesterase histochemistry with diaminobenzidine enhancement was used to describe the morphology of efferents. Under light microscopy, labeled fibers appeared in the distal portion of the saccular nerve, penetrated the basement membrane and formed a horizontal mesh-like plexus near the base of hair cells. Many vertical branchlets with terminal swellings protruded upward toward hair cells from the plexus. Under electron microscopy, dense extracellular labeling was present around efferent terminals, which often formed clusters on hair cells. Labeling was also present around unmyelinated fibers of passage within the sensory epithelium and the distal saccular nerve. These fibers contained coarse microtubules and small vesicles, and often ran in a bundle with other similar fibers. Based on their position within the epithelium, histochemistry and ultrastructural characteristics, these fibers were concluded to be efferents. These fibers became myelinated and unlabeled in the proximal saccular nerve. These results suggest that acetylcholinesterase can be a marker of entire distal unmyelinated portions of efferent fibers and demonstrated abundant efferent innervation in the goldfish saccule.

Estimation of cardiac output by first-pass transit of radiotracers.

To evaluate cardiac function with various tracers to be used for radionuclide scintigraphy, we examined the validity of a simplified method to measure cardiac output (CO) by modifying the equation of Stewart-Hamilton in the radionuclide study. After a bolus injection of I-123 or Tc-99m tracer, the total injection dose and count in the pulmonary artery during the first transit of the tracer were measured to calculate the CO Index. The CO Index was obtained from the integral of the first transit of radiotracers in the pulmonary artery divided by the total injected count. CO was estimated from the regression formula which was obtained by comparing the CO Index with CO measured by the Doppler echocardiographic method. There were close correlations between the CO Index and CO measured by Doppler echocardiography both in the study with I-123 (n = 13, r = 0.85, p < 0.001) and with Tc-99m (n = 17, r = 0.88, p < 0.001). The regression formula varied according to the radionuclide used for the study (CO = 2.29 x (CO Index)(0.634) for I-123 and CO = 3.18 x (CO Index)(0.518) for Tc-99m). CO measured by this method is useful for the assessment of cardiac function with various tracers in routine clinical studies, and this simple method may be utilized for assessment of organ blood flow on the basis of the microsphere model.

[Measurement of retinal circulation in uveitis of Behçet's and Harada's disease].

In order to investigate retinal circulation in patients with Behçet's disease and Harada's disease, we divided 27 patients into three groups; Behçet's group (8 patients), Harada's group (8 patients) and the control group (11 normal subjects). By means of video-densitometric image analysis of fluorescein angiography, we measured the buildup time (BT), time constant of washout rate (TC) and mean circulation time (MCT) for both the retinal artery and vein. The results were as follows: 1) The BT in Behçet group was slightly prolonged compared to that in the control group, while the BT in Harada's disease was shorter than that in the control group. 2) The TC in both the Behçet's and Harada's groups was significantly prolonged compared to that in the control group. 3) The MCT in both Behçet's and Harada's groups was not significantly different from that in the control group. These results suggest that Behçet's disease cases may have normally and compensatory retinal circulation, whatever vasculitis occurs on retinal vessels. On the other hand, choroiditis in Harada's disease has no influence on retinal circulation.

[Acute and chronic effect of moxisylyte hydrochloride on the retinal circulation in diabetes mellitus].

The effect of moxisylyte hydrochloride, a new type alpha 1-blocking vasodilator, on the retinal circulation was investigated in 14 diabetics, using the video-densitometric image analysis of fluorescein angiography. The build-up time (BT) and the mean circulation time (MCT) were compared before and after oral administration of moxisylyte. The BT one hour after oral administration of 30 mg moxisylyte was significantly shorter than that before therapy (artery; before 5.2 +/- 1.5 vs after 4.6 +/- 1.0 sec; p = 0.0001, vein; before 6.9 +/- 1.3 vs 6.3 +/- 1.1 sec; p = 0.0005). The MCT two weeks after oral administration of 90 mg per day moxisylyte was significantly shortened (before 3.6 +/- 2.3 vs after 2.6 +/- 1.4 sec; p = 0.0180). These results suggested that oral moxisylyte improved the retinal circulation and might support the concept that moxisylyte hydrochloride has clinical usefulness in patients with diabetes mellitus.

[Comparison of intraocular penetration level of cefuzonam sodium and cefotiam after intravenous and subconjunctival injection].

We investigated the intraocular penetration of a new Cephem type antibiotic: Cefuzonam sodium (CZON) following intravenous and subconjunctival injection. CZON was administered to 28 eyes in 26 patients by 1 g intravenous injection (IV) and to 11 eyes in 10 patients by 20 mg/0.2 ml subconjunctival injection (SCI). The penetration level of CZON by the IV method was from less than 0.0025-3.35 micrograms/ml into aqueous humor, from less than 0.0025-0.315 microgram/mg into iris tissue and 2.7-157.5 micrograms/ml into serum. The penetration level of CZON by the SCI method was from less than 0.0025-12.8 micrograms/ml into aqueous humor, from less than 0.0025-0.0426 microgram/mg into iris tissue and 1.03-18.5 micrograms/ml into serum. The penetration level of CZON into aqueous humor by SCI was higher than by IV administration. In comparison with the penetration level of CZON and Cefotiam (CTM), both aqueous humor and serum levels of CTM were higher than those of CZON. These results suggested that therapeutic levels in aqueous humor effective against gram-positive and gram-negative pathogens were achieved with the 1 g IV and 20 mg SCI of CZON. However levels effective against Staphylococcus epidermidis were only erratically attained.

BCL-2 counteracts Doppel-induced apoptosis of prion-protein-deficient Purkinje cells in the Ngsk Prnp(0/0) mouse.

The pro-apoptotic factor BAX has recently been shown to contribute to Purkinje cell (PC) apoptosis induced by the neurotoxic prion-like protein Doppel (Dpl) in the prion-protein-deficient Ngsk Prnp(0/0) (NP(0/0)) mouse. In view of cellular prion protein (PrP(c)) ability to counteract Dpl neurotoxicity and favor neuronal survival like BCL-2, we investigated the effects of the anti-apoptotic factor BCL-2 on Dpl neurotoxicity by studying the progression of PC death in aging NP(0/0)-Hu-bcl-2 double mutant mice overexpressing human BCL-2 (Hu-bcl-2). Quantitative analysis showed that significantly more PCs survived in NP(0/0)-Hu-bcl-2 double mutants compared with the NP(0/0) mutants. However, number of PCs remained inferior to wild-type levels and to the increased number of PCs observed in Hu-bcl-2 mutants. In the NP(0/0) mutants, Dpl-induced PC death occurred preferentially in the aldolase C-negative parasagittal compartments of the cerebellar cortex. Activation of glial cells exclusively in these compartments, which was abolished by the expression of Hu-bcl-2 in the double mutants, suggested that chronic inflammation is an indirect consequence of Dpl-induced PC death. This partial rescue of NP(0/0) PCs by Hu-bcl-2 expression was similar to that observed in NP(0/0):Bax(-/-) double mutants with bax deletion. Taken together, these data strongly support the involvement of BCL-2 family-dependent apoptotic pathways in Dpl neurotoxicity. The capacity of BCL-2 to compensate PrP(c) deficiency by rescuing PCs from Dpl-induced death suggests that the BCL-2-like property of PrP(c) may impair Dpl-like neurotoxic pathways in wild-type neurons.

Calcium-activated potassium channels in goldfish hair cells.

1. Characteristics of Ca(2+)-activated K+ channels in the basolateral membrane of hair cells isolated from the caudal part of the goldfish saccular macula were studied mainly with the inside-out mode of the patch clamp method. 2. Several types of Ca(2+)-activated K+ channels differing in unitary conductance were identified. The conductances (n = 156) ranged from 130 to 320 pS (when measured in symmetrical 125 mM KCl) and could be roughly separated into four groups, centred on values of 150, 200, 250 and 300 pS. The pharmacological profile, assessed by, for example, tetraethylammonium blockade, and the relatively large conductance indicated that these channels can be classified as large-conductance Ca(2+)-activated K+ channels (BK channels). The relative permeability of these channels to different ion species was in the order K+ (1.0) > Rb+ (0.8) > NH4+ (0.14) > Na+, Cs+ (< 0.05). 3. Curves relating open state probability to [Ca2+]i, for membrane potentials between -50 and +50 mV, were similar to those observed for BK channels of rat muscle. However, the maximum open state probability (100-1000 microM [Ca2+]i and 50 mV membrane potential) was 0.4-0.9, and always less than 1. 4. These channels had a short arithmetic mean open time ranging from 0.08 to 1.2 ms (0.08-0.5 ms in 88% of cases) and an arithmetic mean shut time ranging from 0.24 to 1.2 ms (10 microM [Ca2+]i and 50 mV membrane potential). The shut intervals were more sensitive to changes in [Ca2+]i and membrane potential than were the open intervals. 5. The distribution of individual open and shut intervals was fitted with the sum of exponential functions. Except for the slowest shut component, which only accounted for less than 1% of shut events, all other components had time constants shorter than 1 ms. As a result of these short open and shut intervals, the current trace had a flickery pattern rather than a burst-interburst pattern. 6. There was a rough correlation between unitary conductance and mean open time, i.e. channels with a large unitary conductance had a longer mean open time. 7. The sensitivity to [Ca2+]i of the Ca(2+)-activated K+ channel in goldfish hair cells was one to two orders of magnitude lower than that of BK channels in rat muscle. Channels with a longer mean open time had a higher Ca2+ sensitivity. 8. The stability of the single Ca(2+)-activated K+ channel kinetics was studied by measuring the 'moving' mean duration of open and shut intervals.(ABSTRACT TRUNCATED AT 400 WORDS)

Morphological and functional aspects of two different types of hair cells in the goldfish sacculus.

1. With the use of whole-cell mode of the patch-clamp method, we examined the electrical responses of hair cells enzymatically isolated from the goldfish sacculus. 2. Hair cells from the rostral saccule had a short cell body and were ovoidal or eggplantlike in shape, whereas hair cells from the caudal saccule had a variable shape. Many had a longer cell body and were cylindrical or gourd-like in shape, but some short hair cells were also present in the caudal saccule. 3. The short hair cells had a resting potential of about -75 mV. In current-clamp experiments, these hair cells elicited damped oscillatory-potential changes of a relatively small amplitude in response to a depolarizing current. A current in the opposite direction produced a slow hyperpolarization, much larger in amplitude. 4. Resonant frequency of the short, or the oscillatory, type of hair cells ranged from 40 to 200 Hz or higher. However, resonance was generally of a poor quality as compared with that noted for hair cells in the turtle cochlea or frog sacculus. 5. The long hair cells had a resting potential of -90 to -100 mV. In current-clamp experiments, these hair cells elicited an all-or-none spike approximately 50 mV in amplitude in response to a depolarizing current. The spike was usually followed by a plateau, which was maintained for the duration of the depolarizing pulse. In some hair cells, damped slow oscillatory waves were evoked at a rate of 5-15 Hz. On the other hand, a hyperpolarizing current produced potential changes much smaller in amplitude. 6. Voltage-clamp experiments showed that Ca2+-activated K+ channel and A-current, especially its high-threshold subclass, were involved in the generation of outward rectification in the oscillatory-type hair cells. On the other hand, Na+, in addition to Ca2+, was involved in the generation of spike in the spike-type hair cells. Spike potentials were elicited even in the presence of tetrodotoxin (TTX), but the rate of rise was slower as compared with the intact spikes. 7. The spike-type hair cells had an inwardly rectifying K+ channel similar to that noted in the tunicate egg and chick vestibular hair cell. However, the oscillatory-type hair cells had an inwardly rectifying channel similar to the hyperpolarization-activated current, Ih, of the rod inner segment, or sinoatrial nodal cell, or lacked the inwardly rectifying channel. Differences in the resting membrane potential between the oscillatory- and spike-type hair cells are probably related to differences in the inwardly rectifying channels. 8. Effects of sound stimulation were simulated by injecting a half-wave rectified sinusoidal current of various frequencies.(ABSTRACT TRUNCATED AT 400 WORDS)