Abstract

MATERIALS AND METHODS

Experimental preparation. Experiments were performed on 93 dorsal column segments obtained from adult male Wistar rats (250–350 gm) ranging in age from 4 to 11 months. After the rats were anesthetized with sodium pentobarbital (40 mg/kg, i.p.), a laminectomy was performed between T3 and T10 to expose the spinal cord. A 25 mm section of cord was removed rapidly and placed in cold (4–7°C) Ringer’s solution. The spinal cord segment was hemisected, and the dorsal column was sectioned longitudinally with microscissors. The dorsal column segment was pinned in an in vitro recording chamber and was perfused constantly (2–5 ml/min drip rate) with Ringer’s solution bubbled with 95% O₂/5% CO₂. The bath medium temperature was maintained at 25 ± 0.5°C with a microprocessor-controlled thermistor (Omega CN9000). Selected experiments (n = 11) were performed at 33°C to verify key results at a higher temperature.

A bipolar platinum wire stimulating electrode was placed on one end of the dorsal column segment, and it delivered a 100 μsec constant current pulse at a supramaximal stimulus intensity, which was 50% greater than that required to elicit a maximal response. The responses were recorded extracellularly by two glass microelectrodes (2–4 μm tip, 5–10 MΩ resistance) filled with 150 mm KCl. The signals were amplified 100× (Axoprobe-1A, Axon Instruments), digitized (ISC-16 A/D converter, R. C. Electronics) at 12 bit resolution, and stored on a microcomputer and VCR. Each sweep of recording had a duration of 8 msec and was digitized to 512 points (i.e., sampling rate of 64 kHz).

Experimental protocol. The dorsal column segment was allowed to stabilize for 90 min after dissection before the experiment was started. A set of recordings was obtained consisting of 100 sweeps at 0.2 Hz. After the control set of recordings, the drug or ion-substituted solutions were infused 15 min before injury. Then the dorsal column segment was injured between the proximal and distal recording sites for 15 sec with a 2 g modified aneurysm clip (1 mm wide) (Dolan and Tator, 1979; Fehlings and Nashmi, 1995; Agrawal and Fehlings, 1996). The drug infusion was continued at least 20 min after injury and then substituted with Ringer’s solution. Response recovery was monitored for at least 2 hr after injury. The same set of control experiments was used for all groups.

Co²⁺ staining of hemisected spinal cord slices for the presence of AMPA/KA receptors. A 30 mm segment of thoracic cord was excised and hemisected in eight male Wistar rats. We used the Co²⁺-uptake staining method of Pruss et al. (1991), with certain modifications, to visualize the presence of AMPA/KA receptors in spinal cord white matter. AMPA/KA stimulation (100 μmkainic acid plus 100 μm AMPA) or compressive injury with a clip exerting a closing force of 2 g or blocking with NBQX (10 μm) plus CNQX (10 μm) was performed at room temperature for 20 min in 5 mm CoCl₂. Co²⁺ was precipitated in 1.0% (NH₄)₂S for 5 min. The hemisected cord was post-fixed in 4% phosphate-buffered formalin for 1 hr and snap-frozen in isopentane. Fifteen micrometer sections were cut with a cryostat and mounted on slides. Silver enhancement of Co²⁺ was performed at 45°C for 30 min in a solution of 0.1% AgNO₃, 292 mm sucrose, 15.5 mm hydroquinone, and 42 mm citric acid, according to the methodology of Pruss et al. (1991).

Western blot analysis of spinal cord white matter. Crude membrane fractions of dorsal column white matter [exclusion of gray matter confirmed by microtubular-associated protein (MAP2; Burgoyne, 1991) immunoblotting; see Figure ​Figure66a] were isolated according to the method of Roberts-Lewis et al. (1994). Briefly, the spinal cord white matter was homogenized in ~10 vol of 50 mm Tris-HCl (4 mm EDTA, pH 7.4, containing 1 μm pepstatin, 100 μm leupeptin, 100 μm phenylmethylsulfonylfluoride, and 10 μg/ml aprotinin) at 4°C. Samples were centrifuged at 400 ×g for 5 min. The pellet was discarded, and the supernatant was centrifuged at 40,000 × g for 20 min at 4°C. The pellet was taken as the crude membrane fraction and was washed with Tris buffer containing 2 mm β-mercaptoethanol and resuspended. Protein quantification was performed by the modified Lowry method (Peterson, 1977). Discontinuous SDS-PAGE was performed using a Bio-Rad mini-protein II electrophoresis cell. For each rat, 10 μg of membrane fraction protein was electrophoresed and electroblotted onto supported nitrocellulose membranes. Blots were blocked (1 hr) with 0.5% nonfat dry milk/0.1% Tween 20 in Tris-buffered saline (TBS) at room temperature and then incubated (1 hr) with rabbit polyclonal antibodies against GluR1, GluR2/3, GluR4, GluR6/7, and KA2 (Upstate Biotechnology, Lake Placid, NY) diluted (1:200) in blocking buffer. Blots were incubated with horseradish peroxidase (HRP)-conjugated goat anti-rabbit (1:4000). After several washes with TBS, immunoreactive proteins were visualized with an enhanced electrochemiluminescence kit (ECL, Amersham, Arlington Heights, IL). Immunoblots of olfactory bulb were used as positive controls for GluR1 and GluR2/3 labeling. To verify that equal amounts of protein were loaded in each lane, the same membranes were reblocked (1 hr) with 0.5% nonfat dry milk/0.1% Tween 20 in TBS at room temperature and then incubated (1 hr) with mouse monoclonal antibody against Neurofilament 200 (Sigma, St. Louis, MO) diluted (1:4000) in blocking buffer. The blots were reincubated with HRP-conjugated goat anti-mouse (1:4000), washed with TBS, and revisualized by ECL.

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Fig. 6.

a, Western blot illustrating MAP2 presence in whole spinal cord (WC) and exclusion in an isolated dorsal column white matter preparation (WM). b, Spinal cord white matter (dorsal column) homogenates (10 μg protein) were subjected to SDS-PAGE and immunoblotted with antibodies to GluR1, GluR2/3, GluR4, GluR6/7, and KA2. As illustrated,GluR4, GluR6/7, and KA2 were detected in spinal cord white matter. c, These immunoblots show equal amounts of protein loading with NF 200 and positive controls for GluR1 and GluR2/3using olfactory bulb.

Immunohistochemistry of spinal cord white matter.Immunohistochemistry was performed according to the method of Martin et al. (1993) in four male Wistar rats. Briefly, after transcardiac perfusion–fixation (4% paraformaldehyde/0.1% glutaraldehyde with 15% picric acid) the spinal cord (n = 4) was removed and frozen in isopentane chilled by dry ice. Transverse and longitudinal 10 μm frozen sections were cut on a cryostat at −18°C, mounted on poly-l-lysine-subbed slides, and dried overnight under vacuum with desiccant. Sections were washed and permeabilized for 30 min in TBS containing 4% heat-inactivated goat serum and 0.4% Triton X-100. The primary antibodies were diluted (1:200) in PBS/0.1% Triton X-100 and used to incubate slides for 48 hr at 4°C in rabbit polyclonal anti-GluR1, GluR2/3, GluR4, GluR6/7, and KA2 (Upstate Biotechnology) and mouse monoclonal glial fibrillary acidic protein (GFAP) (Dimension Laboratories, Mississauga, Ontario, Canada). After successive washes in TBS, the slides were incubated for 30 min in Fluorescent-conjugated 2° antibody fluorescein isothiocyanate (FITC; Molecular Probes, Eugene, OR) for AMPA/KA receptors and in Texas Red for GFAP to identify astrocytes. Control sections were incubated only with the secondary antibody or only with primary antibody. Imaging was performed using a laser confocal microscope (Bio-Rad MRC 600; Bio-Rad, Mississauga, Ontario, Canada) with a krypton–argon ion laser light source and equipped with a Nikon Optiphot upright microscope.

Solutions and drugs. The perfused solutions were bubbled continuously with 95%O₂/5%CO₂. The composition of perfused solutions was (in mm): Ringer’s—124 NaCl, 3 KCl, 1 Na₂HPO₄, 26 NaHCO₃, 1.5 MgSO₄, 1.5 CaCl₂, and 10 glucose; zero calcium—124 NaCl, 3 KCl, 1 Na₂HPO₄, 26 NaHCO₃, 1.5 MgSO₄, 1.5 EGTA, and 10 glucose. NMDA (10 and 100 μm with 10 μm glycine), AMPA (100 μm), kainic acid (100 μm), APV (50 μm), CNQX [10 μm (Research Biochemicals, Natick, MA)], and NBQX [10 μm (Tocris Cookson)] were dissolved in aqueous solution (0.1N NaOH and titrated with HCl, pH 8.0) and then dissolved in Ringer’s solution. The pH of the solutions was maintained at 7.4 and the osmolarity at 290–310.

Data analysis and statistics. Peak-to-peak amplitude of the individual compound action potentials (CAPs) was analyzed by computer after completion of the experiment (Fehlings and Nashmi, 1995; Agrawal and Fehlings, 1996). All data were expressed as the mean ± SE. Significant differences in amplitude (at p < 0.05) between control (Ringer’s solution) and treatment CAPs at a particular time point of the experiment were determined post hoc by the Student Newman–Keuls test after two-way ANOVA. The same set of control experiments was used for all groups, except for data collected at 33°C in which separate controls were generated.

RESULTS

Role of ionotropic glutamate receptors in compressive SCI

Experiments were performed to determine whether ligand-gated ionotropic glutamate receptors are involved in the pathophysiology of traumatic SCI. The NMDA receptor blocker APV (50 μm) and the AMPA/KA receptor blocker CNQX (10 μm) were added to the perfusate to examine for ionotropic glutamatergic effects. The APV+CNQX solution was started 15 min before the 2 g clip compression injury and continued until 20 min after injury. Recovery of CAP amplitude was observed for 2 hr after injury. With the combined administration of APV and CNQX, the recovery of CAP amplitude was significantly improved (91.5 ± 6.4% of preinjury values) as compared with Ringer’s solution (71.4 ± 2.0% of preinjury;p < 0.05) at 1 hr after injury (Fig.​(Fig.1).1). Representative recordings are shown in Figure​Figure11a–c; a graph of normalized CAP amplitude versus time is shown in Figure ​Figure11d.

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Fig. 1.

Effect of ionotropic glutamate receptor blockade on recovery of CAP amplitude after compressive injury. APV (50 μm; NMDA receptor blocker) and CNQX (10 μm; AMPA/KA receptor blocker) (APV+CNQX) were administered in combination and compared with control Ringer’s solution (Ringers). a–c, Representative CAP waveforms from the APV+CNQX group recorded preinjury, 5 min postinjury, and 60 min postinjury (during washout with Ringer’s solution). d, Graph of normalized CAP amplitude versus time. Combined administration of APV (50 μm) and CNQX (10 μm) resulted in improved CAP amplitude recovery postinjury (significant differences in CAP amplitude shown by asterisks). At 60 min postinjury, the CAP amplitude in the APV + CNQX group had recovered to 91.5 ± 6.4% of preinjury values as compared with theRingers group (71.4 ± 2.0% of preinjury).

Role of NMDA receptors in traumatic SCI

To determine to what extent NMDA receptors mediate traumatic spinal cord axonal injury, we examined the effect of the agonist NMDA (10 μm, n = 6; 100 μm,n = 5) and the selective NMDA antagonist APV (50 μm; n = 6). As shown in Figure​Figure22a, administration of NMDA did not exacerbate the effects of traumatic injury. Moreover, the NMDA blocker APV did not improve the recovery of CAP amplitude after compressive trauma to the dorsal column segment (Fig. ​(Fig.22b).

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Fig. 2.

a, Administration of NMDA (10 μm and 100 μm) did not attenuate CAP recovery after traumatic injury. b, The NMDA receptor antagonist APV (50 μm) did not improve recovery of CAP amplitude after compressive injury to the dorsal column segment.

Role of AMPA/KA receptors in traumatic SCI

Experiments were performed to determine the role of AMPA/KA receptors in traumatic SCI. The effect of the selective AMPA/KA receptor blockers NBQX (10 μm) and CNQX (10 μm) and coapplication of AMPA/KA plus antagonists was examined. NBQX, CNQX, or AMPA/KA plus NBQX and CNQX was administered 15 min before the 2 g clip compression injury and continued until 20 min after injury. Recovery of CAP amplitude was observed for 2 hr after injury. NBQX, CNQX, and coapplication of antagonists resulted in significant enhancement of CAP recovery (85.6 ± 2.7%, 86.5 ± 3.9%, and 88.2 ± 7.8% of preinjury values, respectively) as compared with Ringer’s solution (71.4 ± 2.0% of preinjury value; p < 0.05) at 1 hr postinjury. Graphs of normalized CAPs versus time are shown in Figure​Figure33a–c.

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Fig. 3.

Effect of 10 μmCNQX or NBQX or coapplication of AMPA/KA plus antagonists (CNQX and NBQX) on CAP recovery after 2 g clip compression injury.a, Graph of normalized CAP amplitude versus time (significant differences in CAP amplitude between two groups are depicted by asterisks). At 60 min postinjury, the recovery of CAP amplitude in the CNQX group (86.5 ± 3.9% of preinjury) significantly exceeded that of the control Ringer’s solution group (Ringers) (71.4 ± 2.0% of preinjury; p < 0.05). b, Graph of normalized CAP amplitude versus time (significant differences in CAP amplitude between two groups are depicted by asterisks). At 60 min postinjury the recovery of CAP amplitude in theNBQX group (85.6 ± 2.7% of preinjury) significantly exceeded that of the control Ringers group (71.4 ± 2.0% of preinjury; p < 0.05).c, Graph of normalized CAP amplitude versus time (significant differences in CAP amplitude between two groups are depicted by asterisks). At 60 min postinjury the recovery of CAP amplitude in the coapplication group (88.2 ± 7.8% of preinjury) significantly exceeded that of the controlRingers group (71.4 ± 2.0% of preinjury;p < 0.05).

To provide further evidence to support a role for AMPA/KA receptor activation in the pathophysiology of traumatic SCI, the effect of the agonists AMPA (10 and 100 μm) and kainic acid (10 and 100 μm) was examined. Infusion of the test solutions commenced 15 min before the 2 g clip compression injury and continued until 20 min after injury. The effects on CAP amplitude were observed for 2 hr after injury. Infusion of AMPA (100 μm) and kainic acid (100 μm) significantly attenuated the recovery of CAP amplitude to 59.4 ± 1.3% (p < 0.05; n = 5) and 59.0 ± 1.6% (p < 0.05; n = 5) of preinjury values, respectively, as compared with control Ringer’s solution (71.4 ± 2.0%; p < 0.05) (Fig.​(Fig.44a,b). Lower doses of AMPA or kainic acid (10 μm) did not attenuate (p > 0.05) the recovery of CAP amplitude (data not shown). As an additional control, the effect of AMPA and kainic acid on the uninjured dorsal column segment (n = 3; Fig. ​Fig.4)4) was observed. Both AMPA and kainic acid attenuated the CAP amplitude to 86.0 ± 0.8% (p < 0.05) and 85.4 ± 1.2% (p < 0.05) of control values, respectively. During washout with Ringer’s solution, CAP amplitude of the uninjured dorsal column segments returned to baseline levels and remained stable.

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Fig. 4.

Effect of AMPA (100 μm) and kainic acid (100 μm) on CAP amplitude after 2 gclip compression injury. Both AMPA and Kainic Acid resulted in significant exacerbation of traumatic axonal injury when compared with control Ringer’s solution group (Ringers) (asterisks denote significant differences at p < 0.05).

The aforementioned experiments were conducted at 25°C, because at this temperature the dorsal column preparation remains extremely stable physiologically (Agrawal and Fehlings, 1996). To confirm that the results described above could be replicated at more physiological temperatures, a number of experiments (n = 11) were conducted at 33°C. The CNQX-containing solution conferred a significant enhancement of CAP recovery (77.5 ± 1.8%) as compared with Ringer’s solution (64.8 ± 3.2% of preinjury value; p < 0.05). The extent of neuroprotection between Ringer’s solution and drug treatment was similar at 25°C and 33°C.

Co²⁺ uptake in spinal cord slices

Ca²⁺-permeable AMPA/KA receptors in oocytes are permeable to Co²⁺ (McGurk et al., 1991), which does not permeate voltage-sensitive Ca²⁺ channels (Hagiwara and Byerly, 1981), NMDA receptors (Mayer and Westbrook, 1987), or Ca²⁺-impermeable AMPA/KA receptors (Gu and Huang, 1991). Using a histochemical silver-staining method to identify Co²⁺ uptake, Pruss et al. (1991) showed that stimulation with kainic acid causes Co²⁺ influx through Ca²⁺-permeable AMPA/KA receptors in neurons. Using this method, we found that Co²⁺ positively stained glia in spinal cord white matter after incubation with 100 μmkainic acid and 100 μm AMPA or after compressive injury alone (Fig. ​(Fig.55a,c). The postinjury Co²⁺ uptake was blocked by applying the antagonists NBQX (10 μm) and CNQX (10 μm) and is shown in Figure ​Figure55d. In contrast, control spinal cord white matter sections (without AMPA/KA stimulation) showed only low levels of background staining (Fig. ​(Fig.55b).

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Fig. 5.

Longitudinal sections through spinal cord dorsal column stained for AMPA/KA receptors by the Co²⁺uptake technique. Scale bar, 20 μm. a, Two darkly stained astrocytes are shown (arrows). Section incubated with 100 μm kainic acid and 100 μm AMPA before histochemical processing. b, Control section (without AMPA/KA stimulation) of spinal cord dorsal column white matter showing background staining only. c, A darkly stained astrocyte is shown (arrow) in injured dorsal column (untreated with AMPA/KA). d, A dorsal column white matter preparation treated with CNQX and NBQX after clip compression injury showing no Co²⁺ uptake staining.

Immunohistochemistry of spinal cord white matter

Immunohistochemistry was performed on whole spinal cord sections with the goal of determining the subtypes of AMPA or KA receptors present in white matter and their cellular localization. We identified the presence of cells immunoreactive for GluR4, GluR6/7, or KA2 in spinal cord white matter (Fig. ​(Fig.7).7). Double labeling with GFAP identified the majority of these cells as astrocytes. Faint inconsistent labeling with GluR1 was seen. No GluR2/3 immunopositivity in spinal cord white matter was identified. Negative controls (omission of primary antibody and in some cases omission of secondary antibody) showed no immunostaining of any cellular elements (data not shown).

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Fig. 7.

The presence of GluR4 (A, B), GluR6/7 (C), and KA2 (D) immunoreactivity (FITC labeling shown as green) in 10 μm sections of thoracic spinal cord dorsal column. Double labeling with GFAP (Texas Red) confirmed these immunopositive cells to be astrocytes (arrows). Scale bars, 50 μm.

DISCUSSION

In the present study, we have shown that blockade of AMPA/KA but not NMDA receptors improved recovery of CAP amplitude after compressive injury to adult mammalian spinal cord white matter. In support of these findings, infusion of the agonist NMDA did not affect recovery of CAP amplitude after traumatic SCI, whereas administration of AMPA or kainic acid significantly accentuated post-traumatic axonal dysfunction. With AMPA/KA stimulation and injury alone, Co²⁺-positive glia were visualized in sections of dorsal column, providing evidence for the presence of Ca²⁺-permeable AMPA/KA receptors in CNS white matter. With immunohistochemistry and Western blot analysis, we characterized the presence of certain subtypes of AMPA (GluR4) and KA (GluR6/7 and KA2) receptors in thoracic spinal cord white matter. By double labeling with GFAP, these receptors were found directly on periaxonal astrocytes.

Glutamate receptor activation can increase the intracellular Ca²⁺ concentration in neurons and has been implicated in Ca²⁺-mediated cell death in various neurodegenerative disorders (Rothman and Olney, 1987; Regan and Choi, 1991). Ionotropic glutamate receptors are classified into those gated by NMDA and those activated by KA and AMPA. Although NMDA receptors are known to be highly calcium permeable, they are not known to be expressed on axons or glia; accordingly, their role in CNS white matter injury including SCI is doubtful. Thus, our finding that infusion of the agonist NMDA in conjunction with the co-agonist glycine did not exacerbate the extent of post-traumatic axonal dysfunction (Fig. ​(Fig.22a) or that the NMDA antagonist APV did not improve CAP amplitude after injury (Fig.​(Fig.22b) is congruent with the biology of NMDA receptors. Furthermore, these findings are in agreement with the studies ofGomez-Pinella et al. (1989) and Faden and Simon (1988), who found that NMDA antagonists did not ameliorate the extent of tissue loss after traumatic SCI.

The rationale for examining the potential role of AMPA receptors in mediating Na⁺-dependent and Ca²⁺-induced spinal cord white matter degeneration is based on the observation of AMPA receptors, permeable to calcium, on astrocytes (Jensen and Chiu, 1993). Periaxonal glia, in particular astrocytes, are important in modulating axonal signaling (Kriegler and Chiu, 1993) and in regulating extracellular ionic perturbations. We have demonstrated that infusion of either AMPA or kainic acid attenuates CAP amplitude in an in vitro preparation of isolated dorsal column white matter (Fig.​(Fig.44a,b). Furthermore, administration of the AMPA/KA receptor antagonists CNQX or NBQX or coapplication of AMPA/KA plus antagonists is associated with improved recovery of CAP amplitude after compressive injury (Fig. ​(Fig.3).3). The results of coapplication suggests that both AMPA and KA receptors are important in SCI; however, more specific antagonists are required to dissect these mechanisms in greater detail. The results are also in agreement with those of Gill et al. (1992), who found that NBQX was neuroprotective in a rat focal ischemia model, andWrathall et al. (1994), who found that NBQX when administered by intramedullary injection into the rat spinal cord improved locomotor performance after SCI and was associated with sparing of white matter. It is noteworthy that the improvement of CAP amplitude with CNQX or NBQX solutions was not sustained. The affinity of NBQX for KA receptors is ~30 times less than its affinity for AMPA receptors (Sheardown et al., 1990). In contrast, CNQX affects both KA and AMPA receptors, with a slightly greater affect on the former. After 75 min, the CAP amplitude gradually declined (Fig. ​(Fig.33a,b). When AMPA/KA plus antagonists were coapplied, these effects were sustained (Fig.​(Fig.33c), which suggests that both AMPA and KA receptors are involved in traumatic white matter injury.

The majority of experiments conducted in this study were performed at 25°C, because the dorsal column preparations remain extremely physiologically stable under these conditions. Although hypothermia could provide some degree of neuroprotection, both control and test preparations were subjected to the same bath conditions. Accordingly, any neuroprotective effects of a hypothermic extracellular milieu would be controlled; however, to exclude this as a potentially confounding factor, selected experiments (n = 11) were conducted at 33°C. At this temperature, stable recordings could be obtained. The results at 33°C were similar to data obtained at 25°C, as has been reported previously (Agrawal and Fehlings, 1996).

KA-evoked elevation of [Na⁺]_i and [Ca²⁺]_i has been reported in several studies. Lower doses of kainic acid significantly increase the intracellular concentration of sodium and water (Coyle, 1983). This could be one source of neurotoxicity, because there is evidence that removing extracellular Na⁺ or blocking Na⁺ channels in the extracellular environment is neuroprotective (Stys et al., 1992;Agrawal and Fehlings, 1996). Moreover, in some neurons and glia the non-NMDA receptor channels are highly permeable to Ca²⁺(Iino et al., 1990; Gilbertson et al., 1991; Burnashev et al., 1992b). Furthermore, the differences in permeability of Ca²⁺ may be explained by the presence of different subtypes of AMPA/KA receptors in different tissues. With imaging techniques, Keller et al. (1992)demonstrated a large increase in [Ca²⁺]_iinduced by Ca²⁺ influx through AMPA/KA receptor channels expressed in Xenopus oocyte. Burnashev et al. (1992a) showed that unedited homomeric GluR-B channels exhibit a high Ca²⁺permeability in human embryonic kidney cells. It has also been shown that AMPA receptors that lack an edited GluR2 (GluR-B) subtype will be highly permeable to calcium. The present results, which show the absence of GluR2 subtypes in white matter glial cells, suggest that the AMPA receptors are highly calcium permeable.

In contrast to voltage-gated Ca²⁺ channels, Ca²⁺-permeable non-NMDA receptor channels are permeable to a wide range of other divalent cations, including Ba²⁺, Mg²⁺, Sr²⁺, and Mn²⁺ (Iino et al., 1990; Hollmann et al., 1991; Burnashev et al., 1992a), and are indirectly permeable to Co²⁺ (Pruss et al., 1991). In the present study, using the Co²⁺ uptake method we have demonstrated that Ca²⁺ permeable AMPA/KA receptors are found on glial cells and that these receptors may act as a major route for the Ca²⁺ entry (Fig. ​(Fig.5).5). Several explanations can account for the rise in [Ca²⁺]_i with AMPA/KA receptor activation. First, AMPA/KA could activate two populations of channels: one with high permeability to Ca²⁺ and a nonlinear current–voltage (I–V) relationship and the second with linear or outwardly rectifyingI–V relationships and low permeability to Ca²⁺ (Iino et al., 1990). Moreover, the main source of [Ca²⁺]_i elevation on application of KA could be from intracellular stores, i.e., a small influx of Ca²⁺through KA-activated channels could cause Ca²⁺-induced Ca²⁺ release. Finally, activation of Ca²⁺mobilizing systems, including inositol triphosphate-linked mechanism, has been described for nicotinic acetylcholine receptors (Grassi et al., 1993) and potentially could also apply to AMPA/KA receptors.

Non-NMDA ionotropic glutamate receptors seem to be restricted mainly to astrocytes in CNS white matter, although recent work on optic nerve suggests that a small population of O-2A glial precursors in adult CNS white matter express AMPA/KA receptors (Barres et al., 1990). There is evidence that periaxonal astrocytes modulate the ionic environment at the node of Ranvier (Usowicz et al., 1989) and can release substances to modulate excitability of axons. Indeed, axons are known to have GABA receptors, and O-2A glial progenitor cells can synthesize GABA (Barres, 1991), possibly in response to glutamate receptor activation (Gallo et al., 1991). AMPA/KA receptors (GluR1 and GluR3) also may be expressed on axons based on immunoelectron microscopic studies of the hippocampus (Martin et al., 1993) and the bed nucleus of the stria terminalis (Ginsberg et al., 1995). Our results demonstrate clearly that AMPA/KA receptors are present in spinal cord white matter. First, the cobalt staining method showed numerous Co²⁺-positive glia with AMPA and KA stimulation. Second, Western blot analysis demonstrated the presence of GluR4, GluR6/7, and KA2 immunoreactivity in spinal cord white matter. Finally, immunocytochemistry demonstrated numerous GFAP-positive periaxonal astrocytes double-labeled for GluR4, GluR6/7, and KA2 subtypes of AMPA or KA receptors. Thus, the non-NMDA ionotropic glutamate receptor effects in spinal cord axonal injury may be mediated by the GluR4, GluR6/7, and KA2 receptors on astrocytes.

Footnotes

REFERENCES