- Open Access
Selective activation of primary afferent fibers evaluated by sine-wave electrical stimulation
© Koga et al; licensee BioMed Central Ltd. 2005
- Received: 09 February 2005
- Accepted: 25 March 2005
- Published: 25 March 2005
Transcutaneous sine-wave stimuli at frequencies of 2000, 250 and 5 Hz (Neurometer) are thought to selectively activate Aβ, Aδ and C afferent fibers, respectively. However, there are few reports to test the selectivity of these stimuli at the cellular level. In the present study, we analyzed action potentials (APs) generated by sine-wave stimuli applied to the dorsal root in acutely isolated rat dorsal root ganglion (DRG) preparations using intracellular recordings. We also measured excitatory synaptic responses evoked by transcutaneous stimuli in substantia gelatinosa (SG) neurons of the spinal dorsal horn, which receive inputs predominantly from C and Aδ fibers, using in vivo patch-clamp recordings. In behavioral studies, escape or vocalization behavior of rats was observed with both 250 and 5 Hz stimuli at intensity of ~0.8 mA (T5/ T250), whereas with 2000 Hz stimulation, much higher intensity (2.14 mA, T2000) was required. In DRG neurons, APs were generated at T5/T250 by 2000 Hz stimulation in Aβ, by 250 Hz stimulation both in Aβ and Aδ, and by 5 Hz stimulation in all three classes of DRG neurons. However, the AP frequencies elicited in Aβ and Aδ by 5 Hz stimulation were much less than those reported previously in physiological condition. With in vivo experiments large amplitude of EPSCs in SG neurons were elicited by 250 and 5 Hz stimuli at T5/ T250. These results suggest that 2000 Hz stimulation excites selectively Aβ fibers and 5 Hz stimulation activates noxious transmission mediated mainly through C fibers. Although 250 Hz stimulation activates both Aδ and Aβ fibers, tactile sensation would not be perceived when painful sensation is produced at the same time. Therefore, 250 Hz was effective stimulus frequency for activation of Aδ fibers initiating noxious sensation. Thus, the transcutaneous sine-wave stimulation can be applied to evaluate functional changes of sensory transmission by comparing thresholds with the three stimulus frequencies.
- Dorsal Root Ganglion Neuron
- Spinal Dorsal Horn
- Substantia Gelatinosa
- Behavioral Threshold
- Membrane Time Constant
Psychophysical procedures such as the visual analogue scale are commonly used to assess human pain magnitude. However, any of those assessments seem not to be suitable for evaluation of a change in thresholds of each class of afferent fibers, despite of the fact that quantitative analysis of each afferent class is essential for understanding underlying mechanisms of pathological states and evaluation of analgesic chemicals. It now becomes evident that hyperalgesia or allodynia produced by various chronic pain conditions is due to not only a change in threshold of fine afferent fibers but also participation of large myelinated afferents in producing allodynia in inflammation and sciatic nerve transection models [1–3]. Recently, one method that allows us to clarify a change in threshold of each afferent fiber quantitatively has been developed (Neurometer) . That is a method to measure selectively the thresholds of three classes of afferent fibers by applying transcutanous sine-wave stimulation at three frequencies of 2000, 250 and 5 Hz via surface electrodes at a current intensity in the range of 0.01–9.9 mA to the skin. Neurometer is now widely used clinically to evaluate peripheral nerve sensitization and dysfunction in various painful states, including neuropathic pain or an effect of treatment of analgesic drugs [5–9]. Although several lines of evidence suggest the selective stimulation of three distinct afferent fibers by Neurometer, the validity of the method at single cellular level has not been made.
There are three types of sensory afferent fibers that send sensory information to the CNS; unmyelinated C fibers send a long lasting delayed painful sensation, thinly myelinated Aδ fibers send a short and fast painful sensation and the thickly myelinated Aβ fibers send tactile information. Several attempts have been made to identify the types of peripheral sensory fibers activated by the sine-wave stimuli using behavioral pharmacological approaches such as blockade of nerve conduction by local anesthetics or use of topical application of capsaicin, etc. [10–12]. However, no studies have been made to clarify the single neuronal properties such as action potential generation or its frequency of peripheral fibers. Moreover, responses of spinal dorsal horn neurons have not been examined by peripheral stimulation with Neurometer.
The purpose of this study was to clarify the selectivity of the sine-wave stimuli on the activation of sensory afferent fibers in detail. First, we performed behavioral tests with Neurometer to measure the withdrawal thresholds by transcutaneous application of three frequencies of stimuli. Next, we performed intracellular recordings from acutely isolated DRG neurons with attached dorsal roots to examine firing properties of C, Aδ and Aβ fibers. Moreover, using in vivo patch-clamp recordings, we analyzed excitatory synaptic responses evoked by the transcutaneous stimuli in SG neurons.
We first examined the escape and/or vocalization behavior of rats to transcutaneous stimuli using Neurometer. When 250 and 5 Hz stimuli were applied to the left hind limb, rats escaped from the stimuli or vocalized. The thresholds for 250 and 5 Hz stimuli were quite similar, and were averaged to be 0.74 ± 0.06 mA (T250, n = 12) and 0.84 ± 0.12 mA (T5, n = 12), respectively. Next, 2000 Hz stimulation which is used to evaluate Aβ fibers was applied. Although Aβ fibers were thought to convey innocuous information, escape and/or vocalization behavior was also observed at higher intensity. The threshold for 2000 Hz stimulation (2.14 ± 0.28 mA, T2000, n = 12) was more than two times higher than T250 and T5.
Classification of DRG neurons
Comparison of electrophysiological properties of DRG neurons
-63.0 ± 1.5
0.6 ± 0.1
3.1 ± 0.5
1.38 ± 0.01
(n = 15)
-67.7 ± 2.4
5.9 ± 0.8
1.8 ± 0.6
0.63 ± 0.05
(n = 18)
-65.1 ± 1.8
19.6 ± 1.3
0.8 ± 0.2
0.29 ± 0.01
(n = 20)
Action potential generated in DRG neurons by sine-wave stimuli
After classification of DRG neurons, C, Aδ and Aβ neurons were stimulated by sine-wave stimuli with gradual increase in intensity using Neurometer.
2000 Hz Stimulation
250 Hz Stimulation
250 Hz stimulation at intensity below T5/T250 initiated APs in Aδ and Aβ neurons but not in C neurons examined (Figures 2A–C). As shown in figures 2D, the AP frequency of Aβ and Aδ neurons started to increase from 0.3 mA and reached plateau at 2 mA.
5 Hz Stimulation
5 Hz stimulation produced tonic firing in all three classes of DRG neurons examined (Figures 3A–C). As shown figure 3D, in C neurons, APs were elicited at 0.4 mA and the frequency reached plateau at ~1 mA. In Aδ neurons, APs were generated at 0.3 mA and the frequency reached the maximum at 0.8 mA. In Aβ neurons, APs were produced at 0.1 mA and the frequency reached plateau at 0.2 mA. Taken together these three studies shown in figures 1,2,3, the data indicate that C fibers are activated only by 5 Hz stimulation among the three specific frequencies.
Excitatory synaptic responses evoked in SG neurons in vivo by cutaneous noxious stimuli
Excitatory synaptic responses evoked in SG neurons in vivo by transcutaneous sine-wave stimuli
The present study demonstrates that 2000 Hz sine-wave stimulation activates selectively Aβ fibers, and 250 and 5 Hz stimuli excite noxious transmission to SG neurons mediated mainly through Aδ and C fibers, respectively, though 250 Hz stimulation also activates Aβ fibers. Our study is the first to examine the selective activation of sensory transmission by the sine-wave stimuli at the cellular level, and the results support that transcutaneous sine-wave stimuli can be applied to examine clinically the changes of threshold in each subtype of afferent fibers following pathological conditions or after treatment with analgesics based on the combination of three sine-wave stimuli.
Activation of nociceptive transmission by sine-wave stimulation
We observed that the stimulus thresholds producing the escape and/or vocalization behavior in rats with 250 and 5 Hz stimuli were not significantly different, whereas the threshold for 2000 Hz stimulation was two times higher than those of 250 and 5 Hz stimuli. The values of these thresholds are consistent with those of previous study . These observations suggest that transcutaneous stimuli at frequency of 250 and 5 Hz induce pain sensation, and the 2000 Hz stimulation may also induce pain at higher intensity. From the analysis in C and Aδ fibers, which predominantly convey noxious information, we found that 5 Hz stimuli activated both C and Aδ fibers, 250 Hz stimulation activated only Aδ at low intensity (~0.8 mA). Interestingly, Aδ fibers were also activated by 2000 Hz stimulation, although 2000 Hz stimulation is thought to activate Aβ fibers. However, the activation of Aδ fibers by 2000 Hz was observed only at high stimulus intensity (> 2 mA). In in vivo analysis of EPSCs evoked in SG neurons, which receive monosynaptic inputs predominantly from C and Aδ fibers [18–20], we found that 2000, 250 and 5 Hz stimuli significantly increased the frequency of evoked EPSCs at their behavioral thresholds. Therefore, these results indicate that 250 and 5 Hz stimuli, produce nociceptive responses by activation of Aδ fibers and by activation of C and Aδ fibers, respectively. On the other hand, 2000 Hz stimulation at high intensity could activate Aδ fibers and thus initiate noxious sensation. There was no significant difference in the frequencies of EPSCs evoked by 250, 5 and 2000 Hz stimuli at the behavioral threshold (Figure 5D). In the previous behavioral pharmacological study, topical application of capsaicin to the skin, a specific desensitizer of small fibers , increased behavioral thresholds for 250 and 5 Hz but not 2000 Hz stimuli, indicating that 250 and 5 Hz stimuli activate small fibers . This observation is consistent with our results.
Discharge ability of sensory fibers
We observed that C fibers were activated only by 5 Hz stimulation with a maximum frequency of ~3 Hz, Aδ fibers were activated by 250 and 5 Hz (maximum frequency of ~22 Hz with 250 Hz stimulation) and Aβ fibers were activated by all three stimuli (maximum frequency of ~140 Hz with 2000 Hz stimulation, Figures 1,2,3). One of the most important factors for affecting the maximum frequency of sensory fibers is the inactivation of voltage-dependent sodium channels. In other words, discharge frequency of fibers is controlled by the time taken to recover the sodium channels from their inactivation state. Recent studies have shown that TTX-sensitive sodium channels expressed in large diameter DRG neurons exhibit faster recovery from the inactivation than the TTX-resistant ones expressed in small DRG neurons [26–29]. Therefore, it can be speculated that high frequency sine-wave stimuli are unable to initiate APs in small C fibers due to slow repriming of TTX-resistant sodium channels.
Passive membrane property is also an important factor for the ability of neurons to discharge. Previous report has shown that the membrane properties of the three subgroups of rat DRG neurons were varied . In particular, the membrane time constant of C neurons (6.5 ms) is much longer than those of Aδ (2.6 ms) and Aβ (1.8 ms) neurons. On the other hand, the durations of single sine-wave stimuli at frequencies of 2000 Hz and 250 Hz are 0.5 ms and 4 ms, respectively. The membrane time constant is the time required for the voltage change across the membrane to reach ~63% of its final value . Therefore, the longer membrane time constant might contribute to the failure of AP in C neurons with 2000 and 250 Hz stimuli, since the membrane potential is slowly depolarized, resulting that the membrane potential can not reach AP threshold within the short depolarizing cycles with the high frequency stimuli as compared to 5 Hz one. In C fiber of rat DRG neurons, AP failure was increased when repetitive stimulation was applied at high frequencies . Consistent with the lines of evidence, in the present study, there was no firing in most C fibers with 250 Hz and 2000 Hz stimuli even when the high intensity stimuli were applied as described in the results.
Selectivity of specific frequencies of sine-wave stimuli to activate primary afferents
2000 Hz Stimulation
We found that 2000 Hz stimulation selectively activated Aβ fibers at low intensity (< 2 mA). Only at higher intensities (> 2 mA), 2000 Hz stimulation produced APs in Aδ fibers. On the other hand, 2000 Hz stimulation increased EPSC frequency in SG neurons, which are known to receive a few Aβ inputs, at higher stimulus intensity. Therefore, it is conceivable that EPSCs in SG neurons by 2000 Hz stimulation at higher intensities are produced predominantly by activation of Aδ fibers.
250 Hz Stimulation
250 Hz stimulation produced APs in Aδ fibers (with a max discharge frequency of 22.3 ± 5.9 Hz) and Aβ fibers (with a max discharge frequency of 133.4 ± 13.3 Hz). These values of AP frequencies were consistent with those evoked by physiological stimuli . These results suggest that 250 Hz stimulation initiates both nociceptive sensation via Aδ fibers and tactile sensation via Aβ fibers. However, in general when both painful and tactile sensations are produced simultaneously, the painful sensation would only be perceived. Therefore, 250 Hz is thought to be effective stimulus frequency for activation of Aδ fibers initiating noxious sensation.
5 Hz Stimulation
The present study showed that C fibers were activated only by 5 Hz stimulation, but not by other stimulus frequencies. This indicates that 5 Hz stimulation is effective to activate C fibers among the three specific frequencies. Although both Aδ and Aβ fibers were also activated by 5 Hz stimulation, it is conceivable that the activation of Aδ or Aβ fibers by 5 Hz stimulation does not reach sufficient frequency to induce functional sensation. In the present study with 5 Hz stimulation, the maximum AP frequencies were ~3 Hz in C fibers, ~4 Hz in Aδ fibers and ~20 Hz in Aβ fibers (Figures 1,2,3). On the other hand, it has been reported that AP frequencies produced by natural physiological stimuli in rat DRG neurons are: ~5 Hz in C fibers by mechanical nociceptive stimuli, ~15 Hz in Aδ fibers by high threshold mechanical stimuli and ~100 Hz in Aβ fibers by slowly adapting tactile stimuli . Although the AP frequency by 5 Hz stimulation in C fibers in our results was almost similar to the value of AP frequency in C fibers by natural mechanical noxious stimulation, the AP frequencies in Aδ and Aβ fibers by the 5 Hz stimulation were much less than those produced by natural stimuli. Furthermore, the number of C fibers in rat DRG neurons is quite larger than those of Aδ and Aβ fibers (C fiber, ~63%; Aδ fiber; ~25%; Aβ fiber, ~12%) .
In conclusion, we provided electrophysiological evidence that the sine-wave stimulation could differentiate changes in threshold of Aβ, Aδ and C afferent fibers by combining data obtained from 2000, 250 and 5 Hz stimulus protocol. This analysis using Neurometer would be useful for understanding not only changes in primary afferent fibers due to pathological conditions but also the evaluation of clinical treatment of analgesics.
All experiments involving the in vivo study were approved by the Committee of the Ethics on Animal Experiments of Kyushu University and conducted in accordance with the Guiding Principles of the Care and Use of Animals in the Field of Physiological Science of the Physiological Society of Japan.
Animals and Behavioral test
Male Sprague-Dawley rats (6–9-week old), weighing 250–300 g were used for behavioral tests, intracellular recordings and in vivo patch-clamp recordings. A skin patch dispersion electrode was fixed to attach the skin of left hind limb of rats. Transcutaneous nerve stimuli were applied through this electrode using the nociceptive mode of the Neurometer® (NUROTRON INCORPORATED, Baltimore, USA). In this mode, the intensity was automatically increased in step from 0 to 9.99 mA (29 steps for 5 Hz stimulation, 20 steps for 250 Hz and 2000 Hz stimuli). The durations were 2.5 sec for 5 Hz and 2.1 sec for 250 Hz and 0.72 sec for 2000 Hz stimuli. When rats escaped and/or vocalized, the stimulation was immediately stopped and the stimulus intensity was defined as behavioral threshold.
Intracellular recording from DRG neurons
The methods used for the current experiment were similar to those described previously . Under anesthesia with diethyl ether, a rat was decapitated and the lumbar laminectomy was performed. L4-6 DRGs with an attached proximal dorsal root were isolated from the animal. The isolated DRG was submerged in Krebs solution (in mM: NaCl 117, KCl 3.6, CaCl2 2.5, MgCl2 1.2, NaH2PO4 1.2, NaHCO3 2.5 and glucose 11) equilibrated with 95% O2-5% CO2 and maintained at 36 ± 1°C and set in a recording chamber. Intracellular recordings of APs were made from DRG neurons with glass-microelectrodes having a DC tip resistance of 50–100 MΩ, filled with 4 M potassium-acetate. Signals were amplified with a high input-impedance bridge amplifier (Axoclamp 2B; Axon Instruments, Foster City CA, USA). Artifacts were minimized with low-pass (1000 Hz) or notch (250 Hz) filters using pCLAMP program (Axon Instruments). Data from neurons with resting membrane potentials less than – 50 mV and AP amplitudes smaller than 60 mV were excluded in the present study. AP duration was determined at half of the peak amplitude of the AP. Antidromic stimulation (duration 100 μsec) was given to the central end of the dorsal root with a suction electrode. The stimulus intensity was monitored with a digitized output isolator (ss-202J; Nihon Kohden, Tokyo, Japan). The value of conduction velocity was calculated from the latency of AP and the length of the dorsal root retained.
In vivo patch-clamp recording from SG in dorsal horn
The methods for in vivo patch-clamp recording from SG neurons have been described in detailed elsewhere [22, 24]. Briefly, under artificial ventilation, a lumbar laminectomy was performed at the level of L4–L5 and the animal was then placed in a stereotaxic apparatus (Model ST-7, Narishige, Japan). Under a binocular microscope with ×8 ~ × 40 magnification, the dura mater was cut and reflected, and then either L4 or L5 dorsal root was shifted laterally using a glass hook. The pia-arachnoid membrane was cut to make a window to allow the patch electrode into the spinal cord. The patch pipette had a tip resistance of 8–10 MΩ when filled with a solution of the following composition (in mM): Cs2SO4 110, CaCl2 0.5, MgCl2 2, EGTA 5, HEPES 5, Mg-ATP 5, tetraethylammonium 5. Signals were acquired with an Axopatch 200B amplifier (Axon Instruments), low-pass-filtered at 5 kHz. Data were analyzed using Axograph program (Axon Instruments). The surface of the exposed spinal cord was perfused with Krebs solution equilibrated with 95% O2-5% CO2 at 38 ± 0.5°C. Drugs were dissolved in Krebs solution and applied to the perfusing line. Whole-cell patch-clamp recordings could be obtained from in vivo preparations for more than 8 hours and stable recordings were made from single SG neurons for up to 2 hours. After the end of the experiments the animals were killed by exanguination.
Data were presented as mean ± SEM. Statistical significance was determined as P < 0.05 using Dunnett's multiple comparison.
We thank Dr. K. Honda for technical advice with behavioral test, and Dr. J. Yagi and Dr. H. Inokuchi for useful advice on intracellular recording analysis. We also thank Asahikasei Pharma Corporation to provide a Neurometer. This study was supported by the Grants-in Aid for Scientific Research from the Ministry of Education, Science, Sports and Culture to M.Y. and H.F. and in part by a Grant-in-aid for the 21st Century COE Program of Japan.
- Nakatsuka T, Park JS, Kumamoto E, Tamaki T, Yoshimura M: Plastic changes in sensory inputs to rat substantia gelatinosa neurons following peripheral inflammation. Pain 1999, 82: 39–47. 10.1016/S0304-3959(99)00037-8PubMedView ArticleGoogle Scholar
- Okamoto M, Baba H, Goldstein PA, Higashi H, Shimoji K, Yoshimura M: Functional reorganization of sensory pathways in the rat spinal dorsal horn following peripheral nerve injury. J Physiol 2001,532(1):241–250. 10.1111/j.1469-7793.2001.0241g.xPubMed CentralPubMedView ArticleGoogle Scholar
- Woolf CJ, Shortland P, Coggeshall RE: Peripheral nerve injury triggers central sprouting of myelinated afferents. Nature 1992, 355: 75–78. 10.1038/355075a0PubMedView ArticleGoogle Scholar
- Baquis GD: Technology review: the neurometer® current perception threshold (CPT). Muscle Nerve 1999, 22: 523–531. 10.1002/(SICI)1097-4598(199904)22:4<523::AID-MUS16>3.0.CO;2-1View ArticleGoogle Scholar
- Dinh S, Marroquin E, Raj PP: Neuroselective quantification of allodynia by current perception threshold evaluation on CRPS (RSD) patients. Reg Anesth 1997,22(2S):44.Google Scholar
- Katims JJ, Naviasky EH, Ng LKY, Rendell M, Bleecker ML: New screening device for assessment of peripheral neuropathy. J Occup Med 1986, 28: 1219–1221.PubMedGoogle Scholar
- Masson EA, Veves A, Fernando D, Boulton AJM: Current perception thresholds: a new, quick, and reproducible method for the assessment of peripheral neuropathy in diabetes mellitus. Diabetologia 1989, 32: 724–728. 10.1007/BF00274531PubMedView ArticleGoogle Scholar
- Nishimura A, Ogura T, Hase H, Makinodan A, Hojo T, Katsumi Y, Yagi K, Mikami Y, Kubo T: A correlative electrophysiologic study of nerve fiber involvement in carpal tunnel syndrome using current perception thresholds. Clinical Neurophysiol 2004,115(8):1921–1924. 10.1016/j.clinph.2004.03.022View ArticleGoogle Scholar
- Suzuki K, Chung Y, Kobayashi Y, Goto Y: Current perception threshold: A new method for the assessment of peripheral sensory neuropathy in diabetes mellitus. Peripher Nerve 1995, 6: 63.Google Scholar
- Kiso T, Nagakura Y, Toya T, Matsumoto N, Tamura S, Ito H, Okada M, Yamaguchi T: Neurometer measurement of current stimulus threshold in rats. J Pharmacol Exp Ther 2001, 297: 352–356.PubMedGoogle Scholar
- Liu S, Kopacz DJ, Carpenter RL: Quantitative assessment of differential sensory nerve block after lidocaine spinal anesthesia. Anesthesiology 1995, 82: 60–63. 10.1097/00000542-199501000-00009PubMedView ArticleGoogle Scholar
- Oda M, Kitagawa N, Yang BX, Totoki T, Morimoto M: Quantitative and fiber-selective evaluation of dose-dependent nerve blockade by intrathecal lidocaine in rats. J Pharmacol Exp Ther 2005,312(3):1132–1137. 10.1124/jpet.104.076893PubMedView ArticleGoogle Scholar
- Ataka T, Kumamoto E, Shimoji K, Yoshimura M: Baclofen inhibits more effectively C-afferent than Aδ-afferent glutamatergic transmission in substantia gelatinosa neurons of adult rat spinal cord slices. Pain 2000, 86: 273–282. 10.1016/S0304-3959(00)00255-4PubMedView ArticleGoogle Scholar
- Harper AA, Lawson SN: Conduction velocity is related to morphological cell type in rat dorsal root ganglion neurons. J Physiol 1985, 359: 31–46.PubMed CentralPubMedView ArticleGoogle Scholar
- Harper AA, Lawson SN: Electrical properties of rat dorsal root ganglion neurons with different peripheral nerve conduction velocities. J Physiol 1985, 359: 47–63.PubMed CentralPubMedView ArticleGoogle Scholar
- Prabhaker E, Lawson SN: The electrophysiological properties of rat primary afferent neurones with carbonic anhydrase activity. J Physiol 1995,482(3):609–622.View ArticleGoogle Scholar
- Villiere V, McLachlan EM: Electrophysiological properties of neurons in intact rat dorsal root ganglia classified by conduction velocity and action potential duration. J Neurophysiol 1996,76(3):1924–1941.PubMedGoogle Scholar
- Kumazawa T, Perl ER: Excitation of marginal and substantia gelatinosa neurons in the primate spinal cord: Indications of their place in dorsal horn functional organization. J Comp Neur 1978, 177: 417–434. 10.1002/cne.901770305PubMedView ArticleGoogle Scholar
- Sugiura Y, Lee CL, Perl ER: Central projections of identified, unmyelinated (C) afferent fibers innervating mammalian skin. Science 1986, 234: 358–361.PubMedView ArticleGoogle Scholar
- Yoshimura M, Jessell TM: Primary afferent-evoked synaptic responses and slow potential generation in rat substantia gelatinosa neurons in vitro. J Neurophysiol 1989, 62: 96–108.PubMedGoogle Scholar
- Furue H, Katafuchi T, Yoshimura M: Sensory processing and functional reorganization of sensory transmission under pathological conditions in the spinal dorsal horn. Neurosci Res 2004, 48: 361–368. 10.1016/j.neures.2003.12.005PubMedView ArticleGoogle Scholar
- Furue H, Narikawa K, Kumamoto E, Yoshimura M: Responsiveness of rat substantia gelatinosa neurons to mechanical but not thermal stimuli revealed by in vivo patch-clamp recording. J Physiol 1999,521(2):529–535. 10.1111/j.1469-7793.1999.00529.xPubMed CentralPubMedView ArticleGoogle Scholar
- Narikawa K, Furue H, Kumamoto E, Yoshimura M: In vivo patch-clamp analysis of IPSCs evoked in rat substantia gelatinosa neurons by cutaneous mechanical stimulation. J Neurophysiol 2000, 84: 2171–2174.PubMedGoogle Scholar
- Sonohata M, Furue H, Katafuchi T, Yasaka T, Doi A, Kumamoto E, Yoshimura M: Actions of noradrenaline on substantia geltatinosa neurones in the rat spinal cord revealed by in vivo patch recording. J Physiol 2003,555(2):515–526. 10.1113/jphysiol.2003.054932PubMed CentralPubMedView ArticleGoogle Scholar
- Magerl W, Fuchs PN, Meyer RA, Treede RD: Role of capsaicin-sensitive nociceptors in cutaneous pain and secondary hyperalgesia. Brain 2001, 124: 1754–1764. 10.1093/brain/124.9.1754PubMedView ArticleGoogle Scholar
- Black JA, Cummins TR, Plumpton C, Chen YH, Hormuzdiar W, Clare JJ, Waxman SG: Upregulation of a silent sodium channel after peripheral, but not central, nerve injury in DRG neurons. J Neurophysiol 1999, 82: 2776–2785.PubMedGoogle Scholar
- Cummins TR, Waxman SG: Down-regulation of TTX-resistant sodium currents and upregulation of a rapidly repriming TTX-sensitive sodium current in small spinal sensory neurons after nerve injury. J Neurosci 1997, 17: 3503–3514.PubMedGoogle Scholar
- Elliott AA, Elliott JR: Characterization of TTX-sensitive and TTX-resistant sodium currents in small cells from adult rat dorsal root ganglia. J Physiol 1993, 463: 39–56.PubMed CentralPubMedView ArticleGoogle Scholar
- Everill B, Cummins TR, Waxman SG, Kocsis JD: Sodium currents of large (Aβ-type) adult cutaneous afferent dorsal root ganglion neurons display rapid recovery from inactivation before and after axotomy. Neuroscience 2001, 106: 161–169. 10.1016/S0306-4522(01)00258-5PubMed CentralPubMedView ArticleGoogle Scholar
- Shepherd GM: Electronic Properties of Axon and Dendrites. In Fundamental Neuroscience. 2nd edition. Edited by: Squire LR, Bloom FE, McConnell SK, Roberts JL, Spitzer NC, Zigmond MJ. San Diego: Academic Press; 1999:115–137.Google Scholar
- Handwerker HO, Anton F, Reeh PW: Discharge patterns of afferent cutaneous nerve fibers from the rat's tail during prolonged noxious mechanical stimulation. Exp Brain Res 1987,65(3):493–504. 10.1007/BF00235972PubMedView ArticleGoogle Scholar
- Djouhri L, Fang X, Okuse K, Wood JN, Berry CM, Lawson SN: The TTX-resistant sodium channel Nav1.8 (SNS/PN3): expression and correlation with membrane properties in rat nociceptive primary afferent neurons. J Physiol 2003,550(3):739–752. 10.1113/jphysiol.2003.042127PubMed CentralPubMedView ArticleGoogle Scholar
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