Reactive oxygen species mediate TNFR1 increase after TRPV1 activation in mouse DRG neurons
© Ma et al; licensee BioMed Central Ltd. 2009
Received: 09 March 2009
Accepted: 17 June 2009
Published: 17 June 2009
Transient receptor potential vanilloid subtype 1 (TRPV1) is activated by low pH/protons and is well known to be involved in hyperalgesia during inflammation. Tumor necrosis factor α (TNF-α), a proinflammatory cytokine, is involved in nociceptive responses causing hyperalgesia through TNF receptor type 1 (TNFR1) activation. Reactive oxygen species (ROS) production is also prominently increased in inflamed tissue. The present study investigated TNFR1 receptors in primary cultured mouse dorsal root ganglion (DRG) neurons after TRPV1 activation and the involvement of ROS. C57BL/6 mice, both TRPV1 knockout and wild type, were used for immunofluorescent and live cell imaging. The L4 and L5 DRGs were dissected bilaterally and cultured overnight. TRPV1 was stimulated with capsaicin or its potent analog, resiniferatoxin. ROS production was measured with live cell imaging and TNFR1 was detected with immunofluorescence in DRG primary cultures. The TRPV1 knockout mice, TRPV1 antagonist, capsazepine, and ROS scavenger, N-tert-Butyl-α-phenylnitrone (PBN), were employed to explore the functional relationship among TRPV1, ROS and TNFR1 in these studies.
The results demonstrate that TRPV1 activation increases TNFR1 receptors and ROS generation in primary cultures of mouse DRG neurons. Activated increases in TNFR1 receptors and ROS production are absent in TRPV1 deficient mice. The PBN blocks increases in TNFR1 and ROS production induced by capsaicin/resiniferatoxin.
TRPV1 activation increases TNFR1 in cultured mouse DRG neurons through a ROS signaling pathway, a novel sensitization mechanism in DRG neurons.
Inflammation comes with sensitization of specialized sensory neurons that comprise the nociceptive pathway, leading to enhanced pain sensation in response to both noxious and non-noxious stimuli . The transient receptor potential vanilloid 1 (TRPV1) participates in the development of chemical and thermal hyperalgesia in inflammation, through the action of low pH, heat and inflammatory mediators . The most striking feature of TRPV1 knockout mice is the virtual absence of thermal hypersensitivity in the setting of inflammation [3–6]. Inflammation causes the release of inflammatory mediators which lower the threshold of heat stimulation, a process known as heat hyperalgesia depending on TRPV1 activation .
Tumor necrosis factor α (TNF-α) is prominently released during inflammation and plays an important role in hyperalgesia in inflammation. Application of TNF-α enhances calcium currents increasing neuron sensitivity to the neurotoxin capsaicin in cultures of sensory neurons, and anti-TNF therapy produces a profound analgesia [8–11]. TNF-α acts on two distinct subtypes of receptors, TNF receptor type 1 (TNFR1, p55) and TNF receptor type 2 (TNFR2, p75) . TNFR1 but not TNFR2 neutralizing antibodies, as well as antisense RNA against TNFR1, can reduce experimentally induced hyperalgesia [13, 14]. TNFR1 immunoreactivity (IR) has been reported in DRG neurons [15, 16]. TNFR1 is increased in nociceptive DRG neurons and primary afferents by intraperitoneal lipopolysaccharide and after nerve injury in animal models, and in plasma of patients with pain syndromes, supporting an important role for TNFR1 in nociception [17–19].
While reactive oxygen species (ROS) are primarily important for regulating many metabolic cellular activities, excess ROS have been implicated in neuropathic and inflammatory pain [20–23]. The transient but dramatic analgesic effect of free-radical scavengers in pain models suggests that ROS are critically involved in the generation of pain. Some research on the signaling pathways has been directed towards documenting a role for ROS in cell death and the induction of cell proliferation [24–26]. The effects of ROS may be mediated by reversible effects on intracellular proteins which lead to alterations in intracellular signaling pathways. Effects of ROS on aberrant signaling pathways in the nervous system remain to be determined.
Although some reports show that TNF-α sensitizes TRPV1, we are interested in the role that TRPV1 activation might have on TNFR1 as the drive for maintaining nociceptor sensitization. The present study investigated changes in TNFR1 in response to TRPV1 activation in primary DRG neuronal cultures from both TRPV1 knockout and wild type mice while monitoring involvement of ROS as a potential drive in this signaling pathway. Primary DRG neurons were dissected from wild type and TRPV1 knockout C57BL/6 mice. After overnight incubation, DRG cultures were challenged with either capsaicin or resiniferatoxin.
Capsaicin induces TNFR1 staining increases in DRG neurons from wild type mice
Percentage of TNFR1 and TRPV1 positive neurons in primary cultures of DRG neurons from wild type mice
% of total
% of total
9.24 ± 0.27
22.82 ± 1.69
41.04 ± 3.94
14.62 ± 0.72
27.91 ± 2.58
52.89 ± 2.89
16.5 ± 1.37
23.19 ± 2.15
73.63 ± 3.54
Capsaicin induced TNFR1 increase is absent in DRG neurons of TRPV1 deficient mice
Capsazepine blocks capsaicin induced TNFR1 increase in DRG neurons from wild type mice
Capsazepine, a competitive TRPV1 antagonist, was used to determine if capsaicin or resiniferatoxin induced TNFR1 staining in cultured DRG neurons from wild type mice is mediated through TRPV1 receptor activation. The results showed that capsazepine (10 μM, 10 min) blocked TNFR1 increases induced by capsaicin (1 μM, 20 min) or resiniferatoxin (200 nM, 20 min) respectively (Fig. 2A, B) (capsazepine plus capsaicin treated group: 9.74 ± 1.85%, n = 522, P < 0.05 compared with the capsaicin treated group: 14.62 ± 0.72%; capsazepine plus resiniferatoxin treated group: 9.34 ± 0.53%, n = 393, P < 0.01 compared with resiniferatoxin treated group: 16.5 ± 1.37%).
PBN blocks capsaicin induced TNFR1 increase in DRG neurons of wild type mice
PBN blocks TRPV1 activated increases in ROS production in DRG neurons of wild type mice
Capsaicin increases ROS production in DRG neurons of wild type mice
The present study demonstrates that capsaicin increased both the TNFR1 staining and ROS production in cultured DRG neurons from wild type mice through TRPV1 activation. These phenomena did not occur in TRPV1 deficient mice. ROS scavenger PBN and TRPV1 antagonist, capsazepine, blocked both the TNFR1 and ROS increases. We conclude that TRPV1 activation increases TNFR1 through a signaling pathway driven by ROS generation.
Regulation of TNFR1 by capsaicin
Two subtypes of TNF-α receptors, TNFR1 and TNFR2, are expressed in peripheral nerves . TNFR1 is expressed in dorsal root ganglion neurons and plays a potential role in nociception . In present experiment, TNFR1 is positively immunostained in 10% of mouse DRG neurons and almost all of which were small size neurons which suggests a potential role of TNFR1 in transmission of nociception. TNFR1 in mouse DRG neurons is detected after sciatic nerve injury but not in control mice . The process of dissociating and culturing DRG neurons apparently increases expression in the cells somewhat since TNFR1 is not found in normal mouse DRG tissue sections. In rat inflammation or nerve injury models, increases in TNFR1 expression are reported by several other researchers [15, 17, 28–30]. Although there are reports that TNF-α increases TRPV1 expression through TNF-α receptors and TRPV1 induced activity is enhanced by TNF-α administration [31–33], it would be interesting to know if they can reciprocally regulate one another. The interactive relationship of these two types of receptors will be the target of further investigation since the present study suggests TRPV1 activation is inducing TNFR1 increases and/or activation. In the present study using mouse DRG neuronal cultures, TNFR1 was significantly increased after stimulation with capsaicin/resiniferatoxin. The responses to capsaicin and resiniferatoxin were different since resiniferatoxin is a more robust agonist for TRPV1. This result is supported by calcium influx experiments where resiniferatoxin produces a stronger calcium increase . To confirm that TNFR1 increases induced by capsaicin are mediated through TRPV1, TRPV1 knockout mice were employed and additional experiments using capsazepine were also performed. The results of both these experiments showed that capsaicin/resiniferatoxin induced increases in TNFR1 in small size DRG neurons co-expressing TRPV1, and thus are likely to be nociceptors. This novel finding of capsaicin induced TNFR1 increases in cultured mouse DRG neurons has not been reported by other investigators. The result is in agreement with those in a rat inflammation model . In CFA arthritis models in vivo, upregulation of TNFR1 receptors is detected in peripheral joint tissue, DRG neurons, and small fiber bundles within the root entry zone and fibers bordering the trigeminal and spinal cord dorsal horn [28, 34, 35].
During inflammation, high levels of H+ are released from injured tissue and are important mediators activating TRPV1. In fact, there are several other mediators activating TRPV1 such as anandamide and high temperature (43°C) that are present in inflamed tissue targeted by sensory nerve terminals. Thermal hyperalgesia and mechanical allodynia are triggered by TRPV1 over-activation and plastic changes occur in neurons with influxes of ions such as calcium and sodium. One of the changes we find is increasing TNFR1 in TRPV1 stained neurons which would allow neurons to receive information presented in inflammatory conditions of which TNF-α plays an important role. The present study demonstrates the mechanistic linkage between TNFR1 and TRPV1 activation. TNF-α is produced by satellite cells in DRG, Schwann cells in the peripheral nervous system and local macrophage cells which increase TNF-α release from peripheral tissue attracting considerable attention in nociceptive sensation and inflammatory cell invasion during inflammation. TNF-α mRNA increases are observed 24 hours after periganglionic injections of complete Freund's adjuvant . Anti-TNF therapy used in treatment of rheumatoid arthritis produces profound analgesia [8, 11], indicating that TNF-α and its receptors may be good therapeutic targets in other chronic inflammatory pain conditions. The two distinct subtypes of TNF-α receptors have different functions in inflammation. TNFR1 functions mainly in the process that leads to hyperalgesia and most of TNFR2's effects are involved in immunological responses. While depressing the immunological responses is also a way to reduce inflammation induced hyperalgesia, we have chosen to study neuronal TNFR1 effects in this investigation. Significant increases in TNFR1 are relevant based on behavioral evidence showing that antibody against TNFR1 applied to the epineuria abolishes hyperalgesia caused by chronic constriction nerve injury . During inflammation, more TNF-α is released, and TNFR1 expression in neurons is increasing in proportion to the changes in TNF-α release from peripheral tissue and DRG satellite cells [8, 29]. A highly active condition in which ROS, TNF-α and TNFR1 are increasing would cause hypersensitivity of peripheral nerves based on our studies presented here for TRPV1 activation and others in literature.
PBN blocks capsaicin induced TNFR1 increases
ROS are not only endpoint products of TRPV1 activation but also signaling pathway elements. The activation of many types of signaling pathways by ROS involves the direct modification of membrane lipids/proteins or other elements of signaling pathways described for ROS . The present study shows PBN blocks TNFR1 increases induced by capsaicin. It is of considerable interest that ROS are signaling molecules in the regulation of TNFR1 increase after TRPV1 activation. A similar point was held in a study by Gao et al.  that ROS is involved in enhancement of NMDA-receptor phosphorylation in animal pain models. Biologically relevant ROS include the superoxide radical (•O2 -), hydroperoxyl radicals (HO2 •), H2O2 and the hydroxyl radical (•OH). It is not clear at this time which component is acting as the factor regulating the TNFR1 in our experiment. Taking ROS in general, however, ROS play roles either as protein phosphate activators or in activation of transcription factors to increase receptor expression. In our experiment, blocking ROS production also abolished TNFR1 increases. ROS has been shown to mediate TRPV1 and neuropeptide-dependent neurogenic vasodilatation in wild type but not TRPV1 knockout mice .
TRPV1 activation induces increases in ROS production
To determine further if ROS is involved in regulation of TNFR1 increases after TRPV1 activation, we also studied ROS production after TRPV1 activation by capsaicin in the mouse DRG neuronal cultures. We assessed cytosolic oxidant activity with use of CM-H2DCFDA, a redox-sensitive fluorochrome probe to monitor ROS production. CM-H2DCFDA oxidation to DCF is a nonspecific reaction used to monitor generation of biological oxidants that include ROS. It is important to recognize that intracellular conversion of H2DCFDA to DCF occurs in competition with other oxidation reactions. The overall rate of H2DCFDA conversion to DCF therefore reflects a complex, highly dynamic balance between simultaneous rates of oxidant production and oxidant buffering by multiple pathways. We interpret this integrated signal as net oxidant activity under a given condition. The data indicate that ROS production is increased by challenging neurons with capsaicin/resiniferatoxin. The results from TRPV1 deficient mice show no increase in ROS production after capsaicin stimulation. The data for the capsazepine pretreatment experiment also confirmed this finding. These data demonstrate that capsaicin initiates ROS generation through TRPV1 activation. The results are supported in experiments done on synoviocyte cultures showing that ROS production was induced by calcium influxes elicited by TRPV1 activation . It has been established that the cation channel TRPV1 is activated by capsaicin or proton and induces calcium influxes . The effective dose used for activation was selected based on previous studies reporting maximal but non-desensitizing responses [3, 42, 43]. However, the mechanism of generating calcium influx in response to ROS production increase is still unclear. Significant increases in ROS production do not occur in the present study until 30 minutes since ROS levels in cells are tightly regulated. ROS generation during inflammation has attracted increasing attention in the literature. It is also known that the ROS scavenger used to block ROS production also reverses hypersensitivity [23, 44]. While much work has been done in vivo in rat, our work in cultured mouse DRG neurons challenging TRPV1 with capsaicin to increase ROS production is similar to in vivo microenvironment conditions present during inflammation. The finding that PBN abolished ROS production induced by capsaicin in the study further confirms that elevated ROS production is triggered by TRPV1 activation. Thus, ROS are implicated as important functional and potentially therapeutic targets influencing neurotransmitter responses, inflammatory mediator receptors and neurogenic vasodilatation relevant to treatment of inflammation and pain.
The present study reveals that TRPV1 activation increases ROS which act as signaling molecules to increase TNFR1 in mouse DRG neurons. Thus, in conditions of injured or inflamed tissues, TRPV1 activation increases of ROS and inflammatory mediator TNF-α receptor content could enhance peripheral nerve sensitization, inflammatory pain and potentially other pathological events.
This study was performed in accordance with the Guide for the Care and Use of Laboratory Animals published by the National Institutes of Health and was approved by the University of Kentucky Institutional Animal Care and Use Committee.
Primary DRG neuronal cultures
Male and female TRPV1 knockout or wild type C57BL/6 mice (19 – 20 g, Jackson Lab, as a tissue sharing gift from Dr. Lu-Yuan Lee) were used in these experiments . Mice were anesthetized and the vertebral columns were exposed, removed, and put into the ice-cold dissection solution (NaCl 135, KCl 5, KH2PO4 2, HEPES 10, MgSO4 6, CaCl2 1.5, Glucose 10; in mM) bubbled with 100% O2. The L4, L5 DRGs were removed from the lumbar spinal roots and placed into the 30 mm dish with ice-cold dissection solution. After connective tissues were removed, DRGs were digested in fresh enzyme solution (10 mg trypsin+25 mg collagenase in 10 ml dissection solution) in 25 cm2 flask saturated with O2. After shaking in a warm water bath (speed 150 rpm, 35°C) for 1 hour, 4 ml of culture medium (MEM with FBS, antibiotics) were added to the flask. The cells were transferred into a 15 ml centrifuge tube and spun at 800 rpm for 5 minutes. The supernatant was discarded and the cell pellet was re-suspended with culture medium. DRG cells were plated onto poly-L-Lysine pre-coated 12 mm glass-bottom home made tissue culture dish or 12 mm coverslips in 24 well culture plates (0.2 ml of cell suspension per well). Cultured DRG neurons were maintained in an incubator with 5% CO2, 37°C overnight and all experiments performed on the subsequent day.
Dissociated DRG neurons were cultured on coverslips in 24-well plates overnight. Cells were stimulated with capsaicin (1 μM) or resiniferatoxin (200 nM) for 30 minutes and then the media was replaced with Dulbecco’s phosphate buffered saline (DPBS) for 90 minutes. In some experiments, ROS scavenger PBN was applied for 90 minutes before capsaicin stimulation, or TRPV1 antagonist capsazepine (10 μM) was administered 10 minutes before capsaicin stimulation. At the end of incubation, cells were washed with 0.1 M phosphate buffered saline (PBS, pH7.4) 3 times × 5 minutes and fixed with 4% paraformaldehyde in 0.1 M PBS for 30 minutes. After washing with PBS, cells were incubated with 3% normal donkey serum in PBS plus 0.02% Triton X-100 for 30 minutes to block non-specific protein binding. Then, cells were incubated overnight with the primary antibody diluted in PBS TritonX-100 plus 1% normal donkey serum at 4°C. The anti-TRPV1 receptor antibody (VR1 P-19, Santa Cruz, and affinity purified goat polyclonal antibody against a peptide mapping near the N-terminus of VR1 of rat origin producing a single band in western blots) was diluted 1:100. The anti-TNFR1 receptor antibody (TNF-R1 H-5, Santa Cruz), a mouse monoclonal antibody raised against amino acids 30–301 mapping within the extracellular domain of TNF-R1 of human origin producing a single band in western blots, was diluted 1:50. After overnight incubation, the coverslips were rinsed in PBS 3 times × 5 minutes and incubated with FITC-donkey-anti-goat antibody, diluted 1:1000 and Texas Red-donkey-anti-mouse antibody, diluted 1:800 in PBS Triton-X plus 1% normal donkey serum for 1 hour at room temperature. For staining controls, primary antibodies were omitted. The coverslips were washed again 3 times × 5 minutes. Thereafter, the coverslips were mounted face down onto slides with mounting medium. Five different areas were picked randomly from each coverslip for pictures. MetaMorph offline software was used for digital image data analysis.
Determination of ROS production by H2DCFDA fluorescent probe
All experiments were done at room temperature. Cells were kept at room temperature for 30 min before replacing culture medium with DPBS, pH 7.4. On the day of the experiment, the ROS-sensitive fluorescent dye, 5-(and-6)-chloromethyl-2', 7'-dichlorodihydrofluorescein diacetate, acetyl ester (CM-H2DCFDA, Invitrogen) was freshly reconstituted. Cells were pre-loaded with CM-H2DCFDA in DPBS at a final concentration of 4 μM for 30 min. The loading buffer was removed and replaced with DPBS allowing 20 min to 2 h recovery time for cells to exhibit low levels of esterase activity. ROS production was monitored for 30 minutes in the live cell imaging experiment. Cells were stimulated with bath application of capsaicin (1 μM) or resiniferatoxin (200 nM) and in some cases neurons were pretreated 10 minutes with TRPV1 antagonist capsazepine (10 μM) before beginning the recording and capsaicin stimulation. ROS scavenger N-tert-Butyl-α-phenylnitrone (PBN, 2 mM) was administered for 90 minutes before capsaicin stimulation.
The change in fluorescent intensity over time is proportional to DCF accumulation, an index of net oxidant activity in the cytoplasm. Fluorescent imaging was performed using an Eclipse 2000-S microscope (Nikon) equipped with a high sensitivity digital monochrome Cool SNAP ES camera (Photometrics, Tucson, AZ) controlled by MetaMorph software (Molecular Devices, Sunnyvale, CA). DCF was excited at 480 nm and emitted light was collected using a 520 nm long pass filter. The photos were captured under 10 ms exposure at 1 min intervals for 30 min. Emissions from DCFH-free buffer are not detectable under these conditions, and background correction is not required. Photooxidation artifact was controlled by conducting experiments in a darkened laboratory and by standardizing excitation parameters to minimize the cumulative delivered energy. The baseline fluorescent intensity was determined prior to exposing the cells to experimental inducements. MetaMorph offline software (Molecular Devices, Sunnyvale, CA) was used for image data analysis.
Trypsin, poly-L-Lysine, capsaicin, resiniferatoxin, capsazepine and N-tert-Butyl-α-phenylnitrone were obtained from Sigma-Aldrich (St. Louis, MO). Collagenase was purchased from Roche Applied Science (Indianapolis, IN). 5-(and-6)-chloromethyl-2', 7'-dichlorodihydrofluorescein diacetate, acetyl ester and DPBS were purchased from Invitrogen (Carlsbad, CA). Antibody against TRPV1, antibody against TNFR1, FITC-donkey-anti-goat antibody and Texas Red-donkey-anti-mouse antibody were obtained from Santa Cruz Biotechnology (Santa Cruz, CA). Mounting medium was purchased from Vector Laboratories (Burlingame, CA).
All data were expressed as mean ± SEM. Comparisons among multiple means were analyzed with the one-way ANOVA. Post hoc test was analyzed with the Newman-Keuls Multiple Comparison test. A P < 0.05 was considered significant.
The authors are grateful for the following University of Kentucky College of Medicine and Department of Physiology support:
(1) These studies were funded by the Dean's Start-Up Funds.
(2) Animals were acquired through tissue sharing with Dr. Lu-Yuan Lee.
(3) ROS imaging support was provided by Jeff Smith and Dr. Michael Reid.
- Millan MJ: The induction of pain: an integrative review. Prog Neurobiol 1999, 57: 1–164. 10.1016/S0301-0082(98)00048-3PubMedView ArticleGoogle Scholar
- Caterina MJ, Julius D: The vanilloid receptor: a molecular gateway to the pain pathway. Annu Rev Neurosci 2001, 24: 487–517. 10.1146/annurev.neuro.24.1.487PubMedView ArticleGoogle Scholar
- Caterina MJ, Leffler A, Malmberg AB, Martin WJ, Trafton J, Petersen-Zeitz KR, Koltzenburg M, Basbaum AI, Julius D: Impaired nociception and pain sensation in mice lacking the capsaicin receptor. Science 2000, 288: 306–313. 10.1126/science.288.5464.306PubMedView ArticleGoogle Scholar
- Chuang HH, Prescott ED, Kong H, Shields S, Jordt SE, Basbaum AI, Chao MV, Julius D: Bradykinin and nerve growth factor release the capsaicin receptor from PtdIns(4,5)P2-mediated inhibition. Nature 2001, 411: 957–962. 10.1038/35082088PubMedView ArticleGoogle Scholar
- Davis JB, Gray J, Gunthorpe MJ, Hatcher JP, Davey PT, Overend P, Harries MH, Latcham J, Clapham C, Atkinson K, et al.: Vanilloid receptor-1 is essential for inflammatory thermal hyperalgesia. Nature 2000, 405: 183–187. 10.1038/35012076PubMedView ArticleGoogle Scholar
- Moriyama T, Iida T, Kobayashi K, Higashi T, Fukuoka T, Tsumura H, Leon C, Suzuki N, Inoue K, Gachet C, et al.: Possible involvement of P2Y2 metabotropic receptors in ATP-induced transient receptor potential vanilloid receptor 1-mediated thermal hypersensitivity. J Neurosci 2003, 23: 6058–6062.PubMedGoogle Scholar
- Zhang X, Li L, McNaughton PA: Proinflammatory mediators modulate the heat-activated ion channel TRPV1 via the scaffolding protein AKAP79/150. Neuron 2008, 59: 450–461. 10.1016/j.neuron.2008.05.015PubMedView ArticleGoogle Scholar
- Feldmann M: Development of anti-TNF therapy for rheumatoid arthritis. Nat Rev Immunol 2002, 2: 364–371. 10.1038/nri802PubMedView ArticleGoogle Scholar
- Nicol GD, Lopshire JC, Pafford CM: Tumor necrosis factor enhances the capsaicin sensitivity of rat sensory neurons. J Neurosci 1997, 17: 975–982.PubMedGoogle Scholar
- Pollock J, McFarlane SM, Connell MC, Zehavi U, Vandenabeele P, MacEwan DJ, Scott RH: TNF-alpha receptors simultaneously activate Ca2+ mobilisation and stress kinases in cultured sensory neurones. Neuropharmacology 2002, 42: 93–106. 10.1016/S0028-3908(01)00163-0PubMedView ArticleGoogle Scholar
- Sorkin LS, Doom CM: Epineurial application of TNF elicits an acute mechanical hyperalgesia in the awake rat. J Peripher Nerv Syst 2000, 5: 96–100. 10.1046/j.1529-8027.2000.00012.xPubMedView ArticleGoogle Scholar
- MacEwan DJ: TNF receptor subtype signalling: differences and cellular consequences. Cell Signal 2002, 14: 477–492. 10.1016/S0898-6568(01)00262-5PubMedView ArticleGoogle Scholar
- Parada CA, Yeh JJ, Joseph EK, Levine JD: Tumor necrosis factor receptor type-1 in sensory neurons contributes to induction of chronic enhancement of inflammatory hyperalgesia in rat. Eur J Neurosci 2003, 17: 1847–1852. 10.1046/j.1460-9568.2003.02626.xPubMedView ArticleGoogle Scholar
- Sommer C, Schmidt C, George A: Hyperalgesia in experimental neuropathy is dependent on the TNF receptor 1. Exp Neurol 1998, 151: 138–142. 10.1006/exnr.1998.6797PubMedView ArticleGoogle Scholar
- Schafers M, Sorkin LS, Geis C, Shubayev VI: Spinal nerve ligation induces transient upregulation of tumor necrosis factor receptors 1 and 2 in injured and adjacent uninjured dorsal root ganglia in the rat. Neurosci Lett 2003, 347: 179–182. 10.1016/S0304-3940(03)00695-5PubMedView ArticleGoogle Scholar
- Shubayev VI, Myers RR: Axonal transport of TNF-alpha in painful neuropathy: distribution of ligand tracer and TNF receptors. J Neuroimmunol 2001, 114: 48–56. 10.1016/S0165-5728(00)00453-7PubMedView ArticleGoogle Scholar
- Li Y, Ji A, Weihe E, Schafer MK: Cell-specific expression and lipopolysaccharide-induced regulation of tumor necrosis factor alpha (TNFalpha) and TNF receptors in rat dorsal root ganglion. J Neurosci 2004, 24: 9623–9631. 10.1523/JNEUROSCI.2392-04.2004PubMedView ArticleGoogle Scholar
- George A, Buehl A, Sommer C: Tumor necrosis factor receptor 1 and 2 proteins are differentially regulated during Wallerian degeneration of mouse sciatic nerve. Exp Neurol 2005, 192: 163–166. 10.1016/j.expneurol.2004.11.002PubMedView ArticleGoogle Scholar
- Maihofner C, Handwerker HO, Neundorfer B, Birklein F: Mechanical hyperalgesia in complex regional pain syndrome: a role for TNF-alpha? Neurology 2005, 65: 311–313. 10.1212/01.wnl.0000168866.62086.8fPubMedView ArticleGoogle Scholar
- Kim HK, Park SK, Zhou JL, Taglialatela G, Chung K, Coggeshall RE, Chung JM: Reactive oxygen species (ROS) play an important role in a rat model of neuropathic pain. Pain 2004, 111: 116–124. 10.1016/j.pain.2004.06.008PubMedView ArticleGoogle Scholar
- Salvemini D, Wang ZQ, Zweier JL, Samouilov A, Macarthur H, Misko TP, Currie MG, Cuzzocrea S, Sikorski JA, Riley DP: A nonpeptidyl mimic of superoxide dismutase with therapeutic activity in rats. Science 1999, 286: 304–306. 10.1126/science.286.5438.304PubMedView ArticleGoogle Scholar
- Tal M: A novel antioxidant alleviates heat hyperalgesia in rats with an experimental painful peripheral neuropathy. Neuroreport 1996, 7: 1382–1384. 10.1097/00001756-199605310-00010PubMedView ArticleGoogle Scholar
- Wang ZQ, Porreca F, Cuzzocrea S, Galen K, Lightfoot R, Masini E, Muscoli C, Mollace V, Ndengele M, Ischiropoulos H, Salvemini D: A newly identified role for superoxide in inflammatory pain. J Pharmacol Exp Ther 2004, 309: 869–878. 10.1124/jpet.103.064154PubMedView ArticleGoogle Scholar
- Bae YS, Kang SW, Seo MS, Baines IC, Tekle E, Chock PB, Rhee SG: Epidermal growth factor (EGF)-induced generation of hydrogen peroxide. Role in EGF receptor-mediated tyrosine phosphorylation. J Biol Chem 1997, 272: 217–221. 10.1074/jbc.272.51.32071PubMedView ArticleGoogle Scholar
- Irani K, Xia Y, Zweier JL, Sollott SJ, Der CJ, Fearon ER, Sundaresan M, Finkel T, Goldschmidt-Clermont PJ: Mitogenic signaling mediated by oxidants in Ras-transformed fibroblasts. Science 1997, 275: 1649–1652. 10.1126/science.275.5306.1649PubMedView ArticleGoogle Scholar
- Sundaresan M, Yu ZX, Ferrans VJ, Irani K, Finkel T: Requirement for generation of H2O2 for platelet-derived growth factor signal transduction. Science 1995, 270: 296–299. 10.1126/science.270.5234.296PubMedView ArticleGoogle Scholar
- Ohtori S, Takahashi K, Moriya H, Myers RR: TNF-alpha and TNF-alpha receptor type 1 upregulation in glia and neurons after peripheral nerve injury: studies in murine DRG and spinal cord. Spine 2004, 29: 1082–1088. 10.1097/00007632-200405150-00006PubMedView ArticleGoogle Scholar
- Inglis JJ, Nissim A, Lees DM, Hunt SP, Chernajovsky Y, Kidd BL: The differential contribution of tumour necrosis factor to thermal and mechanical hyperalgesia during chronic inflammation. Arthritis Res Ther 2005, 7: R807–816. 10.1186/ar1743PubMed CentralPubMedView ArticleGoogle Scholar
- Sakuma Y, Ohtori S, Miyagi M, Ishikawa T, Inoue G, Doya H, Koshi T, Ito T, Yamashita M, Yamauchi K, et al.: Up-regulation of p55 TNF alpha-receptor in dorsal root ganglia neurons following lumbar facet joint injury in rats. Eur Spine J 2007, 16: 1273–1278. 10.1007/s00586-007-0365-3PubMed CentralPubMedView ArticleGoogle Scholar
- Xu JT, Xin WJ, Zang Y, Wu CY, Liu XG: The role of tumor necrosis factor-alpha in the neuropathic pain induced by Lumbar 5 ventral root transection in rat. Pain 2006, 123: 306–321. 10.1016/j.pain.2006.03.011PubMedView ArticleGoogle Scholar
- Constantin CE, Mair N, Sailer CA, Andratsch M, Xu ZZ, Blumer MJ, Scherbakov N, Davis JB, Bluethmann H, Ji RR, Kress M: Endogenous tumor necrosis factor alpha (TNFalpha) requires TNF receptor type 2 to generate heat hyperalgesia in a mouse cancer model. J Neurosci 2008, 28: 5072–5081. 10.1523/JNEUROSCI.4476-07.2008PubMedView ArticleGoogle Scholar
- Hensellek S, Brell P, Schaible HG, Brauer R, Segond von Banchet G: The cytokine TNFalpha increases the proportion of DRG neurones expressing the TRPV1 receptor via the TNFR1 receptor and ERK activation. Mol Cell Neurosci 2007, 36: 381–391. 10.1016/j.mcn.2007.07.010PubMedView ArticleGoogle Scholar
- Khan AA, Diogenes A, Jeske NA, Henry MA, Akopian A, Hargreaves KM: Tumor necrosis factor alpha enhances the sensitivity of rat trigeminal neurons to capsaicin. Neuroscience 2008, 155: 503–509. 10.1016/j.neuroscience.2008.05.036PubMedView ArticleGoogle Scholar
- Holmes GM, Hebert SL, Rogers RC, Hermann GE: Immunocytochemical localization of TNF type 1 and type 2 receptors in the rat spinal cord. Brain Res 2004, 1025: 210–219. 10.1016/j.brainres.2004.08.020PubMedView ArticleGoogle Scholar
- Spears R, Oakes R, Moore C, Bellinger LL, Hutchins B: A determination of tumor necrosis factor expression in TMJ inflammation with the use of microarray analysis. J Dent Res 2003, 82: 807–813. 10.1177/154405910308201009PubMedView ArticleGoogle Scholar
- Amaya F, Samad TA, Barrett L, Broom DC, Woolf CJ: Periganglionic inflammation elicits a distally radiating pain hypersensitivity by promoting COX-2 induction in the dorsal root ganglion. Pain 2009, 142: 59–67. 10.1016/j.pain.2008.11.013PubMed CentralPubMedView ArticleGoogle Scholar
- Maher P, Schubert D: Signaling by reactive oxygen species in the nervous system. Cell Mol Life Sci 2000, 57: 1287–1305. 10.1007/PL00000766PubMedView ArticleGoogle Scholar
- Gao X, Kim HK, Chung JM, Chung K: Reactive oxygen species (ROS) are involved in enhancement of NMDA-receptor phosphorylation in animal models of pain. Pain 2007, 131: 262–271. 10.1016/j.pain.2007.01.011PubMed CentralPubMedView ArticleGoogle Scholar
- Starr A, Graepel R, Keeble J, Schmidhuber S, Clark N, Grant A, Shah AM, Brain SD: A reactive oxygen species-mediated component in neurogenic vasodilatation. Cardiovasc Res 2008, 78: 139–147. 10.1093/cvr/cvn012PubMedView ArticleGoogle Scholar
- Hu F, Sun WW, Zhao XT, Cui ZJ, Yang WX: TRPV1 mediates cell death in rat synovial fibroblasts through calcium entry-dependent ROS production and mitochondrial depolarization. Biochem Biophys Res Commun 2008, 369: 989–993. 10.1016/j.bbrc.2008.02.155PubMedView ArticleGoogle Scholar
- Larrucea C, Castro P, Sepulveda FJ, Wandersleben G, Roa J, Aguayo LG: Sustained increase of Ca+2 oscillations after chronic TRPV1 receptor activation with capsaicin in cultured spinal neurons. Brain Res 2008, 1218: 70–76. 10.1016/j.brainres.2008.04.035PubMedView ArticleGoogle Scholar
- Ni D, Lee LY: Lack of potentiating effect of increasing temperature on responses to chemical activators in vagal sensory neurons isolated from TRPV1-null mice. Am J Physiol Lung Cell Mol Physiol 2008, 295: L897–904. 10.1152/ajplung.90385.2008PubMed CentralPubMedView ArticleGoogle Scholar
- Wood JN, Winter J, James IF, Rang HP, Yeats J, Bevan S: Capsaicin-induced ion fluxes in dorsal root ganglion cells in culture. J Neurosci 1988, 8: 3208–3220.PubMedGoogle Scholar
- Khattab MM: TEMPOL, a membrane-permeable radical scavenger, attenuates peroxynitrite- and superoxide anion-enhanced carrageenan-induced paw edema and hyperalgesia: a key role for superoxide anion. Eur J Pharmacol 2006, 548: 167–173. 10.1016/j.ejphar.2006.08.007PubMedView ArticleGoogle Scholar
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