Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

N/OFQ modulates orofacial pain induced by tooth movement through CGRP-dependent pathways

BMC Neuroscience volume 22, Article number: 25 (2021) Cite this article

Abstract

Background

Nociceptin/orphanin FQ (N/OFQ) has been revealed to play bidirectional roles in orofacial pain modulation. Calcitonin gene-related peptide (CGRP) is a well-known pro-nociceptive molecule that participates in the modulation of orofacial pain. We aimed to determine the effects of N/OFQ on the modulation of orofacial pain and on the release of CGRP.

Methods

Orofacial pain model was established by ligating springs between incisors and molars in rats for the simulation of tooth movement. The expression level of N/OFQ was determined and pain level was scored in response to orofacial pain. Both agonist and antagonist of N/OFQ receptor were administered to examine their effects on pain and the expression of CGRP in trigeminal ganglia (TG). Moreover, gene therapy based on the overexpression of N/OFQ was delivered to validate the modulatory role of N/OFQ on pain and CGRP expression.

Results

Tooth movement elicited orofacial pain and an elevation in N/OFQ expression. N/OFQ exacerbated orofacial pain and upregulated CGRP expression in TG, while UFP-101 alleviated pain and downregulated CGRP expression. N/OFQ-based gene therapy was successful in overexpressing N/OFQ in TG, which resulted in pain exacerbation and elevation of CGRP expression in TG.

Conclusions

N/OFQ exacerbated orofacial pain possibly through upregulating CGRP.

Background

Orofacial pain induced by tooth movement, highly prevalent among orthodontic patients [1], is characterized by a cascade of inflammatory reactions in periodontal tissues that eventually elicits pain sensation [2]. As is well documented, orofacial pain sensation is initiated at periodontal sensory terminals, modulated at trigeminal ganglia (TG), replayed at trigeminal nucleus and finally reaches sensory cortex via thalamus [2]. Particularly, TG undergo dramatic adaptations in response to orofacial pain [3, 4]. Specifically, abundant proteins are upregulated and downregulated in concert to modulate orofacial pain [5, 6].

Nociceptin/orphanin FQ (N/OFQ) is derived from a precursor, prepronociceptin (PNOC), the sequence of which shares similar structural features to precursors of classical opioid peptides [7]. The receptor of N/OFQ, also designated as ORL1, belongs to the opioid receptor family and is widely distributed in both central and peripheral nervous system, especially abundant in pain modulation regions [8,9,10,11]. Unlike other members of opioid family, N/OFQ plays a crucial role in pain modulation in a bidirectional manner, exhibiting either pro- or anti-nociceptive effects, which depends on a series of complex factors including pain quality, administration routes and dosages [12,13,14,15]. Our previous study elucidated the pro-nociceptive effect of N/OFQ in periodontal tissue for orofacial pain [16]. However, it is still largely unknown the effects of N/OFQ on orofacial pain in TG.

Calcitonin gene-related peptide (CGRP), a 37-amino-acid neuropeptide, is widely distributed in central and peripheral nervous system [17, 18]. It is well documented that CGRP has an essential role in the modulation of orofacial pain, especially migraine [19, 20]. Our previous study revealed that CGRP played an important role in the modulation of orofacial pain [21]. A further study showed that CGRP was co-expressed with N/OFQ in TG, suggesting their possible interactions in pain modulation [22].

Therefore, in this study, we aimed to explore the specific role of N/OFQ in the modulation of orofacial pain and its impacts on CGRP expression.

Methods

Animals

In total, 357 male Sprague–Dawley rats (200–250 g) were obtained from the Animal Experimental Center at Sichuan University (Additional File 1: Table S1). They were maintained in the animal facility and kept in an air-conditioned room at 21 °C with a 12 h light–dark cycle. Standard rat chow and water were provided ad libitum. Animal experiments were performed in accordance with protocols that were approved by the ethical committee of the State Key Laboratory of Oral Diseases, Sichuan University (WCCSIRB-D-2015–006). Following general anesthesia with intraperitoneal injection of sodium pentobarbital (30 mg·kg−1), rats were placed in supine positions, and intraoral NiTi alloy closed-coil springs were ligated between left upper first molars and incisors to mimic orthodontic tooth movement. Four initial force levels were used in this study, i.e., 0, 20, 40 and 80 g. Force magnitudes were determined through a force meter (Tiantian, Changsha, China). Rats were euthanized by decapitation following anesthesia with pentobarbital sodium (50 mg·kg−1) six hours following drug administrations. Rats that did not receive any intervention were regarded as the baseline control for each group.

Drug administration into TG

The administration of drugs and lentivirus vectors into TG was conducted according to our previous study with modifications that shaving was not performed to avoid its impact on behavioral testing [23]. Following general anesthesia with intraperitoneal injection of sodium pentobarbital (30 mg·kg−1), the injected region was disinfected with 75% ethanol. The injected position is between tympanic bulla and the posterior edge of mandibular ramus. The injected direction is middle upper, perpendicular to the long axis of rat body and 15 degree to coronary plane. When the needle reached trigeminal fossa, the drug was slowly injected at a constant speed. The injection process should last 1 min, and the needle should be remained in situ for 1 min before withdrawn. UFP-101 ([Nphe1, Arg14, Lys15] N/OFQ-NH2) is a specific peptide antagonist of N/OFQ which has been reported to have high efficacy and durability in vivo [24]. Specifically, 15 μl nociceptin (10 nM), 15 μl UFP-101 (10 nM) or 15 μl normal saline was administered right after 40-g spring placement (0 h) and on 1st day, 3rd day, 5th day and 7th day to evaluate the effects of N/OFQ on pain and CGRP expression. N/OFQ-overexpressing lentivirus vector suspension (10 μl), blank vector suspension (10 μl) or normal saline (10 μl) was administered into TG one week after spring placement to assess the effects of N/OFQ-based gene therapy on pain.

Orofacial pain assessment (rat grimace scale, RGS)

The assessment of orofacial pain was performed through rat grimace scale (RGS) six hours following drug administrations, strictly according to our previous study [25]. In brief, rats were placed in transparent cubicles and videotaped for 30 min using a camera (Canon, Japan). For each session, 10 images of facial expressions for each rat were extracted using an emotional picture capture software (RODENT FACE FINDER). The RGS scoring was performed based on the facial expression changes in orbit, nose, ear and whisker (Fig. 1). Values of 0, 1, or 2 were given according to the degree of the four RGS action units (eyes, ears, nose and whiskers), which was scored in duplicate and independently by two researchers who are blind to the group information and any disagreement was solved by discussion. The scores of four action units were averaged as the score of each photograph, and the mean score of the extracted 10 photographs was calculated as the final RGS score reflecting the level of pain. The surrogate pain levels were obtained by subtracting the baseline RGS scores from the ones for testing sessions.

Fig. 1
figure 1

Facial expression changes of rats in RGS scoring. a–d Facial expression changes in the context of no pain. e–h Facial expression changes in the context of pain. The RGS scoring was performed based on the facial expression changes in orbit, nose, ear and whisker (indicated by boxes and arrows). Note that the eyes were round, ears were flat, noses were bulged and whiskers showed no tendency of bunching in the context of no pain. In contrast, eyes were squeezed, ears were folded, noses were flattened and whiskers tended to bunch in pain condition

Full size image

Tissue processing and analysis

For immunostaining, V1/V2 of TG were placed in liquid nitrogen and cryosectioned at a thickness of 10 μm by using microtome (Thermo Fisher Scientific, USA). The tissue samples were immunostained with primary antibodies against CGRP (1:200, Ab36001, Abcam, Cambridge, UK) and FITC-labelled rabbit anti-goat secondary polyclonal antibody IgG (1:100, Ab150077, Abcam, Cambridge, UK). Image observation and acquisition were performed using a fluorescence microscope under the 200X lens (Leica, Germany).

For western blot, V1/V2 of TG tissue samples were homogenized through RIPA lysis buffer with PMSF (Beyotime Biotechnology, China). Following electrophoretic separation, proteins were transferred onto PVDF membranes and blocked with 5% skim milk in TBST solution. Afterwards, sealed PVDF membranes were incubated in the primary polyclonal antibody against FLAG (F1804, Sigma, USA), N/OFQ (Ab216413, Abcam, Cambridge, UK) or β-actin (SC-69879, Santa-cruz, USA), then washed with TBST and incubated with secondary polyclonal antibody goat anti-mouse IgG (SC-2005, Santa-cruz, USA). The protein blot densities were analyzed using ImageJ Software (NIH, Bethesda).

Simple Western (WES) analysis was performed on a WES system (ProteinSimple, WS-2471). The V1/V2 of TG tissues were homogenized with RIPA lysis buffer plus PMSF (Beyotime Biotechnology, China). After dilution and degeneration, the extracted proteins, along with the primary polyclonal antibody against CGRP (Ab36001, Abcam, Cambridge, UK), N/OFQ (Ab216413, Abcam, Cambridge, UK) or β-actin (SC-69879, Santa-cruz, USA), horseradish peroxidase (HRP)-conjugated secondary polyclonal antibody IgG (PS-MK15, Protein Simple, USA) and chemiluminescent substrate, were put into the microplate as instructed. The target band intensity of Western Blot results was analyzed using Compass Software. The specificity of antibodies was pre-validated by the antibody manufacturer Abcam (https://www.abcam.com/nociceptin-antibody-ab216413.html). Moreover, in our study, the specificity of primary antibodies was validated according to their corresponding proteins’ specific molecular sizes (20 kD for N/OFQ and 14 kD for CGRP).

Real-time PCR was conducted to determine the mRNA levels of N/OFQ (PNOC gene) and CGRP (Calca gene) with GAPDH being the reference. PCR was performed using specific primers for rat CGRP (forward primer: 5′-GAAGAAGAAGCTCGCCTACTGG-3′, reverse primer: 5′-CTGTCCAAGCTAGAGCCCTCA-3′, expected size: 110 bp) and PNOC (forward primer: 5′-GCTCACGTCCGCTGCTCTTTA-3′, reverse primer: 5′-TCCACCTCATCGGCCTCATCT-3′, expected size: 147 bp). Total RNA was extracted from TG via Trizol RNA Extraction Kit (Pufei, Shanghai, China) and cDNA reversely transcribed through the M-MLV test kit (M1705, Promega). The expressions were quantified in a LightCycler480 (Roche, Switzerland) RT-PCR platform with the SYBR Premix Ex Taq (Takara, Dalian, China). The thermal profile was set at 95 °C for 30 s, followed by 40 cycles at 95 °C for 5 s and then at 60 °C for 30 s.

Lentivirus vector construction

The lentivirus vector was constructed as previously described [23]. As shown in Fig. 5a, a lentivirus vector GV320 (Shanghai Genechem, China) containing red fluorescence (Cherry) and vector marker (3FLAG) was recombined with rat PNOC gene. PNOC was expressed under ubiquitin promoter, and m-cherry under SV40 promoter. Thus, the two genes were under two independent promoters. The specific sequences retrieved from GenBank (NM_013007) are displayed in Additional file 2. The recombined sequence was amplified with PCR and DNA sequencing performed for sequence verification. Viral vectors were packaged and harvested by transfecting 293 T cells, followed by visualization through fluorescence microscope and verification of PNOC expression through WB. The viral titer was determined to be 2 × 108 TU/ml. All the procedures involving use of lentivirus vectors were performed in the laboratory with biosafety level 2 (BSL2) containment according to General Guidelines for Biosafety in Microbiology and Biomedical Laboratories (WS233-2002).

Statistical analysis

Results are depicted as mean ± standard error of the mean (SEM). Two-way ANOVA with repeated measures were used to analyze the effects of force magnitudes (0, 20, 40 and 80 g), time (0, 1, 3, 5, 7 and 14 days) and their interactions on RGS scores and the expression levels of N/OFQ. One-way ANOVA with Bonferroni post hoc test was employed to analyze the differences in PNOC expression, CGRP expression and orofacial pain among different time points in each group. Pearson’s correlation test was used to analyze the relevance between N/OFQ expression, CGRP expression and RGS scores. All the statistical analyses were performed in SPSS 19.0 and Graphpad Prism 6.0, with a p value less than 0.05 being considered as statistical significance.

Results

Orofacial pain elevated N/OFQ expression in TG

We found that orofacial pain-like behaviors indicated by RGS scores was elicited following tooth movement and started to increase on 1st day, peaked on 3rd day, decreased on 5th day and returned to baseline level on 7th or 14th day (Fig. 2a). The two-way ANOVA with repeated measures revealed that RGS scores were significantly influenced by time (p < 0.001), force magnitude (p = 0.005) and their interactions (p < 0.001). The one-way ANOVA revealed that RGS scores were significantly different on 1st day (p < 0.01) and 3rd day (p < 0.05). Areas under curve (AUCs) were similar between 0-g group and 20-g group (p > 0.05), while significantly higher in the 40-g group (p < 0.05) and 80-g group (p = 0.001) (Fig. 2b).

Fig. 2
figure 2

The effect of tooth movement on orofacial pain level and N/OFQ expression. The rats were respectively treated with the force of 0 g, 20 g, 40 g and 80 g (n = 30 for each group, n = 5 for each group each day). a Temporal changes of RGS scores in all the force groups. Two-way ANOVA with repeated measures were used to analyze the effects of force magnitudes, time and their interactions on the RGS scores. One-way ANOVA was used to analyze RGS scores in different force groups at different timepoint (*p < 0.05, **p < 0.01, 0 g group vs. 20 g group vs. 40 g group vs. 80 g group). b One-way ANOVA with Bonferroni post hoc test was used to analyze the area under curve (AUC) of RGS scores (*p < 0.05, 40 g group vs. 0 g group, 80 g group vs. 0 g group). c Western blot analysis for the quantification of N/OFQ expression in trigeminal ganglia, with β-actin being the internal reference. The images were cropped using Adobe Photoshop software, and full-length blots/gels are presented in Additional file 3: Figure S1. d Temporal changes of N/OFQ expression in all the force groups. Two-way ANOVA with repeated measures were used to analyze the effects of force magnitudes, time and their interactions on the expression levels of N/OFQ. One-way ANOVA was used to analyze N/OFQ expression levels in different force groups at the same timepoint (*p < 0.05, **p < 0.01, 0 g group vs. 20 g group vs. 40 g group vs. 80 g group). e One-way ANOVA with Bonferroni post hoc test was used to analyze the AUC of the expression level of N/OFQ (*P < 0.05, 40 g group vs. 0 g group, 80 g group vs. 0 g group)

Full size image

As displayed in Fig. 2c, d, our results revealed that the expression levels of N/OFQ started to increase on 1st day following orthodontic tooth movement. The one-way ANOVA revealed that N/OFQ expression was significantly different on 1st day (p < 0.01), 3rd day (p < 0.01), 5th day (p < 0.05), 7th day (p < 0.01) and 14 day (p < 0.05). Areas under curve (AUCs) were similar between 0-g group and 20-g group (p > 0.05), while significantly higher in the 40-g group (p < 0.001) and 80-g group (p = 0.001) (Fig. 2e). Thus, a force magnitude of 40 g was used for the following experiments.

The effects of N/OFQ agonist and antagonist on pain modulation and CGRP expression

As depicted in Fig. 3, two-way ANOVA with repeated measures indicated that the RGS scores were significantly influenced by different groups (p < 0.05) and time (p < 0.05). The RGS scores were significantly higher in the N/OFQ agonist group than in the normal saline (NS) group on 3rd day, 5th day and 7th day (p < 0.01). Moreover, the RGS scores were significantly lower in the antagonist UFP-101 group than in the NS group on 3rd day, 5th day and 7th day (p < 0.01).

Fig. 3
figure 3

The effects of N/OFQ receptor agonist and antagonist on pain modulation. The rats were respectively injected with N/OFQ receptor agonist (N/OFQ), antagonist (UFP-101) and normal saline (NS) after 40-g spring placement (n = 8 for each group). Temporal changes of RGS scores in NS group, N/OFQ group and UFP-101 group were shown in the figure. One-way ANOVA with Bonferroni post hoc test was employed to analyze the effects of N/OFQ, UFP-101 and NS on RGS scores. (**p < 0.01, NS group vs. N/OFQ group, NS group vs. UFP-101 group, N/OFQ group vs. UFP-101 group)

Full size image

As displayed in Fig. 4a and b, more CGRP-positive neurons were detected in the N/OFQ group and fewer CGRP-positive neurons were observed in the UFP-101 group. Two-way ANOVA with repeated measures indicated that CGRP expression was significantly influenced by different groups (p < 0.05) and time (p < 0.05). The expression levels of CGRP were significantly higher in the N/OFQ group than in the NS group on 3rd day, 5th day and 7th day (all p < 0.05), and significantly lower in the UFP-101 group than in the NS group on 1st day, 3rd day, 5th day and 7th day (all p < 0.05) (Fig. 4c).

Fig. 4
figure 4

The effects of N/OFQ receptor agonist and antagonist on CGRP expressions. The rats were respectively injected with N/OFQ receptor agonist (N/OFQ), antagonist (UFP-101) and normal saline (NS) after 40-g spring placement (n = 18 for each group, n = 3 for each group each day). a CGRP immunostaining in trigeminal ganglion of rats in NS group, N/OFQ group and UFP-101 group (3rd day). The images were acquired at the resolution of 300dpi. b Western blot analysis of CGRP expression in trigeminal ganglion of rats in NS group, N/OFQ group and UFP-101 group using WES. The images were cropped using Adobe Photoshop software, and full-length blots/gels are presented in Additional file 3: Figure S2. c Temporal changes of CGRP expression level in NS group, N/OFQ group and UFP-101 group. One-way ANOVA with Bonferroni post hoc test was employed to analyze the effects of N/OFQ, UFP-101 and NS on CGRP expressions. (*p < 0.05, NS group vs. N/OFQ group, NS group vs. UFP-101 group, N/OFQ group vs. UFP-101 group)

Full size image

Successful transduction of PNOC-overexpressing lentivirus vectors into TG

As shown in Fig. 5a, the lentivirus vector carried cherry fluorescence protein and we used this fluorescence signal for the detection of virus transduction. As displayed in Fig. 5b, the PNOC-overexpressing lentivirus vectors were able to transduce 293 T cells, as evidenced by the cherry fluorescence. This overexpression was functionally successful as the N/OFQ-3FLAG fusion protein was detected (Fig. 5c). Moreover, immunofluorescence staining showed that lentivirus vectors were transduced at trigeminal ganglia (Fig. 5d).

Fig. 5
figure 5

Construction of PNOC overexpression lentivirus vector. a The map of GV320 vector. b Successful transduction of lentiviral vector into 293 T cells as shown by fluorescence microscopy that most cells were marked by enhanced red fluorescence protein (Cherry). The image was acquired at the resolution of 300dpi. c Western blot analysis of 293 T cells transfected with positive reference (SURVIVIN-3FLAG-GFP, 48KD) [1], not transfected [2], and transfected with PNOC lentiviral vectors (N/OFQ-3FLAG, 23KD) [3]. d Immunofluorescence image of TG in rat stained with cherry, which indicates successful transfection with PNOC lentivirus. The image was acquired at the resolution of 300dpi

Full size image

Two-way ANOVA with repeated measures indicated that the expression level of both PNOC gene and N/OFQ protein were significantly influenced by different groups (p < 0.05) and time (p < 0.05). The real-time PCR revealed that the expression level of PNOC gene was significantly higher in the PNOC-lenti-OE group (denoting PNOC-overexpressing lentivirus transduction) than in the Ctrl-lenti group (blank lentivirus vector) on 3rd day, 5th day, 7th day and 14th day (all p < 0.05) (Fig. 6a). The western blot showed that the level of N/OFQ protein was significantly higher in the PNOC-lenti-OE group than in the Ctrl-lenti group and the NS group on 3rd day, 5th day and 7th day (all p < 0.05) (Fig. 6b, c).

Fig. 6
figure 6

The effects of PNOC overexpression lentivirus vector on PNOC and N/OFQ expression. The rats were respectively administered with PNOC overexpression lentivirus (PNOC-lenti-OE), control lentivirus (ctrl-lenti) and normal saline (NS) one week prior to 40-g force application (n = 15 for each group, n = 3 for each group each day). a Temporal changes of PNOC mRNA expression level in trigeminal ganglia of rats in PNOC lentivirus group and control lentivirus group. One-way ANOVA with Bonferroni post hoc test was employed to analyze the effects of control lentivirus and PNOC overexpression lentivirus on PNOC mRNA expression. (*p < 0.05, **p < 0.01, ctrl-lenti group vs. PNOC-lenti-OE group). b Temporal changes of N/OFQ expression in trigeminal ganglia of rats in NS group, control lentivirus group and PNOC lentivirus group. One-way ANOVA with Bonferroni post hoc test was employed to analyze the effects of normal saline, control lentivirus and PNOC overexpression lentivirus on N/OFQ expression. (*p < 0.05, PNOC-lenti-OE group vs. NS group, PNOC-lenti-OE group vs. ctrl-lenti group). c Western blot analysis of N/OFQ expression in trigeminal ganglion of rats in NS group, control lentivirus group and PNOC lentivirus group using WES (NS normal saline, CV control lentivirus, V PNOC lentivirus). The images were cropped using Adobe Photoshop software, and full-length blots/gels are presented in Additional file 3: Figure S3

Full size image

The effects of N/OFQ overexpression on CGRP expression and pain modulation

As displayed in Fig. 7a, two-way ANOVA with repeated measures indicated that the CGRP expression was significantly influenced by different groups (p < 0.05) and time (p < 0.05). The expression level of CGRP was significantly higher in the PNOC-lenti-OE group than in the Ctrl-lenti group on 3rd day, 5th day, 7th day and 14th day (all p < 0.05). Moreover, as depicted in Fig. 7b, the trend of the changes in expressions of CGRP and N/OFQ were highly positively correlated (r = 0.925).

Fig. 7
figure 7

The effects of PNOC overexpression on CGRP expressions and pain modulation. The administration of lentivirus or saline was performed one week prior to force application (40 g). a Temporal changes of CGRP mRNA expression in trigeminal ganglia in control lentivirus group and PNOC lentivirus group (n = 15, n = 3 for each group each day). One-way ANOVA with Bonferroni post hoc test was employed to analyze the effects of control lentivirus and PNOC overexpression lentivirus on CGRP mRNA expression. (*p < 0.05, **p < 0.01, ctrl-lenti group vs. PNOC-lenti-OE group). b Changes in PNOC expression and CGRP expression in PNOC lentivirus group exhibited high correlation (r = 0.925). c Temporal changes of RGS scores in NS group, control lentivirus group and PNOC lentivirus group (n = 8 for each group). One-way ANOVA with Bonferroni post hoc test was employed to analyze the effects of normal saline, control lentivirus and PNOC overexpression lentivirus on RGS scores. (**p < 0.01, PNOC-lenti-OE group vs. NS group, PNOC-lenti-OE group vs. ctrl-lenti group). d Difference value of orofacial pain level and N/OFQ expression level between PNOC lentivirus group and control lentivirus group. The trends of the two curves are similar and highly correlated (r = 0.994)

Full size image

RGS scoring revealed that pain levels were significantly higher in the PNOC-lenti-OE group than in the Ctrl-lenti group and the NS group on 3rd day, 5th day, 7th day and 14th day (all p < 0.01) (Fig. 7c). Then, we plotted the difference values between PNOC-lenti-OE and Ctrl-lenti groups against time for RGS scores and N/OFQ expression level. We found that the changes in difference values of RGS scores and N/OFQ expression level displayed high consistency which were most prominent on 7th day. Pearson’s correlation test showed that the trend of the difference values for RGS scores and N/OFQ expression level were highly positively correlated (r = 0.994) (Fig. 7d).

Discussion

In this study, we found that N/OFQ expression was elevated in response to orofacial pain elicited by tooth movement. N/OFQ could exacerbate orofacial pain and elevate CGRP expressions while UFP-101 alleviated orofacial pain and downregulate CGRP expressions. Furthermore, overexpression of PNOC gene that upregulated N/OFQ in trigeminal ganglia was able to exacerbate pain level and increase CGRP expression level in trigeminal ganglia.

Orofacial pain, a constellation of various painful conditions in orofacial regions, includes migraine, trigeminal neuralgia, headaches, dental pain and tooth-movement pain [26, 27]. Of particular, orofacial pain induced by tooth movement is a type of inflammatory pain at periodontal tissues due to force application [25]. It is well accepted that tooth movement elicits orofacial pain by obstructing periodontal blood vessels that in turn initiate a cascade of inflammatory response [28]. In the present study, we used NiTi-closed coil springs to elicit tooth-movement-related orofacial pain. Notably, several studies have suggested that constant forces cannot be delivered by NiTi-closed coil springs, which could be partially attributed to the tooth movement that changed the length of the springs. Thus, it is more appropriate to state “initial force”. On the whole, however, this tooth-movement animal model has been well-documented and validated by many previous studies, including ours [28,29,30]. We previously revealed that tooth-movement-induced orofacial pain was initiated by a force above 20 g and that pain level differed among rats receiving different force magnitudes [2]. But it is still largely unknown whether this paradigm works similarly between force magnitude and the expression level of N/OFQ in TG. Notably, we found that pain level and N/OFQ expression level were upregulated in the 0-g group, which could be attributed to the painful stimulus induced by bulky intraoral springs [25]. Furthermore, the AUCs of pain and N/OFQ were similar between the 0-g group and the 20-g group, while significantly higher in the 40-g group and 80-g group, indicating that the threshold force that could incite the tooth-movement-dependent upregulation of pain level and N/OFQ lies between 20 and 40 g, which is consistent with our previous study [25]. Therefore, we suggest that 40-g force could be sufficient to elicit orofacial pain and an elevation of N/OFQ expression in trigeminal ganglia.

N/OFQ and its receptor are the fourth opioid family member discovered so far [31]. Despite high sequence similarity between N/OFQ and other opioid ligands, the lacking of an N-terminal tyrosine renders N/OFQ to have a negligible affinity for the three classical opioid receptors, thereby making it functionally distinct from the classical opioid ligands (e.g., morphine) [32]. Though NOP receptor inhibits voltage-gated calcium channels and activates inward potassium channels coupled to pertussis toxin-sensitive Gi/o proteins, thereby impacting on the neurotransmitter release and neuronal excitability like other opioid receptors, the pain-modulatory effects mediated by N/OFQ-NOP are more complicated [31]. N/OFQ has been revealed to exhibit either pro- or anti-nociceptive effects, depending on a series of complex factors such as pain quality, doses and administration routes [12,13,14,15]. In terms of rodents, N/OFQ system exhibits antinociceptive effects when peripherally and spinally activated, while pronociceptive effects after supraspinal activation. Therefore, the net effect of systemically administered NOP agonists on nociception is dependent on relative contribution of peripheral, spinal and supraspinal sites of action, which varies between rodents and non-human primates [33]. The sensation of orofacial pain induced by tooth movement is initially received by the sensory terminals at periodontium, transmitted to TG, relayed to trigeminal nucleus at medulla oblongata and projected to sensory cortex via thalamus [2]. Our previous studies have reported that N/OFQ participates in pain modulation at periodontium and trigeminal nucleus caudalis [16, 34]. Although previous findings have demonstrated that N/OFQ and its receptor are actively expressed in neuronal cells of trigeminal ganglia and our previous study found an indirect evidence that N/OFQ could modulate the expression of a key nociceptor (P2X3) on trigeminal neurons [22, 35], its pain-modulatory role at TG is still largely unknown. Our results revealed that intra-ganglionic administration of N/OFQ exacerbated pain while that of UFP-101 alleviated pain, suggesting that N/OFQ plays a pro-nociceptive role in orofacial pain induced by tooth movement. Moreover, elevated pain level caused by PNOC overexpression lentivirus was strongly correlated with increased N/OFQ expression, strongly supporting the promotive role of N/OFQ in pain modulation. This finding was consistent with our previous studies where we found that periodontal administration of N/OFQ antagonist UFP-101 was able to alleviate pain in rats and that N/OFQ could upregulate the expression of a nociceptor P2X3 [16, 35]. However, Borgland et al. revealed that N/OFQ inhibited calcium currents of trigeminal neurons, supporting its antinociceptive role in TG [36]. We attribute this disagreement to the fact that N/OFQ was able to inhibit calcium currents in only a subpopulation of trigeminal neurons in the study by Borgland et al. [36].

CGRP is a well-known pronociceptive molecule for orofacial pain [37]. The upregulation and release of CGRP are the hallmarks during pain episodes of orofacial pain [38]. The release of CGRP to peripheral tissues could induce neurogenic inflammation that exacerbates pain [39, 40]. And we found CGRP was upregulated and released to periodontal tissues in response to orofacial pain in our previous studies [21, 41, 42]. However, current evidence on the interaction between CGRP and N/OFQ is generally lacking, especially in the aspect of pain modulation. Previous studies have shown that N/OFQ were abundantly expressed with a high degree of coexpression with CGRP both in dorsal root ganglion and trigeminal ganglion, suggesting that N/OFQ modulated primary sensory nociception through interacting with CGRP [22, 43]. In trigeminal neurons, N/OFQ-NOP system has been reported to impact on stimulated CGRP release, whereas how N/OFQ interacts with CGRP in response to pain stimuli is largely unknown [44, 45]. In our present study, we found that N/OFQ upregulated while UFP-101 downregulated the expression level of CGRP in trigeminal ganglia, supporting the notion that N/OFQ has a pronociceptive role in trigeminal ganglia via promoting CGRP expression and release, thus facilitating transmission of pain signals. Noteworthily, UFP-101 actively decreased the amount of CGRP protein by approximately 60% on 1st day, which was attributed to the accumulative effect of UFP-101 administered respectively at baseline and 1st day.

In terms of methodology of this study, facial expressions have been widely used to evaluate pain level of non-verbal experimental animals, among which RGS is a standardized behavioral coding system demonstrated to have high accuracy and reliability [46]. Interestingly, the RGS scores were greater for the NS group in Fig. 3 than that in 40-g group of Fig. 2a since 3rd day, which can be mainly attributed to the fact that the rats of Fig. 3 received drug injection that aggravated their pain level, thus leading to generally higher RGS scores. The integration of viral gene into host genome on one hand is beneficial for stable expression, which makes it a promising gene therapeutic tool for a variety of pain conditions, especially for chronic pain [47,48,49]. Our previous study revealed that administration of lentivirus containing shRNA aiming at knocking down TRPV1 or ASIC3 was effective in alleviating orofacial pain [50, 51]. In our present study, transduction of PNOC overexpression lentivirus was successful in overexpressing N/OFQ in trigeminal ganglia and the overexpression was stable on 3rd day, 5th day and 7th day, but not on 14th day. We attribute this decrease of N/OFQ expression on 14th day to built-in analgesic pathways that were activated at the late stage of orofacial pain. Notably, the increase in N/OFQ did not reach statistical significance on 1st day (Fig. 6b), which might be significantly different if the virus was injected earlier (e.g., two weeks before spring placement). We showed that the overexpression of N/OFQ was able to upregulate CGRP expression and exacerbate orofacial pain induced by tooth movement. Moreover, the N/OFQ expression levels and pain levels were highly correlated with each other, further reinforcing the aforementioned results. Notably in Fig. 4c, the expression level of CGRP in NS group was slightly increased on 1st day, but significantly decreased on 3rd and 5th day, suggesting that trigeminal injection inhibited CGRP expression in TG. In contrast, the expression level of CGRP was significantly higher in N/OFQ group, which revealed that N/OFQ upregulated CGRP expression in TG.

Though our study firstly revealed the modulatory role of N/OFQ system in tooth-movement-induced orofacial pain which is dependent on CGRP, there are some limitations in this study. Although CGRP has been well-documented as a pronociceptive factor in TG neural system, and our previous study has validated the pain-modulatory effect of CGRP on tooth-movement-induced pain, direct evidence on the regulatory role of CGRP on tooth-movement-induced pain in our present study was not validated. Besides, while gain-of-function study conducted using PNOC overexpression lentivirus suggested the pro-nociceptive effect of N/OFQ in trigeminal ganglia, the knockdown of PNOC may be more important to validate the therapeutic value of N/OFQ. Moreover, the role of NOP receptor and its relationship with orofacial pain and CGRP expression need specific investigations. Therefore, based on above limitations, further studies digging into more thorough pain-modulatory mechanisms of N/OFQ-NOP system are expected.

Conclusions

Taken together, we suggest that N/OFQ modulate orofacial pain induced by tooth movement possibly through CGRP-dependent pathways.

Availability of data and materials

All data generated or analysed during this study are included in this published article and its supplementary information files.

References

  1. Long H, Zhou Y, Pyakurel U, Liao L, Jian F, Xue J, et al. Comparison of adverse effects between lingual and labial orthodontic treatment. Angle Orthod. 2013;83(6):1066–73.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Long H, Wang Y, Jian F, Liao LN, Yang X, Lai WL. Current advances in orthodontic pain. Int J Oral Sci. 2016;8(2):67–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Zhu Y, Wang S, Long H, Zhu J, Jian F, Ye N, et al. Effect of static magnetic field on pain level and expression of P2X3 receptors in the trigeminal ganglion in mice following experimental tooth movement. Bioelectromagnetics. 2017;38(1):22–30.

    Article  CAS  PubMed  Google Scholar 

  4. Liu S, Liu L, Jiang Y, Zhou J, Hu H, Wu Z, et al. Effect of endomorphin-2 on orofacial pain induced by orthodontic tooth movement in rats. Eur J Oral Sci. 2019;127(2):408–16.

    Article  CAS  PubMed  Google Scholar 

  5. Yang Z, Cao Y, Wang Y, Luo W, Hua X, Lu Y, et al. Behavioural responses and expression of P2X3 receptor in trigeminal ganglion after experimental tooth movement in rats. Arch Oral Biol. 2009;54(1):63–70.

    Article  CAS  PubMed  Google Scholar 

  6. Yang Z, Wang Y, Luo W, Hua X, Wamalwa P, Wang J, et al. Trigeminal expression of N-methyl-D-aspartate receptor subunit 1 and behavior responses to experimental tooth movement in rats. Angle Orthod. 2009;79(5):951–7.

    Article  PubMed  Google Scholar 

  7. Mollereau C, Simons MJ, Soularue P, Liners F, Vassart G, Meunier JC, et al. Structure, tissue distribution, and chromosomal localization of the prepronociceptin gene. Proc Natl Acad Sci USA. 1996;93(16):8666–70.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Yamamoto T, Nozaki-Taguchi N, Sakashita Y, Kimura S. Nociceptin/orphanin FQ: role in nociceptive information processing. Prog Neurobiol. 1999;57(5):527–35.

    Article  CAS  PubMed  Google Scholar 

  9. Mollereau C, Mouledous L. Tissue distribution of the opioid receptor-like (ORL1) receptor. Peptides. 2000;21(7):907–17.

    Article  CAS  PubMed  Google Scholar 

  10. Neal CR Jr, Mansour A, Reinscheid R, Nothacker HP, Civelli O, Watson SJ Jr. Localization of orphanin FQ (nociceptin) peptide and messenger RNA in the central nervous system of the rat. J Comp Neurol. 1999;406(4):503–47.

    Article  CAS  PubMed  Google Scholar 

  11. Pettersson LME, Sundler F, Danielsen N. Expression of orphanin FQ/nociceptin and its receptor in rat peripheral ganglia and spinal cord. Brain Res. 2002;945(2):266–75.

    Article  CAS  PubMed  Google Scholar 

  12. Agostini S, Eutamene H, Broccardo M, Improta G, Petrella C, Theodorou V, et al. Peripheral anti-nociceptive effect of nociceptin/orphanin FQ in inflammation and stress-induced colonic hyperalgesia in rats. Pain. 2009;141(3):292–9.

    Article  CAS  PubMed  Google Scholar 

  13. Chen X, Geller EB, Adler MW. Nociceptin/orphanin FQ blocks the antinociception induced by mu, kappa and delta opioid agonists on the cold water tail-flick test. Eur J Pharmacol. 2007;557(1):32–6.

    Article  CAS  PubMed  Google Scholar 

  14. Depner UB, Reinscheid RK, Takeshima H, Brune K, Zeilhofer HU. Normal sensitivity to acute pain, but increased inflammatory hyperalgesia in mice lacking the nociceptin precursor polypeptide or the nociceptin receptor. Eur J Neurosci. 2003;17(11):2381–7.

    Article  PubMed  Google Scholar 

  15. Rizzi A, Nazzaro C, Marzola GG, Zucchini S, Trapella C, Guerrini R, et al. Endogenous nociceptin/orphanin FQ signalling produces opposite spinal antinociceptive and supraspinal pronociceptive effects in the mouse formalin test: pharmacological and genetic evidences. Pain. 2006;124(1–2):100–8.

    Article  CAS  PubMed  Google Scholar 

  16. Shan D, He Y, Long H, Zhou Y, Liu H, Xu R, et al. The effects of blocking N/OFQ receptors on orofacial pain following experimental tooth movement in rats. Aust Orthod J. 2016;32(2):206–10.

    PubMed  Google Scholar 

  17. Eftekhari S, Salvatore CA, Calamari A, Kane SA, Tajti J, Edvinsson L. Differential distribution of calcitonin gene-related peptide and its receptor components in the human trigeminal ganglion. Neuroscience. 2010;169(2):683–96.

    Article  CAS  PubMed  Google Scholar 

  18. Warfvinge K, Edvinsson L. Cellular distribution of PACAP-38 and PACAP receptors in the rat brain: relation to migraine activated regions. Cephalalgia Int J Headache. 2020;40(6):527–42.

    Article  Google Scholar 

  19. Deng H, Li GG, Nie H, Feng YY, Guo GY, Guo WL, et al. Efficacy and safety of calcitonin-gene-related peptide binding monoclonal antibodies for the preventive treatment of episodic migraine—an updated systematic review and meta-analysis. BMC Neurol. 2020;20(1):57.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Bree D, Mackenzie K, Stratton J, Levy D. Enhanced post-traumatic headache-like behaviors and diminished contribution of peripheral CGRP in female rats following a mild closed head injury. Cephalalgia Int J Headache. 2020;40(7):748–60.

    Article  Google Scholar 

  21. Long H, Liao L, Gao M, Ma W, Zhou Y, Jian F, et al. Periodontal CGRP contributes to orofacial pain following experimental tooth movement in rats. Neuropeptides. 2015;52:31–7.

    Article  CAS  PubMed  Google Scholar 

  22. Hou M, Uddman R, Tajti J, Edvinsson L. Nociceptin immunoreactivity and receptor mRNA in the human trigeminal ganglion. Brain Res. 2003;964(2):179–86.

    Article  CAS  PubMed  Google Scholar 

  23. Long H, Liao L, Zhou Y, Shan D, Gao M, Huang R, et al. A novel technique of delivering viral vectors to trigeminal ganglia in rats. Eur J Oral Sci. 2017;125(1):1–7.

    Article  CAS  PubMed  Google Scholar 

  24. Calo G, Guerrini R, Rizzi A, Salvadori S, Burmeister M, Kapusta DR, et al. UFP-101, a peptide antagonist selective for the nociceptin/orphanin FQ receptor. CNS Drug Rev. 2005;11(2):97–112.

    Article  CAS  PubMed  Google Scholar 

  25. Liao L, Long H, Zhang L, Chen H, Zhou Y, Ye N, et al. Evaluation of pain in rats through facial expression following experimental tooth movement. Eur J Oral Sci. 2014;122(2):121–4.

    Article  PubMed  Google Scholar 

  26. Shinal RM, Fillingim RB. Overview of orofacial pain: epidemiology and gender differences in orofacial pain. Dent Clin North Am. 2007;51(1):1–18, v.

    Article  PubMed  Google Scholar 

  27. Long H, Gao M, Zhu Y, Liu H, Zhou Y, Liao L, et al. The effects of menstrual phase on orthodontic pain following initial archwire engagement. Oral Dis. 2017;23(3):331–6.

    Article  CAS  PubMed  Google Scholar 

  28. Gao M, Long H, Ma W, Liao L, Yang X, Zhou Y, et al. The role of periodontal ASIC3 in orofacial pain induced by experimental tooth movement in rats. Eur J Orthod. 2016;38(6):577–83.

    Article  PubMed  Google Scholar 

  29. Horinuki E, O’Hashi K, Kobayashi M. In vivo Ca(2+) imaging of the insular cortex during experimental tooth movement. J Dent Res. 2020;100(3):276–82.

    Article  PubMed  CAS  Google Scholar 

  30. Tsuchiya T, Hasegawa N, Yugawa M, Sasaki A, Suda N, Adachi K. Different therapeutic effects of CO(2) and diode laser irradiation on tooth movement-related pain. Front Neurol. 2020;11:481.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Kiguchi N, Ding H, Ko M-C. Central N/OFQ-NOP receptor system in pain modulation. Adv Pharmacol. 2016;75:217–43.

    Article  CAS  PubMed  Google Scholar 

  32. Thompson AA, Liu W, Chun E, Katritch V, Wu H, Vardy E, et al. Structure of the nociceptin/orphanin FQ receptor in complex with a peptide mimetic. Nature. 2012;485(7398):395–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Schröder W, Lambert DG, Ko MC, Koch T. Functional plasticity of the N/OFQ-NOP receptor system determines analgesic properties of NOP receptor agonists. Br J Pharmacol. 2014;171(16):3777–800.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  34. Liao L, Hua X, Long H, Ye N, Zhou Y, Wang S, et al. Expression patterns of nociceptin in rats following experimental tooth movement. Angle Orthod. 2013;83(6):1022–6.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Wang Y, Long H, Jian F, Li X, Yang X, Zhao Z, et al. Nociceptin/orphanin FQ up-regulates P2X(3) receptors in primary cultures of neonatal rat trigeminal ganglion neurons. Eur J Oral Sci. 2015;123(6):409–15.

    Article  CAS  PubMed  Google Scholar 

  36. Borgland SL, Connor M, Christie MJ. Nociceptin inhibits calcium channel currents in a subpopulation of small nociceptive trigeminal ganglion neurons in mouse. J Physiol. 2001;536(Pt 1):35–47.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Afroz S, Arakaki R, Iwasa T, Oshima M, Hosoki M, Inoue M, et al. CGRP induces differential regulation of cytokines from satellite glial cells in trigeminal ganglia and orofacial nociception. Int J Mol Sci. 2019;20(3):711.

    Article  CAS  PubMed Central  Google Scholar 

  38. Thalakoti S, Patil VV, Damodaram S, Vause CV, Langford LE, Freeman SE, et al. Neuron-glia signaling in trigeminal ganglion: implications for migraine pathology. Headache. 2007;47(7):1008–23.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Yuan H, Spare NM, Silberstein SD. Targeting CGRP for the prevention of migraine and cluster headache: a narrative review. Headache. 2019;59(Suppl 2):20–32.

    Article  PubMed  Google Scholar 

  40. Zhou Y, Long H, Ye N, Liao L, Yang X, Jian F, et al. The effect of capsaicin on expression patterns of CGRP in trigeminal ganglion and trigeminal nucleus caudalis following experimental tooth movement in rats. J Appl Oral Sci Rev FOB. 2016;24(6):597–606.

    Article  Google Scholar 

  41. Long H, Shan D, Huang R, Liu H, Zhou Y, Gao M, et al. Bite force measurements for objective evaluations of orthodontic tooth movement-induced pain in rats. Arch Oral Biol. 2019;101:1–7.

    Article  PubMed  Google Scholar 

  42. Liang H, Hu H, Shan D, Lyu J, Yan X, Wang Y, et al. CGRP modulates orofacial pain through mediating neuron-glia crosstalk. J Dent Res. 2020;100(1):98–105.

    Article  PubMed  CAS  Google Scholar 

  43. Mika J, Li Y, Weihe E, Schafer MKH. Relationship of pronociceptin/orphanin FQ and the nociceptin receptor ORL1 with substance P and calcitonin gene-related peptide expression in dorsal root ganglion of the rat. Neurosci Lett. 2003;348(3):190–4.

    Article  CAS  PubMed  Google Scholar 

  44. Capuano A, De Corato A, Tringali G, Currò D, Dello Russo C, Navarra P. Buprenorphine inhibits bradykinin-induced release of calcitonin gene-related peptide from rat trigeminal neurons via both mu-opioid and nociceptin/orphanin peptide receptors. Eur J Pharmacol. 2009;609(1–3):45–50.

    Article  CAS  PubMed  Google Scholar 

  45. Capuano A, Currò D, Dello Russo C, Tringali G, Pozzoli G, Di Trapani G, et al. Nociceptin (1–13)NH2 inhibits stimulated calcitonin-gene-related-peptide release from primary cultures of rat trigeminal ganglia neurones. Cephalalgia Int J Headache. 2007;27(8):868–76.

    Article  CAS  Google Scholar 

  46. Sotocinal SG, Sorge RE, Zaloum A, Tuttle AH, Martin LJ, Wieskopf JS, et al. The Rat Grimace Scale: a partially automated method for quantifying pain in the laboratory rat via facial expressions. Mol Pain. 2011;7:55.

    PubMed  PubMed Central  Google Scholar 

  47. Kanao-Kanda M, Kanda H, Liu S, Roy S, Toborek M, Hao S. Viral vector-mediated gene transfer of glutamic acid decarboxylase for chronic pain treatment: a literature review. Hum Gene Ther. 2020;31(78):405–14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Guedon JM, Wu S, Zheng X, Churchill CC, Glorioso JC, Liu CH, et al. Current gene therapy using viral vectors for chronic pain. Mol Pain. 2015;11:27.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  49. Sakuma T, Barry MA, Ikeda Y. Lentiviral vectors: basic to translational. Biochem J. 2012;443(3):603–18.

    Article  CAS  PubMed  Google Scholar 

  50. Guo R, Zhou Y, Long H, Shan D, Wen J, Hu H, et al. Transient receptor potential Vanilloid 1-based gene therapy alleviates orthodontic pain in rats. Int J Oral Sci. 2019;11(1):11.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  51. Yang H, Shan D, Jin Y, Liang H, Liu L, Guan Y, et al. The role of acid-sensing ion channel 3 in the modulation of tooth mechanical hyperalgesia induced by orthodontic tooth movement. Neuroscience. 2020;442:274–85.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

Not applicable.

Funding

This work was supported by National Natural Science Foundation of China (NSFC, No. 82071147), Sichuan Science and Technology Program (Nos. 2018JY0558, 2021YJ0428 & 2018SZ0232), Research Grant of Health Commission of Sichuan Province (Nos. 19PJ233 and 20PJ090), CSA Clinical Research Fund (CSA-02020–02), and Research and Develop Program, West China Hospital of Stomatology, Sichuan University (No. LCYJ2020-TD-2 & WCHS-201704).

Author information

Author notes

  1. Xinyu Yan and Han Han authors contributed equally to this work.

Authors and Affiliations

  1. Department of Orthodontics, State Key Laboratory of Oral Diseases, National Clinical Center for Oral Research, West China Hospital of Stomatology, Sichuan University, No. 14, Section 3, Ren Min Nan Road, Chengdu, 610041, China

    Xinyu Yan, Han Han, Shizhen Zhang, Yanzhu Lu, Linghuan Ren, Yufei Tang, Xiaolong Li, Fan Jian, Yan Wang, Hu Long & Wenli Lai

Authors
  1. Xinyu Yan
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Han Han
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Shizhen Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Yanzhu Lu
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Linghuan Ren
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Yufei Tang
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Xiaolong Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Fan Jian
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Yan Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Hu Long
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Wenli Lai
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

In this study, LW and LH were mainly responsible for topic proposal and theoretical guidance, YX and HH were in charge of experiment conduction, ZS and LY contributed to data collection and statistical analysis, RL and TY were responsible for article writing and proofreading, LX and WY took charge of graphic production, JF contributed to polishment and revision of the manuscript. All authors have read and approved the manuscript.

Corresponding authors

Correspondence to Hu Long or Wenli Lai.

Ethics declarations

Ethics approval and consent to participants

Animal experiments were approved by the ethical committee of the State Key Laboratory of Oral Diseases, Sichuan University (WCCSIRB-D-2015-006).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1.

Grouping of experimental animals.

Additional file 2:

Rat PNOC overexpression sequence. The specific sequences were retrieved from GenBank (NM_013007), with red indicating PNOC mRNA sequence, and ACCGGT is AgeI enzyme cutting site.

Additional file 3: Figure S1.

Full results of Western blot analysis for the quantification of N/OFQ expression in trigeminal ganglia. Figure S2. Full results of Western blot analysis of CGRP expression in trigeminal ganglion of rats in NS group, N/OFQ group and UFP-101 group. Figure S3. Full results of Western blot analysis of N/OFQ expression in trigeminal ganglion of rats in NS group, control lentivirus group and PNOC lentivirus group.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yan, X., Han, H., Zhang, S. et al. N/OFQ modulates orofacial pain induced by tooth movement through CGRP-dependent pathways. BMC Neurosci 22, 25 (2021). https://doi.org/10.1186/s12868-021-00632-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12868-021-00632-5

Keywords

BMC Neuroscience

ISSN: 1471-2202

Contact us