Abstract
Chronic inflammatory temporomandibular disorder (TMD) pain has a high prevalence, and available nonspecific treatments have adverse side effects. ECa 233, a standardized Centella asiatica extract, is highly anti-inflammatory and safe. We investigated its therapeutic effects by injecting complete Freund’s adjuvant (CFA) into right temporomandibular joint of mice and administering either ibuprofen or ECa 233 (30, 100, and 300 mg/kg) for 28 days. Inflammatory and nociceptive markers, bone density, and pain hypersensitivity were examined. CFA decreased ipsilateral bone density, suggesting inflammation localization, which ipsilaterally caused immediate calcitonin gene-related peptide elevation in the trigeminal ganglia (TG) and trigeminal subnucleus caudalis (TNC), followed by late increase of NaV1.7 in TG and of p-CREB and activation of microglia in TNC. Contralaterally, only p-CREB and activated microglia in TNC showed delayed increase. Pain hypersensitivity, which developed early ipsilaterally, but late contralaterally, was reduced by ibuprofen and ECa 233 (30 or 100 mg/kg). However, ibuprofen and only 100-mg/kg ECa 233 effectively mitigated marker elevation. This suggests 30-mg/kg ECa 233 was antinociceptive, whereas 100-mg/kg ECa 233 was both anti-inflammatory and antinociceptive. ECa 233 may be alternatively and safely used for treating chronic inflammatory TMD pain, showing an inverted U-shaped dose–response relationship with maximal effect at 100 mg/kg.
Similar content being viewed by others
Introduction
Orofacial pain is the most prevalent and debilitating condition affecting the craniofacial region, accounting for approximately 10–15% of all pains1. Temporomandibular disorder (TMD) pain is a major pathological condition (roughly 15–20% of the orofacial pain) causing widespread chronic pain in the orofacial area2. The trigeminal pain pathway is linked to orofacial pain development. Pain signals travel through the peripheral processes of the first-order sensory neurons in the trigeminal ganglia (TG) in the peripheral nervous system (PNS) and are conveyed through their central processes to the second-order sensory neurons in the trigeminal subnucleus caudalis (TNC) in the central nervous system (CNS). In acute inflammatory orofacial pain, TG neurons primarily release calcitonin gene-related peptide (CGRP)—an inflammatory mediator and a neurogenic inflammatory marker—into TG and TNC after excessive uncontrolled inflammation. In chronic pain, the released CGRP in TG is implicated in the increased expression of voltage-gated sodium ion channel 1.7 (NaV1.7)—a pain hypersensitivity marker in PNS—causing peripheral sensitization3. The released CGRP in TNC is also associated with enhanced expression of activated microglia and phosphorylated cAMP response element-binding protein (p-CREB)—a marker for nociceptive activity and pain hypersensitivity in CNS—causing central sensitization4. This proposed mechanism results in development of orofacial pains, including TMD pain.
TMD pain results from multiple factors affecting the temporomandibular joint (TMJ) such as trauma or occlusal changes5. Because the pathophysiology of chronic TMD pain remains unclear, it is typically managed by nonspecific treatments, such as nonsteroidal anti-inflammatory drugs (NSAIDs), resulting in unpredictable outcomes and/or adverse effects6. Although widely used, NSAIDs produce many known adverse effects, including gastrointestinal irritation and kidney injury7. Thus, new treatment innovations particularly focus on the use of traditional herbal medicines that may treat chronic inflammatory TMD pain without adverse side effects. The herbal plant Centella asiatica (L.) Urban (Indian pennywort, Gotu kola, or Bua-bok) reportedly exhibits anti-inflammatory and antinociceptive effects8. Its major bioactive constituents are triterpenoid glycosides including asiaticoside and madecassoside8,9. However, its effects remain inconsistent9. This inconsistency could be explained by the greatly varying amounts of the herb’s active components, depending on many factors such as cultivation methods and climate. Hence, researchers established a standardized C. asiatica extract through guided isolation by controlling the manufacturing process; subsequently, the standardized extract of C. asiatica, namely, ECa 233, was obtained. ECa 233 is a white/off-white powder with ≥ 80% w/w of triterpenoid glycosides, with a consistent madecassoside-to-asiaticoside ratio of 1.5 ± 0.5:19.
Both acute and subchronic toxicity tests revealed that ECa 233 is very safe to use10. ECa 233 did not induce nor inhibit the activities of drug-metabolizing enzymes, which eliminate and/or detoxify major drug groups such as paracetamol and NSAIDs; hence, ECa 233 does not interfere with major drug metabolisms9,10. Moreover, ECa 233 has neuropharmacological activities such as anti-inflammation and antinociception. Its antinociceptive activity was explored in a tail flick test, showing that ECa 233 reduced pain responses11. In patients with aphthous ulcers, an oral paste containing ECa 233 considerably reduced ulcer-associated pain and inflammation12. These effects might occur through the antinociceptive and anti-inflammatory mechanisms of ECa 233. Further, some studies have investigated the anti-inflammatory activities of C. asiatica extract in acute inflammatory pain such as in osteoarthritis of knee joints13. Recently, our group reported the anti-inflammatory activities of C. asiatica extract in a mouse model of acute temporomandibular joint osteoarthritis in which ECa 233 could inhibit pathogenesis in the affected joint by modulating the local expression of transient receptor potential vanilloid 1 (TRPV1) and acid-sensing ion channel subunit 3 (ASIC3)14.
Although ECa 233 has beneficial effects, its underlying mechanisms remain poorly explored. Therefore, we aimed to elucidate its effects and underlying mechanisms on chronic inflammatory TMD pain induced by unilaterally injecting complete Freund’s adjuvant (CFA) into the right TMJ of mice. Our study might be the first to demonstrate the benefits of C. asiatica extract on chronic inflammatory TMD pain.
Results
Descriptive results
Weight
After 28 days of CFA-induced TMD pain, there was no difference in weight between the Sham, Ibu, CFA, 30ECa, 100ECa, and 300ECa groups (Fig. 1).
Orofacial pain sensitivity
Figure 2 illustrates the time course of behavioral pain responses of the different groups tested by 0.04 g von Frey filament for mechanical hyperalgesia and 0.05 ml cold acetone for cold allodynia. We tested each side 12 times and then recorded the response scores according to the following criteria: no response = 0, occurrence of head withdrawal = 0.25, occurrence of face grooming once = 1, and occurrence of face grooming > 3 times = 1.5. We added all response scores on each side to obtain the total response score; the maximum response score was 18. The Sham group, which was injected with NSS into the right TMJ, showed the lowest pain response scores; the response remained constant at the baseline level throughout the whole experiment. However, the CFA group developed a significant pain hypersensitivity on the ipsilateral side of the CFA injection at post-CFA-injection days 14, 21, and 28 with both von-Frey and cold acetone tests, and on the contralateral side at post-CFA-injection day 28 also with both von-Frey and cold acetone tests when compared with the Sham group. In the Ibu, 30ECa, and 100ECa groups, pain hypersensitivity significantly decreased on the ipsilateral side, but not in the 300ECa group, at post–CFA-injection days 14, 21, and 28 with both von-Frey and cold acetone tests. On the contralateral side, pain hypersensitivity significantly decreased in the Ibu, 30ECa, and 100ECa groups at post–CFA-injection day 28 for both von-Frey and cold acetone tests, compared with that in the CFA group. Thus, CFA injection induced pain hypersensitivity, including mechanical hyperalgesia and cold allodynia, initially on the ipsilateral side of the injection and later on the contralateral side. In addition, ibuprofen, which was used as a positive control treatment, and ECa 233 at 30 and 100 mg/kg doses significantly and equally reduced pain hypersensitivity that developed bilaterally, while there was no statistical difference among the three groups at any days measured.
Structural changes in TMJ
Figure 3 depicts the bone density of the condylar head of TMJ on the ipsilateral and contralateral sides measured by micro-CT. Although CFA-induced pain hypersensitivity developed early on the ipsilateral side and later on the contralateral side, the bone density of the CFA group significantly reduced only on the ipsilateral side at post–CFA-injection days 21 and 28, compared with that of the Sham group. Considering that bone density reduction is a major sign of TMJ tissue inflammation, CFA-induced inflammation could cause pathology in the condylar head of the right TMJ, consistent with pain hypersensitivity on the ipsilateral side. Meanwhile, the pain hypersensitivity on the contralateral side seemed not to be induced by the pathology in the contralateral TMJ because no bone density reduction was observed. Compared with the Sham group, only the Ibu and 100ECa groups did not exhibit bone density reduction at post–CFA-injection days 21 and 28. Pain hypersensitivity was also reduced in the 30ECa group; however, this group as well as the CFA and 300ECa groups showed bone density reduction without significant difference among the three groups. Thus, both 30 and 300 mg/kg doses of ECa 233 could not prevent the pathology caused by CFA, whereas 0.14 g/kg ibuprofen and 100 mg/kg ECa 233 effectively prevented the pathology at all of the time points after CFA injection and also reduced pain hypersensitivity.
Inflammation and nociceptive activity changes in TG
Expression of CGRP in TG
Figures 4 and 9 illustrate the expression of CGRP in bilateral TGs. CFA injection immediately and significantly enhanced the CGRP expression in the ipsilateral TG at post–CFA-injection days 3, 7, and 14, but not in the contralateral TG, compared with Sham. These data supported the idea that CFA-induced inflammation on the ipsilateral side immediately activates nociceptors, possibly causing pain hypersensitivity on the same side. Although the 30 and 300 mg/kg doses of ECa 233 could not reduce the enhanced expression of CGRP, ibuprofen and 100 mg/kg ECa 233 effectively prevented the enhanced CGRP expression at post–CFA-injection days 3, 7, and 14 compared with the CFA injection. Thus, 100 mg/kg dose of ECa 233 effectively inhibited inflammation in TG.
Expression of NaV1.7 in TG
Figures 5 and 9 show the NaV1.7 expression in bilateral TGs. In the CFA group, NaV1.7 expression was late yet significantly enhanced in the ipsilateral TG at post–CFA-injection days 21 and 28, but not in the contralateral TG. The immediate enhancement of CGRP and later enhancement of NaV1.7 corresponded well with the early development of pain hypersensitivity on the ipsilateral side. However, the late development of pain hypersensitivity on the contralateral side seemed to be not associated with the contralateral TG activity because no inflammation and nociceptive activities were observed. Although the 30 and 300 mg/kg doses of ECa 233 could not reduce the enhanced expression of NaV1.7, ibuprofen and 100 mg/kg ECa 233 effectively prevented the enhanced NaV1.7 expression compared with the CFA injection. Thus, 100 mg/kg dose of ECa 233 effectively prevented peripheral sensitization and pain hypersensitivity in TG.
Inflammation and nociceptive activity changes in TNC
Expression of CGRP in TNC
Figures 6 and 9 depict the CGRP expression in bilateral TNCs in all groups. Similar to that in TG, CFA injection immediately and significantly enhanced the expression of CGRP in the ipsilateral TNC at post–CFA-injection days 3, 7, and 14, but not in the contralateral TNC. Hence, CFA-induced inflammation on the ipsilateral side immediately activated the trigeminal pain pathway, but not on the contralateral side. Although 30 and 300 mg/kg ECa 233 could not reduce the enhanced expression of CGRP in the ipsilateral TNC, ibuprofen and 100 mg/kg ECa 233 effectively reduced the enhanced CGRP expression compared with the CFA injection. Therefore, 100 mg/kg ECa 233 effectively inhibited the inflammation in TNC.
Expression of p-CREB in TNC
Figures 7 and 9 show the expression of p-CREB in bilateral TNCs in all groups. In the CFA group, the expression of p-CREB significantly increased later than that of CGRP on the ipsilateral side at post–CFA-injection days 14, 21, and 28, and on the contralateral side at post–CFA-injection day 28 compared with that in the Sham group. The enhanced expression of p-CREB on both sides corresponded well with the pain hypersensitivity on each side. Thus, the underlying mechanisms of the bilateral pain hypersensitivity development most likely came from the overstimulation of both TG (in the PNS) and TNC (in the CNS) on the ipsilateral side and of only the TNC on the contralateral side. Although 30 and 300 mg/kg ECa 233 could not reduce the enhanced expression of p-CREB on both sides, ibuprofen and 100 mg/kg ECa 233 effectively abolished the enhanced p-CREB expression on both sides compared with the CFA injection. Thus, 100 mg/kg dose of ECa 233 effectively prevented central sensitization and pain hypersensitivity in TNC.
Expression of activated microglia in TNC
Figures 8 and 9 present the expression of activated microglia in bilateral TNCs in all groups. In the CFA group, the expression of activated microglia in TNC was later significantly increased on the ipsilateral side at post–CFA-injection days 14, 21, and 28, and on the contralateral side at post–CFA-injection day 28 compared with that in the Sham group. The increase in the expression of the activated microglia in TNC was similar to that in the expression of p-CREB in TNC; hence, CFA-induced inflammation activated the ipsilateral pain pathway. However, on the contralateral side, the p-CREB expression increased, but the CGRP expression did not increase; thus, the pain signals triggering both the contralateral TNC neurons and microglia possibly came from the ipsilateral TNC neurons or higher relay stations. Although 30 and 300 mg/kg ECa 233 could not reduce the expression of activated microglia on both sides, ibuprofen and 100 mg/kg ECa 233 effectively abolished the enhanced expression of activated microglia on both sides compared with the CFA injection. Therefore, 100 mg/kg dose of ECa 233 effectively inhibited the inflammation in TNC.
Discussion
This is the first in vivo study of the standardized extract of C. asiatica (ECa 233) reporting that ECa 233 could attenuate pain hypersensitivity in chronic inflammatory TMD in male mice induced by CFA injection. Despite inducing many side effects, such as gastrointestinal irritation and kidney injury, the NSAID ibuprofen is currently the standard treatment for TMD pain15.
After receiving ibuprofen and ECa 233 (30 and 100 mg/kg), the mice had lower pain response scores. However, only ibuprofen and 100 mg/kg ECa 233 could protect the TMJ from bone density changes and prevent the increased expression of inflammation- and nociception-associated proteins in the TG (PNS relay station) and TNC (CNS relay station) of the trigeminal pain pathway. Although the pathophysiology of chronic inflammatory TMD pain remains unclear, other studies hypothesized that TMD results from the local release of inflammatory irritants caused by tissue damage or external irritants such as CFA. Clinically, however, many patients with TMD have no apparent signs of local inflammation or tissue damage16, and TMD pain can widely spread within the orofacial area17.
In our TMD model, CFA caused an excessive uncontrolled inflammation mimicking the osteoarthritis-induced TMD pain18. Owing to the inflammation at the injected TMJ, the TMJ’s condylar head degenerated with lowered bone density, leading to osteoarthritis-induced pain hypersensitivity19. Consistent with the previous studies, we showed that the unilateral CFA injection induced chronic inflammation in the ipsilateral joint and nervous system (both PNS and CNS); hence, hyperalgesia and allodynia occur on the ipsilateral side. However, through our lengthened observation into the chronic phase of pain (28 days after the CFA injection), our study also demonstrated changes that occurred in the contralateral CNS, causing pain hypersensitivity on the contralateral side, as first reported by our group recently, indicative of a mirror-image pain20.
When stimulated by noxious stimuli, CGRP drives the sensitization at TG and TNC in the chronic phase of the TMD pain, as evidenced by the increased expression of NaV1.7 in TG and that of p-CREB in TNC. In a previous study, injecting CGRP into the rat’s TMJ promoted changes in p38 MAP kinases and ERK in TG and c-Fos in TNC after 2 h of injection, indicating peripheral and central sensitizations, respectively21. Meanwhile, pain hypersensitivity and neuronal activity in the trigeminal system in response to CFA-induced pain in the masseter muscle were attenuated by a CGRP antagonist22. In our study, CGRP was enhanced only in the early stage of inflammation in the ipsilateral TG and TNC, but not in the contralateral TG and TNC; thus, the pain signals stimulating the contralateral TNC (as evidenced by the late enhancement of the expressions of p-CREB and activated microglia at post–CFA-injection day 28) would originate from the ipsilateral TNC or other higher relay stations, eventually producing pain hypersensitization at post–CFA-injection day 28 on the contralateral side. Therefore, our data supported that TMD pain could occur despite the lack of inflammatory signs as in the mirror-image pain.
In particular, NaV had implicated chronic pain including NaV1.7, NaV1.8, NaV1.9. However, in terms of insight into function, NaV1.7, which is related to communication in nociceptive peripheral afferents, has a hereditary loss-of-function mutation that triggers pain hypersensitivity without causing other neurodevelopmental changes23. In an animal model, successful NaV1.7 suppression in the lumbar dorsal root ganglia was associated with decreased thermal hyperalgesia in the inflammatory state, decreased tactile allodynia in the neuropathic state, and no modifications to the animals' regular motor function23,24. Therefore, in our study the increased expression of NaV1.7, a pain hypersensitivity marker in TG, would lower stimulation threshold and provoke ectopic discharge, causing peripheral sensitization3. Moreover, activation of p-CREB, a molecular marker of pain transmission and pain hypersensitivity in TNC4, may be a key step for developing a synaptic plasticity–dependent activity that ultimately increases pain perception25. The role of activated microglia in TNC and spinal cord is related to pain hypersensitivity, particularly mechanical hyperalgesia following inflammation26. Persistent PNS inflammation is a major cause of activated microglia in CNS. Activated microglia release proinflammatory cytokines and chemokines, leading to widespread inflammatory responses. Our study revealed expressions of NaV1.7, p-CREB, and activated microglia in the 100ECa and Ibu groups significantly decreased compared with that in the CFA group. Thus, the 100-mg/kg dose of ECa 233 could prevent pain sensitization, possibly by reducing the CGRP and NaV1.7 expressions, thereby reducing the behavioral pain responses and pain hypersensitivity.
Consistent with other supporting results, C. asiatica extracts and active ingredients had shown both anti-inflammatory and antinociceptive effects. For example, 100 mg/kg dose of C. asiatica inhibited foot edema in carrageenan and prostaglandin-induced hind foot pain in rats, similar to the activity of ibuprofen treatment8. C. asiatica also significantly decreased proinflammatory cytokine (TNF-α and interleukin 6) expression in lipopolysaccharide-induced HEK-293 cell inflammation27. Moreover, oral madecassoside administration could reduce the clinical pain scores of mice with an induced rheumatoid arthritis and also minimize prostaglandin, COX-2, and proinflammatory cytokine infiltrations27. Indeed, madecassoside promotes anti-inflammation and protects the joint from destruction. Moreover, asiaticoside has an antinociceptive effect, seen when oral treatment of asiaticoside reduced pain in mice with capsaicin-induced paw pain28. Therefore, ECa 233, which contains ≥ 80% w/w of triterpenoid glycosides with a 1.5:1 ratio of madecassoside and asiaticoside, possesses both anti-inflammatory and antinociceptive activities, resulting in the reduction of inflammatory responses in both PNS and CNS and behavioral pain responses; however, the effective dose of both activities demonstrated an inverted U-shaped dose–response relationship with the maximal effect at 100 mg/kg dose.
At a low dose of 30 mg/kg, ECa 233 showed an effect comparable with that of 100 mg/kg ECa 233 on pain hypersensitivity alleviation, but it did not reduce the expression of inflammation-associated proteins; thus, the antinociceptive activity of ECa 233 started to manifest at the low dose. The 30 mg/kg dose of ECa 233 contains approximately 15 mg/kg dose of madecassoside and 10 mg/kg dose of asiaticoside9. Madecassoside at 40 mg/kg (not 10 and 20 mg/kg) could reduce inflammation, thereby lowering pain scores and protecting the joint from destruction; hence, madecassoside exhibits an anti-inflammatory activity27. Meanwhile, asiaticoside at 10 mg/kg (not 5 mg/kg) could alleviate pain in capsaicin-induced pain; hence, asiaticoside has an antinociceptive activity13. Therefore, the possible mechanism is that at the dose of 30 mg/kg, ECa 233 could exert the antinociceptive effect, thereby reducing the behavioral pain responses; however, it could not reduce inflammatory responses and prevent osteoarthritis development at the CFA-injected TMJ. ECa 233 at the dose of 100 mg/kg containing approximately 49.5 mg/kg concentration of madecassoside and 33 mg/kg concentration of asiaticoside not only reduced the pain responses but also reduced inflammatory responses and prevented osteoarthritis development.
At the low dose of ECa 233 (30 mg/kg), the antinociceptive activity, which might originate from the asiaticoside activity, was perhaps caused by the increased activity of gamma aminobutyric acid (GABA), which is the major inhibitory neurotransmitter of CNS. The activity of glutamic acid decarboxylase, which is involved in GABA synthesis, is increased by an aqueous extract of C. Asiatica29. Moreover, asiatic acid, which is an active metabolite of asiaticoside, interacts with GABAB receptor to inhibit synaptic transmission. The increased GABA activity of CNS might cause pain hypersensitivity reduction. However, the GABA expression does not directly relate to the inflammatory markers30 and also may not be associated with the expression of inflammation-associated proteins in the pain pathway.
Interestingly, high-dose ECa 233 treatment (300 mg/kg) did not exhibit beneficial effects. One of the reasons could be that the plant products contain other constituents, which at a high dose, exert some antagonistic or inhibitory effects. ECa 233 could enhance brain-derived neurotrophic factor (BDNF) and N-methyl-D-aspartate receptor (NMDAR) in the hippocampus, cerebral cortex, and spinal cord9. BDNF facilitated pain transmission and contributed to pain hypersensitivity development31 via the postsynaptic NMDAR to modulate nociceptive signaling in TNC32. After BDNF antagonist injection in mice with formalin-induced pain, pain hypersensitivity decreased33. Intrathecal NMDAR antagonist injection in nerve injury-induced neuropathic pain reduced pain hypersensitivity34. Therefore, BDNF and NMDAR were involved in some aspects of pain hypersensitivity, possibly in the central sensitization. Thus, at a high dose (300 mg/kg), ECa 233 may facilitate pain transmission, counteracting its antinociceptive and anti-inflammatory effects. All these mechanisms could perhaps inhibit the beneficial effects of the major constituents, possibly owing to which the highest dose of ECa 233 exhibited results similar to those of the control group.
Therefore, the inverted U-shaped dose–response relationship of ECa 233 might indicate one of the factors responsible for pain hypersensitivity reduction. Hence, the effective dose of C. asiatica extract should be limited to moderate doses to achieve beneficial effects in chronic inflammatory TMD pain. The recommended dose of ECa 233 in this study is 100 mg/kg, which showed both antinociceptive and anti-inflammatory effects by preventing the anatomical changes in the condylar head of TMJ and hindering the expression of inflammation- and nociception-associated proteins in the TG and TNC. These findings provide basic knowledge of ECa 233 effects on inflammation and nociception, supporting ECa 233 development as an antinociceptive and anti-inflammatory drug or a dietary supplement for pain treatment.
Our study's limitations include not using the rotarod test for evaluating ECa 233 additional behavioral side effects, and consideration of the subjective meaning of pain. Moreover, NaV implicated in pain such as NaV1.8, NaV1.9 in the trigeminal pathway should be further studied.
In conclusion, C. asiatica has antinociceptive and anti-inflammatory effects on chronic inflammatory TMD pain within a specific therapeutic range. Despite the very limited therapeutic dose of ECa 233, it has potent effects and a high safety profile. Therefore, ECa 233 can be safely used as an antinociceptive and anti-inflammatory agent in chronic pain management, although further investigation is still required.
Methods
Animals
We used 6-week-old healthy male mice (n = 144, weighing 25–30 g, which were purchased from the Nomura Laboratory Animal Center, Thailand. All mice were housed under conditions of controlled humidity (40%–70%), temperature (23 °C ± 1 °C), and light (12 h day/12 h night cycle), with free water and food access. All study protocols were performed in accordance with relevant guidelines and regulations and were approved by the Animal Care and Use Committee of the Faculty of Medicine Siriraj Hospital, Mahidol University (Approval No.: SI-ACUP014/2561). All experimental procedures conformed to the Animal Research: Reporting In Vivo Experiments (ARRIVE) guidelines for animal experiment35. The sample size was estimated to provide 80% power (1 − β) with a 95% confidence interval (α = 0.05)36. According to previous study, CFA-induced TMJ pain animal model was treated with ibuprofen treatment as a positive control13,37 . A total of 144 mice were used for the study, randomly divided into six groups (n = 24/group):
-
1.
Sham (Sham): 10 µl of 0.9% normal saline solution (NSS) injection
-
2.
Negative control (CFA): 10 µl of 50% CFA injection
-
3.
Positive control (Ibu): 10 µl of 50% CFA injection + ibuprofen (0.14 g/kg)
-
4.
30 mg/kg ECa 233 (30ECa): 10 µl of 50% CFA injection + ECa 233 (30 mg/kg)
-
5.
100 mg/kg ECa 233 (100ECa): 10 µl of 50% CFA injection + ECa 233 (100 mg/kg)
-
6.
300 mg/kg ECa 233 (300ECa): 10 µl of 50% CFA injection + ECa 233 (300 mg/kg)
To evaluate pain hypersensitivity, we used 54 animals (9 animals/group) for the behavioral pain response tests at pre–CFA-injection day and post–CFA-injection days 3, 7, 14, 21, and 28. At each time point of post–CFA-injection days 3, 7, 14, 21, and 28, 90 animals (3 animals/group/time point) were used for evaluating the structural changes caused by CFA-induced inflammation in bilateral TMJs by assessing the bone density through micro–computed tomography (micro-CT) and the expression of proteins related to the inflammatory and nociceptive activities in TG (CGRP and NaV1.7) and TNC (CGRP, p-CREB, and activated microglia) through immunohistochemistry.
Development of TMD
To induce temporomandibular pain, we injected the mice with sodium pentobarbital (60 mg/kg) intraperitoneally for anesthesia and then with 10 µl of NSS-dissolved 50% CFA (1 mg/ml) (F5881; Sigma-Aldrich, St. Louis, MO, USA) unilaterally into the right TMJ. The anatomical landmark for the injection was described in a previous study20,38. Briefly, we identified TMJ by palpation and trimmed the surrounding local hair using a pair of scissors. We subsequently inserted a 30-gauge needle through the facial skin until the needle tip reached the zygomatic arch. We slowly advanced the needle until it passed under the edge of the arch and ultimately entered into the joint space. When the needle reached the joint space, we slowly injected 10 µl of 50% CFA, via a Hamilton syringe, over a period of 5 s.20,38.
Behavioral test
We performed two series of behavioral pain response tests [using 0.04 g of von Frey filament for mechanical hyperalgesia and 0.05 ml of cold acetone (− 5 °C) for cold allodynia with an interval of at least 30 min. At pre–CFA-injection day and post–CFA-injection days 3, 7, 14, 21, and 28, the mice underwent tests at their whisker pads of both ipsilateral and contralateral sides. We tested each side 12 times and then recorded the response scores according to the following criteria: no response = 0, occurrence of head withdrawal = 0.25, occurrence of face grooming once = 1, and occurrence of face grooming of > 3 times = 1.518,20. We added all response scores on each side to obtain the total response score; the maximum response score was 18.
Micro-CT of TMJ
Animals were deeply anesthetized and then transcardially perfused with 250 ml of ice-cold phosphate-buffered solution (PBS; 0.1 M, pH 7.4). The head of the mice was decapitated, immersed in 4% paraformaldehyde in PBS (0.1 M, pH 7.4), and placed horizontally in a micro-CT scan (µCT 35 Sanco Medical AG, Bruetteisellen, Switzerland). We scanned the condylar head of TMJ using an X-ray at 30–70 kVp. Thereafter, we sliced the condylar head of TMJ and selected the slices from the start of the condylar head to the neck of the ramus. Normally, approximately 150–250 sections or slices are obtained39. The condylar head of TMJ was analyzed by measuring the bone density of each mouse in every group at different time points (post–CFA-injection days 3, 7, 14, 21, and 28).
Inflammatory and nociceptive activities in TG and TNC
The mice were deeply anesthetized and perfused with the same conditions used for the micro-CT. We located TG and TNC using the brain atlas of Paxinos and Keith40. TG and TNC were then extracted bilaterally and immersed in 4% paraformaldehyde in PBS (0.1 M, pH 7.4) immediately. Tissue processing and paraffin embedding procedures were also performed. We transversely sliced 5-μm thick sections using a microtome (Global Medical Instrumentation Inc., Ramsey, MN, USA) and deparaffinized them before immunostaining by immunohistochemistry. The TG paraffin sections were stained with neuroinflammatory markers rabbit monoclonal anti-NaV1.7 antibody (AB5390; Merck KGaA, Darmstadt, Germany) and rabbit polyclonal anti-CGRP antibody (SC-57053; Santa Cruz Biotech, Dallas, TX, USA), whereas the TNC sections were immunolabeled with a rabbit polyclonal anti-p-CREB antibody (SC-81486; Santa Cruz Biotech, Dallas, TX, USA), rabbit polyclonal anti-CGRP antibody (SC-57053; Santa Cruz Biotech, Dallas, TX, USA), and rabbit polyclonal anti-OX42 antibody (SC-52; Santa Cruz Biotech, Dallas, TX, USA) for the expression of activated microglia.
Briefly, the TG and TNC sections were warmed with antigen retrieval solution (citrate buffer; Dako, Glostrup, Denmark) in a microwave oven. The endogenous peroxidase activity was inhibited with Dako Peroxidase Blocking Reagent (Dako) for 5 min and then blocked with an antibody diluent (Dako) for 10 min to prevent nonspecific staining. Further, we incubated the sections with the primary antibodies at 4 °C overnight, followed by the secondary antibody (goat anti-rabbit-IgG antibody conjugated with horseradish peroxidase). We used the EnVision™ Detection System (Dako) for signal visualization and a light microscope (Carl Zeiss Microimaging GmbH, AxioVision 40 version 4.8.2.0, Germany) for peroxidase activity site detection. We also evaluated the nociceptive activity in TG and TNC individually and independently and blindly analyzed each datum by the mean number of positive neuron expression at each time point.
For TG analysis, we used three mice from each group at each time point and selected five sections per TG tissue (5th, 10th, 15th, 20th, and 25th sections) of each mouse. We counted the neurons in each whole TG section and then summed and averaged the numbers of counted neurons from all sections in one mouse. The ratio of positive neurons per total number of neurons and the mean value of each experimental group (n = 3/group/time point) were calculated. For TNC analysis, we used the same three mice from each group at every time point and selected five sections per TNC tissue (5th, 10th, 15th, 20th, and 25th sections) of each mouse. We counted the positive cells (brown dots) at laminas I and II of the TNC sections and then summed and averaged the numbers of brown dots from all sections in one mouse. Thereafter, the mean value of each experimental group (n = 3/group/time point) was analyzed.
Statistical analysis
All statistical data were analyzed using SPSS version 26.0 (IBM, Chicago, IL, USA). The Kolmogorov–Smirnov test was used for testing normal data distribution. Possible statistically significant differences between groups were determined using two-way analysis of variance with Fisher’s least significant difference post hoc test. All analyses were performed using the two-tailed hypothesis testing method. In addition, P < 0.05 was considered statistically significant. Data are shown as mean ± standard error of the mean.
Data availability
The datasets generated and analyzed during the current study are available from the corresponding author on a reasonable request.
Change history
21 July 2023
A Correction to this paper has been published: https://doi.org/10.1038/s41598-023-39016-6
References
Häggman-Henrikson, B. et al. Increasing gender differences in the prevalence and chronification of orofacial pain in the population. Pain 161, 1768–1775. https://doi.org/10.1097/j.pain.0000000000001872 (2020).
van Selms, M. K. A., Wiegers, J. W. & van der Meer, H. A. Temporomandibular disorders, pain in the neck and shoulder area, and headache among musicians. J. Oral Rehabil. 47, 132–142. https://doi.org/10.1111/joor.12886 (2020).
Ibi, M. Inflammation and temporomandibular joint derangement. Biol. Pharm. Bull. 42, 538–542. https://doi.org/10.1248/bpb.b18-00442 (2019).
Edelmayer, R. M., Brederson, J. D., Jarvis, M. F. & Bitner, R. S. Biochemical and pharmacological assessment of MAP-kinase signaling along pain pathways in experimental rodent models: A potential tool for the discovery of novel antinociceptive therapeutics. Biochem. Pharmacol. 87, 390–398. https://doi.org/10.1016/j.bcp.2013.11.019 (2014).
Romero-Reyes, M. & Uyanik, J. M. Orofacial pain management: Current perspectives. J. Pain Res. 7, 99–115. https://doi.org/10.2147/jpr.s37593 (2014).
Nascimento, M. M. et al. Physical therapy and anesthetic blockage for treating temporomandibular disorders: A clinical trial. Med. Oral, Patol. Oral Cirugia Bucal 18, e81-85. https://doi.org/10.4317/medoral.17491 (2013).
Irvine, J., Afrose, A. & Islam, N. Formulation and delivery strategies of ibuprofen: Challenges and opportunities. Drug Dev. Ind. Pharm. 44, 173–183. https://doi.org/10.1080/03639045.2017.1391838 (2018).
Huang, S. S. et al. Antinociceptive activities and the mechanisms of anti-inflammation of asiatic Acid in mice. Evid.-Based Complement. Altern. Med. 2011, 895857. https://doi.org/10.1155/2011/895857 (2011).
Anukunwithaya, T., Tantisira, M. H., Tantisira, B. & Khemawoot, P. Pharmacokinetics of a standardized extract of Centella asiatica ECa 233 in rats. Planta Med. 83, 710–717. https://doi.org/10.1055/s-0042-122344 (2017).
Chivapat, S., Chavalittumrong, P. & Tantisira, M. H. Acute and sub-chronic toxicity studies of a standardized extract of Centella asiatica ECa 233. Thail. J. Pharm. Sci. 35, 55–64 (2011).
Ketkomol, P., Towiwat, P., Tantisira, B. & Tantisira, M. Anti-nociceptive effects of standardized extract of centella asiatica ECa 233 in tail flick test. Thail. J. Pharmacol. 34(1), 196–203 (2012).
Ruengprasertkit, C., Hongprasong, N., Tantisira, B. & Tantisira, M. H. Preliminary study of effects of a standardized extract of Centella asiatica ECa233 on minor aphthous ulcers. CU Dent. J. 33, 131–142 (2010).
Micheli, L. & Di Cesare Mannelli, L. Intra-articular route for the system of molecules 14G1862 from Centella Asiatica: Pain relieving and protective effects in a rat model of osteoarthritis. Nutrients 12, 1618. https://doi.org/10.3390/nu12061618 (2020).
Rotpenpian, N. et al. A standardized extract of Centella asiatica (ECa 233) prevents temporomandibular joint osteoarthritis by modulating the expression of local inflammatory mediators in mice. J. Appl. Oral Sci. 29, e20210329. https://doi.org/10.1590/1678-7757-2021-0329 (2021).
Wang, J. et al. Evaluation of anti-inflammatory and analgesic effects of synthesized derivatives of ibuprofen. Chem. Biol. Drug Des. 85, 623–632. https://doi.org/10.1111/cbdd.12316 (2015).
Gil-Martínez, A., Paris-Alemany, A., López-de-Uralde-Villanueva, I. & La Touche, R. Management of pain in patients with temporomandibular disorder (TMD): Challenges and solutions. J. Pain Res. 11, 571–587. https://doi.org/10.2147/jpr.s127950 (2018).
Gil-Martínez, A. et al. Chronic temporomandibular disorders: Disability, pain intensity and fear of movement. J. Headache Pain 17, 103. https://doi.org/10.1186/s10194-016-0690-1 (2016).
Krzyzanowska, A. & Avendaño, C. Behavioral testing in rodent models of orofacial neuropathic and inflammatory pain. Brain Behav. 2, 678–697. https://doi.org/10.1002/brb3.85 (2012).
Xu, L. et al. A time-dependent degeneration manner of condyle in rat CFA-induced inflamed TMJ. Am. J. Transl. Res. 8, 556–567 (2016).
Rotpenpian, N. & Tapechum, S. Evolution of mirror-image pain in temporomandibular joint osteoarthritis mouse model. J. Appl. Oral Sci. 29, e20200575. https://doi.org/10.1590/1678-7757-2020-0575 (2021).
Cady, R. J., Glenn, J. R., Smith, K. M. & Durham, P. L. Calcitonin gene-related peptide promotes cellular changes in trigeminal neurons and glia implicated in peripheral and central sensitization. Mol. Pain 7, 94. https://doi.org/10.1186/1744-8069-7-94 (2011).
Romero-Reyes, M., Pardi, V. & Akerman, S. A potent and selective calcitonin gene-related peptide (CGRP) receptor antagonist, MK-8825, inhibits responses to nociceptive trigeminal activation: Role of CGRP in orofacial pain. Exp. Neurol. 271, 95–103. https://doi.org/10.1016/j.expneurol.2015.05.005 (2015).
Yang, Y. et al. Nav1.7-A1632G mutation from a family with inherited erythromelalgia: enhanced firing of dorsal root ganglia neurons evoked by thermal stimuli. J. Neurosci. 36(28), 7511–7522. https://doi.org/10.1523/JNEUROSCI.0462-16.2016 (2016).
Emery, E. C., Luiz, A. P. & Wood, J. N. Nav1.7 and other voltage-gated sodium channels as drug targets for pain relief. Expert Opin. Ther. Targets 20, 975–983. https://doi.org/10.1517/14728222.2016.1162295 (2016).
Duenes, S. L., Thompson, R., Chang, Z., Okamoto, K. & Bereiter, D. A. Psychophysical stress increases the expression of phospho-CREB, Fos protein and neurokinin-1 receptors in superficial laminae of trigeminal subnucleus caudalis in female rats. Neurosci. Lett. 486, 207–210. https://doi.org/10.1016/j.neulet.2010.09.054 (2010).
Adães, S. et al. Glial activation in the collagenase model of nociception associated with osteoarthritis. Mol. Pain 13, 1744806916688219. https://doi.org/10.1177/1744806916688219 (2017).
Liu, M. et al. Anti-rheumatoid arthritic effect of madecassoside on type II collagen-induced arthritis in mice. Int. Immunopharmacol. 8, 1561–1566. https://doi.org/10.1016/j.intimp.2008.06.011 (2008).
Ayumi, R. R. et al. Antinociceptive activity of asiaticoside in mouse models of induced nociception. Planta Med. 86, 548–555. https://doi.org/10.1055/a-1144-3663 (2020).
Awad, R. et al. Effects of traditionally used anxiolytic botanicals on enzymes of the gamma-aminobutyric acid (GABA) system. Can. J. Physiol. Pharmacol. 85, 933–942. https://doi.org/10.1139/y07-083 (2007).
Xu, D. et al. Participation of pro-inflammatory cytokines in neuropathic pain evoked by chemotherapeutic oxaliplatin via central GABAergic pathway. Mol. Pain 14, 1744806918783535. https://doi.org/10.1177/1744806918783535 (2018).
Takeda, M. et al. Brain-derived neurotrophic factor enhances the excitability of small-diameter trigeminal ganglion neurons projecting to the trigeminal nucleus interpolaris/caudalis transition zone following masseter muscle inflammation. Mol. Pain 9, 49. https://doi.org/10.1186/1744-8069-9-49 (2013).
Ding, H. et al. BDNF promotes activation of astrocytes and microglia contributing to neuroinflammation and mechanical allodynia in cyclophosphamide-induced cystitis. BioMed Cent. 17, 19. https://doi.org/10.1186/s12974-020-1704-0 (2020).
Richner, M. & Pallesen, L. T. Sortilin gates neurotensin and BDNF signaling to control peripheral neuropathic pain. Sci. Adv. 5, eaav9946. https://doi.org/10.1126/sciadv.aav9946 (2019).
Pagadala, P. et al. Loss of NR1 subunit of NMDARs in primary sensory neurons leads to hyperexcitability and pain hypersensitivity: Involvement of Ca(2+)-activated small conductance potassium channels. J. Neurosci. 33, 13425–13430. https://doi.org/10.1523/jneurosci.0454-13.2013 (2013).
Kilkenny, C., Browne, W. J., Cuthill, I. C., Emerson, M. & Altman, D. G. Improving bioscience research reporting: The ARRIVE guidelines for reporting animal research. PLoS Biol. 8, e1000412. https://doi.org/10.1371/journal.pbio.1000412 (2010).
Dolan, J. C., Lam, D. K., Achdjian, S. H. & Schmidt, B. L. The dolognawmeter: A novel instrument and assay to quantify nociception in rodent models of orofacial pain. J. Neurosci. Methods 187, 207–215. https://doi.org/10.1016/j.jneumeth.2010.01.012 (2010).
Kerins, C. A., Carlson, D. S., McIntosh, J. E. & Bellinger, L. L. Meal pattern changes associated with temporomandibular joint inflammation/pain in rats; analgesic effects. Pharmacol. Biochem. Behav. 75, 181–189. https://doi.org/10.1016/s0091-3057(03)00072-8 (2003).
Kim, S. H. & Son, C. N. Infliximab partially alleviates the bite force reduction in a mouse model of temporomandibular joint pain. J. Korean Med. Sci. 30, 552–558. https://doi.org/10.3346/jkms.2015.30.5.552 (2015).
Kuroki, Y. et al. In vivo morphometric analysis of inflammatory condylar changes in rat temporomandibular joint. Oral Dis. 17, 499–507. https://doi.org/10.1111/j.1601-0825.2010.01782.x (2011).
Paxinos, G. & Franklin, K. B. G. The Mouse Brain in Stereotaxic Coordinates (Elsevier, 2011).
Acknowledgements
This research is supported by Prince of Songkla University Scholarship, the Thailand Research Fund through the Royal Golden Jubilee PhD program (Grant No. PHD 0058/2561), and Siriraj Research Fund (SRF) type 1, the Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand (Grant Number (IO) R016331041). We would like to thank Assist. Prof. Dr. Aunwaya Kaewpitak for her kind suggestion and also Assist. Prof. Dr. Thanaporn Rungruang for the molecular techniques in this study.
Author information
Authors and Affiliations
Contributions
N.P. participated in the study concept and design, funding acquisition, data analysis, data interpretation, manuscript drafting, critical revision of the manuscript, and the final review of the manuscript. N.R. participated in data acquisition, data analysis, and data interpretation of all the studies, and manuscript drafting. A.V., W.C., and C.C. participated in data acquisition, data analysis, and data interpretation of all the studies. A.W. and S.T. participated in the study concept and design, and the final review of the manuscript. K.T. and M.T. participated in the study concept and design, and the final review of the manuscript.
Corresponding author
Ethics declarations
Competing interests
N.P. is currently an instructor at Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand. He has received a research grant (R016331041) from Siriraj Research Fund (SRF) type 1, Faculty of Medicine Siriraj Hospital, Mahidol University. Other authors declare no financial relationships or activities with any organizations that might have an influence on the submitted work.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
The original online version of this Article was revised: The original version of this Article contained errors in the names of the authors Nattapon Rotpenpian, Aree Wanasuntronwong, Sompol Tapechum, Anchalee Vattarakorn, Chit Care, Wongsathit Chindasri, Kanokwan Tilokskulchai, Mayuree H. Tantisira & Narawut Pakaprot, which were incorrectly given as Rotpenpian Nattapon, Wanasuntronwong Aree, Tapechum Sompol, Vattarakorn Anchalee, Care Chit, Chindasri Wongsathit, Tilokskulchai Kanokwan, Tantisira H. Mayuree & Pakaprot Narawut.
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/.
About this article
Cite this article
Rotpenpian, N., Wanasuntronwong, A., Tapechum, S. et al. Standardized Centella asiatica (ECa 233) extract decreased pain hypersensitivity development in a male mouse model of chronic inflammatory temporomandibular disorder. Sci Rep 13, 6642 (2023). https://doi.org/10.1038/s41598-023-33769-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-023-33769-w
- Springer Nature Limited