Relationship between Pain Behavior and Changes in KCNA2 Expression in the Dorsal Root Ganglia of Rats with Osteoarthritis

Objective. To investigate the relationship between pain behavior and potassium voltage-gated channel subfamily A member 2 (KCNA2) expression in dorsal root ganglia (DRGs) of rats with osteoarthritis (OA). Methods. Male Sprague-Dawley rats were randomly divided into three groups: blank control group (group C), normal saline group (group S), and group OA. Paw withdrawal mechanical threshold (PWMT) and paw withdrawal thermal latency (PWTL) were measured one day before injection and one, two, four, and six weeks after injection. At one, two, four, and six weeks after injection, pathological knee joint changes and activated transcription factor-3 (ATF-3) and KCNA2 expressions in DRGs were analyzed. Results. Compared with preinjection, PWMTand PWTL at two, four, and six weeks after injection were significantly decreased in the group OA (P< 0.05 or 0.01). Compared with group C, PWMTand PWTL at two, four, and six weeks after injection were significantly decreased in the group OA (P< 0.05 or 0.01). In the group OA, slight local articular cartilage surface destruction was found at week one. /e cartilage surface destruction gradually developed, and the exacerbation of cartilage matrix reduction and bone hyperplasia were increasingly aggravated and eventually evolved into advanced OA in the second to sixth weeks. Compared with group C, ATF-3 expression was significantly increased, and KCNA2 expression was significantly decreased in the group OA at two, four, and six weeks after injection (P< 0.05 or 0.01). Compared to baseline, ATF-3 expression was significantly increased, and KCNA2 expression was significantly decreased in the group OA (P< 0.05 or 0.01). Conclusion. Pain behavior in OA rats was associated with decreased KCNA2 expression in DRGs.


Introduction
OA is a common disease in the aging population which affects bones and motor system; its incidence rate in people who are 65 years old and above is more than 50%, and its prevalence rate in people who are 75 years old and above is approximately 80% [1]. Pain is the most important symptom of OA, and it is also the main cause that affects the human health and causes disability [1,2]. However, little is known about the pathogenesis of OA pain, and thus, there is a lack of targeted treatment and measures to control OA pain. Nonsteroidal anti-inflammatory drugs [3,4] and opioids [5,6] have a certain effect on relieving OA pain, but longterm use of these drugs has great side effects, and they cannot fundamentally reverse or delay the progression of the disease [7][8][9][10]. Although surgery is effective in relieving pain in patients with advanced OA, surgery itself can cause pain and increase the financial burden on the patient. erefore, studying the pathogenesis of OA pain and exploring the possible targets for prevention and treatment of OA pain have a great research value and clinical significance.
Studies have shown that OA causes not only changes in the local nerve distribution [11,12] but also damage to the DRGs [11,13]. However, increased excitability of neurons in DRGs caused by injury is an important mechanism of chronic pain. e results of some researches [14][15][16] have confirmed that OA pain has similar characteristics as neuropathic pain (NP), but whether the mechanism of OA pain is similar to that of NP remains unclear. Recent studies have indicated that downregulation and dysfunction of KCNA2 are one of the important pathogeneses of NP [17,18]. Furthermore, other researches have demonstrated that changes in the expression and function of voltage-gated sodium channel in DRGs are related to hyperalgesia in OA pain [19,20]. erefore, we hypothesized that KCNA2 in DRGs is related to changes in pain behavior in OA animal models. is paper aims to study the relationship between pain behavior and KCNA2 expression in DRGs of rats with OA and to provide a theoretical basis for further exploring the pathogenesis of OA pain.

Animals and Grouping.
As the decrease of estrogen is an important pathogenesis of osteoarthritis, we choose male rats in order to eliminate the interference of estrogen to animal model. A total of 144 male Sprague-Dawley rats (aged 7-8 weeks, weight 230−270 g) were acquired from Guangdong Experimental Animal Center (qualified number: 44007200052028). en, they were randomly equally divided into the following three groups: blank control group (group C), normal saline group (group S), and group OA.

Model Establishment.
According to literatures [21][22][23][24] and slightly modified techniques, intraperitoneal injection of 6% sodium pentobarbital was administered in rats (60 mg/kg). After sufficient anesthesia, fur on the left knee joint was shaved off, disinfected by medical iodine, and then deiodinated by 75% ethanol. e puncture needle was inserted into the joint cavity through the lateral part of the infrapatellar ligament. e group OA received intra-articular injection of 4% monosodium iodoacetate (MIA) (Macklin Biochemical Technology Co. Shanghai, China) 2 mg (dissolved in 50 μL normal saline) [21][22][23], group S was injected with the same volume of normal saline, and group C was only subjected to articular cavity puncture without injection.

Pain Behavior.
After preadapting for 30 min, pain behavior in rats was measured one day before intra-articular injection and one, two, four, and six weeks after injection. Based on references [17,25,26] and slightly altered, Aesthesio Von-Frey filaments (Ugo Basile, Gemonio, Italy) with different folding forces (2,4,6,8,10,15,26, and 60 g) were applied to stimulate the midpoint of the left paw. e filament was applied for a period of ≤4 s, and the procedure was repeated five times at 30 s intervals, and three or more positive reaction fold forces were recorded as withdrawal mechanical threshold (PWMT). According to some other studies [17,27,28], the left paw of the rat was irradiated with a laser heat source lamp of infrared thermal pain tester (RWD, San Diego, USA) at a temperature of 55°C. e time from the start of irradiation to the foot-licking phenomenon in the rat was recorded. A cut-off time of 60 s was used to avoid tissue injury. e irradiation was repeated three times at 10 min intervals, and the average value of three measurements was considered as paw withdrawal thermal latency (PWTL).

Knee Joint Histopathology.
e left knee joint tissue was obtained after injection into the articular cavity at one, two, four, and six weeks, fixed in 4% paraformaldehyde for 48 h, and then placed in a decalcified solution. e fluid was changed every three days, and the articular tissue was cut into 8-μm-thick paraffin sections for use after two weeks. e above paraffin sections were dewaxed and hydrated for further dyeing. Hematoxylin-Eosin staining (Biyuntian Biotechnology Research Institute, China) was performed, and it included the following steps: adding Hematoxylin dyeing solution for 10 min, 1% hydrochloric acid alcohol differentiation after water wash for 5−10 s, and adding eosin dyeing solution for 1−3 min. Safranin O-Fast Green staining (Beijing Baiao Laibo Technology Co., Ltd., China) was performed, and it included the following steps: Hematoxylin staining for 5 min, hydrochloric acid alcohol differentiation after water wash for 5−10 s, washing and then add strengthening green solution for 3 min, quick rinsing with 1% acetic acid for 10−15 s, and staining with Safranin O solution for 2-3 min. e stained sections were dehydrated, waxed, and sealed, and then they were observed under a microscope.

Expression of ATF-3 in DRGs.
e animals were killed at one, two, four, and six weeks after the intra-articular injection: the rat's thoracic cavity was cut open quickly, the left ventricle was inserted, and the right atrium was cut open, and 4% paraformaldehyde was injected for fixation. e DRGs at L3-5 of the left lumbar vertebra of the rat were obtained for frozen section. e sections were rewarmed at room temperature for 30 min. en, the sections were blocked by the rupture solution containing 0.2% Triton X-100 and 5% goat serum at room temperature for 2 h, and the corresponding primary antibodies of rabbit-anti-rat ATF-3 (GTX129120, 1 : 200, GeneTex, Radnor, USA) and mouse anti-rat NeuN (GTX30773, 1 : 200, GeneTex, Radnor, USA) were added dropwise at 4°C overnight. On the next day, the sections were removed and rinsed, and the corresponding fluorescent secondary antibodies of donkey antirabbit (AB141637, 1 : 1000, ermo Fisher, Waltham, USA) and goat-anti-mouse (ab150113, 1 : 1000, Abcam, London, UK) were added; they were incubated for 2 h at room temperature and stained with Hoechst 33342 (Sigma, St. Louis, USA) for 10 min. On observation by confocal microscopy after the sections were sealed, the neurons were green, ATF-3 were red, and image analysis was performed using Image J software (NIH, MA, USA).

Expression of KCNA2 in DRGs.
e L3-5 DRGs tissue on the left side of the rat was obtained at one, two, four, and six weeks after articular cavity injection and stored in a refrigerator at −80°C. All samples were cut to pieces, added with tissue lysis fluid, fully homogenized on ice, and lysed. en, they were centrifuged at 12,000 r/min for 30 min at 4°C. e supernatant was obtained, and the protein concentration was determined by the bicinchoninic acid assay balanced. en, it was denatured in boiling water and stored in a refrigerator at −20°C for use. e same amount of protein samples was obtained for electrophoresis. e proteins were separated and transferred to a polyvinylidene fluoride membrane, and it was blocked by 5% skim milk at room temperature for 1 h. Rabbit-anti-rat KCNA2 polyclonal antibody (GTX54835, 1 : 1000, GeneTex, Radnor, USA) was added dropwise, incubated at 4°C overnight, and rinsed after removal.
en, horseradish peroxidaseconjugated goat-anti-rabbit secondary antibody (ZDR-5118, 1 : 1000, Zhongshan Jinqiao Biotechnology Co., Ltd., Beijing, China) was added and incubated for 2 h at room temperature. ECL Western Blotting Substrate kit ( ermo Fisher, Waltham, USA) was used for color rendering, and analysis was performed by Image J Software.

Statistical Analysis.
All data were analyzed with SPSS 20.0 statistical software package (SPSS Inc., IL, USA) and presented as mean ± standard deviation (SD). All data were graphed by Excel 2010 (Microsoft, MA, USA). e pain behavior data were analyzed by the repeated-measures analysis of variance (ANOVA). e comparison between groups of PWMT and PWTL was performed respectively by the multiplex analysis and the simple effect test, and intragroup comparison was performed using the least-significant difference (LSD) test.
e remaining data were analyzed by the one-way ANOVA followed by the LSD test. P < 0.05 was considered statistically significant.

Changes in Pain Behavior in the ree Groups of Rats.
Compared with baseline, PWMT and PWTL were significantly lower in the group OA (P < 0.05 or 0.01) at two, four, and six weeks after intra-articular injection; PWMT and PWTL were lowest at four weeks (P < 0.01). ere was no significant difference in PWMT and PWTL between four and six weeks after OA model establishment (P > 0.05). Compared with group C, at two, four, and six weeks, PWMT and PWTL were significantly decreased in the group OA (P < 0.05 or 0.01) (see Figure 1).

Histopathological Changes in the Knee Joints in the ree
Groups of Rats. In group OA, the local cartilage surface was incomplete and opaque, the proteoglycan in the cartilage matrix was uniformly stained red, the subchondral cortical bone and trabecular bone were uniformly stained green, and the tidal line was clear at one week. At two weeks, cartilage surface damage was aggravated. It was observed that the cartilage matrix was reduced, the subchondral cortical bone and trabecular bone were increased, and some tidal lines were blurred. At four weeks, cartilage damage was further aggravated, local bone was exposed, the joint cavity was narrow, the cartilage matrix was reduced greatly, the extent of subchondral cortical bone and trabecular bone was further expanded than that at two weeks, and the tidal line was unclear. At six weeks, the articular cartilage was severely damaged, the exposed bone surface was augmented, the cartilage matrix was extensively decreased, the subchondral cortical bone and trabecular bone were enlarged, and part of the bone was convex to the joint cavity. In group C, the articular cartilage surface was intact and smooth at one, two, four, and six weeks, with clear articular chondrocytes and a visible tidal line and absence of hyperosteogeny ( Figure 2).

Expression of ATF-3 in DRGs in the ree Groups of Rats.
In order to determine whether the DRGs of rats with OA were involved, L3-5 DRGs on the same side as intra-articular injection were collected for analysis of the ATF-3 expression.
e results showed that the expression of ATF-3 in DRGs was significantly increased at two, four, and six weeks after the injection with MIA compared to before the injection (P < 0.05 or 0.01), and compared with group C, the expression of ATF-3 in DRGs in the group OA was significantly increased at two, four, and six weeks after the intraarticular injection (P < 0.05 or 0.01) (Figure 3).

Expression of KCNA2 in DRGs in the ree Groups of Rats.
We further explored the expression of KCNA2 in DRGs. e results indicate that the expression of KCNA2 was significantly decreased at two, four, and six weeks after intra-articular administrated with MIA than baseline (P < 0.05 or 0.01), and compared with group C, the expression of KCNA2 in DRGs in the group OA was significantly decreased at two, four, and six weeks (P < 0.05 or 0.01) (Figure 4).

Discussion
OA is a common and frequently observed disease in the clinic, and pain is the main reason that affects the life of patients. However, the mechanism of OA pain is very complicated, and little is known about this mechanism at present, which results in certain difficulties in the prevention and treatment of OA.

Scientific and Reasonable Establishment of Animal Model.
Intra-articular injection of MIA into the unilateral knee joint in rats destroyed the articular cartilage, the synovial membrane, and ligament to some extent and changed the original stability of the joint, thus leading to the development of OA. ese pathological changes are similar to those in human OA. Because chronic deterioration of joints is associated with chronic pain behavior, this model can assess the changes in pain in animal models. e model has a short modeling period, is stable and reliable, requires a simple operation, and has a high success rate. erefore, it is widely used in OA research [24,29,30]. According to several previous studies [11, 21-23, 31, 32], we selected the dose, concentration, and volume of MIA. is study showed that pathological changes occurred in the knee joint of rats in the Pain Research and Management 3 OA group within one week after intra-articular injection of MIA, and the pathological changes after four weeks were similar to those in advanced human OA. Furthermore, pain behavioral changes of rats were apparent in group OA, indicating that the OA model was successfully established.

Changes of Pain Behavior in OA Model Rats.
Fernihough et al. [24] reported that, compared with partial medial meniscectomy, the pain behavioral changes in the knee joint OA model constructed by intra-articular MIA injection were more similar to those in OA patients. Furthermore, another study provided evidence that both MIA and meniscal transection models in rats are similar to those of human knee OA, but inflammation may play a greater role in the development of pain behavior in the meniscal transection model [33]. Kim et al. [29] reported that, compared with the saline group, the PWMT and PWTL in the OA group were significantly decreased. e above results suggest that the characteristic of OA pain is similar to that of NP. Pain hypersensitivity and pain allergies are the two prominent symptoms of NP. is study showed that PWMT and PWTL of rats in the group OA were significantly decreased than those in group C after two weeks of intraarticular injection of MIA, and they reached a peak at four weeks after intra-articular injection, suggesting that OA pain had similar characteristics to NP and that pain allergy and hypersensitivity were involved in the pathogenesis of OA pain.

e Involvement of DRGs in Changes of Pain Behavior in OA Rats.
e DRGs serve as a relay station for the pain signal transmission process. When a peripheral nerve is injured, the DRGs, as the first level neurons, receive the incoming pain signal and transmit it to the dorsal horn of the spinal cord and higher centers. Furthermore, Albayrak et al. reported that pulsed radiofrequency therapy to DRG contributes to reducing the degree of pain in patients with persistent postsurgical pain after total knee arthroplasty [34]. erefore, DRGs play an important role in the pathogenesis of OA pain [13,35]. Joint inflammation is a major clinical problem and a main cause of debilitating chronic pain, characterized by pronounced mechanical hyperalgesia and persistent pain at rest [36]. Pain mechanisms require the sensitization of primary sensory neurons, whose cell bodies are located in DRG, and involve several media-tors that trigger particular signal-transduction pathways. A great part of these pathways imply the activation of transcription factors, in which gene expression becomes altered. In particular pathological conditions, DRGs are actually responsible for the synthesis of signaling molecules involved in reaction cascades that can ultimately lead to phenomena like survival or regeneration [37]. Activating transcription factor 3 (ATF-3) has been suggested as acting as an "adaptive response" due to its ability to respond differently according to the cellular context [38]. ATF-3, which shows low expression under normal conditions, increases rapidly when the cells are stimulated by various pathophysiological processes [39]. It is the earliest transcription factor that is expressed during a cellular stress response, and its increased expression often indicates tissue damage. Its inclusion in anti-and proapoptosis mechanisms [40], cell survival [41], regeneration [42], and neuroprotection [43] signaling events has been reported. In a p-Akt-mediated survival pathway, the ATF-3/c-Jun heterodimer has been suggested to promote nerve elongation and inhibit apoptosis in neurons under death stress such as nerve injury [44]. Nowadays, ATF-3 is mostly assumed as a neuronal injury marker, after its expression was found to be highly induced in several models of neuropathic pain [45][46][47]. e results of our study showed that ATF-3 expression was significantly increased in DRGs of rats after two weeks of intra-articular injection with MIA into the knee joint, thus indicating that the neurons were damaged. However, data on ATF-3 expression in In group C, the articular cartilage surface was smooth and there was no crack formation, the cells were normal and arranged regularly, the tidal line was clear, and there was no bone hyperplasia. In the group OA, with the development of the OA, the destruction of cartilage surface is aggravated and even bone exposure occurred, the increasing exacerbation of cartilage matrix reduction and bone hyperplasia was apparent, the tidal line gradually blurred, and pathological changes showed typical advanced OA manifestations at four to six weeks. primary afferents in different models of inflammatory pain have not always been consistent [48][49][50]. For example, intraplantar injection of complete Freund's adjuvant (CFA) did not induce any ATF-3 expression, suggesting there is no neuronal damage associated [48,49]. Interestingly, in the collagen-induced arthritis and monoiodoacetate-induced osteoarthritis joint pain models, ATF-3 was also expressed in DRG neurons [51,52], suggesting some degree of neuronal damage is occurring. Taking into account these controversial data and the sparse information available on the role of ATF-3 in pain processing, its expression was shown to be either increased or decreased depending on the neuronal populations, indicating ATF-3-expressing cells' size distribution and colocalization with isolectin B4 (IB4) or calcitonin generelated peptide (CGRP) [50].

e Relationship between the Expression of KCNA2 in DRG Neurons and Pain Behavior in OA Model Animals.
Injury to the neurons in DRGs may cause changes in the expression or function of ion channels on the membrane [17,20]. e Kv channel is one of the important ion channels that play important roles in maintaining the resting membrane potential and action potential repolarization, and it is closely related to the excitability of neurons. e Kv channel is a tetramer composed of the α subunit superfamily and the β auxiliary subunit. Kv channels can be divided into 12 subfamilies according to the α subunit, 1−12, where, in the α subunit, Kv1.2 (KCNA2) of the Kv1 subfamily is highly expressed in DRGs [53,54]. Decreased expression of KCNA2 in DRGs contributes to hyperalgesia in NP and increases the expression of KCNA2 to attenuate the symptoms of NP [17]. Recently, Zhao et al. [18] demonstrated that, in the chronic pain rat model created by spinal nerve ligation, the expression of KCNA2 in DRGs was significantly decreased, and the Kv current was decreased, which caused abnormal excitation and discharge of neurons and led to peripheral sensitization of pain. e results of our study showed that the expression of KCNA2 in DRGs of rats in the group OA was decreased compared with that of rats in group C since two weeks after MIA injection, and the difference was most significant at four to six weeks. Since the changes in pain behavior were basically consistent with the trend of KCNA2, we believe that the pain behavior of OA rats was related to the decrease in KCNA2 expression in DRGs. However, this study did not further study the changes of pain behavior in OA model rats after reversing the downregulation of KCNA2 expression in DRGs. In addition, there are many potential mechanisms that cause the change of KCNA2 expression in DRG neurons in other chronic pain animal models [18,55,56], and this is not clear in OA model animals. However, we have not carried out further research in this field. In the future, we will conduct more in-depth research on the previously mentioned issues.

Summary
In conclusion, this study confirmed that the nature of OA pain is similar to that of NP and demonstrated the occurrence and development of OA pain are associated with the decreased expression of KCNA2 in DRG neurons.

Data Availability
e data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest
e authors declare that they have no conflicts of interest.