Introduction

Primary osteoarthritis (OA) refers to the development of OA without any known underlying factors, conditions, or injuries. Aging is a significant risk factor for OA, and during the aging process, there are progressive changes in joint tissues, including articular cartilage, subchondral bone, synovium, and ligaments. These changes involve increased matrix degradation, altered cell metabolism, impaired tissue repair mechanisms [1], and chronic low-grade inflammation [2,3,4,5]. In knee OA, which is commonly associated with aging, the articular cartilage gradually deteriorates, becoming thinner and exhibiting structural abnormalities. This compromises its ability to absorb shock and distribute load, resulting in joint pain and dysfunction. The subchondral bone also undergoes remodeling, including thickening and sclerosis, contributing to joint stiffness and further impacting cartilage health. Inflammation in the synovial membrane increases, leading to the production of inflammatory mediators that contribute to cartilage degradation and joint inflammation [6].

Our understanding of primary OA is derived from both clinical and preclinical research. In vivo preclinical animal models that focus mainly on genetic- or injury-induced OA have been particularly useful for two key purposes: investigating the underlying mechanisms of OA and evaluating the effectiveness of various treatment options. However, clinical studies of primary OA have shown variability in the actual onset of the disease, in the rate of OA progression, and in the severity of OA in different individuals. Thus, while inbred mouse models have provided valuable insights into OA mechanisms, they lack the genetic complexity of the human population [7, 8], and provide only limited insights into the natural development of the disease. Studying OA using a single genome compromises generalization and translation of findings [9]. The UM-HET3 mouse model, generated through a specific crossbreeding strategy (Fig. 1A), offers a genetically heterogeneous population that better represents genetic diversity. The UM-HET3 mouse model was selected by the Intervention Testing Program (ITP) at the National Institute of Aging (NIA) for studies of anti-aging drugs and was used in several studies to map genes controlling skeletal morphology [10,11,12,13] (https://phenome.jax.org/projects/ITP1). A previous study has shown that UM-HET3 male mice (from one ITP center) developed age-related OA, but exhibited a high degree of variability, showing no significant effects of the tested ITP treatments [14]. In the current study we used 182 stifles of UM-HET3 mice from three ITP centers and explored both sexes.

Fig. 1
figure 1

OARSI scoring of stifles from UMHET3 mouse model. A UM-HET3 is a genetically diverse mouse model, generated via 4way cross of (BALB/cByJ × C57BL/6J) F1 mothers and (C3H/HeJ × DBA/2J) F1 fathers. Each of the offspring is genetically unique but shares 50% of its genetic material with every other UM-HET3 mouse. B Shown are representative knee joint samples that were processed for safranin-O-red, or (C) H&E staining of the synovial membrane that were categorized based on the OARSI scoring system [15,16,17]

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Since OA occurrence intensifies with age, evaluating the presence and severity of OA becomes a crucial factor in assessing the effectiveness of compounds designed to prolong life by influencing pathways that might also play a role in OA development. Therefore, this study aimed to assess the severity of OA associated with aging in genetically diverse male and female mice and to investigate whether the severity of this age-related OA was altered in mice treated with specific agents from the ITP study. Specifically, since common cellular processes are shared between OA and aging, such as mitochondrial dysfunction, oxidative stress, increased inflammation, and accumulation of senescent cells [18], we focused on two compounds that enhance mitochondrial function. Mitochondrial dysfunction and imbalanced production of reactive oxygen species (ROS) are considered contributing factors to OA development [19,20,21]. Impaired mitochondrial function in chondrocytes is linked to various cellular mechanisms involved in energy regulation, inflammation, and pro-catabolic responses [22].

Two compounds that affect mitochondrial function were tested by the ITP centers, methylene blue (MB) and mitoquinone (MitoQ). Neither MB nor MitoQ altered lifespan in UM-HET3 mice [23]. MB, an FDA-approved drug used to treat methemoglobinemia, has been shown to enhance mitochondrial function and has demonstrated beneficial effects in animal models of OA [24]. Intra-articular injection of MB in rat and rabbit OA models improved joint symptoms, protected cartilage, and reduced inflammation [25] [26]. MitoQ, a mitochondria-targeted antioxidant [27,28,29], also suppressed ROS production and ATP synthesis in an osteochondral explant model [30] .Here we report the prevalence of primary OA and the effects of lifelong mitochondrial function enhancement on knee joint tissues during aging in the UM-HET3 mice [31].

Methods

Animals

UM-HET3 male and female mice were produced by a cross between (BALB/cByJ × C57BL/6J)F1 mothers (JAX stock #100009) and (C3H/HeJ × DBA/2J)F1 fathers (JAX stock #100004). Detailed housing conditions were specified elsewhere [32]. All the ITP sites used the same supplier of bedding and food was prepared centrally and shipped simultaneously to all sites (https://www.nia.nih.gov/research/dab/interventions-testing-program-itp). The mice were housed in plastic cages with metal covers and furnished with corn-cob bedding under similar environmental conditions in all sites (21-23°C temperature, 40-60% humidity and 12-hour light/dark cycle). Cages were adequately ventilated, and the mice were relocated to new cages at least every 7 days. Male mice were accommodated in groups of three per cage, while female mice were housed in groups of four per cage. Mice had unrestricted access to water and food. Mice were euthanized by controlled CO2 inflow to a chamber. Whole body was fixed and preserved in 4% formaldehyde solution prepared in 1X phosphate-buffered saline at 40C. Specific pathogen free status was quarterly assessed in each site. All experiments were approved by the Institutional Animal Care and Use Committee (IACUC) of each site (The Jackson Laboratory in Bar Harbor, Maine (TJL), the University of Michigan at Ann Arbor (UM), and the University of Texas Health Science Center at San Antonio (UT).

Interventions (diets): Pharmacological grade MB and MitoQ were mixed in irradiated Purina test Diet 5LG6 at a concentration of 28 mg kg−1 (28 ppm) and 100 mg kg−1 (100 ppm) of diet respectively [23, 33]. The same batch of food was supplied to all the sites. The mice were fed MB containing food from 4 months and MitoQ from 7 months of age [23].

Micro computed tomography (micro-CT)

Right hind limbs were dissected (n=182, male control=47, female control=45, male MB=22, female MB=24, male MitoQ=22 and female MitoQ=22). Legs were washed three times in 1X PBS and proceed to Micro-CT in accordance to the American Society for Bone and Mineral Research (ASBMR) guidelines [34]. Intact femur and tibia including the knee joint were scanned using a high-resolution SkyScan micro-CT system (SkyScan 1172, Kontich, Belgium) containing 10-M digital detector set at a 10W energy level (100kV and 100 μA), with a 0.5 mm aluminum filter with a 9.7μm image voxel size. Subchondral bone (SCB) parameters were taken in the distal femur below the articular cartilage (AC) avoiding cortical bone and included bone volume fraction (bone volume/tissue volume, (BV/TV %), trabecular thickness (Tb.Th, mm), trabecular number (Tb.N, 1/mm), and bone mineral density (BMD, g/cc). Subchondral bone plate (SCBP) thickness and BMD were measured at the proximal tibia. Data reconstruction was done using NRecon software, and data analysis using CTAn software. 3D images were obtained using CT Vox software.

Histology

Following micro-CT scanning, intact hindlimbs were decalcified in 10% EDTA for 3-4 weeks. Decalcification was stopped when the bones were found soft and confirmed in random samples by x-ray. Decalcified samples were thoroughly washed in running tap water, dehydrated using graded alcohol series and xylene, and processed for paraffin embedding and sectioning. Samples were sectioned in a coronal plane to 5-µm sections. Sections from the mid coronal region were used for histological analyses. Safranin-O-red staining was used for scoring the AC of the knee joint, including the presence and maturation stage of osteophytes as well as the ectopic chodrogenesis and ossification. H&E staining was used to score inflammation of synovial membrane, and overall morphology. For all the scoring systems, six typical mid coronal sections covering approximately 80-µm were chosen, subjected to staining, and the mean score of sections were taken for calculations.

Osteoarthritis score

Cartilage damage at medial and lateral tibio-femoral joints was evaluated by two blinded observers using the Osteoarthritis Research Society International (OARSI) scoring system [15]. The cartilage damage quantification by safranin-O-red consisted 0, 0.5, 1-6 scores; Osteophyte maturity was scored 0, 1-4 according to previously described method [16], where 0 as no osteophyte detected; 1 when osteophytes were composed of pre-cartilaginous lesion; 2 when osteophytes were composed predominantly of cartilage; 3 when osteophytes were composed of mixed cartilage and bone; and 4 when osteophytes were composed predominantly of bone. Synovitis was scored 0, 1-3 from H&E-stained sections based on the thickness of the synovial cell lining layer and the cell density within this layer [35]. 0 being the thinnest synovial cell lining layer and low cell density (1-2 cell layers), 1 with 3-5 cell layers, 2 with 6-8 cell layers, and 3 being the thickest synovial cell lining layer (>8 layers) and high cell density. Ectopic chondrogenesis was scored 0 when it was undetectable, 1 when it was found in the synovium and or the capsule, and 2 when it extended into the surrounding ligament and or muscle [36].

Immunohistochemistry

At least three sections of the mid coronal region per mouse and an overall 15 samples per sex were used for IHC staining. Following deparaffinization and rehydration, the tissue sections were treated with citrate-based antigen unmasking solution (H-3300, Vector Laboratories, Inc, California, USA). Then endogenous peroxidase activity was inactivated by BLOXALL endogenous blocking solution (SP-6000, Vector Laboratories, Inc, California, USA). After blocking using the protein block solution (ab64226, Abcam, Massachusetts, USA), the sections were incubated overnight with the primary antibodies at 4°C over-night, stained with rabbit specific HRP/DAB(ABC) detection kit (PK-4001/SK-4100, Vector Laboratories, Inc, California, USA) and counterstained by hematoxylin (Sigma, Missouri, USA)). For IHC, primary antibodies were against iNOS (1:300, PA3030A, Invitrogen, Massachusetts, USA), MMP-13 (1:50, 18165-1-AP, Proteintech, Illinois, USA), NLRP3 (1:300, PA5-88709, Invitrogen, Massachusetts, USA), β‐galactosidase (1:400; #ab196838, Abcam), and p16 (1:100; #PA30670, Invitrogen). Section images were acquired by DMRXE universal microscope with objective imaging gigapixel montaging workstation (Leica Biosystems, IL, USA) and analyzed using Fiji Image J where positive cells were manually labeled to allow automatic counting process (Version 1.5r; NIH, Maryland, USA). Quantification was performed by calculating the percent of positively stained cells for respective markers of the total number of chondrocytes confined within 20-µm immediately proximal to femoral condyle and distal to the tibial plateau surface.

Statistical analysis

Individual descriptive statistics (e.g., means, medians, interquartile ranges) were calculated overall and by group for each outcome. The main effects for treatment and sex, as well as the interaction between the two, were estimated using linear regression (for continuous outcomes) and ordered logistic regression (for categorical outcomes). For each pairwise combination of categorical variables, Spearman’s rank correlation coefficients were computed overall and within treatment and sex, with adjustment for the family wise error rate using the method of Benjamini and Hochberg [37]. Comparisons between sex-specific correlations within each treatment were made using the Fisher r-to-z transformation. Principal component analyses were conducted for continuous multivariate outcomes by treatment and sex, with any instance of missing data being imputed using the regularized iterative PCA algorithm [38]. Finally, no difference was found in data distribution of samples of the same sex, coming from different centers. The data was normally distributed for each center and there was no difference in the frequency distribution of the different traits between samples from different centers for each sex. Data analysis was conducted in R v4.1.3

Results

Prevalence of primary OA in UM-HET3 mice: assessed the integrity of the AC at the distal femur and proximal tibia (Fig. 1B) and the state of the synovial membrane at the medial and lateral sides of the joint (Fig. 1C). The scores of control male and female mice varied both between and within sexes.

Cumulative AC (cAC) scores across all the knee joint (medial and lateral sides of both the tibia and the femur, that can reach a maximal score of 24) revealed significant difference between male and female mice which developed primary OA to varying degrees (OR 2.15, CI [1.289, 3.609], Fig. 2A,B). However, there was no sex differences within treatment for MB (OR 1.15, CI [0.619, 1.863]) or MitoQ (OR 1.227, CI [0.669, 1.834]).

Fig. 2
figure 2

Prevalence and severity of OA in UM-HET3 mice during aging. The frequency of cAC scores at the medial (A, B) and lateral (C, D) sides of the knee joints from control (CTL males n=47, CTL females n=45), MB- (males n=22, females n=24), and MitoQ-treated (males n=22, females n=22) mice. The odd ratio (OR) and the coefficient interval 95% upper (U) and lower (L) of the main effects for treatment and sex, as well as the interaction between the two, were estimated using ordered logistic regression, are indicated in the tables

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cAC scores, specifically at the medial side of the tibia and the femur (that can reach a maximal score of 12) revealed significant differences between sexes (OR 2.425, CI [1.443, 4.076], Fig. 2C, D). Across all mice, treatment with MB significantly reduced the outcomes (OR 0.429, CI [0.213, 0.866]). On the other hand, MitoQ-treated mice did not show significantly different cAC scores at the medial knee joint (OR 0.903, CI [0.424, 1.924]). In females, 11% of control mice showed no OA with age. Treatment with MB or MitoQ increased that ratio to 25% and 23%, respectively, with no effect on the proportion of mice scored 1≤X≤3 in female mice. Approximately 64% of control females, 67% of MB-treated females, and 69% of MitoQ-treated females exhibited an accumulative score of 4≤X≤6 OA.

cAC scores, specifically at the lateral side of the tibia and the femur (that can reach a maximal score of 12) revealed no difference between sexes (OR 1.161, CI [0.695, 1.939], Fig. 2E, F). Approximately 66% of control males, 86% of MB-treated males, and 82% of MitoQ-treated males exhibited a cAC score of 1≤X≤3 OA in the lateral side. In females, treatment with MitoQ associated with 14% of cAC score of 0 and 87% of cumulative AC score of 1≤X≤3. Overall, we found that at the lateral side of the knee joint, treatment significantly differed between sexes. Male mice had 3.575X the odds of female mice of having a high cAC scores (OR 3.575, CI [1.045, 12.226]). Likewise, MitoQ-treated male mice had 3.557X higher odds (OR 3.557, CI [1.539, 20.066]) of having a high cAC score than females.

AC scores correlate with osteophytosis, synovitis and ectopic chondrogenesis

We investigated the relationships between cAC scores (of whole joint; medial and lateral femur and tibia) and three other factors: synovitis (cumulative scores of medial and lateral joint) (Fig. 3A, B), osteophytosis (cumulative scores of medial and lateral joint) (Fig. 3C,D) and ectopic chondrogenesis (Ec.Chond, cumulative scores of medial and lateral joint) (Fig. 3E,F). Score distribution for each of the aforementioned factors was plotted in supplement figure 7. There was no significant difference in the correlation between AC score and synovitis in males versus females (Fig. 3A,B). In the MitoQ group, but not MB, there were significant differences (p=0.0117) in the correlations between cAC and synovitis in males compared to females (Fig. 3G). Notably, we found a significant presence of ossification within the synovial membrane with over 80% of the animals exhibited ectopic chondrogenesis and ossification at the site of the synovial membrane. This ossification greatly affects the precision of evaluating synovial features such as fibrin deposition, vascularization, fibrosis, or perivascular edema, as described in Minten et al [39], which were applied to human samples. Nevertheless, we present synovial membrane sections from both control male and female mice (Supplement Figure 8) to illustrate the vascularization and fibrosis of the synovial membrane.

Fig. 3
figure 3

Correlations between cumulative AC (cAC) scores and synovitis, osteophytosis, or ectopic chondrogenesis (Ec.Chond). Correlations between cAC scores and synovitis in male (A) and female (B) mice. Correlations between cAC scores and osteophyte formation in male (C) and female (D) mice. Correlations between cAC scores and ectopic chondrogenesis in in male (E) and female (F) mice. A summary table of the Z score differences between each correlation along with the p values (G). CTL males n=47, CTL females n=45, MB males n=22, MB females n=24, MitoQ males n=22, MitoQ females n=22

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We used a semiquantitative method to score the degree of osteophytes present in the medial and lateral sides of the knee joint. In male mice, osteophytosis did not correlate with cAC scores (Fig. 3C,D). However, there were significant differences in the correlations between AC score and ostephytosis in males as compared to females (p=0.044) (Fig. 3G). Lastly, there were no correlations between ectopic chondrogenesis and cAC scores in either sex for mice treated with MitoQ or MB (Fig. 3E,F).

AC scores correlate with markers of inflammation in chondrocyte

We used immunohistochemistry (IHC) approach to determine the levels of inflammatory markers in AC chondrocytes of control mice. Three inflammatory markers were selected including MMP-13, iNOS, and the NLRP3 inflammasome. We found significant direct correlations between the AC scores and the protein levels of MMP-13, iNOS, and NLRP3 in chondrocytes at the medial part of the knee joint in both male and female mice (Fig. 4A, supplement figure 1). Similar correlations were found in the lateral part of the knee joint, although, not all were significant (Fig. 4B). As expected, synovitis score correlated with the protein levels of iNOS, and NLRP3 at the synovial membrane at the medial part of the joint (Fig. 4C, supplement figure 2). Finally, we found significant direct correlations between AC scores and the protein levels of markers of cell cycle arrest including p16 and ß-galactosidase in chondrocytes (supplement figure 3).

Fig 4
figure 4

Correlations between cumulative AC scores and markers of inflammation. Correlations between cumulative AC scores at the medial (A) and lateral (B) side of the joint with the levels of MMP13 (males n=21, females n=15), iNOS (males n=19, females n=19), and NLRP3 (males n=17, females n=15) in AC chondrocytes. (C) Sections of the medial synovial membrane in control mice immunostained with iNOS (males n=19, females n=19), and NLRP3 (males n=17, females n=15)

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SCB morphology in aged UM-HET3 mice was not modified by MB or MitoQ treatment

We examined the morphology of the subchondral bone (SCB) and subchondral plate (SCBP) using micro-CT analysis (Table 1, supplement figure 4). All parameters tested, including SCB volume (bone volume/total volume, BV/TV) in femur (Fig. 5A) or tibia (Fig. 5E), SCB trabecular thickness (Tb.Th) in femur (Fig. 5B) or tibia (Fig. 5F), or subchondral bone mineral density (BMD) in femur (Fig. 5C) or tibia (Fig. 5G) significantly deferred between sexes but were not altered with treatment. Similarly, tibial SCBP Th (Fig. 5H) or BMD (Fig. 5I), significantly deferred between sexes, and MitoQ treatment significantly increased SCBP BMD (p=0.0438) compared to controls. We found that morphological traits of the SCB in the femur correlated significantly to those of the tibia, indicating that both SCB compartments are regulated in a similar manner (supplement figure 5).

Table 1 SCB morphology of male and female mice determined by micro-CT. Bone volume/total volume (BV/TV), trabecular thickness (Tb.Th), and bone mineral density (BMD)
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Fig. 5
figure 5

Subchondral bone (SCB) and subchondral plate (SCP) morphology analyzed by micro-CT. A 2D image of a micro-CT scan indicating the knee joint regions of interest that were analyzed including the SCB of the distal femur, SCB of the proximal tibia, and the SCB plate of the proximal tibia. Parameters assessed by micro-CT included femur (B) bone volume/total volume (BV/TV), (C) trabecular thickness (Tb.Th), and (D) SCB mineral density (BMD). Likewise, tibia BV/TV (E), Tb.Th of the tibia SCB (F), and tibia SCB mineral density (G). SCB plate (SCBp) thickness (H), and SCBp bone mineral density (I), were determined at the proximal tibia. Data presented as mean ± SEM, p values are indicated. CTL males n=44, CTL females n=44, MB males n=22, MB females n=24, MitoQ males n=22, MitoQ females n=22. SCB phenotypic measurements from PCA of both male (J) and female (K) mice. Positively correlated variables point to the same side of the plot; negatively correlated variables point to opposite sides of the plot. Length and color of arrows indicate contribution of the variable to the overall variance of the data. Arrows that are close together are strongly positively correlated, arrows that are about 90 degrees (orthogonal) to each other are uncorrelated, and those far away (such as 180 degrees) are strongly negatively correlated

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Results from principal component analyses (PCA) suggest that much of the variation in micro-CT measures across samples occurs in two dimensions (70%) (Fig. 5J, K). In both males and females, the strongest influencing measurements included femur SCB BV/TV, femur SCB BMD, and tibia SCB BV/TV for the first component, while femur SCB Tb.Th had substantial influence on the second component. There was a strong positive correlation between femur and tibial measurements with the exception of strong negative correlations with both tibia and femur SCB trabecular spacing (Tb.Sp). Surprisingly, PCA indicate that measurements for the tibia SCBP were largely orthogonal. In males, contributions from tibia SCB Tb.Th and tibia SCBP BMD were not as strong, nor were tibia SCB Tb.Th and tibia SCB Tb.Sp in females. Finally, we did not find significant interactions between SCBP morphology and the cAC scores at the lateral or medial of the tibia (supplement figure 6).

Discussion

OA, a widespread and chronic joint disorder, is marked by ongoing deterioration of cartilage, alterations in subchondral bone, bone marrow lesions, damage to the meniscus, and synovitis. In the current study we utilized 182 stifles of genetically diverse UM-HET3 mice to model the prevalence and severity of primary OA during aging in male and female mice. We found that at the medial side of the knee joint 90% of control female and 85% of control male mice developed primary OA to varying degrees, accompanied by synovitis, osteophytosis, and calcified menisci. Interestingly, 64% of control females showed cAC scores of 1≤X≤3, and only 43% of males showed scores at that range in the medial side of the knee joint.

Both male and female control mice showed significant correlations between AC scores and synovitis. In control female mice we found significant correlation between osteophytosis and AC scores. Notably, osteophytes contribute to both the functional properties of affected joints and clinically relevant symptoms. They are closely associated with cartilage damage, although they can also develop without explicit cartilage damage [40]. The precursor cells for osteophyte formation are debatable and include mesenchymal stem cells in the periosteum [41] or synovium-derived cells [42]. The TGFβ superfamily of growth factors and macrophages play important roles in osteophyte induction [43]. In control males, osteophytosis did not correlate with AC scores.

The progression of osteoarthritis, triggers inflammatory reaction, characterized by increased expression of the inflammatory markers in AC chondrocytes and cells of the synovial membrane. Specifically, we report significant correlations between protein levels of MMP13, iNOS, and NLRP3 in AC chondrocytes and synovial membrane at the medial knee joint in both male and female mice. Release of inflammatory factors interfere with the anabolic and catabolic activities of chondrocytes and may lead to cell death [44, 45].

Previous studies have reported that mitochondrial dysfunction and oxidative stress contribute to OA development [46]. In chondrocytes, the production of mitochondrial ROS has been linked to a marked increase in cyclooxygenase, a powerful catabolic inflammatory agent [47] and MMP-13 [48], highlighting their potential role in degradation of the AC. Earlier research has established the significant role of oxidants in modulating metabolic processes in cartilage [49,50,51]. Together, it is expected that inhibiting excessive ROS accumulation can protect against chondrocyte damages and slow down OA progression. Further, mitochondria in chondrocytes are mechanically connected to the cell membrane through f-actin, facilitating their movement and distribution in the cytosol [52]. This connection between mitochondria and the cytoskeleton plays a crucial role in managing energy and ROS production [50], as well as maintaining calcium balance [53] and controlling mitochondrial apoptotic factors [54]. In light of these evidence, we studied the effects of lifelong treatment with MB or MitoQ on the natural history of primary OA in UM-HET3 mice.

MB and MitoQ affect oxidative stress in tissues of the knee joint via different mechanisms. MB ameliorates oxidative stress via stimulation of Nrf2 and its translocation to the nucleus in both in chondrocytes and synoviocytes and exerts anti-inflammatory effects in the synovium and neurons that innervate the knee joint [25]. Evidence from the current study indicate that lifelong treatment with MB lowered the cAC scores compared to controls, suggesting that it may alter the natural history of primary OA in UM-HET3 mice. MitoQ, on the other hand, functions as a mitochondrial antioxidant [55]. Its lipophilic moiety allows MitoQ to concentrate within mitochondria up to a thousand times more than other general antioxidants [56]. MitoQ is known for its protective effects against diseases related to oxidative damage. In a study using a model of bovine cartilage explants subjected to mechanical stress, MitoQ significantly reduced the production of ROS [30]. Furthermore, MitoQ treatment was found to mitigate the breakdown of the extracellular matrix (ECM), reduce oxidative stress, and lessen the inflammatory response in chondrocytes. This was observed in a mouse model of OA induced by destabilizing the medial meniscus (DMM) [57] and was likely due to its activation of the NRF2 pathway and the promotion of mitophagy in chondrocytes. In the current study we found that MitoQ-treated male mice had higher lateral, but not medial, cAC scores compared to female mice. Additionally, mice treated with MitoQ, regardless of sex, showed lower measures for SCB Plate BMB in Tibia.

In this study, we report on the prevalence and severity of primary OA in the genetically diverse UM-HET3 mice. We also examined how treating these mice with the antioxidants MB and MitoQ from early adulthood into old age impacts the development of primary OA. Our research has certain limitations, including the fact that we only examined mice at one age range (22-25 months). We established the validity of our model by showing correlations between OA features and indicators of inflammation, synovitis, and osteophyte formation. However, our study did not explore the direct causes of these conditions. We also recognize that our research does not delve into the cellular or molecular mechanisms that might trigger or advance OA. Nevertheless, our findings demonstrate that primary OA in UM-HET3 mice reflects the prevalence and severity seen in human primary OA. This suggests that these mice are a suitable model for testing systemic treatments that could influence aging processes, particularly in the context of develo** primary OA.

Conclusions

Our study offers detailed insights into the prevalence and severity of primary OA in aged UM-HET3 mice, mirroring the patterns observed in human primary OA. We demonstrate a link between the degeneration of AC and synovitis, and also uncover sex-specific associations between osteophyte development and AC scores. Additionally, our research sheds light on the impact of MB and MitoQ treatments on primary OA's prevalence and severity. Both treatments reduced the odds ratio (OR) for the onset of primary OA, but only MB showed a significant reduction in the OR in the medial knee joint. Overall, our findings confirm that UM-HET3 mice are an effective model for evaluating systemic treatments aimed at influencing aging processes, especially in relation to the development of primary OA.