Achint Jain,Royana Singh,Saurabh Singh,Sanjay Singh

1Department of Pharmaceutics,Indian Institute of Technology;2Departmant of Anatomy;3Departmant of Orthopedics, Institute of Medical Sciences,Banaras Hindu University,Varanasi-221 005,U.P.India;4National Institute ofPharmaceutical Education&Research,Raebareli-229 010,U.P.India.

Diacerein protects against iodoacetate-induced osteoarthritis in the femorotibial joints of rats

Achint Jain1,4,Royana Singh2,Saurabh Singh3,Sanjay Singh1,✉

1Department of Pharmaceutics,Indian Institute of Technology;2Departmant of Anatomy;3Departmant of Orthopedics, Institute of Medical Sciences,Banaras Hindu University,Varanasi-221 005,U.P.India;4National Institute of
Pharmaceutical Education&Research,Raebareli-229 010,U.P.India.

The present study was undertaken to investigate the effect of diacerein on the histopathology of articular cartilage and subchondral bone of the femorotibial joint in rats.Osteoarthritis was induced in rats after single intra-articular injection of sodium iodoacetate.Rats were sacrificed 1,2,4,and 8 weeks post intra-articular injection to evaluate the progression of histopathogenesis of osteoarthritis.Diacerein was orally administered(15 mg/kg)once daily post 1 and 2 weeks of iodoacetate injection in two groups,respectively,for up to 12 weeks.Articular cartilage and subchondral bone of the rats of both groups were examined after 8 and 12 weeks,respectively.Quantitative histological analyses were performed by scoring these sections as per the OARSI system.Chondroitin sulfate was also estimated in articular cartilage by decrease in absorbance of methylene blue on complexation with chondroitin sulfate using a spectrophotometer.Intra-articular injection of iodoacetate induced loss of articular cartilage with progressive subchondral bone sclerosis and degeneration.Based on histopathological and biochemical findings,diacerein treatment showed chondroprotective effect.Furthermore,the chondroprotective effect of diacerein was found to be more pronounced after 12 weeks as compared to 8 weeks in both cases(i.e.,post 1 and 2 weeks of iodoacetate injection). Similar results were observed by investigation of chondroitin sulfate during biochemical study,showing the chondroprotective effect.In conclusion,diacerein exhibits chondroprotective effect in rats with late onset of action.

diacerein,osteoarthritis,articular cartilage,chondroitin sulfate,histopathology

Introduction

Osteoarthritis(OA)is a chronic degenerative joint disease characterized by destruction of the articular cartilage,subchondral bone alterations and synovitis. Though the hip,ankle,shoulder and small joints of the hands and feet may be involved,the most common joints to be affected are the knee joints.The WHO estimates that 10% of the world population over 55-60 years of age has symptomatic OA[1-3].According to the Center for Disease Control and Prevention,about 27 million U.S.adults suffer from OA;this may increase to up to 35 million by 2030[4].In India,it is the second most common joint problem with a prevalence of 22% to 39%[5-6].

The hallmark of the disease is progressive degeneration of articular cartilage and subsequent joint space narrowing.OA is a major therapeutic challenge because of the lack of effective therapies which may alter the natural course of OA progression.Pharmacological treatment strategies for OA usually include acetamino-phen which is a poorly effective drug and non-steroidal anti-inflammatory drugs which are more effective than acetaminophen but have a higher risk profile[7].Thus,current treatment recommendations for OA are intended to provide patients with symptomatic relief only.There is no generally accepted drug or structure modifying agent for OA.

Diacerein(4,5-diacetoxy-9,10-dihydro-9,10-dioxo-2-anthracenecarboxylic acid)is a novel chondroprotective agent intended for the treatment of OA.It is a semi-synthetic anthraquinone derivative.Diacerein is converted into rhein before reaching the systemic circulation.Rhein selectively inhibits the synthesis of interleukin-1(IL-1)beta and downregulates the production of nitric oxide(NO),both of which are responsible for cartilage degeneration.Rhein does not inhibit the production of PGE2;therefore,no gastrointestinal toxicity is observed[8-12].

Very few experimental rat models are available to study the course and outcome of OA.One of the best characterized rat models for analyzing the effects of drugs on the pathology of OA involves the injection of the metabolic inhibitor monosodium iodoacetate into the femorotibial joint of rats.This inhibits the activity of glyceraldehyde-3-phosphate dehydrogenase in chondrocytes,resulting in disruption of glycolysis and eventual cell death.The progressive loss of chondrocytes results in histological and morphological changes of the articular cartilage that closely resemble the degeneration seen in OA patients[13-15].OA involves a complex cascade interaction of biochemical and biomechanical factors which alters pathology of all articular tissues[16].Therefore,for assessment of a structure modifying agent for the treatment of OA,histopathology of articular cartilage,subchondral bone and other structures of an affected joint becomes important.

Chondroitin sulfate is a type of glycosaminoglycan (GAG)which forms a major component of articular cartilage.Chondroitin sulfate is widely distributed to the extracellular matrix of body tissue.It is reported to modify the chondrocyte death process and to maintain the metabolic process of cartilage matrix[17-18]. Several studies have shown that the concentration of Chondroitin sulfate is decreased at the site of osteoarthritic lesions,which is normally characterized by softening and erosion of cartilage[19-20].Thus,the estimation of chondroitin sulfate in articular cartilage along with histopathology could be an important investigation for supporting the chondroprotective effect of structure modifying agent in treatment of OA.

Many clinical trials, of 6 months to 3 years of duration,studying the safety and efficacy of diacerein in terms of its symptomatic as well as chondromodulating effect have been reported[8,21-23].Disease modifying characteristics for chondroprotective activity was also reported in a biochemical study conducted in surgically induced OA in dogs[19].Our literature search suggested that the chondroprotective or structure modifying actions of diacerein have not been supported by a histopathologic study using a suitable rat model based on cartilage destruction.Therefore,the present study was undertaken to evaluate the chondroprotective and structure modifying effect of diacerein on femorotibial joint using IA induced OA rat model along with concurrent estimation of chondroitin sulfate in articular cartilage.

Materials and methods

The study was performed using adult Charles Foster ratsaged 12-14 weeks(200±20 g).Rats were maintained in a controlled room temperature(22±2°C)with a 12:12 hours light-dark cycle from birth.They had access to food and water ad libitum.Rats used in this study were maintained and treated in accordance with the CPCSEA guidelines for laboratory rat facilities(CPCSEA Guidelines,2003).The experimental protocol was approved by the Institutional Ethics Committee of Banaras Hindu University,Varanasi,India.

Seventy-two rats of either sex were randomized under ether anesthesia to receive a single intraarticular injection of 40 μL of sodium iodoacetate(2 mg/joint) or an equivalent volume of normal saline through the patellar ligament using a 27-gauge needle,into the left knee of each rat.Then,diacerein[0.3% dispersion in sodium carboxymethyl cellulose(NaCMC)]was orally administered at a daily dose of 15 mg/kg of body weight[24-25]1 or 2 weeks post the intraarticular injection. The day of iodoacetate injection was counted as day 1.

Histology

Rats were euthanized by high dose of anesthesia and the knee joints of 4 rats at a time were taken.The femorotibial joint of each rat was removed by cutting halfway through the femur and tibia.The joint was opened for gross examination and then subjected for histopathologic sections.The rats were sacrificed at the indicated time points and tissue sections were prepared for light microscopy using standard procedures. Soft tissues around the femorotibial joint were removed from the medial and lateral joint capsule. Tissues were fixed overnight with 10% phosphate-buffered formalin and then decalcified for a maximum of 16 hours in water containing 7%w/v A lCl3.6H2O,5% formic acid and 8.5% HCl.The decalcified knee joints were washed overnight in 0.1 M phosphate buffer(pH 7.4)and then incubated in 15% sucrose and 0.1 Mphosphate buffer for 24 hours.The tissues were dehydrated using gradient alcohol.Paraffin blocks of the tissues were prepared after treating them with xylene. Serial 6 μm thickness sections of the tissue were taken and stained with hematoxylin&eosin(H&E)using standard protocol[26].Tissue sections were observed under a microscope(Olympus CH20i,Japan)[23,27].Each of the sections was scored per the Osteoarthritis Research Society International(OARSI)system for quantitative histological analyses.The entire tissue section of each slide was considered in applying the staging parameter of the OARSI system[28].

Biochemical study

The femorotibial joint was removed for biochemical evaluation after the rats were euthanized by a high dose of anesthesia.Articular cartilage was obtained from the joint using a scalpel blade to cut as deeply as possible without removing underlying bone.Samples were removed from the posterior surface of the patella or from the condyles and patellar groove of the femur.Ethanol fractions were prepared from cartilage samples digested in phosphate buffer pH 7 containing trypsin for 16 to 20 hours at 37°C and then homogenized for 1-2 minutes. Insoluble debris was removed by brief centrifugation. Supernatant was brought to 40%,50%&80% ethanol, respectively,by addition of ethanol and aqueous 20% potassium acetate solution.At each step,supernatant was allowed to stand overnight at 4°C and centrifuged. All precipitates were pooled,dissolved in water and used for determination of chondroitin sulfate[19,20].Chondroitin sulfate was indirectly estimated by decrease in absorbance of methylene blue on complexation with chondroitin sulfate using a spectrophotometer[29].

Statistical analysis

The results were expressed as mean values±standard deviation.One way analysis of variance(ANOVA)followed by Student-Newman-Keuls test was applied to examine the data of different studies.In all cases, P＜0.05(*)was considered to be significant.

Results

Normal femorotibial joints were compared with the osteoarthritic joints(Fig.1).Microphotographs of the control femorotibial joints showed normal articular cartilage(Fig.1A).The articular surface was smooth and without any fissures or debris attached to it.The femoral condyles were separated by meniscus from the tibial plateau.One week post iodoacetate injection, thinning,irregularity,and loss of surface hyaline cartilage of the joints were observed(Fig.1B).Widening of the intraarticular space was a common finding in the entire joint injected with iodoacetate.Diminished hemopoietic tissue was found in the trabecular space in the subchondral region;the tidemark representing the boundary between calcified and non-calcified region was also lost.Loss of bony spicules and sclerosis of the subcortical bone was also exhibited.

The progression of disease is shown inFig.2. Different stages of moderate to advanced OA were seen due to the metabolic inhibitory effect of iodoacetate.Two weeks post iodoacetate treatment,the tissues completely broke down(Fig.2A,B,andC). Multifocal,denuded cartilage was observed with a large number of necrotic chondrocytes.Deep fissures and cracks were observed,which reached down to the deep calcified zone.Moreover,chondrocyte degeneration was found on the surface layer,which was clearly evidenced by the empty chondrons.Four weeks post iodoacetate treatment,advanced stages of OA were observed(Fig.2D,E,andF),marked by loss of surface cartilage with subchondral bone collapse and fragmentation.Subchondral hemopoetic tissues were replaced by fibrous tissue.The bony trabeculae collapsed due to extreme thinning and degeneration, which led to an increase in interosseous space,(Fig. 2D,E).Eight weeks post iodoacetate treatment (Fig.2G,H,andI),there was well-defined subchondral cyst formation within the subchondral bone, demarcated by fibrous tissue.Regenerated chondrocyte cell nests were dispersed without normal arrangements. A large number of degenerative necrotic chondrocytes with pyknotic nuclei and sometimes partly dissolved cytoplasm were present.An increase in interosseous spaces,with a break in the bony spicules in between, resulted in confluence of the interosseous space and large cyst formation.

Diacerein treated rats,when compared with the control rats,had the same degree of OA at1 and 2 weeks post injection of iodoacetate(Fig.3and4).The femoro-tibial joints exhibited early to moderate levels of OA 1 week postiodoacetate injection(Fig.3A).Healing was evident by 8 weeks post diacerein treatment and the degree of OA changes regressed at 12 weeks(Fig.3BandC).Degenerating chondrocytes were not seen in diacereinrats.Similarly, the femorotibial joint,2 weeks post iodoacetate injection, showed moderate-to-advanced OA and was compared with diacerein treated rats(Fig.4A).Regeneration of cartilage, as evident by new chondrocyte cell nests and other structure modifications,was evident after diacerein treatment (Fig.4B,CandD).The degree of regeneration was better at 12 weeks than at 8 weeks.The chondrocyte regeneration was at faster rate than the degeneration,evidenced by pyknotic chondrocytes seen at both 8 and 12 weeks.The chondrocytes exhibited regeneration.Finally,the score values for quantitative histological analyses are summarized inTable 1.Scores for each section were calculated on the basis of individual grading values and staging of respective sections.

Fig.1 Comparison of normal femorotibial joint with osteoarthritic joint.A:Photomicrograph of a normal(treated with saline as vehicle) Charles Foster rat tibiofemoral joint.The articular surface is smooth.The femoral condyles are separated by meniscus from the tibial plateau.The normal structure of cartilage is organized in three well-ordered zones:the superficial,the mid zone and the deep zone(S,M,D).The subchondral(SC) bone,articular bone plate(AP)and the trabecular bone(TB)are clearly observed.The trabecular space(TS)is filled with hemopoitic tissue.(Grade 0, Stage 0).H&E A1x20(panoramic view),A2x100,A3x400.B:Photomicrograph of a treated Charles Foster rat femorotibial joint 1 week post IA injection.The articular space between the two ends has widened.The femoral condyles articular surface shows irregularity(arrow).The tibial plateau shows thinning(arrow head)as well as an irregular hyaline cartilage surface(arrow).The subchondral space show diminished hemopoietic tissue with bony spicule loss;(Grade 2-2.5,Stage 2).H&E x20(panoramic view).

OA induction caused significant reduction in chondroitin sulfate concentration in a time dependent manner.Chondroitin sulfate concentration in the articular cartilages of diacerein treated rats was found to be higher, compared to the control rats(i.Further,chondroitin sulfate concentration was even higher after treatment for 12 weeks,compared to 8 weeks(Fig.5).

Discussion

Fig.2 Progression of disease(OA)after IA in jection.A and B:Femorotibial joint 2 weeks post IA injection.The articular surface exhibits multifocal denuded cartilage with fissures extending deep into the mid zone.Large numbers of necrotic chondrocytes are seen(White arrow head).C: Chondrocytes degeneration exhibited by empty chondrons in the surface cartilage(White arrow);(Grade 3-3.5,Stage 3).H&E,A x100,B,C x400.D and E:Femoral condyle 4 weeks post IA injection showing marked loss of cartilage from the surface associated with subchondral bone collapse and fragmentation.Large areas of subchondral hemopoietic tissue are replaced by fibrous tissue(*).Marked bony trabeculae loss and collapse leading to formation of large interosseous spaces(black triangle)are seen.F:Irregular margin of the surface cartilage is visualized as well as irregular margin of the matrix of the regenerative fibrocartilage.(White asterisk),(Grade 4-4.5,Stage 3).H&E.D x100.E,F x400.2G-Tibial condyle 8 weeks post IA injection showing extensive degeneration of the articular cartilage and the subchondral bone(arrow head)H and I:Complete loss of the cartilage and large cysts within the subchondral region(*).Articular cartilage erosion(arrow).Cortical area show fibrous tissue formation(double arrow).Associated large number of degenerative(necrotic)chondrocytes(arrow head).Regeneration of chondrocytes cell nest dispersed without normal arrangement(triangle). Subchondral cyst due to cartilage cell proiferation within the subchodral bone(*),(Garde 5-5.5,Stage 4).H&E.x20,x100,x400.

Fig.3 Effect of treatment of diacerein after post 1 week IA in jection.A:Femorotibial joint 1 week post IA injection showing mild to moderate OA changes.Note the degenerating chondrocyte(Arrow)and loss of the cellular matrix;(Grade 2.5,Stage 2).B:Eight weeks after DC treatment which begun 1 week post IA injection.Regeneration of the cartilage is evident by the cell nest(arrow)within the articular cartilage.Cortical bone formation with microvasculature evident(by bold Arrow head);(Grade 2,Stage 2).C:Twelve weeks after DC treatment which begun 1 week post IA injection.Cell cartilage is well-organized;(Grade 1.5,Stage 2)H&E.x400.

Iodoacetate induced experimental OA in rats has been reported as a useful rat model of osteoarthritis in terms ofsimilar time dependent degeneration of the articular cartilage and subchondral bone to that in humans[27]. Degeneration was evident as early as 1 week post iodoacetate injection accompanied by osteoclastic and osteoblastic activity in the subchondral region.An intimate relation was exhibited by the degenerating articular cartilage and the subchondral bone,which was similar to earlier findings[1,14].According to Kraan et al.(2007), progression of OA leads to subchondral bone sclerosis and/or formation of osteophytes[30].These types of damage were observed 4 weeks post injection of iodoacetate.Rats showed no regenerative changes 1 and 2 weeks post diacerein treatment.Eight weeks post diacerein treatment,regeneration became apparent and further improved at 12 weeks post diacerein treatment.It may be suggested that these regenerative effects of diacerein could be attributed to the slow onset of action of the drug.The difference in chondroprotection and regeneration after 1 and 2 weeks of iodoacetate injection shows that the earlier diacerein treatment commences,the better the regeneration of OA associated lesions[31].All the above findings were well supported and explained by scoring done for tissue sections for each specimen (Table 2).Pelletier et al.(2010)reported that diacerein decreased the inhibitory effect of IL-1 on the synthesis of collagen and proteoglycans[32].Loss of these parts of cartilage matrix by induction of OA was observed in the current study and regeneration of these structures was evident due to the chondroprotective effect of diacerein.

Fig.4 Effect of treatment of diacere in after post 2 week IA in jection.A:Femorotibial joint 2 weeks post IA injection.The articular surface exhibits multifocal denuded cartilage with fissures extending deep into the deep layer.Large numbers of necrotic chondrocytes were seen(black arrow); (Grade 3.5,Stage 3).x200 B-Eight weeks after DC treatment was begun 2 weeks post IA injection.C,D:Twelve weeks after treatment was begun 2 weeks post IA injection.Regeneration of the cartilage is evident by the cell nest(small black arrow)within the articular cartilage.Note,in the subchondral region,the bone regeneration is poor.The hemopoitic tissue is being pushed to the center(*).Few necrotic chondrocytes are seen(down arrow));(Grade 1.5-1,Stage 2-1).H&E,x400.

In the present study,chondroitin sulfate was estimated as cartilage matrix biomarker along with the histological study to assess the chondroprotective effect of diacerein. Chondroitin sulfate concentration in the articular cartilage of OA induced rats(i.e.group 2 to 5)was foundto be significantly reduced in comparison to normal rats. This indicates loss of cartilage matrix due to the destructive action of iodoacetate when used as chemical agent for inducing osteoarthritis.The drug treated rats showed less loss of cartilage matrix,which may be due to the larger amount of chondroitin sulfate in these rats.

Table 1 OA score of tissue sections for quantitative histological analyses:OARSI system

Fig.5 Concentrations of CS in the articular cartilage of the treatment groups.All values are reported as Mean±SD(n=4;ANOVA), *P≤0.01 compared to Group 2(arthritic control;post 7thday IA injection);†P≤0.05 compared to Group 3(arthritic control;post 14thday IA injection); **P≤0.001 compared to all other group except Group 7.

Although clinical reports about the chondroprotective effect of diacerein are available,this work hasproven that the effect is at the site of chondrocytes.The present study has elucidated the chondroprotective effect of the diacerein on the tibiofemoral joint by histological examination.The study also suggests that the chondroprotective effect of diacerein is evident after prolonged treatment.

Table 2 OA score of tissue sections for quantitative histological analyses:OARSI system

In conclusion,injection of iodoacetate induces loss of chondral cartilage with subchondral bone lesions that mimic human OA.A clear relationship between the cartilage damage and the subjacent damage to the underlying subchondral bone was evident.The therapeutic effect of diacerein was better when the treatment was started post one week,rather than 2 week, of intraarticular injection of iodoacetate.The effect of diacerein was more pronounced after 12 weeks of treatment in comparison to eight weeks.This reflects that onset of therapeutic action is delayed.These results may be extrapolated to humans with the suggestion that the treatment efficiency would progress better if diacerein is used during the earlier phase of OA.Studies with direct evidence from the human cartilage showing effect of diacerein need to be explored in the future.

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is thankful to University Grant Commission,New Delhi for the financial support in the form of Senior Research Fellowship.The authors are thankful to Dr.Reddy’s Laboratories Ltd.(Hyderabad, India)for providing diacerein as gift sample.

✉Corresponding author:Sanjay Singh,Professor,Department of Pharmaceutics,Indian Institute of Technology,Banaras Hindu University,Varanasi-221 005,U.P.India,Tel:+91-542-6702712, E-mail:ssingh.phe@iitbhu.ac.in,drssinghbhu@gmail.com.

Received 23 June 2013,Revised 02 October 2013,Accepted 30 June 2014,Epub 28 June 2015

R684 Document code:A

The authors reported no conflict of interests

©2015 by the Journal of Biomedical Research.All rights reserved.

10.7555/JBR.29.20130092