EXPERIMENTAL STUDY OF THE ACTION OF COX-2 SELECTIVE NONSTEROIDAL ANTI-INFLAMMATORY DRUGS AND TRADITIONAL ANTI-INFLAMMATORY DRUGS IN BONE REGENERATION

OBJECTIVE: The aim of this study is to compare the effects of traditional nonsteroidal anti-inflammatory drugs with nonsteroidal anti-inflammatory drugs that are selective cyclooxygenase-2 (COX-2) inhibitors in the process of bone regeneration in a rat model. MATERIALS AND METHODS: Forty-four Wistar strain rats were subjected to osteotomy of the right femur and randomly divided into 3 groups according to the drug to be given (diclofenac, rofecoxib, or placebo). Each group was divided into 2 subgroups according to the time to euthanasia after the surgery. The animals of Subgroup 1 were submitted to euthanasia 2 weeks after surgery, and those of Subgroup 2, underwent euthanasia 4 weeks after surgery. Radiographic examinations and bone callus histomorphometry were analyzed. RESULTS: No intergroup statistical difference was found in the bone callus area or in bone formation area 2 and 4 weeks after surgery. Intra-group analysis concerning the bone neoformation area inside the callus showed a significant difference within the diclofenac group, which presented less tissue. CONCLUSIONS: Fracture consolidation in Wistar rats occurs within less than 2 weeks, and the use of nonsteroidal antiinflammatory drugs does not significantly influence this process.


INTRODUCTION
Prostaglandins (PGs) are local, autacoid hormones formed by the oxygenation of arachidonic acid (AA) from cell membranes from which it is removed by phospholipase A2 (PLA2).Prostaglandins are produced by cyclooxygenase (COX), an enzyme also known as prostaglandin H2 synthase (PGHS).Cyclooxygenase is responsible for 2 reactions involving AA: the first reaction converts AA into the highly unstable Prostaglandin G2, and the second converts Prostaglandin G2 into Prostaglandin H2.Each tissue metabolizes Prostaglandin H2 in a different manner according to the enzymes in it, generating different active metabolites of this substance.[3][4][5][6][7][8][9][10] Until recently it was thought that the AA concentration, and therefore the action of phospholipase A2, was the limiting factor for the production of PGs. 11It is now known that the limiting stage is the one mediated by COX.
At first it was thought that only 1 type of COX existed.It was only in the beginning of the 1990s that studies in cells of rat ovaries 12 produced the first evidence for a second isoform of COX.At the same time, the conclusion was reached that the already known isoform, now called cyclooxygenase-l (COX-1), is constitutive, meaning that it can be found regularly in tissues, while the other isoform, called cyclooxygenase-2 (COX-2), is expressed only through signaling. 13Finally in 1992the COX-2 gene was cloned. 14he fact that COX-1 is expressed constitutively while COX-2 is expressed in events such as inflammation suggests a more physiologic role for the first enzyme, while COX-2 would be more important in the production of PGs in pathological processes.][17][18][19] However, it is known that COX-2 is not involved only in inflammatory processes.It is also important in a series of physiological processes such as child birth labor, when it acts by promoting mechanisms that facilitate uterine contractions. 9,15rostaglandins play an important role in bone metabolism.Recent studies have shown that in COX-2 knockout mice compared to COX-1 knockout mice, there is also a decrease in bone resorption in response to parathyroid hormone (PTH). 20In cultures of human cells, it has been shown that PTH is responsible for an increase in COX-2 expression and, consequently, of PGs in bone tissue. 10t lower concentrations, 10 PGs seem to have an effect on the formation of bone tissue. 21,22Studies have shown that the production of lamellar bone induced by mechanical stress is mediated by COX-2. 23,24t is increasingly believed that PGs are important in bone repair, since tissue levels of PGs increase between Day 3 and Day 14 after fracture in rabbit tibias. 25racture consolidation is a complex process involving intramembranous bone formation and direct differentiation of mesenchymal cells into osteoblasts, as well as endochondral ossification, when the bone matrix is deposited onto cartilage.
A study that used COX-2 knockout mice showed that both types of ossification are impaired by the absence of this enzyme.The most striking point in this study was the persistence of mesenchymal cells in the site of the fracture, 26 pointing to an important role of PGs in the differentiation of these cells into osteoblasts.The study also pointed to a possible role of PGs in the recruiting of mesenchymal cells as well as in remodeling of the bone scar or callus.
Based on these experimental findings and because of the use of selective COX-2 inhibitors in medical practice, it is important to study their effects of on the process of bone regeneration.

OBJECTIVE
The objective of this study is to compare the effects of using traditional nonsteroidal anti-inflammatory drugs (NSAIDs) and NSAIDs that are selective COX-2 inhibitors in the process of bone regeneration in a rat model.We analyzed radiographic findings and histomorphometric data of the callus related with the time to regeneration of the fracture and bone neoformation area inside the callus.

MATERIAL AND METHODS
Forty-four Wistar strain rats weighing 341 ± 31 grams (mean ± SD) were used for this study.The rats were kept in controlled conditions of temperature and lighting and with no restriction on food or water.All rats were submitted to an osteotomy of the right femur with a mechanical saw and osteotome.The rats were then randomly divided into 3 groups (1, 2, and 3) according to the drug to be given.Each group was divided into 2 subgroups according to the time to euthanasia after the surgery: Subgroup 1 2 weeks (14 days) after the surgery and Subgroup 2 4 weeks (28 days) after the surgery as follows: placebo (P), P.1 Group 2 weeks and P.2 Group 4 weeks; diclofenac (D) D.1 Group 2 weeks and D.2 Group 4 weeks; and rofecoxib (R), R.1 Group 2 weeks and R.2 Group 4 weeks.
Thirteen animals were not included in the study: 9 due to infection and 4 due to bone fixation failure (Kirschner wire migration).All groups included 5 rats each, except for the R.1 Group, which included 6 animals.
The rats in the P groups received orally 1.25 mL/kg of a solution made of 2 parts of condensed milk and 1 part of water, once daily, at the same time every day.The animals in the D groups received a similar solution of 3 mg/ kg diclofenac sodium (a nonselective COX inhibitor), while the rats in the R groups received rofecoxib (a selective COX-2 inhibitor) at a dose equivalent to 1 mg/kg.6][17] The animals were weighed once a week for drug dose adjustment.
Fracture.All animals were anesthetized using thiopental and ketalar.The right hind limb of each rat was prepared for surgical procedure.After assembling the surgi- cal table in a laminar air flow environment, the animal was positioned, and a 2% iodine solution was first used externally as an antiseptic.A 2.5-cm incision was made along the femoral diaphysis.The subcutaneous and muscular planes were incised until the bone plane was reached.
The femur was exposed, a small mechanical saw was used to weaken the cortical bone layer (Figure 1), and an osteotome was used to finish the osteotomy (Figure 2).
Intramedullary bone fixation was performed using a 1.25mm diameter Kirschner wire and an electric drill (Figures 3  and 4).The wound was closed using 4-0 nylon sutures.
The animals of Subgroups 1 (P.1, D.1, and R.1) were subjected to radiologic examination 15 days after osteotomy and 30 minutes prior to euthanasia.The animals of Subgroups 2 (P.2, D.2, and R.2) underwent a radiologic examination 2 and 4 weeks after osteotomy; the second exam was performed 30 minutes prior to euthanasia.Radiographs were taken to enable the analysis of bone union in the fracture area.Each radiograph was evaluated independently by 2 orthopedists blinded to the procedure.
After euthanasia, the femur was extracted without removing the Kirschner wire, placed in a glass container with approximately 100 mL of a 10% formol solution, and sent for histomorphometric analysis of the bone callus.A single pathologist experienced in bone tissue analysis performed the anatomical and pathological assessment.This histomorphometric assessment was blinded and measured the bone callus area and the neoformation areas inside the callus in square micrometers (Carl Zeiss AxioVision software).
The statistical analysis of the callus area and the bone neoformation area inside the callus among the 2-week subgroups (P.1 vs D.1 vs R.1) and among the 4-week subgroups (P.2 vs D.2 vs R.2) was performed using the nonparametric Kruskall-Wallis and Dunn tests.For intragroup analysis (P.1 vs P.2; D.1 vs D.2; R.1; R.2), the Mann-Whitney test was used.We considered P < 0.05 to indicate a statistically significant difference.The total area, by individual animal, of the bone callus area and of the bone neoformation area inside the callus for each group is listed in Tables 5,6,7, and 8.

RESULTS
Radiological examination.The orthopedists had difficulty in analyzing the X-rays.When asked to evaluate consolidation, quality of consolidation, and mechanical strength of the callus, they could only define whether consolidation was present or not.Both considered that all animals presented radiographic signs of consolidation in the examinations performed at 2 and 4 weeks after osteotomy.
Histomorphometric examination.In the Subgroup 1 (euthanasia at 2 weeks after osteotomy) no statistical difference was found concerning the bone callus area (Figure 5) or the bone neoformation area inside the callus P = 0.838 and P = 0.366, which was confirmed by the Dunn test (Tables 1 and 3, Figure 6).In the Subgroup 2 (euthanasia at 4 weeks) there was no statistical difference in the bone callus area or in the bone neoformation area inside the callus (P = 0.9254 and P = 0.858, respectively (Tables 1 and 3).
No significant intragroup difference was found regarding the amount of callus formation (Table 2).The intragroup analysis of the amount of bone neoformation area inside the callus showed a significant difference within the diclofenac group only (Table 4), which had less organized bone tissue.

DISCUSSION
The radiographic examination proved to be very difficult to analyze, possibly because no comparison parameter was adopted.Since the orthopedists felt comfortable only to define presence of consolidation or absence of union of fragments, the radiograph examinations were useful for   documentation purposes only.The relative stabilization obtained with the intramedullary fixation with no immobilization should have resulted in a large amount of callus, but at the end of the fourth week after osteotomy, we observed bone consolidation with no hypertrophic callus (Figure 7).Probably, a large bone callus would be seen later in this experimental model. 21,24 Regarding the callus area, the histomorphometric analysis showed no differences between subgroups (P.1 vs D.1 vs R.1 and P.2 vs D.2 vs R.2) at either 2 weeks or 4 weeks after osteotomy.This led us to believe that the administration of selective or nonselective non steroidal anti-inflammatory agents does not interfere with bone regeneration measured as the amount of callus formation in Wistar rats.Despite the findings of other clinical and experimental studies, [21][22][23][24][25][26] this model demonstrated that the administration of usually recommended doses of selective or nonselective non steroidal anti-inflammatory agents does not interfere in the ossification after bone osteotomy in the Wistar rat.
Analyzing the amount of callus formation, we did not find intragroup differences in comparing subgroups 1 and 2 (euthanasia 2 weeks and 4 weeks after osteotomy).In this model bone regeneration after bone osteotomy occurs in 2 weeks.
Concerning the comparison between the intragroup bone neoformation areas (organized bone tissue inside the bone callus), we found a significant difference within the diclofenac (D) group, since the average area of the 4-week group (subgroup 2) was smaller than that of the 2-week group (subgroup 1).It is possible that simultaneous inhibition of COX-1 and COX-2 may explain this phenomenon, but further research should be undertaken to explain this finding.

CONCLUSIONS
Bone consolidation in Wistar rats occurs by 2 weeks after osteotomy, and the use of selective or nonselective nonsteroidal anti-inflammatory drugs does not interfere in the amount of callus formation between 2 and 4 weeks after the osteotomy.The inhibition of COX-1 and COX-2 may restrain the production of well-organized bone neoformation areas inside the callus.OBJETIVO: Comparar os efeitos do uso de antiinflamatórios não-esteróides tradicionais (AINES) e AINES que são inibidores seletivos da ciclooxigenase-2 (COX-2), no processo de regeneração óssea em ratos.

Figure 2 -
Figure 2 -End of the femur osteotomy with manual saw

Figure 3 -
Figure 3 -Intramedullary nail fixation of the femur

Table 3 -
Intergroup comparison of bone neoformation area among the groups with at 4 and 2 weeks after osteotomy

Table 2 -
Intragroup comparison of bone callus area related to the time of sacrifice (2 vs 4 weeks after osteotomy)

Table 1 -
Intergroup comparison of bone callus area among the groups withat 4 and 2 weeks after osteotomy

Table 8 -
Total area (µm²) ofAbsolute Values of bone neoformation, by animal, area of the groups with at 2 weeks after osteotomy

Table 7 -
Total area (µm²) ofAbsolute Values of bone neoformation, by animal, area of the groups with 4 weeks after osteotomy

Table 6 -
Total area (µm²)Absolute Values of bone callus, by animal, area of the groups at 2 weeks after osteotomy with 2 weeks

Table 5 -
Absolute ValuesTotal area (µm²) of bone callus, by animal, area of the groups awith t 4 weeks after osteotomy