Autoimmune diseases refer to problems with the acquired immune systems reactions. In an autoimmune reaction, antibodies and immune cells accidently target the bodies’ healthy tissues, which signaling the body to attack them. Researchers reported that there are more than 80 illnesses caused by autoimmunity  . An autoimmune disease affects approximately 8% of the world population, 78% of whom are women  . Studies have shown that autoimmunity causes pathogenesis of more than 100 diseases. Approximately 1-2% of the world’s population has rheumatoid arthritis and affects 45 out of every 3000 people who have autoimmune diseases. Although there are many diseases that cause chronic arthritis, rheumatoid arthritis (RA) is a chronic systemic disease, which damages the connective tissues irreversibly, gradually leading to a loss of ability to work and causing disability. This terminal illness requires permanent treatment which is highly expensive   .
To investigate the therapeutic influence of ibuprofen and Boigor-10 on experimentally induced mice with rheumatoid arthritis (RA).
1) To induce RA in animal model and determine the structural changes on vertebrae of the mice based on the clinical findings and joint microstructural test.
2) To investigate the changes on vertebrae and joints in experimentally induced RA animals after treatment of Ibuprofen and Boigor-10.
This experiment includes 60 mice bought from the Training and Industrial Center of Traditional Medicine who are 6 - 8 weeks old. Parts of this study, which were conducted on human organs, were carried out at The National Center of Coroner’s Investigation, National Center for Maternal and Child Health, Maternity Hospital I, II, & III, Ulaanbaatar Songdo Hospital, and Anatomical Department of Mongolian National University of Medical Science (MNUMS).
60 mice in the study were divided into three groups and the study was done for duration of 60 days.
• Group 1: Control group with induced arthritis.
• Group 2: Group who used Boigor-10 medication.
• Group3: Group who used Ibuprofen medication.
1) Histology test or biopsy
Sixty mice in the study were eliminated and the vertebral column was surgically removed. The biopsy test was performed using Light Microscope MBC-2, at 4 × 10, 10 × 10, 20 × 10, and 40 × 1 magnification.
The following steps were scheduled:
• Fixation: fixed in 10% neutralized formalin solution for 48 hours.
• Bone decalcification: The first method of nitric acid was employed to decalcify the bones.
• Block preparation method: Tissue-Tek VIP 5 Jr Automatic transmission apparatus was used. Dehydration, lucidification, Pouring Paraffin method, Mayer’s hematoxylin-eosin staining methods were employed.
2) Collagen induced arthritis
We carried out our experimental study according to the collagen-induced RA protocols of David D. Brand, Kary A. Latham, Edward F. Rosloniec    Collagen is a fibrous protein that, at normal physiological conditions, is insoluble. Consequently, we used diluted acetic acid to keep CII in solution for use in the CIA model (in order to make solution of 10 mm diluted acetic acid, we added 1ml cold acetic acid into 1739 ml distilled water and mixed for 5 min). 2.5 ml of the solution was also used for solubilizing the collagen II.
3) Solubilizing collagen II
We added 5 mg collagen II into a 2.5 ml-diluted solution of acetic acid (2 - 4 mg dilute acetic acid/ml collagen).
Preparation of emulsion:
• Added 2.5 ml diluted collagen II into 2.5 ml solution of Complete Freund’s Adjuvant (CFA).
• Solubilized collagen II and CFA were mixed with a ratio of 1:1, kept the lid tightly closed and dipped into the ice every 30 seconds. When a drop from the emulsion was put into water, the emulsion didn’t scatter on water surface. This verified that the emulsion formed was stable.
4) Immunization of mice
Emulsified collagen II was injected on a carefully chosen tissue site at about 1 - 2 cm distal from the base of the tail. The depth of the needle was 0.5 cm and 50 μl volume of the EC II was slowly injected intradermallyin every mouse.
After immunization we evaluated the incidence of arthritis.
The following is a scoring of Arthritis severity (individually):
• Score 0―Normal (no evidence of erythema and swelling).
• Score 1―Mild inflammation (Erythema and mild swelling) confined to the tarsals or ankle joint.
• Score 2―Inflammation from mild to average (Erythema and mild swelling) extending from the ankle to the tarsals.
• Score 3―From the intermediate to severe inflammation (Erythema and moderate swelling) extending from the ankle to metatarsal joints.
• Score 4―Severe inflammation (Erythema and severe swelling) encompass the ankle, foot, and digits, or ankylosis of the limb.
5) Boigor-10 influence on collagen induced RA inflammation
Sixty mice in the study were divided into three groups: The control group (Group I), Ibuprofen group (Group II), and Boigor-10 group (Group III). Distilled water was given orally to Group I, 17 mg/kg of Ibuprofen for Group II, and Boigor-10 for Group III (36 mg/kg) respectively, using the arthritis severity score between 0 - 4.
6) Determining the toxic effects of Boigor-10
This experiment had been carried out on 20 white-headed BalB/C mice, which weighed 16 - 22 gr. We used the Prozorovski B.P. (1978) rapid method to determine the median effective dose. The preparation was administered to the mice with the ratio of 1:1 intravenously. The median effective dose was LD50 = 1.42 (1.24 - 1.61) g/kg and it referred to the low toxic classification of Sydorov K.G.
7) The statistical processing of the outcomes
A statistical and mathematical calculation outcome of the biopsy and protocols (body weight, arthritis severity score) during the experiment was done using SPSS-16.0. To analyze the data, the following menus were employed: Descriptive Statistics, Compare Means, Correlation, Regression and Microsoft Office Excel, Adobe Photoshop CS3, References-Endnote X4 were used to create the figures respectively. The arithmetic mean and its errors, maximal and minimum values, and standard slop results were used on statistical analysis  .
Study of Ibuprofen and Boigor-10 treatment for experimentally induced RA and structural changes on vertebral column.
Body weight changes in control group with induced RA:
One of the most important incidents that give information on evaluating the experiments outcome is the body weight change in the control group. We weighed all the mice in the study prior to the start date of the study and since then, we weighed the mice every week. All groups of mice were weighed a total of 9 times (Table 1 and Table 2).
The arthritis severity was scored in three groups. Based on our findings, the control group and the Boigor-10 group had arthritis severity difference of p < 0.001. According to the Student’s criteria, the difference between the control group and Ibuprofen group was p < 0.001, which was statistically significant. There was no statistical significance between the Boigor-10 and Ibuprofen group (Figure 1).
Table 1. Body weight comparison of control and treatment group.
Figure 1. Comparison of arthritis severity between control group and treatment group.
Table 2. Arthritis severity comparison of control and treatment group.
Microstructures Changes of Vertebral Bone (after 56 days) in Control Group:
After 56 days of immunization, pannus accumulation was formed on every mice vertebral surface, the number of cavities in medullary ossium rubra had decreased and the cells contained in it also decreased dramatically. We found that the trabeculs had vanished and replaced with cartilage in whole.
When viewed through a microscope at 200× and 400× magnification, we found the following changes: the perichondrium of cartilage that covers the vertebral body surface became thin, and its chondroblast cells shapes were oval, the acidification of the cytoplasm had decreased dramatically, and trabeculs had vanished and were replaced with cartilage.
When viewed through a microscope at 200× and 400× magnification, the perichondrium of cartilage that covers the vertebral body surface became thin, and its chondroblast cells shapes were oval, the acidification of the cytoplasm had decreased and there was space between isogenous cells /nests/ and cells inside it (Figure 2).
The Structural Changes (after 56 days) on Intervertebral Cartilaginous Disks of Control Group
The collagen fibers of intervertebral cartilages disk become sparse in induced RA mice. Some cartilaginous disks of the vertebrae were destroyed and there was an empty space instead. When the nucleolus pulpous was cut, the cartilage disks were destroyed and had evaporated.
Microstructural Changes on Vertebra after Ibuprofen Treatment
Looking at the mice that were treated with Ibuprofen through a microscope at 100× and 200× magnification, the perichondrium of cartilage that covers the vertebral body surface and the cartilaginous layers of perichondrium lamellas had thickened. There was an intense process of forming new cartilage tissues. The chondroblast cell shapes and the acidification of the cytoplasm became normal and formed numerous isogenous/nests/cells.
Therefore, we concluded that ibuprofen treatment ceased the cartilage damage of the vertebral body surface and pannus accumulation process. It also intensified the regeneration of vertebral body and trabecular growth (Figure 3).
Figure 2. Intervertebral joint microstructure in the control group (after 56 days). Staining: Hematoxylin-eosin. Magnification at: А ×40, Б ×100, В ×200.
Figure 3. Intervertebral joint microstructure of mice in the Ibuprofen group. Staining: Hematoxylin-eosin. Magnification at: А ×40, Б ×100, В ×200.
The Structural Changes on Intervertebral Disk after Ibuprofen Treatment
The collagen fibers of intervertebral cartilaginous disk become sparse in mice induced with RA. Some cartilaginous disks of the vertebrae were destroyed and there was an empty space instead. When the nucleolus pulpous was cut, the cartilage discs were destroyed and had vanished. But the intervertebral disks of the mice that were treated with Ibuprofen were regenerated, the connective tissue cells and nucleolus pulpous deposition in the central part were surrounded by bundles of connective tissue fibers.
Microstructural Changes on Vertebrae after Boigor-10 Treatment
After Boigor-10 treatment, there was a decrease in pannus depositions and a damage on the surface of cartilage of the vertebral body. In addition, the Boigor-10 treatment intensified the regeneration process on vertebral body cartilages. When viewed through a microscope at 100× and 200× magnification, the perichondrium that covers adjacent vertebral body surfaces had thickened, and its chondroblastic cells shapes and the cytoplasmic acidification became normal (Figure 4).
Figure 4. Intervertebral joint microstructure of mice in Boigor-10 Group. Staining: Hematoxylin-eosin. Magnification at: А ×40, Б ×100, В ×200.
Structural Changes on Intervertebral Cartilaginous Disk after Boigor-10 Treatment
The collagen fibers of Intervertebral cartilaginous disk become sparse in mice induced with RA. Some cartilaginous disks of the vertebrae were destroyed and there was an empty space instead. When the nucleous pulposus was cut, the cartilage discs were destroyed and had evaporated. But the intervertebral disks of the mice that were treated with Boigor-10 were regenerated, the connective tissue cells and nucleous pulposus deposition in the central part surrounded by bundles of connective tissue fibers were the same as the mice Group III who had ibuprofen treatment.
For the collagen induced RA, we conducted our research according to the “Protocol for the Successful Induction of Collagen-Induced Arthritis (CIA) in Mice” by David D. Brand, Kary A. Latham, Edward F. Rosloniec published on 17th May, 2007. On the first day of the experiment, we emulsified collagen II and Complete Freund’s Adjuvant (CFA) with the ratio of 1:1 and injected 50 μl volume intradermally in every mouse-tail. The experiment work protocols were written based on arthritis severity score system, body weight changes, and biopsy test results.
According to David D. Brand, Linda K. Myers (2002) study, the first symptoms of joint inflammation occurred on the 11th day and clinical manifestations of arthritis appeared on the 35th day  .
According to the study of Edward F, Rosloniec (2007), in DBA/1 and most strain mice, the clinical manifestations of arthritis detected on day 18 - 21 and arthritis incidence was 80% - 100%. As for Campbell (2000) experimental study, the arthritis clinical manifestation started after 3.5 weeks, the arthritis incidence occurred on week 6 - 8 and the severity scores reached 10 - 12  .
From the 21st day to the 60th day, Boigor-10 was given to the Group Ibuprofen and I was given to Group II orally. Arthritis was detected in all mice after 15 - 17 days of immunization of collagen II.
As for Collagen-induced RA study of G. Dariimaa and E. Bayarmaa (2011), the arthritis was detected in all mice from days 16 - 18 and the arthritis average severity score was 3.25 on the 16th day, 4.03 on the 18th day and 5.18 on the 20th day respectively. In the study of collagen-induced RA of A. Pagmadulam, E. Bayarmaa (2012), detection of arthritis started from day 16 - 18th, the arthritis severity score in all mice was 3.25 on the 16th day, 4.03 on the 18th day and 5.18 on the 20th day. Looking at the result of Collagen-induced RA study of G. Dariimaa and E. Bayarmaa (2011) and A. Pagmadulam, E. Bayarmaa (2012), we noticed that when comparing the experimental group mice which had collagen induced RA to the healthy group mice, the body weight increased by a little. Therefore, we concluded that all these study results were similar to this study.
The collagen induced experimental arthritis study (2013) of B. Hongorzul, E. Bayarmaa showed that from the first day through the 21st day of the experiment, the body weight of healthy mice increased (n = 8) by 0.92 gr on average, while the control group mice body weight decreased by 2.15 gr. This result was possibly different due to the variety of methods that can be used with collagen-induced arthritis. Clinical manifestation results were similar to prior research results in Mongolia. We relate these findings to the breed or strain of the experimental animal.
According to the traditional medicine in Mongolia, the Influence of Traditional Medicine Senden-4 on Animal Model of Rheumatoid Arthritis [RA] study was carried out by researchers S. Soyolmaa, Z. Ariunaa and S. Oldokh. In this study, joint arthritis was induced by injecting 0.2 ml solution of 4% papain and 0.1 ml tsistein solution of 0.03 m in the 1st, 4th and 7th weeks. The induced RA was treated by Traditional medicine Senden-4. The arthritis severity, histological examination and blood tests were taken and determined Senden-4 traditional medicines action against inflammation.
We induced RA in mice treated with Boigor-10 and Ibuprofen and compared the result to the vertebral structure of the control group. After 56 days of immunization, pannus accumulation was formed on every vertebral surface, the number of cavities in medullary ossium rubra had decreased and the cells contained in it had also decreased dramatically. Trabeculs of the vertebral body had disappeared and were replaced with cartilage on the whole. After the treatments of Boigor-10 and Ibuprofen, the vertebral shapes became accurate, the pannus accumulation had disappeared, and the number of cavities in medullary ossium rubra and cells contained had increased. There was also an appearance of growing trabeculas in the vertebral body.
As for the results of collagen-induced RA study of G. Dariimaa and E. Bayarmaa (2011), Score 4 or the severity symptoms wasn’t revealed. Infiltration of inflammatory cells in the cavities, the growth of connective tissue, and the joint surface cartilages had eroded by the pannus in joint biopsy test, which were similar to our results.
In the study results of Collagen-induced RA of A. Pagmadulam, E. Bayarmaa (2012), the joint biopsy test of the limbs on the 21st day of the experimental, the synovial membrane had thickened greatly due to excessive proliferation. Therefore, it had infiltration in inflammatory tissues with lymphocytes, and pannus formation chondrocytes had developed, and joint surfaces had thickened. This conveys that we induced experimental model of RA successfully.
The collagen induced experimental arthritis study (2013) of B. Hongorzul, E. Bayarmaa showed that there was no changes in joint tissues of healthy mice in the biopsy test while the experimental group were treated with Derveger Jirgeruu and Sodium salicylate solution. The results in this study showed that the joint tissues had a score of 2.45 synovial membrane proliferation and formed cartilaginous tissue damages.
Shin-Yao Chen, Chao-Liang Wu study showed the following results, on the 16th day of their experiment, the joint biopsy test score was 3, cartilage had formed and bone tissue was damaged, and inflammatory cells had infiltrated the bone  . Further results of Shin Yoshino study, conveys that on the 21st day of biopsy test, showed changes in the arthritis severity score which scored 2.
In a pharmacological study on Mana-4 medicine carried out by Ch. Chimedragchaa (2002), they determined that Mana-4 forms and figures immune-regulation and inflammatory processes properly, strengthens cell membranes and antioxidants and intensifies cell regeneration  . Tsend-Ayush (1998) investigated Gurvan-Uriin Tan which had anti-clotting influence  .
B. Uuganbayar (2013) conducted pharmacological study on Garid-5, (a traditional medicine) and identified its reactions against bacteria’s such as: Staphylacocus aureus, Escherichai coli, Shigella dysenteriae, Pseudomonas aeruginasa, Proteus microbus, BaciIIus anthraci, Enterococc facialis, Klebsiella and Enterococcgallinarum, Escherichai coli bacteria which are resistant to many drugs  . These were similar to our findings.
1) The clinical manifestation score of experimentally induced RA increased to 2.37 ± 0.10 for the control group. Generated pannus deposition on cartilaginous disks of vertebrae destroyed the cartilage disks.
2) The clinical manifestation score decreased to 1.63 ± 0.11, 1.58 ± 0.11 respectively, after Ibuprofen and Boigor-10 treatments of RA, decreasing the processes of cartilage damage and pannus deposition. It also intensified the regeneration of the vertebral cartilage.
 Jacobson D.L., Gange, S.J., Rose, N.R. and Graham, N.M. (1997) Epidemiology and Estimated Population Burden of Selected Autoimmune Diseases in the United States. Clinical Immunology and Immunopathology, 84, 223-243.
 Kong, Y., Sarosi, I., et al. (1999) Activated T Cells Regulate Bone Loss and Joint Destruction in Adjuvant Arthritis through Osteoprotegerin Ligand. Nature, 402, 304-309.
 Brand, D.D., Myers, L.K., Whittington, K.B., et al. (2002) Detection of Early Changes in Autoimmune T Cells Phenotype and Function Following Intravenous Administration of Type II Collagen in a TCR-Transgenic Model. Journal of Immunology, 168, 490-498.
 Chen, S.Y., et al. (2011) Amelioration of Rat Collagen-Induced Arthritis through CD4+ T Cells Apoptosis and Synovial Interleukin-17 Reduction by Indoleamine 2,3-Dioxygenase Gene Therapy. Human Gene Therapy, 22, 145-154.