Background: In recent years, natural compounds have been shown to play an important role in cancer prevention and early-stage therapy. Flavanones, a class of polyphenolic compounds present in plants, vegetables, seeds, fruit peels, and flowers, have been identified to possess anticancer, antioxidant, anti-inflammatory, and antibacterial bioactivities. Cancer has become a major global economic and public health challenge. According to international statistics, one in four individuals (22.8%) die from non-communicable diseases, while one in six (16.8%) die from cancer. Aim: To investigate the effect of a flavanone (5,2’,3’-trihydroxy-6,7-methylenedioxyflavanone) isolated from Iris tenuifolia on the migration of liver cancer cells. Materials and Methods: The study was conducted at the Institute of Biomedicine, Mongolian National University of Medical Sciences. The effect of the flavanone (5,2’,3’-trihydroxy-6,7-methylenedioxyflavanone) on cancer cell migration was evaluated in vitro using the scratch assay. Human liver cancer cells (HepG2) were revived and stabilized before experiments were performed. Results: HepG2 cells were treated with a 2.5 μg/mL concentration of the flavanone for 24 hours. In the control group, an initial scratch width of 0.9 mm was reduced to 0.65 mm after 24 hours due to cell proliferation and migration into the denuded area. However, treatment with the 2.5 μg/mL flavanone concentration resulted in the complete inhibition of cell migration. Conclusion The flavanone isolated from Iris tenuifolia effectively suppresses the migration of liver cancer cells.

Background: In recent years, scientists have found that certain natural compounds have significant potential in cancer prevention and early-stage cancer treatment. Flavanones, a class of polyphenolic compounds found in plants, vegetables, seeds, fruit peels, and flowers, have been identified to possess anticancer, antioxidant, anti- inflammatory, and antibacterial bioactivities. Cancer has become a major global challenge in terms of both economic and public health concerns. Global statistics indicate that 22.8% of deaths are attributed to non-communicable diseases, and 16.8% are caused by cancer, accounting for one in four and one in six deaths, respectively. Aim : To investigate anticancer effects of Iris Tenuifolia-derived flavanone on cancer cell lines. Materials and Methods : The study was conducted at the Bio-Medical Research Institute of the Mongolian National Uni versity of Medical Sciences, investigating the effect of flavanones on cancer cell viability under in vitro conditions using the MTT assay. In the study, colon, liver, and lung cancer cells were cultured, stabilized, and used for the experiments. Colorectal cancer cells (MC38), liver cancer cells (HepG2), and lung cancer cells (A549) were revived, cultured, and stabilized for use in the experimental procedures. Statistical analysis of the results was performed using Microsoft Excel 2010, and graphs were generated using GraphPad Prism 8. Differences between groups were analyzed using Student’s t-test, and a p-value of <0.05 was considered statistically significant. Results : We treated MC38, HepG2, and A549 cancer cells with different concentrations of flavanone (2.5 µM, 5 µM, and 10 µM) for 24 to 48 hours to evaluate cell viability. Flavanone inhibited A549 cell viability by 2.5 μM-10%, 5 μM-25%, and 10 μM-38%, respectively. For HepG2 cells, flavanone treatment at concentrations of 5-10 µM reduced cell viability by 28–58%. No statistically significant effect on the viability of MC38 cells was observed following treatment with flavanone at concentrations ranging from 2.5 to 10 µM. Additionally, although MC38 inhibited cell viability in a dose-de pendent manner in cell cultures, it had a statistically significant effect at higher concentrations of 30-200 μM (p<0.01). Conclusion Flavanone inhibits the cancer cell viability in a dose and time dependent manner

Background: In recent years, natural compounds have been shown to play an important role in cancer prevention and early-stage therapy. Flavanones, a class of polyphenolic compounds present in plants, vegetables, seeds, fruit peels, and flowers, have been identified to possess anticancer, antioxidant, anti-inflammatory, and antibacterial bioactivities. Cancer has become a major global economic and public health challenge. According to international statistics, one in four individuals (22.8%) die from non-communicable diseases, while one in six (16.8%) die from cancer. Aim: To investigate the effect of flavanone (5,2’,3’-trihydroxy-6,7-methylenedioxyflavanone) isolated from Iris tenuifolia on the migration of lung cancer cells. Materials and Methods: The study was conducted at the Institute of Biomedicine, MNUMS. The effect of flavanone (5,2’,3’-trihydroxy-6,7-methylenedioxyflavanone) on cancer cell migration was evaluated in vitro using the scratch assay. Human lung cancer cells (A549) were revived and stabilized before experiments were performed. Results: We treated A549 cancer cells with different concentrations of flavanone (1.25 μg/ml, 2.5 μg/ml) for 24 hours and analyzed them using the scratch assay. A cell-free gap of 0.9 mm in width was created, and after 24 hours, A549 cells migrated and proliferated into the gap, reducing its width to 0.25 mm. Treatment with 2.5 μg/ml flavanone completely inhibited cell migration. Conclusion Flavanone isolated from Iris tenuifolia inhibits lung cancer cell migration in a doseand time-dependent manner.

Traditional drug Jonlon-5 have been widely used in the clinical practice for recent years in traditional medicine. The study was conducted on the experimental animal wistar rats by the carrageenan induced mice paw edema (Winter et al. 1962, Vogel, 2002) methods. We performed chemical and pharmacological investigation was based and implemented scientific research laboratory of Institute of Traditional Medicine and Technology. The Jonlon-5 significantly (P<0.05) inhibited carrageenan induced rat paw edema as compared to control group. TNF-α secretion was magnified by carrageenan injec¬tion (387.2 pg/ml). TNF-α secretion was reduced, com¬parable to carrageenan group, as a respond to extract administration. Administration of Jonlon-5 significantly reduced inflammatory mediator secretion TNF-α by 20.8%, IL-1 β – 41.7%, to be close to inhibition level of Indo¬methacin administration. Jonlon-5 significantly decreased (P<0.05) of serum malondialdehyde (MDA) 16.5% in animal model.

Background: The prescription of Shar gaa made from the Curcuma longa L., Tribulus terrestris L., Cortex Phellodendri L., Gardenia jasminoides L. By reviewing a lot of relative research papers and the pharmacological dictionaries, we summarized the conclusion that the efficiency components of the Shar gaa extract is effective to control the infection of bacteria and the fungi, to relieve skin inflammation and pain.Aim:We conducted the control experiment to discuss thecontrol effect of the Shar gaa extract to the fungi and the bacteria. Materials and methods:We carried out susceptibility test to fungus and bacterium using medicine dilution method and cup-plate method on the sand clan proof agar culture and nutrient agar culture. The fungi inhibition results show that the Shar gaa extract has the significant restrain effects to all of experimental fungi. It has the better effects to the Microsporum lanosum M.grpseum、T.rubrum、M. canis、C.albicans、Pityrosporum than the 20% Ethanol control group (P<0.05). Meanwhile, it has the same affects with the CAILE extract (P>0.05). In addition, the Shar gaa extract of high concentration has no significant difference with the one of the low concentration. This phenomenon demonstrated the truth that the Shar gaa extract has no concentration diversity to inhibit the fungi (P>0.05). On the other hand, the bacterium inhibition results demonstrate that the weak restrain effects of the Shar gaa extract. Regard to the gram positive bacteria (mainly including the S.aureas, Bacillus anthraci, Staphylococcus), the Shar gaa extract has the less effect to control the bacteria than the Penicillin group (P<0.05) and to the gram negative bacteria (the Pseudomonas) the Shar gaa extract has the less effect to control the bacteria than the Gentamicin group (P<0.05). Invalid of the drug-resistant E. coli and the P.mirabilis the Shar gaa extract group. The 20% Ethanol on bacterial group had no inhibitory effect. Conclusion: The Shar gaa extract possessed favourable inhibitory effect to frequent fungus and relative weak inhibitory effect to general bacterium in clinic. The research achievement not only expanded the new type of the Shar gaa -4 tan, but also developed the new usage of the Shar gaa-4 tan. It is to have the potential guide significance to clinical application.

Introduction. Garidi-5, a traditional medicine composed of 5 herbs including Terminalia chebula Retz., Aconitum Kusnezoffii Reichb., Acorus calamus L., Saussurea lappa L., and musk of Moschus moschiferus, has been used in traditional Mongolian medicine as an analgesic and antibacterial medicine. The present work was undertaken to evaluate the traditional drug Garidi-5 for its analgesic and anti-inflammatory activity.Materials and Methods. The method of Winter et al. was used to study acute inflammation. Rats in groups of five each were treated with vehicle, Garidi-5 (20, 80 and 200 mg/kg, p.o.) and Indometacin (10 mg/kg) one hour prior to Carrageenan injection. 0.1 ml of 1% Carrageenan was injected into the subplantar tissue of left hind paw of each rat. Swelling of carrageenan injected foot was measured at 0, 0.5, 2, 4 h using Plethysmometer (UGO Basile, Italy)). The right hind paw was injected with 0.1 ml of vehicle.Results. The Garidi-5 (20, 80 and 200 mg/kg) significantly (P<0.01) inhibited carrageenan induced rat paw edema as compared to control group. Maximum inhibition of paw edema was observed with Garidi- 5 (80 and 200 mg/kg) at 4 h when compared to the control group (Tab.1). In assay data, the TNF-α, IL-1β and IL-6 secretion in serum were highly elevated by carrageenan induction but administration of Garidi-5 signifi cantly reduced serum secretion of inflammatory mediatorsas compared to vehicle group (Tab. 2).Conclusion. In conclusion, Traditional drug Garidi-5 have anti-in flammatory properties. The potential efficacy of Garidi-5 to treat inflammation is based in a part on the hy pothesis that it will suppress the proinflammatory cytok ines resulting in less oedema.

Introduction. Garidi-5, a traditional medicine composed of 5 herbs including Terminalia chebula Retz. Aconitum Kusnezoffii Reichb., Acorus calamus L., Saussurea lappa L., and musk of Moschus moschiferus, has been used in traditional Mongolian medicine as an analgesic and antibacterial medicine. The present work was undertaken to evaluate the traditional drug Garidi-5 for its analgesic and anti-inflammatory activity.Materials and Methods. The method of Winter et al. was used to study acute inflammation. Rats in groups of five each were treated with vehicle, Garidi-5 (20, 80 and 200 mg/kg, p.o.) and Indometacin (10 mg/kg) one hour prior to Carrageenan injection. 0.1 ml of 1% Carrageenan was injected into the subplantar tissue of left hind paw of each rat. Swelling of carrageenan injected foot was measured at 0, 0.5, 2, 4 h using Plethysmometer (UGO Basile, Italy)). The right hind pawwas injected with 0.1 ml of vehicle.ResultsThe Garidi-5 (20, 80 and 200 mg/kg) significantly (P<0.01) inhibited carrageenan induced rat paw edema as compared to control group. Maximum inhibition of paw edema was observed with Garidi-5 (80 and 200 mg/kg) at 4 h when compared to the control group (Tab.1). In assay data, the TNF-α, IL-1β and IL-6 secretion in serum were highly elevated by carrageenan induction but administration of Garidi-5 signifi cantly reduced serum secretion of inflammatory mediators as compared to vehicle group (Tab. 2). ConclusionIn conclusion, Traditional drug Garidi-5 have anti-in flammatory properties. The potential efficacy of Garidi-5 to treat inflammation is based in a part on the hy pothesis that it will suppress the proinflammatory cytok ines resulting in less oedema.

Shoulder pain is the third common areas of musculoskeletal pain. Shoulder pain was originated from pathology which neck and upper thoracic spines and destabilize movement of shoulder girdle. Treatment of chronic shoulder pain was used by acupuncture in recent time. Therefore research studies increased and we made search Medline and found articles on biomechanics of shoulder complaint, when we consolidated articles on biomechanics of shoulder complaint. Then we coordinated results of consolidated articles to theory of the Chinese acupuncture meridians and collaterals. Findings of coordination biomechanics of shoulder complaints to theory of the Chinese acupuncture meridians and collaterals studies to improve diagnostics and acupuncture treatment of shoulder pain.

Garidi-5, a traditional medicine composed of 5 herbs including Terminalia chebula Retz., Aconitum Kusnezoffii Reichb., Acorus calamus L., Saussurea lappa L., and musk ofMoschus moschiferus, has been used in traditional Mongolian medicine as an analgesic and antibacterial medicine. The aim of the study was to evaluate the central and peripheral analgesic action of traditional mongolian drug Garidi-5 in experimental animal models. Analgesic activity was assessed by tail flick method (for central action) and l acetic acid- induced writhing test (for peripheral action). Garidi-5 extract (20 mg/kg, 80, 200mg/kg p.o.) and aspirin (100 mg/kg) showed significant peripheral analgesic activity (p<0.05). Garidi-5 extract (20 mg/kg, 80, 200mg/kg p.o.) and Morphin (10 mg/kg, i.p.) also showed significant central analgesic activity (p<0.05). Conclusion: Biological activity substances were detected in the Traditional drug Garidi-5. Traditional drug Garidi-5 has analgesic effects.