Background Diabetes is a metabolic disorder that is characterized by chronic high blood glucose levels that causes complications in the eyes, kidneys, heart, vessels and nerves. Currently diabetic nephropathy is the most significant long-term complications in terms of morbidity and mortality for individual patients with diabetes. Honey bee venom can be considered as a natural remedy for diabetes due to its blood glucose levels lowering and lipid-regulating effect on diabetic rabbits. Aim The aim of this study was to investigate the effect of Mongolian honey bee venom (Apis mellifera) on renal dysfunction in alloxan induced diabetic rabbits. Material and Method Twenty two Chinchilla rabbits were divided into three groups: control (n=6), diabetic (n=8), and bee venom treated (n=8). The diabetic group was injected with 5% solution of Alloxan monohydrate 100 mg/kg intravenously behind the ear for 2 minutes to induce diabetes. The bee venom treated group received a bee sting (a sting contains 0.2-0.5 ml of bee venom) on their hind paw every day after their diagnosis of diabetes. Result Bee venom treatment (BVT) led to the following changes: compared to the diabetic group, the bee venom treated group’s blood glucose levels lowered between 14.9% and 26.5%; the plasma creatinine and urea levels were decreased respectively by 19,8% and 14.8%. Blood urea nitrogen (BUN) levels were reduced by 14.8%. Conclusion: Treatment with Mongolian bee venom lowered the blood glucose levels and prevents the renal dysfunction in alloxan induced diabetic rabbits

Introduction In 19th century, researchers proved at biochemical level the healing properties of bee products such as bee venom, honey, royal jelly, pollen, propolis and wax. The object of our research is the Apis cerena’s venom properties1-2. Asiatic honey bee or Apis cerana is small honey are small honey bees of southern and southeastern Asia, such as China, India, Japan, Malaysia, Nepal, Bangladesh and Papua New Guinea3. This species is also known as the Himalayan hive honeybee. This species is the sister species of Apis koschevnikovi, and both are in the same sub¬genus as the Western (European) honey bee, Apis mellifera4. Goal The purpose of our research is to study property and potential of bee venom and its effect on immune system. Heal¬ing property of Apis cerana was high. This study proves that bee venom therapy stimulates immunity. Materialis and Methods The research was conducted at the Scientific Research Center of “Monos” Institute of Traditional Medicine and in biochemical Laboratory of “Khuljborjigon” Clinic. For the experiment, we used 23 perfectly healthy mice of same sex and size which meets standards of laboratory testing. We put a bee sting to 0.5 ml of 10% red blood cell (RBC) solution and measured time of heamolysis to de¬fine bee venom potential/capability by Shkenderov S., Ivanov Ts., (1985) method. Following Erne (1963), Kovalev I.E.,(1976), Petrov’s (1980) methodology of studying effects on immune system, we have stung bee venom to 23 mice on the acupuncture point of hind paw every other day in total 3 times. On third day of the experiment, we in¬jected into vein 2ml of 10 % sheep’s RBC to stimulate the immunity. On the fifth day, we defined weight of pancreas, number of pancreatic cells, pancreatic index, and haemagglutination titre. Results Potential of bee venom is determined by speed of heamolysis when bee sting is placed in the 0.5 ml of 10% RBC solution. If we place one bee sting into 1ml of RBC solution then the speed of heamolysis is 46 seconds, when two stings are place speed is 38 seconds and when 3 stings placed then time is 30. Compare to usual speed of heamolysis which is 60 seconds, change in time depending on the number of bee stings proves the effectiveness of bee venom (Table 1). In figure 3, the number of spleen cells of control group’s was 142.71±55.51*106/ml. this is 1.2 times lower compare to normal group which is 172.67±135.5*106/ml. BVT group’s number of spleen cells was 329.78±187.78*106/ml and 1.61 times bigger than in control group. In comparison to control group, haemagglutina¬tion titre of BVT group was 1.13 times higher (BVT group 54.86±19.95%; control group 50±8.83%, p<0.05) and this indicates that BV has immunity stimulating effect. Conclusions From our experiment we can conclude the following 1. Apis mellifera’s bee venom has high treating effect. 2. Bee venom therapy has immunity stimulating activity.

The aim of this study is to investigate biological activity compounds in Mongolian traditional medicinal plants, such as Leonurus Sibiricus L., Ephedra Przewalskii Stapt. and Lonicera Altaica Pall. In the phytochemical research, biological active substance was determined by using paper chromatography and thin-layer chromatography, on silica gel plats. We determined the total content of phenolic compound by the Folin–Ciocalteu method, total alkaloid, and tannin by titrimetric method and total fl avonoid by spectrophotometric method. The following biological active substances were detected: catechin, ephedrine, anthocyan and rutin. As a result of our research, it was determined that the total alkaloids was 0.02 percent, tannin was 9.03 percent in herba Ephedra Przewalskii Stapt , total phenolic compound was 3.3 percent in Leonurus Sibiricus L. and total fl avonoid was 6.6 percent in fruits Lonicera Altaica Pall. Key words: Leonurus Sibiricus L., Ephedra Przewalskii Stapt., Lonicera Altaica Pall., thinlayer chromatography, phytochemical INTRODUCTION Ephedra przewalskii is a species of Ephedra that is native to Central Asia, Mongolia,Pakistan, and parts of China ( Gansu, Inner Mongolia, Ningxia, Qinghai, and Tibet) [1][2]. Ephedra przewalskii is widely distributed in desert regions of Mongolia such as khobdo, Dornogovi, and Mongol Altai [3]. Ephedrae herba has been used in traditional Chinese, Mongolia and Japanese (Kampo) medicine from ancient times. In Mongolia, Ephedra przewalskii herba has traditionally been used by indigenous people for a variety of medicinal purposes, including treatment of asthma, hay fever, and the common cold [4]. Herba of Ephedra przewalskii are considered to be rich source of a large amount of bioactive substances like alkaloids, catechin, fatty oil and carbohydrate [3]. Leonurus Sibiricus L., is a member of the family Lamiaceae, is widely distributed in forested area and desert regions of Mongolia such as Khangai, Khuvsgul, Khentii Mongol Daguur, and Mongol Altai [5]. In traditional Mongolian medicine aerial parts of Leonurus Sibiricus L., used for treatment of diseases of heat reduction, removal of poisonous diseases, soothing and reducing hypertension. Aerial parts of Leonurus Sibiricus L.are considered to be rich source of a large amount of bioactive substances like fl avonoids, alkaloids, tannin and organic acids [5]. In mongolia has described four species of Lonicera Altaica Pall (Caprifoliaceae). Their habitats are khuvsgul, khangai, Khentii, khobdo, Mongolian altai, and depression of great lakes, mongol daguur and the Gobi-altai (three Beauty of gobi) region of the country. Lonicera altaica in Mongolian traditional medicine is reputed for its treatment of liver, stomach and cardiac disorders, Moreover, it is known for its rejuvenation action [6]. Fruit of Lonicera Altaica Pall. is considered a rich source of bioactive substances like fl avonoids, anthocyanins, vitamin C and amino acids [6].

The biologically active food supplement products were produced in the form natural raw materials for powder, tablets, pellets, capsule, juice and extract preparation. Osteoporosis disease is increasing among the population of the world in recent years. Therefore, calcium supplement is used more often for prevention of this disease. Osteoporosis is now widely recognized as a public health problem since this disease, which increases bone fragility and thereby the risk of fractures, is associated with high mortality, morbidity and medical expenses throughout the world. We obtained new “Eghomon” supplement which reduces osteoporosis. We determined by quantitative analysis, the calcium ion and mineral composition is a crystal structure in this supplement. In the study, we used titrimetric, X-ray fl uorescence and X-ray diffractometer spectroscopy methods. The following mineral elements such as, Ca, P, Mg, Fe, Mn, Al, Na, K, Si, Ti were contained in the Eghomon supplement. Additionally, we determined the concentration of calcium ion 22.9 percent in the supplement. INTRODUCTION Mineral ions such as calcium, phosphorus, magnesium, copper, zinc, etc.., play a tremendous role in the metabolic processes of the human body, including tissue, fl uid, and bone. In each are they function to promote and maintain normal body function with a wide range of activities including assisting in body hydration, enzyme activation, maintenance of pH, as cofactors in blood coagulation, controlling neuromuscular excitability, as well as promoting the stability of bones and teeth, and many other functions. Calcium is the most abundant mineral in the human body, most of which (98%) is present in the skeleton. The concentration of calcium ion in the blood is very important for the development and preservation of strong bones and teeth. Absorption of too much calcium in the blood may lead to the leaching of calcium from the bones and teeth. The absorption of calcium is controlled, in part, by vitamin D. Growing children in particular need an ample supply of calcium for the development of strong bones. Milk, which is a good natural source of calcium and which is consumed primarily by children, is usually fortifi ed with vitamin D to promote calcium absorption. Similarly, outdoor recess for elementary school children is mandated by law in many states because exposure to sunshine allows the body to synthesize vitamin D. In later adulthood, particularly among women, the level of calcium in the blood may decrease to the point where calcium is removed from the bones and teeth to replace the blood calcium, making the bones and teeth much weaker and more susceptible to fracture. This condition is known as osteoporosis and can become very serious, causing shrinking if the skeleton and severe arthritis. For this reason, calcium supplements are often prescribed in an effort to maintain the proper concentration of calciumion in the blood. Although the results are not yet conclusive, recent reports indicate 100mg of calcium ion, taken orally on a daily basis, may serve to prevent osteoporosis. Typically, such calcium supplements consist of calcium carbonate, calcium citrate and calcium lactate. MATERIALS AND METHODS We conducted used in the study of natural biologically active food supplements Eghomon. The researchers invented new Eghomon supplement in the institute of traditional medicine and technology of Mongolia. Eghomon is composed from horse bones and eggshells. It is a calcium preparation.

Traditional medicine describes common flu as excessof blood and bile heat combined with microbes which results infectious heat. Deva-5is a decoction used which treats infectious heat. The aim of this study is to analyze components of Deva-5 decoction by traditional methods. Deva- 5 is composed of Gentianadecumbens L., Terminalia Chebula Retz., Polygonium bistorta L., Momordica cochinchinensis (Lour) and Chiazospermum erectum Bernh.It has a cool power and dispels infectious heat andkills microbes. The main component of the decoctionis Gentiana decumbens L. Ithas a sweat taste and clears heat, kills microbes, and cures typhus. Medical practitioners of Mongolia, Tibet, and Tuva use Gentiana decumbens L.as a substitution to deva (sngo-de-ba).It has a bitter taste and a cool power. It also has antimicrobial and heat clearing effects. All components of Deva-5 decoction have a cool power and the decoction is compounded by power.

INTRODUCTION:Alcohol (EtOH) use disorders (AUDs) represent a substantial public health problem worldwide. Over 76million people present with AUDs 2.5 million deaths were attributed to alcohol (World Health Organization,2010). Channadshelshi has been used for treatment of alcohol-related, liver disease and intoxication intraditional medicine.GOAL:To determine effect of channadshelshi on voluntary alcoholic wistar rats.MATERIALS AND METHODS:To examine acute toxicity of Channadselshi were used V.P.Prozorovsky express method (1978) andOECD (2001).Voluntary EtoH consumption measurement (two-bottle choice, intermittent access to EtOH paradigm inwistar rats). Water and 20% ethanol were presented in 200 mlgraduated plastic cylinders with stainlesssteeldrinking spouts.The experiment period was 10 weeks total. EtOH consumption was expressed asgrams of EtOH consumed per kilogram of body weight/day.Elevated plus maze. Anxiety associated with EtoH withdrawalwas measured on EPM The mazewaselevated 1 m above the floor and contained four 50 cm long, 10 cmwidearms arranged at rightangles. The closed arms had opaque walls 30cm high, extending the length of the arm. At the time of thetest, eachanimal was placed in the center of the maze facing an open arm andallowed to explore for a5 min session. During this 5 min test session, theanimal’s number of arm entries and time spent in eacharm per entry was recorded on a camera.Pentylenetetrazol (PTZ) 100 mg/kg dose used in this study was determined as the dose that inducedseizures and protection against mortality in miceThe experimental protocol was approved by the Ethics Committee of the MNUMS. (№ 14-11/1À)RESULTS:LD50 of Channadselshi extract was found to be LD50=2.58 (2.1-3.2) gr/kg by V.P.Prozorovsky expressmethod (1978). Channadselshi was no acute toxic by OECD (2001).Ten and four weeks oral administration of Channadselshi (200 mg/kg) significantly (P<0.01) decreasedthe consumption of ethanol and significantly (P<0.01) increased time spent in open arm (EPM) involuntary alcoholic wistar rat compare to control.The time (sec) of latency the generalized convulsion were significantly (P<0.01) increased ofChannadselshi compare to control. The percent of protection against mortality were 80% in PTZinduced seizure in mice.CONCLUSIONS:1. Our study showed that Channadselshi hasreduced consumption of ethanol in voluntary alcoholicwistar rat.2. Channadselshi has central nervous system protection effect against PTZ induced seizure in mice.

Background: Wound healing mechanisms still unclear. Wounds are physical injuries that result in an opening or breaking of the skin. Proper healing of wounds is essential for the restoration of disrupted anatomical continuity and disturbed functional status of the skin. This is a product of the integrated response of several cell types to injury. Wound healing is a complex process that results in the contraction and closure of the wound and restoration of a functional barrier.Goal: The purpose of this study was to determine burn wound healing activity of Calvacin. Materials and Methods:We used in study as colored reaction thin layer chromatography (TLC) and UV-spectrophotometer methods to determine active compounds in the three component drug "Calvacin".In research were inducted 20 healthy white mice and 40 rats. Investigation was based and implemented at scientific research laboratory of Traditional Medical Science Technology and Production Corporation and Institute of Veterinary medicine of pathological laboratory. The study protocol was approved by the Ethics Committee of the Ministry of Health.Results:Results of the phytochemical investigations showed that contained in the new drug "Calvacin" determined the presence of bioactive substances such as flavonoids, saponin, tannin, curcuminoids, organic acids and minerals. Substance was absorbed 25.7% in 40 grade ethanol, 27.1% in 70 grade, 22.2% in 96 grade and 19.6% in sterile water. We was established quality quantities of Calvacin in the drug amount summary flavonoids 1% and determined by UV spectrophotometer method. Proceeding from the absorption maximum of the substances analyzed the wave length of detection was determined as 370nm. In the result of mineral study of the "Calvacin", Ca^2.3%, P-6.17%, K-5.58%Burn wound healing time is control group 35±0.1 days, on 26±0.1 day animals of Calvacin group, but animals of Vishinski's ointment group 33±0.1 (p<0.05).Conclusions:1. The phytochemical investigations contained in the "Calvacin" drug determined the presence of bioactive substances such as flavonoids, saponin, tannin, curcuminoids, organic acids and minerals.2. Calvacin preparation has less toxic and significantly stimulate experimentally induced wound contract.

IntroductionNowadays the risk factors for thrombosis include blood stasis, vessel wall injury, and hypercoagulability, as proposed by Virchow over 150 years ago. We chose to study affect of Zomoshin 6 tan to the model of thrombosis formed in experimental animal. It was written in books and sudar that it has action of treating some type’s disease such as blood diluting, meeting frozen blood and treating some gynecological disease.PurposeTo study affect of Zomoshin-6 tan deep vein thrombosis model formed in experimental animal.Material and Methods30 male rats of wistar bread with 180-220 gram of weight for control group, experimental group or Zomoshin-6 tan and comparative group Warfarin. Thirty rats were equally divided into 3 groups: Group 1 received saline alone, Group 2 received Zomoshin-6 (200 mg/kg), and Group 3 received Warfarin as a positive control (0.25 mg/kg), seven days prior to the assessment of thrombus formation. Thrombus formation was also assessed histopathologically. Thrombi were detected in all rats after experimentallyinduced thrombosis.ResultsHistological analysis demonstrated the presence of thrombosis in the interior vena cava (IVC) of the control group, which contained fibrin, erythrocytes, and leucocytes and obstructed the lumen. Only a small amount of fibrin clot, containing a few leucocytes and large numbers of erythrocytes, were observed in the Zomoshin-6-treated group. The thrombus formed in the IVC of Warfarin-treated animals consisted of fibrin clot, which was mostly attached to the wall, with few leucocytes but abundant erythrocytes. These findings suggest that Zomoshin-6 is an effective antithrombotic agent.Conclusion:Zomoshin-6 tan has an action of inhibing thrombosis forming of vein in experimental animal.

BackgroundThese study made us to investigate the drug row material of Mongolian traditional medicine such us Tribulus terrestris, Malva neclecta Wall and Eriocheir sinensis compounded preparation named “Malbus”. Investigated us preparations steel using for treatment of kidney and urinetract deseases, it is one of effective in Mongolian traditional drug preparations.Material and MethodsThe experimental protocol was approved by the Ethics Review Committee at the Ministry Health of Mongolia. In research we used 20 healthy mice and 60 Wistar rats. Investigation was based and implemented at scientific research laboratory of Traditional Medical Science Technology and Producttion Corporation and pathological laboratory of Institute Veterinary medicine. Chemically acting substances is steroid saponin content in Malbus compound was detected by using thin layerchromatography (TLC) and its value was determined by UV-spectrophotometry. The acute oral toxicity study was according to the method Prozorovsky (1978). The toxic nephrosis was produced using Gentamicin (80 mg/kg) rats by using Neugarten’s method (1983).ResultsThe ethanolic extract results of the phytochemical investigations showed that conteined in the “Malbus” determined the presence of bioactive substances such as flavonoids, steroid saponins. The ethanolic extract of Malbus was found to be LD50 of 16.3 g/kg. Toxic nephrosis was induced in Wistar rats administered preparation Malbus dose 80 mg/kg, 160 mg/kg, and 240 mg/kg. Blood levels of creatinine, uric acid, and urea were siginificantly reduced by Malbus treatment compared tocontrol. Histological study revealed that Malbus was effective for treatment of nephritis in rats induced by gentamicin.Conclusions:1. The ethanolic extract of “Malbus” compound determined the presence of bioactive substances such as flavonoids, steroid saponins.2. LD50 of Malbus 16.3 g/kg, the preparation is has nephroprotective effect on experimental Gentamicine induced nephrosis in rats.

Background: In traditional medicine, Jur Ur-4 Tang, which is widely used for the treatment of diabetes, has been technologically processed and transformed into a modern pharmaceutical form as soluble granules. Therefore, it is essential to evaluate the pharmacological effects of the soluble granules derived from Jur Ur-4 Tang. Aim: To study the effect of granules extracted from Jur ur-4 Tang in a model of type 2 diabetes mellitus in experimental rats. : Materials and Methods : T2DM in rats was induced by a high-fat diet and a low-dose streptozotocin (STZ 35 mg/kg). Then, oral gavage administration of three different doses of Granule (450 mg/kg, 900 mg/kg) was given to T2DM rats. Experimental results showed that Granule dramatically reduced the levels of fasting blood glucose, fasting blood insulin, and GLUT4. Results:: In the glucose tolerance test, granules at doses of 450 and 900 mg/ kg significantly reduced blood glucose levels at 60 and 120 minutes (p < 0.01). Additionally, the soluble granules at all tested doses significantly decreased blood insulin levels and increased GLUT4 expression (p<0.01). Conclusion The granules lower blood glucose levels.