AIM: To study the cerebra damaged by long-term administration of prednisone,and investigate the preventive effects of compound danqi (CD) in rats. METHODS: 40 SD rats were randomly divided into 5 groups with 8 rats each group. Group 1 was control (NS group),other groups were oral gavages prednisone ( 2.7 mg?kg -1 ?d -1 ) first,and then plus vehicle (GC group),or plus CD at dose of 2.5 , 5.0 or 10.0 g?kg -1 ?d -1 ,respectively,once a day for 12 weeks. At the experimental endpoint,animals were drawn blood from right ventricle under anesthesia. The left half cerebrum was milled in 10% homogenate to test the content of mono-amine oxidase (MAO),superoxide dismutase (SOD) and acetylcholinesterase (AchE). The right half cerebrum was for histological observation. RESULTS: The concentration of SOD and AchE decreased,yet MAO increased significantly in GC group. Moreover,histopathology showed that the structure of cerebrum cortex became thinner and hippocampi was in disorder. Dropsical and necrotic nerve cells were found. Yet CD could prevent the changes of nerve centre in prednisone tats. CONCLUTION: Cerebra damage occurs in four-month-old male Sprague-Dawley rats after prednisone-treated for 12 weeks. The treatment of CD in different dose can prevent the damage.

Aim To study the characteristics of osteoporosis induced by long-term administration of prednisone, and investigate the preventive effects of compound stanozolol (CS) on the adverse reactions in male rats. Methods Twenty-four four-month-old male Sprague-Dawley rats were randomly divided into 3 groups with 8 rats per group. Group 1 was control (NS group), other groups were oral gavages prednisone (2.7 mg?kg -1?d -1) first, and then plus vehicle (GC group) or plus CS (combination of Stanozolol 0.5 mg?kg -1?d -1 + Calciofon 0.5 g?kg -1?d -1 + Vitamin D 3 250 U?kg -1?d -1), once a day for 12 weeks. At the experimental endpoint, animals were drawn blood from right ventricle under anesthesia. The tibia, ulna and thighbone were collected to test for parameters related to bone.The undecalcified longitudinal proximal tibia metaphyseal sections were cut and stained with Masson-Goldner's Trichrome (5-?m thickness) for osteoclasts analysis, unstained sections (8-?m thickness) for the cancellous bone histomorphometric and fluorochrome labeling analysis. The measured parameters were used to calculate the percent trabecular area (Tb.Ar%), trabecular thickness (Tb.Th), trabecular number (Tb.N), trabecular separation (Tb.Sp), percent labeled perimeter (L.Pm%), Mineral apposition rate (MRA), bone formation rate (BFR/TV, BFR/BV, BFR/BS), unit area osteoclast number (Oc.N/BV) and Percent osteoclast number surface perimeter (OcP/BS). The desiccant left ulnar was dissolved in hydrochloric acid to test the content of Ca 2+ and hydroxyproline. Length and width of the thigh bone were tested to observe the instance of bone growing. Results Compared with NS group, bone weight, contents of bone hydroxyproline and Ca 2+decreased remarkably in GC group and the bone histomorphometric parameters also showed bone lose significantly.The effects of CS in prednisone rats showed that CS prevented bone loss effectively.Conclusions Bone loss occured in four-month-old male Sprague-Dawley rats after prednisone-treated for 12 weeks. CS could prevent bone loss effectively by inhibiting bone resorption and advancing bone formation.

BACKGROUND: Since chronic liver disorders are associated with bone loss commonly, it is very significant to probe into the prevention of such bone loss for the treatment of osteoporosis.OBJECTIVE: To study the mechanism of glycyrrhizic acid on prevention and treatment of bone loss induced by liver fibrosis in mice.DESIGN: Randomized and controlled study in which the experimental animals were taken as the objects.SETTING: Experimental animal center, central experimental room and pharmacological research room of a universityMATERIALS: The experiment was performed from January to September 2001. Forty common-grade PCR mice of either sex were employed, weighted varied from 20 to 22 g, provided by Experimental Animal Center of the Institution. According to mass-equivalence principle, 4 groups were randomized, named as control, model group, the treatment with colchicine group(CL group) and the treatment of glycyrrhizic acid group(GA group-) with 10 mice in each group.METHODS: Except the control group, in the model group, CL group and GA group, the subcutaneous injection with 400 g/L carbon tetrachloride prepared with peanut oil was given for 5 weeks to induce liver fibrosis in mice. Afterward, the treatment was applied with carbon-tetrachloride peanut-oil solution 10 mL/kg, colchicum autumnale solution 0. 1 g/kg and glycyrrhizic acid solution 0. 1 mg/kg successively. At the end of the experiment, the eyeball was extirpated for blood collection. The serum was separated to assay the various relevant biochemical indexes of liver injury, observe the changes in liver pathological tissues and measure bone calcium(Ca2+) content of femur and the contents of other bone trace elements as well as bone oxyproline hydroxyproline (Hyp).Effects of glycyrrhizic acid on the contents of bone trace elements in mice of every group.RESULTS: The levels of serum aspartate aminotransferase(AST) and alanine aminotransferase(ALT) in CL group and GA group were lower than those in the model group( P < 0. 01 ). The level of albumin and ratio between albumin and globulin in the model group were lower than those in CL group and GA group( P < 0.01, P < 0.05) . The content of bone calcium in CL group and GA group were lower than that in the control group ( P < 0. 05),but that was higher than the model group( P < 0.05) . The unit contents of copper(Cu2+ ), magnesium(Mg2+) and zinc(Zn2+) in the right femur of the model group were all higher than the control group ( P < 0.01 ), but the contents of those in GA group were not indicated significant differences compared with the control group ( P > 0.05 ). The liver pathological changes of mice in GA group were obviously milder compared with the model group ( P < 0.01 ) and it was shown with VG staining the severity of hyperplasia of liver collagenous fibers was remarkably milder compared with the model group( P < 0.01).CONCLUSION: The extractive solution of glycyrrhizic acid induces medical metabolic enzyme in the liver, enhances detoxification of liver, protects liver to maintain protein metabolic level and maintains the normal metabolism of bone to promote bone Ca2+ and balance between oxyproline hydroxyproline (Hyp) and trace elements of bone so as to prevent and treat bone loss.

AIM To study the relationship between hepatic fibrosis and osteoporosis and to determine the preventive effects of Glycyrrhizin on bone loss in mice. METHOD Forty PCR Mice were randomly divided into 4 groups. Group A mice were controls; Group B mice were given sc injection of 40% CCl 4 10 ml?kg -1 once per 5 days as fibrosis model group; Group C were given orally colchicine of 0 01 mg?kg -1 plus CCl 4 sc, Group D were given Glycyrrhizin(GL) of 100 mg?kg -1 orally plus CCl 4 sc. The four groups were treated for 42 days. The liver injury indexes were measured and the mineral elements and Hydroxyproline of the femur were determined. RESULT Compared with group A, the serum enzymes of alanine aminotransferase (ALT), aspartic acid aminotransferase (AST) were markedly increased and serum albumin (Alb) and A/G(Alb/(total protein Alb) were decreased significantly in group B whose liver slides also showed typical liver cirrhosis. The dried weight of femur in the cirrhosis mice was markedly reduced and the bone Calcium content and bone Hydroxyproline content were also significantly decreased in group B. Bone copper and bone magnesium were increased in group B. In group D, GL inhibited markedly the decrease of the serum enzymes and increased Calcium content and Hydroxyproline content of the bone compared with group B. The bone mass loss was prevented effectively by Glycyrrhizin. CONCLUSION The bone mass was lost in mice with chronic hepatic injury induced by CCl 4 and Glycyrrhizin can prevent bone loss which was accompanied by chronic hepatic injury in mice.

AIM: To study the time dose effects of liver damnification induced by CCl 4 in rats. METHODS: The SD rats were given sc injection 60% CCl 4 twice a week to induced liver damage. After the first week, one proportion animals were killed. The contents of serum alanine aminotransferase (ALT), aspartic acid aminotransferase (ALT), hyaluronic Acid (HA), total protein (TP) and albumin (Alb) were investigated, and the thymus, liver, spleen, kidney, and the adrend gland were weighed. On the other hand, the liver tissue was studied with histopathological to observe the degrees of inflammatory activity and fibrous hyperplasia. In the coming the third, fifth, seventh, ninth week, the different proportion animals were done as the above. RESULTS: In the first week, the level of serum ALT were significantly increased; in the third week, the hepatic cells were occurred fattiness denaturalization; in the fifth week, the histopathological showed the necrotic hepatic cells obviously; in the seventh week, the histopathological displayed that the liver turned into fibrotic; and in the ninth week, the liver changed into hepaticfibrosis induced by CCl 4. CONCLUSION: The injection (sc) of 60% CCl 4 will cause diverse hepatic injury with the dissimilar durative time in rats.

AIM:To study the (rat's) osteoporosis induced by long-term administration of prednisone,and investigate the prophylactic effects of Salvia miltiorrhiza Beg in male rats. METHODS: Twenty-four SD rats were randomly divided into four groups such as control group,prednisone group and Danshen(Salvia miltiorrhiza Bge) group,with 8 rats per group.control group was treated with normal saline,other groups with prednisone at dose of(2.7) mg/kg first,and then prednisone group with normal saline group with Salvia miltiorrhiza Bge at dose of 5.0 g/kg,respectively,once a day for 12 weeks.At the experimental endpoint,bone histomorphometric analysis of thighbone were performed in undecalcified sections,the contet of Ca~(2+) and oxyproline hydroxyproline of ulnar bone were to be measured.length and width of the thighbone were to be tested. RESULTS: Bone histomorphometric parameters showed bone loss was significant to prednisone group(P

AIM: To establish the hyperlipemic rat model by long-term gastric perfusion of intralipid and investigate the effects of hyperlipidemia on bone. METHODS: Eighteen SD rats were randomly divided into control group (C) and high-fat-diet group (HDF), with 9 rats per group. Rats of C group were treated orally with normal saline, and rats in HDF group were oral gavage of intralipid at dose of 5.0 mL/kg, once a day for 20 weeks. At the end of experiment, their serum levels of lipid were measured. Bone histomorphometric analysis of thighbone was performed in undecalcified sections, and the length and width of ulnar were measured. RESULTS: Compared with the C group, serum TC and low density lipoproteins (LDL) were increased (P

AIM: To study the effects of Ginseng fiber on hepatic fibrosis induced by CCl 4 in mice. METHODS: Forty PCR Mice were randomly divided into 4 the control group, the NS group, the colchicine group and the Ginseng fiber groups. Rats in control group were treated by daily oral gavage with vehicle. Rats in other three groups were given SC injection of 40% CCl 4 10 ml?kg -1 and treated by either daily oral gavage with vehicle, or colchicine at 0.1 ml?kg -1, or Ginseng fiber at 10 g?kg -1 for 42 d. The liver injury indexes were measured. RESULTS: Compared with control group, the serum enzymes of alanine aminotransferase (ALT), aspartic acid aminotransferase(AST) were markedly increased but serum albumin (Alb) and A/G were decreased distinctly in CCl 4 group whose liver slides also showed typical liver cirrhosis. Ginseng fiber markedly prevented CCl 4-induced increases in liver weight, serum ALT and TP. Ginseng fiber lightened the hepatic pathological necrosis resulting from CCl 4. The preventive effect of Ginseng fiber was identical to that of colchicine. CONCLUSION: Ginseng fiber can prevent hepatic fibrosis induced by CCl 4 in mice.

AIM: To study the relationship between hepatic fibrosis and osteoporosis, and observe the preventive effects of ginseng fiber on bone loss. METHODS: Forty PCR mice were randomly divided into 4 groups. The mice in control group were treated by daily oral gavage with vehicle. The mice in other three groups were given SC injection of 40% CCl_4 10 ml?kg -1 and treated by either daily oral gavage with vehicle, colchicine, or ginsen hair for 42 d. The liver injury indexes were measured and the mineral elements and hydroxyproline of femur were determined. RESULTS: Compared with the control group, the serum enzyme activity of alanine aminotransferase (ALT), aspartic acid aminotransferase (AST) markedly increased and serum albumin (Alb) and A/G distinctly decreased in CCl_4 group whose liver slides also showed typical liver cirrhosis. The dried weight of femur markedly reduced and the bone calcium content and bone hydroxyproline content significantly decreased in CCl_4 group. Bone copper and bone magnesium increased in CCl_4 group. Ginseng fiber markedly decreased the serum enzyme activity of ALT and increased the bone calcium content and bone hydroxyproline content. The preventive effects of ginseng fiber was similar to that of colchicine. CONCLUSION: The bone mass is lost in mice with chronic hepatic injury induced by CCl_4. Ginseng fiber can prevent bone loss and hepatic fibrosis induced by CCl_4 in mice.

AIM: To study the effects of epimedium pubescens flavonoids (EF) on the skeleton in ovariectomized rats. METHODS: Forty 4.5-month-old Sprague-Dawley female rats were randomly divided into 4 groups. Rats in sham group were sham-operated and treated by daily oral gavage with vehicle. Rats in other three groups were bilaterally ovariectomized (OVX) and treated by either daily oral gavage with vehicle, or diethylstilbestrol (DES) at 22.5 ?g?kg~ -1?d~ -1, or EF at 300 mg?kg~ -1?d~ -1 for 90 days. Bone histomorphometric analysis of the proximal tibial metaphysis (PTM), fifth lumbar vertebrae (LV5) and tibial shaft (Tx) was performed in undecalcified sections. The left femur was collected to determine bone weight, contents of calcium (Ca) , phosphorus (P ) and hydroxyproline. The uterine weight and the uterine luminal epithelial thickness (ULET) were determined. RESULTS: A significant increase in contents of Ca and P of femur was found in EF group. A tendency of increase was found in %Tb.Ar of PTM, but no significant change was found in bone histomorphometric parameters of LV5 and Tx in EF group. EF had no effect on uterine weight and ULET. CONCLUSION: EF can prevent OVX-induced bone mineral loss of femur, but does not prevent bone loss of PTM and LV5.