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OBJECTIVE:To study the effects of different drying technologies and slicing on the quality of Tetrastigma hemsley-anum,and optimize the drying methods for T. hemsleyanum. METHODS:2 treatment methods(slicing and no slicing)and 5 dry-ing methods(drying in the shade,drying in the sunlight,hot-air drying,microwave drying and freeze drying)were respectively ad-opted for the T. hemsleyanum root. After drying for 3.5-213.0 h,using the total flavonoids,total polyphenols,polysaccharides andβ-sitosterol as indexes,effects of different drying technologies on the quality of T. hemsleyanum were comparatively analyzed. RE-SULTS:Compared with no slicing,sliced T. hemsleyanum can shorten the drying time and reduce the loss of active ingredients. In the 5 drying methods,freeze drying was the best for keeping the active ingredients in T. hemsleyanum. After drying,the contents of total flavonoids,polysaccharides,total polyphenols and β-sitosterol were 18.5 mg/g,92.7 mg/g,9.19 mg/g and 0.344 mg/g respec-tively,followed by microwave drying,hot-air drying,drying in the shade and drying in the sunlight. The contents of active ingredi-ents had statistical significance by each drying methods (P<0.05 or P<0.01). CONCLUSIONS:Different drying technologies have obvious effects on the quality of T. hemsleyanum. Slicing and hot-air drying at 60 ℃ were suggested as suitable method for T. hemsleyanum in terms of cost,content of active ingredients and practicability.
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Objective To investigate the effects of ISO-1, a selective MIF tautomerase activity inhibitor, on liver metastasis in a BALB/c mouse model of colonic cancer. Methods Micmporous migration assay was used to determine the effect of ISO-1 on the invasion abilities of CT26 cells. Orthotopic transplantation of fresh colonic tumor fragments into the hernial sac of cecum was used in a BALB/c mouse model of eolorectal cancer. Thirty mouse models were divided into three groups and treated respectively with ISO-1 (0. 2 ml, 20 mg/kg), 5% DMSO and NS ( normal sodium) twice a week, iutraperitoneally. After 4 weeks, mice were sacrificed and the whole livers were made into serial slices to detect the occurrence of liver metastasis. Serum MIF tautomerase activities were measured using L-dopachrome methyl ester, ELISA was used to test serum VEGF concentrations. Immunohistochemical staining of CD31 was used for comparing microvascular density (MVD) of tumor tissues. Results 100 μmol/L ISO-1 treatment for 24 hours significantly reduced the average number of the cells penetrating polycarbonates, ( 151 ± 19 ) vs. ( 178 ± 9 ), P<0. 01. Serum MIF tautomerase activities were significantly inhibited after ISO-1 treatment (51% vs. 81%, P <0. 01 ). Compared with DMSO and NS treatment, ISO-1 decreased the occurrence of liver metastasis ( 10% ,60% and 70% ,respectively;x2 = 8. 30, P < 0. 05 ). Also ISO-1 decreased serum VEGF levels ( 15 ± 7 ) pg/ml, ( 63 ± 11 ) pg/ml and ( 67 ± 8 ) pg/ml, respectively; P < 0. 01 and the MVD of tumor tissues (17±4) ,(36±7) and( 38±5) ,respectively; P<0. 01. Conclusion In vitro ISO-1 inhibits the invasion ability of CT26 cells. In vivo ISO-1 reduces the occurrence of liver metastasis, possibly by a mechanism of inhibiting MIF tautomerase activities, down-regulating the expression of VEGF and reducing MVD.
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Objective To determine MIF expression in normal colorectal mucosa,colorectal adenoma and colorectal carcinoma, and the relationship between MIF and the clinical pathologic features of colorectal carcinoma.MethodsMIF expression was determined by immunohistochemical staining ELISA was used to detect the level of MIF in serum samples. Results The percentage of MIF expressing epithelial cells and MIF positive expression intensity were progressively increased in normal colorectal mucosa, colorectal adenoma and colorectal carcinoma. There was significant difference among three groups (P
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0 05). Between the patients with high level of serum HBV-DNA and the ones with low level of serum HBV-DNA, both the quantity and positive rate of HBV-DNA in PBMC had a significant difference (P