ABSTRACT
The ethyl acetate part of the alcoholic extract of Cordia dichotoma fruits was purified by a combination of normal-phase silica gel column chromatography, Sephadex LH-20 gel column chromatography and semi-preparative HPLC, and the structure was identified by modern spectroscopic techniques (UV, IR, MS, NMR). A total of 10 compounds were isolated and identified as cordilide (1), (S)-2-hydroxy-3-(4′-hydroxyphenyl) propanoic acid (2), vanillic acid (3), p-coumaric acid (4), 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one (5), benzoic acid (6), p-hydroxypropiophenone (7), p-hydroxyacetophenone (8), 5′-methoxyevofolin B (9) and vanillin (10). Among them, compound 1 is a pair of new phenylpropanoid enantiomers, and compounds 3, 6, 8 and 9 were isolated for the first time from the genus.
ABSTRACT
Silica gel column chromatography, reversed phase C18 column chromatography, Sephadex LH-20 gel column chromatography, high performance liquid chromatography and medium performance semi preparative liquid chromatography were performed to separate and purify the chemical constituents of Hypericum lagarocladum N. Robson. Spectroscopic methods such as MS and NMR combined with physicochemical properties were applied in identifying the structures of the isolated compounds. A total of 11 compounds were isolated and identified as hyperlagarone A (1), hyperpatulone E (2), hyperbeanol G (3), uralione D (4), tomoeone F (5), pyramidatone A (6), tomoeone A (7), tomoeone B (8), hyperbeanol C (9), hyperbeanol A (10), and hypercohone G (11), respectively. Compound 1 is a new polycyclic polyprenylated acylphloroglucinol derivative, and compounds 2-11 are isolated from this plant for the first time. 11 compounds were tested for glucose uptake in L6 cells, and the results showed that compounds 7 and 8 had significant effect on glucose uptake.
ABSTRACT
Objective To investigate the value of diffusion weighted imaging combined with contrast-enhanced MRI(CE-MRI)in activity of sacroiliitis of patients with ankylosing spondylitis(AS).Methods The AS patients diagnosed in Beijing Jishuitan Hospital were selected as the experimental group,and healthy volunteers were selected as the control group.The AS group was divided into the active group and the stable group according to the clinical diagnostic criteria.All subjects were examined with both MRI plain scan and CE-MRI of bilateral sacroiliac joints.ROIs were drawn in the lesion region and the ADC values and signal intensity enhancement rate(△SI)were recorded.△SI and ADC value among the active AS group,chronic group and control group was compared and analyzed.The clinical diagnostic criteria was regarded as the gold standard for the active AS group and the chronic group.The ROC curve was used to evaluate the value of ADC,△SI,ADC, and ADC combined with △SI can detect the efficiency of AS activity.Results Ninety-eight AS patients were enrolled in this study,including 63 cases in the active AS group,35 cases in the chronic AS group,and 23 cases in the control group.The ADC values of the active group,the chronic group and the control group were(1.35 ±0.17)×10-3mm2/s,(1.07±0.20)×10-3mm2/s,(0.36±0.14)×10-3mm2/s,respectively,and ΔSI values were (2.42±0.80)%,(1.28 ± 0.34)% and(0.74 ± 0.22)%.There were significant differences in ΔSI and ADC values among the three groups(F=216.559,56.522.P=0.000).When ADC values were used to assess the activity of AS,the area under the ROC curve was 0.809 and the optimal diagnostic threshold was 1.35×10-3 mm2/s,the sensitivity and specificity of AS activity were 57.1% and 94.3%.When ΔSI values were used,the area under the ROC curve was 0.837 and the sensitivity and specificity were 71.40% and 97.10% with the optimal diagnostic threshold of 1.79%.When ΔSI values were combined with the ADC values,the area was 0.963 and the sensitivity and specificity were 74.6% and 94.3%.Conclusion In assessment of the activity of AS,DWI combined with CE-MRI is most valuable.
ABSTRACT
Objective To investigate the value of diffusion weighted imaging combined with contrast-enhanced MRI(CE-MRI)in activity of sacroiliitis of patients with ankylosing spondylitis(AS).Methods The AS patients diagnosed in Beijing Jishuitan Hospital were selected as the experimental group,and healthy volunteers were selected as the control group.The AS group was divided into the active group and the stable group according to the clinical diagnostic criteria.All subjects were examined with both MRI plain scan and CE-MRI of bilateral sacroiliac joints.ROIs were drawn in the lesion region and the ADC values and signal intensity enhancement rate(△SI)were recorded.△SI and ADC value among the active AS group,chronic group and control group was compared and analyzed.The clinical diagnostic criteria was regarded as the gold standard for the active AS group and the chronic group.The ROC curve was used to evaluate the value of ADC,△SI,ADC, and ADC combined with △SI can detect the efficiency of AS activity.Results Ninety-eight AS patients were enrolled in this study,including 63 cases in the active AS group,35 cases in the chronic AS group,and 23 cases in the control group.The ADC values of the active group,the chronic group and the control group were(1.35 ±0.17)×10-3mm2/s,(1.07±0.20)×10-3mm2/s,(0.36±0.14)×10-3mm2/s,respectively,and ΔSI values were (2.42±0.80)%,(1.28 ± 0.34)% and(0.74 ± 0.22)%.There were significant differences in ΔSI and ADC values among the three groups(F=216.559,56.522.P=0.000).When ADC values were used to assess the activity of AS,the area under the ROC curve was 0.809 and the optimal diagnostic threshold was 1.35×10-3 mm2/s,the sensitivity and specificity of AS activity were 57.1% and 94.3%.When ΔSI values were used,the area under the ROC curve was 0.837 and the sensitivity and specificity were 71.40% and 97.10% with the optimal diagnostic threshold of 1.79%.When ΔSI values were combined with the ADC values,the area was 0.963 and the sensitivity and specificity were 74.6% and 94.3%.Conclusion In assessment of the activity of AS,DWI combined with CE-MRI is most valuable.
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effect of salvianolic acid B (SAB) on the proliferation of human embryonic lung fibroblast MRC-5, and the secretion of procollagen I and endogenous transforming growth factor-beta1, (TGF-beta1).</p><p><b>METHODS</b>The MRC-5 cells were randomly divided into four groups as follows: the control group: cells cultured with DMEM but with no TGF-beta1, or SAB; the TGF-beta1, group: cell cultured with 10 ng/mL TGF-beta1; the SAB1 group: cell cultured with medium with 10 ng/mL TGF-beta1 and 1 pmol/L SAB; the SAB2 group: cell cultured with medium with 10 ng/mL TGF-beta1, and 10 pmol/L SAB. The proliferation of cells was assayed by MTT incorporation. The concentration of amino-terminal propeptide of type I procollagen (PINP), a marker of collagen synthesis, was measured by radioimmunoassay. The endogenous TGF-beta1, levels were measured using ELISA.</p><p><b>RESULTS</b>The optical density, procollagen I contents, and endogenous TGF-beta1, levels significantly increased when compared with those of the control group (P<0.05). Compared with the TGF-beta1, group, the optical density was obviously lowered, the procollagen I contents and endogenous TGF-beta1, levels significantly decreased in the SAB1 group and the SAB2 group, and better in the SAB2 group, showing statistical difference (P<0.05).</p><p><b>CONCLUSIONS</b>SAB could inhibit the proliferation of MRC-5 cells induced by TGF-beta1 and attenuate the roles of secreting collagen and endogenous TGF-beta1. It had the potential of postponing or delaying the progressive developing of pulmonary fibrosis.</p>
Subject(s)
Humans , Benzofurans , Pharmacology , Cell Proliferation , Cells, Cultured , Collagen Type I , Metabolism , Fibroblasts , Cell Biology , Lung , Cell Biology , Embryology , Transforming Growth Factor beta1 , PharmacologyABSTRACT
Objective To investigate the influence of iodine excess on expression of TRAIl/TRAIL-sR1 in NOD and Balb/c mice and to study the effect of TRAIl/TRAIL-sR1 on the pathogenesis of experimental autoimmune thyroiditis(EAT). Methods Both Balb/c and NOD mice were divided randomly into control and iodine excess group by feeding with water containing no NaI or 0.05% Nal. The mice were sacrificed after 8 weeks. TRAIL and TRAIL-sR1 mRNA levels were detected by RT-PCR. The function, morphology and apoptosis of thyroids were also observed by ELISA and Tunnel stain. Results Treated by HI, enlarged follicles and flattened epithelium by accumulation of colloid were found in thyroids of both NOD and Balb/c mice. But significant lymphoid cell infiltration and local fibrosis were only found in thyroids of NOD HI group. The relative weight of thyroids of NOD mice in HI group[(104.8±14.5)mg/kg]was heavier than that of control group [(71.8±20.4)mg/kg]. The level of TT4 declined in HI group[(30.77±3.59)mmol/L]compared with control group[(36.43±2.66)mmol/L], meanwhile, the level of TSH was higher in HI group[(6.98±0.66)μg/L]than that in control group [(5.55±0.56)μg/L]. The difference being statistically significant(t=7.773,-9.526,-4.458, all P < 0.05). The relative weight of thyroids of Balb/c mice of HI group[(155.8±20.8)mg/kg]also heavier than that of control group [(105.1±22.0) mg/kg]. The level of TT4 droped in HI group [(19.75±3.32) mmoL/L]was higher than that in control group[(23.46±6.21)mmoL/L], the level of TSH in HI group[(4.14±1.71)μg/L]was higher than that in control group[(3.55±1.41)μg/L], the difference being statistically significant(t=7.554,-7.239,3.140, all P< 0.05). A great deal of apoptotie ceils observed in NOD (3.97±0.91) and Balb/c mice (1.05±0.45) by Tunnel stain were greater than control groups (0.21±0.15, 0.10±0.03), the difference being statistically significant in beth of the two species(t=-7.167,-17.772, both P < 0.05). The apoptosis index of thyroid follicular epithelium in NOD was obviously higher than Balb/c(t=-7.625, P<0.05). The level of TRAIL mRNA did not remarkably change in Balb/c between control group(0.000 59±0.000 39) and HI group(0.001 24±0.000 46, t=-1.940, P>0.05), but it increased apparently in NOD mice HI group(0.018 88±0.005 77) than that of control group(0.009 61± 0.00591, t=-2.71, P<0.05). The level of the expression of TRAIL-sR1 mRNA increased in HI groups of NOD (0.000 53±0.000 15) and Balb/c mice(0.000 42±0.000 09) than that in control groups of NOD(0.000 28± 0.000 05) and Balb/c mice (0.000 17±0.000 06) and the differences were statistically significant between the two species(t=3.050,3.990, all P<0.05). The differences of the expression of TRAIL and TRAIL-sR1 mRNA between the two species were significant(t=-3.37,-4.76, all P<0.05). Conclusions Iodine excess induces colloid goiter in beth species of mice and thyroiditis in NOD mice. The increase of TRAIL and TRAIL-sR1 influenced by iodine excess is one of the molecular bases of follicular epithelium apoptosis and inflammation in thyroids. Genetic factor is a key factor in the pathogenesis of thyroiditis.
ABSTRACT
Undifferentiated and differentiated 3T3-L1 adipocytes were treated with 100 ng/ml tumor necrosis factor-?(TNF-?),and peroxisome proliferator-activated receptor-?2 (PPAR-?2) mRNA expression and adiponectin secretion in cultured cells were measured.The results showed that TNF-?suppressed PPAR-?2 mRNA expression and adiponeetin secretion in 3T3-L1 adipocytes (P