1.A new benzamide derivative from rice fermentation of Streptomyces sp. CPCC 202950.
Shan-Shan CHANG ; Ming-Hua CHEN ; Ren-Zhong WANG ; Ye-Xiang WU ; Guo-Hong YANG ; Biao DONG ; Li-Yan YU ; Zeng-Ping GAO ; Shu-Yi SI
China Journal of Chinese Materia Medica 2017;42(11):2097-2101
Eight compounds were isolated from the rice fermentation of Streptomyces sp. CPCC 202950 by a combination of various chromatographic techniques including column chromatography over silica, Sephadex LH-20, flash C₁₈, and reversed-phase HPLC. Their structures were identified as 3-[(3'-amino-3'-oxoprop-1'-en-2'-yl)oxy]benzamide (1), m-hydroxybenzamide (2), leptosphaepin (3), 5-methyluracil (4), feruloylamide (5), p-hydroxyphenylacetoamide (6), vanillamide (7), cyclo (L-val-L-ala) (8). Among them, 1 was a new benzamide analogue, and 2 was a new natural product. In the preliminary assays, none of the compounds 1-8 exhibited obvious inhibition of HIV-1 protease activity, and toxic with the Hela, HepG2, and U2OS cells. (IC₅₀ > 10 μmol•L⁻¹).
2.Effects of Maternal Marginal Iodine Deficiency on Interactions between Cerebellar Bergmann Glia Cells and Purkinje Cells in Rat Offspring.
Ye YU ; Jing DONG ; Yuan WANG ; Yi WANG ; Hui MIN ; Zhong Yan SHAN ; Wei Ping TENG ; Jie CHEN
Biomedical and Environmental Sciences 2017;30(12):932-937
Iodine deficiency (ID) during early pregnancy has an adverse effect on children's psychomotor and motor function but the mechanism has not been clarified. Therefore, our aim was to study the effect of maternal marginal ID on cerebellar neurodevelopment and the underlying mechanism. After obtaining marginal ID rats, we examined interactions between Bergmann glia cells (BGs) and Purkinje cells (PCs) using immunofluorescence and expression of the glutamate transporter and receptor by western blot. Our results showed that marginal ID reduced the number of contacted points between BGs and PCs, and disturbed expression of the glutamate transporter and receptor. Our results support the hypothesis that marginal ID inhibits interactions of BGs-PCs, which may be involved in abnormal regulation of the glutamate transporter and receptor.
3.Estimation Study of New Cancer Cases and Deaths in Wuwei, Hexi Corridor Region, China, 2018.
Bo Yu CAO ; Cheng Yun LI ; Feng Lan XU ; Xiao Qin LIU ; Yan Xu YANG ; Jing LI ; Cai Yun GAO ; You Ming RONG ; Rong Cheng LI ; Ya Li LI ; Shan ZHENG ; Ya Na BAI ; Yan Cheng YE
Biomedical and Environmental Sciences 2017;30(11):829-833
Population-based cancer registration data were collected to estimate the cancer incidence and mortality in Wuwei, Hexi Corridor Region, China in 2018. We used the 2011-2013 data to predict the number of new cases and deaths in 2018 and the 2003-2013 data to analyze trends in cancer incidence and mortality. The goal is to enable cancer prevention and control directions. Our results indicated that stomach cancer is the most common cancer. For all cancers combined, the incidence and mortality rates showed significantly increasing trends (+2.63% per year; P < 0.05 and +1.9% per year; P < 0.05). This study revealed a significant cancer burden among the population of this area. Cancer screening and prevention should be performed after an epidemiological study of the cause of the cancer is completed.
China
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Female
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Humans
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Incidence
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Male
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Neoplasms
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classification
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epidemiology
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mortality
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Population Surveillance
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Registries
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statistics & numerical data
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Rural Population
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Urban Population
4.Comparison of chemical constituents in different parts of Gardenia jasminoides based on multiple wavelength HPLC-DAD.
Ri-Chuan XIAO ; Guang-Ming LUO ; Li-Hua DONG ; Yu-Ye ZHU ; Ji-Xiao ZHU ; Feng-Bo ZHANG ; Shan-Na WU
China Journal of Chinese Materia Medica 2017;42(23):4636-4640
Seven compounds(deacetylasperulasidic acid methyl ester, gardenoside, chlorogenic acid, geniposide, crocin-Ⅰ, crocin-Ⅱ, chikusetsu saponin Ⅳa)were determined simultaneously by multiple wavelength HPLC with diode array detector(DAD) in different parts of Gardenia jasminoides. The results showed that these components in different parts of G. jasminoides had a different distribution, and there was a large difference in content of each component. Geniposide was mainly distributed in fruits and leaves; chikusetsu saponin Ⅳa was mainly distributed in roots and stems; crocus glycosides existed mainly in fruits; chlorogenic acid had a higher distribution in leaves and stems; gardenoside had a higher distribution in leaves and roots, while ceacetylasperulasidic acid methyl ester had a higher distribution in roots and stems. Based on the analysis of the chemical composition and content difference in different parts of G. jasminoides, the basis for the comprehensive utilization and quality evaluation of resources of G. jasminoides was provided.
5.Purifying process of gynostemma pentaphyllum saponins based on "adjoint marker" online control technology and identification of their compositions by UPLC-QTOF-MS.
Dong-Dong FAN ; Yan-Hui KUANG ; Li-Hua DONG ; Xiao YE ; Liang-Mian CHEN ; Dong ZHANG ; Zhen-Shan MA ; Jin-Yu WANG ; Jing-Jing ZHU ; Zhi-Min WANG ; De-Qin WANG ; Chu-Yuan LI
China Journal of Chinese Materia Medica 2017;42(7):1331-1337
To optimize the purification process of gynostemma pentaphyllum saponins (GPS) based on "adjoint marker" online control technology with GPS as the testing index. UPLC-QTOF-MS technology was used for qualitative analysis. "Adjoint marker" online control results showed that the end point of load sample was that the UV absorbance of effluent liquid was equal to half of that of load sample solution, and the absorbance was basically stable when the end point was stable. In UPLC-QTOF-MS qualitative analysis, 16 saponins were identified from GPS, including 13 known gynostemma saponins and 3 new saponins. This optimized method was proved to be simple, scientific, reasonable, easy for online determination, real-time record, and can be better applied to the mass production and automation of production. The results of qualitative analysis indicated that the "adjoint marker" online control technology can well retain main efficacy components of medicinal materials, and provide analysis tools for the process control and quality traceability.
6.Value of DAPK Gene Methylation Patterns in the Diagnosis of Leukemia.
Song-Shan YE ; Xian-Juan LIU ; Bing-Yu MAO ; Lei YANG ; Geng QIU
Journal of Experimental Hematology 2016;24(3):687-692
OBJECTIVETo screen the differential methylation patterns of tumor suppressor gene DAPK and evaluate its value as a biomarker for the diagnosis of leukemia.
METHODSThe methylation status of DAPK gene promoter's CpG island was analyzed in the genomes of normal human white blood cells and HL-60, U937 and Jurkat cell lines by bisulfite sequencing PCR (BSP). The effectiveness of differential methylation patterns of DAPK gene for diagnosis of leukemia was verified in the leukemia cell lines and peripheral blood samples by methylation specific PCR (MSP).
RESULTSThe methylation pattern of DAPK gene in different cell genomes displayed that the degree of unmethylation in normal cell genome was higher than that of leukemia cell lines. The differential CpG sites were found and could be used to differentiate HL-60 and the other 3 cell lines by MSP. Meanwhile, the differential methylation patterns in clinical specimens could distinguish acute non-lymphocytic leukemia (ANLL) and other types of leukemia by MSP. The diagnostic sensitivity, specificity and accuracy were 59.1%, 100% and 82.7% respectively. No relationship was found between MSP diagnosis results and clinical pathological typing.
CONCLUSIONThe differential methylation patterns of DAPK gene as potential tumor biomarker for diagnosis of leukemia can enrich the means of diagnosis of leukemia, provide idea and basis for finding all kinds of tumor's DNA methylation biomarkers in the future.
Biomarkers, Tumor ; genetics ; CpG Islands ; DNA Methylation ; Death-Associated Protein Kinases ; genetics ; HL-60 Cells ; Humans ; Jurkat Cells ; Leukemia ; diagnosis ; genetics ; Polymerase Chain Reaction ; Promoter Regions, Genetic
7.Improvement and Evaluation on Bisulfite Modification of DNA for DNA Methylation Detection.
Song-Shan YE ; Xian-Juan LIU ; Jun-Ran HOU ; Bing-Yu MAO ; Geng QIU
Journal of Experimental Hematology 2016;24(2):611-615
OBJECTIVETo establish a rapid and convenient method of DNA modification by bisulfite sodium for the detection of DNA methylation.
METHODSThrough increasing the bisulfite sodium concentration and the temperature of treatment, cutting down the modification time, besides using glassmilk to adsorb the DNA in the purification and recovery, to improve the methods of DNA modification. Efficiency of cytosine converted to thymine in MAGE-A3 gene and DAP-K gene fragments were analyzed by bisulfite sequencing PCR in order to evaluate the DNA modification effect among the improved method, traditional method and kit method.
RESULTSThe operating time of test was shortened to about 3 hours by the improved method; conversion rate of unmethylated cytosine to thymine was over 99%; compared with the traditional method and kit method, there was no significant difference (χ(2) = 0.0564, P > 0.05); the improved method was only for the unmethylated cytosine conversion modification, and there was no significant difference in process of methylated cytosine converted to thymine comparing with the traditional method (χ(2) = 0.0149, P > 0.05).
CONCLUSIONThe improved method has high efficiency of DNA modification and has no significant effect on excessive modification;meanwhile, it has many advantages such as time-saving and easy to operate etc.
Cytosine ; chemistry ; DNA ; chemistry ; DNA Methylation ; Polymerase Chain Reaction ; Sulfites ; chemistry ; Thymine ; chemistry
8.Observation of low-dose HA/HAA regimen as induction chemotherapy on elderly patients with acute myeloid leukemia.
Dijiong WU ; Baodong YE ; Jianping SHEN ; Yiping SHEN ; Shengyun LIN ; Zhiping HU ; Qinghong YU ; Zhiyin ZHENG ; Laijun PENG ; Shan LIU ; Conghua JI ; Yunfei LUO ; Xiaowen WEN ; Keding SHAO ; Yu ZHANG ; Yanting GAO ; Dan CHEN ; Yuhong ZHOU
Chinese Journal of Hematology 2014;35(3):256-259
9.The potential effects of linalool on enantioselective skin permeation of norgestrel.
Yi RONG ; Wen-Ying YU ; Xia GUO ; Shan-Shan ZENG ; Zheng-Rong SHEN ; Su ZENG ; Jin-Cui YE
Acta Pharmaceutica Sinica 2014;49(8):1175-1180
The purpose of this study is to investigate the enantioselectivity of norgestrel (NG) transdermal permeation and the potential influence of linalool and lipids on the enantioselectivity. In vitro skin permeation studies of NG across the excised rat skins were performed with Valia-Chien diffusion cells, and the permeation samples were analyzed by enantioselective HPLC. The possible enantioselective permeation of NG across intact rat back skin and lipids extracted rat back skin and the influence of linalool were evaluated. The skin permeation rate of dl-NG was two times higher than that of l-NG when donor solutions (EtOH/H2O 2 : 8, v/v) containing l-NG or dl-NG. It may be mainly attributed to the solubility discrepancy between enantiomer and racemate. The enantioselective permeation of dl-NG across intact rat skin was observed when the donor solutions containing dl-linalool. The permeation flux of l-NG was 22% higher than that of d-NG. But interestingly, the enantioselective permeation of dl-NG disappeared under the same experimental condition except that the lipid extracted rat skin was used. Attenuated total reflection-fourier transform infrared spectroscopy analysis of stratum corneum showed that the wave number for asymmetric CH2 stretching vibrations of lipids treated with dl-linalool was greater than that of the control. The results indicated that the enantioselective permeation of NG may be contributed by the interaction between dl-linalool and lipids. More than half of lipids were composed of ceramides. The stereospecific interaction maybe existed among chiral enhancer (linalool), lipids (ceramides) and/or chiral drugs (NG).
Administration, Cutaneous
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Animals
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Lipids
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pharmacology
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Monoterpenes
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pharmacology
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Norgestrel
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pharmacokinetics
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Rats
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Skin Absorption
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drug effects
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Spectroscopy, Fourier Transform Infrared
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Stereoisomerism
10.Effect of FGF-21 on learning and memory ability and antioxidant capacity in brain tissue of D-galactose-induced aging mice.
Yin-Hang YU ; Gui-Ping REN ; Yao-Nan LIU ; Su-Su QU ; Fu-Liang BAI ; Tong ZHANG ; Wen-Fei WANG ; Gui-You TIAN ; Xian-Long YE ; De-Shan LI
Acta Pharmaceutica Sinica 2014;49(7):1000-1006
This study aims to investigate the effects of fibroblast growth factor 21 (FGF-21) on learning and memory abilities and antioxidant capacity of D-galactose-induced aging mice. Kunming mice (37.1 +/- 0.62) g were randomly divided into normal control group, model group and FGF-21 high, medium and low dose groups (n = 8). Each group was injected in cervical part subcutaneously with D-galactose 180 mg x kg(-1) x d(-1) once a day for 8 weeks. At the same time, FGF-21-treated mice were administered with FGF-21 by giving subcutaneous injection in cervical part at the daily doses of 5, 2 and 1 mg x kg(-1) x d(-1). The normal control group was given with normal saline by subcutaneous injection in cervical part. At seventh week of the experiment, the learning and memory abilities of mice were determined by water maze and jumping stand tests. At the end of the experiment, the mice were sacrificed and the cells damage of hippocampus was observed by HE staining in each group. Reactive oxygen species (ROS), malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT) and total antioxidant capacity (T-AOC) in the brain of mice were determined. The results showed that different doses of FGF-21 could reduce the time reaching the end (P < 0.01 or P < 0.05) and the number of touching blind side (P < 0.01 or P < 0.05) in the water maze comparing with the model group. It could also prolong the latency time (P < 0.05) and decrease the number of errors (P < 0.01 or P < 0.05) in the step down test. The result of HE staining showed that FGF-21 could significantly reduce brain cell damage in the hippocampus. The ROS and MDA levels of three different doses FGF-21 treatment group reduced significantly than that of the model group [(5.58 +/- 1.07), (7.78 +/- 1.92), (9.03 +/- 1.77) vs (12.75 +/- 2.02) pmol (DCF) x min(-1) x mg(-1), P < 0.01 or P < 0.05], [(2.92 +/- 0.71), (4.21 +/- 0.81), (4.41 +/- 0.97) vs (5.62 +/- 0.63) nmol x mg(-1) (protein), P < 0.01]. Comparing with the model group, the activities of SOD, GPx, CAT and T-AOC of the three different doses FGF-21 treatment groups were also improved in a dose-dependent manner. This study demonstrates that FGF-21 can ameliorate learning and memory abilities of D-galactose induced aging mice, improve the antioxidant abilities in brain tissue and delay brain aging. This finding provides a theoretical support for clinical application of FGF-21 as a novel therapeutics for preventing aging.
Aging
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drug effects
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Animals
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Antioxidants
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metabolism
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Brain
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drug effects
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Catalase
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metabolism
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Fibroblast Growth Factors
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pharmacology
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Galactose
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Glutathione Peroxidase
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metabolism
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Hippocampus
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drug effects
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Malondialdehyde
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metabolism
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Maze Learning
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drug effects
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Memory
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drug effects
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Mice
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Superoxide Dismutase
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metabolism

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