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1.
Yi Chuan ; 41(11): 1009-1022, 2019 Nov 20.
Article Zh | MEDLINE | ID: mdl-31735704

Quinoa (Chenopodium quinoa Willd, 2n=36) is an annual crop belonging to the genus Chenopodium in Amaranthaceae, and originated from the Titicaca lake of the Andes region in the South America. Due to its high nutritional values and adapted tolerance to various abiotic stresses, quinoa was considered a crop with high application potential, but improvement is still needed for the development and utilization of crop. Therefore it attains the attention of biological scientists and breeders. In recent years, with the pursuit of better health and higher quality of life, the consuming of quinoa grains has increased dramatically. Cultivation and breeding of quinoa has received more attention to ensure global food security as well. On the basis of our multiple years of experience in quinoa germplasm collection which were evolution from Andes region, the focus of this review is on the nutritional quality and application of quinoa, species origination and evolution, domestication by human, and genetic breeding progress and trends, so that a better understanding of quinoa values can be achieved. We aim to help increase farmers' income in poverty areas and ensure national food security by promoting development of quinoa industry in China.


Chenopodium quinoa , Domestication , Plant Breeding , Nutritive Value
2.
Exp Ther Med ; 14(2): 1568-1576, 2017 Aug.
Article En | MEDLINE | ID: mdl-28810622

It is acknowledged that contrast-induced nephropathy (CIN) is a common cause of acute renal insufficiency after cardiac catheterization and affects mortality and morbidity. To date, it is unknown whether oral N-acetylcysteine (NAC) is able to prevent contrast-induced nephropathy (CIN) in patients undergoing coronary angioplasty. A meta-analysis of randomized controlled trials was performed to assess the effects of NAC in the prevention of CIN in patients following coronary angioplasty. A total of 19 studies published prior to January 2015 that investigated the efficacy of oral NAC for the prevention of CIN were collected from Medline, Cochrane and Embase databases and conference proceedings from cardiology and nephrology meetings. The primary point of investigation was CIN, and the secondary points were renal failure requiring dialysis, mortality and length of hospitalization. The meta-analysis was performed using fixed- or random-effect models according to heterogeneity. Up to January 2015, 19 randomized placebo-controlled clinical trials met the inclusion criteria for the meta-analysis, including 4,514 patients. The pooled data showed that oral NAC did not reduce the CIN incidence [relative risk 0.84, 95% confidence interval (CI) 0.65-1.10; P=0.20], without heterogeneity among trials (I2=29%). Thus, the present meta-analysis suggests that oral NAC therapy is not effective as an alternative treatment to prevent CIN in patients following angioplasty. Further high quality randomized clinical controlled trials are required to confirm the usage and availability of this treatment.

3.
Arch Virol ; 161(1): 219-22, 2016 Jan.
Article En | MEDLINE | ID: mdl-26497175

The first complete genome sequence of calla lily chlorotic spot virus (CCSV) from Lijiang in northwestern Yunnan Province was obtained using RT-PCR with designed primers. The genome of CCSV isolate LJ-1-Yunnan is tripartite. The small (S) RNA is 3182 nucleotides (nt) in length and encodes a nonstructural protein (NSs, 1383 nt) and a nuclear nucleocapsid (N, 834 nt), separated by an 836-nt intergenic region (IGR). The medium (M) RNA is 4749 nt in length and encodes a nonstructural movement protein (NSm, 930 nt) and a glycoprotein (GnGc, 3,372 nt), also separated by a 349-nt IGR. The large (L) RNA is 8912 nt in length and encodes a predicted RNA-dependent RNA polymerase (RdRp, 8652 nt). The nucleotide sequences of the three viral RNA segments are 92-94 % identical to the published CCSV genome sequence, and the amino acid sequences of the encoded proteins are 96-98 % identical. However, the IGRs of the S and M RNAs are less similar, with 86 and 72 % identity, respectively. Genome sequence comparisons and phylogenetic analysis indicate that the Lijiang CCSV isolate is a unique tospovirus isolate that differs from CCSV isolates in other geographic regions.


Genome, Viral , Nicotiana/virology , Plant Diseases/virology , Tospovirus/isolation & purification , Base Sequence , China , Molecular Sequence Data , Phylogeny , Tospovirus/classification , Tospovirus/genetics , Viral Proteins/genetics
4.
Scand J Clin Lab Invest ; 75(1): 85-91, 2015 Jan.
Article En | MEDLINE | ID: mdl-25465803

BACKGROUND: Recent reports have shown that miR-145 concentration correlates with infarct size. In this paper, we attempt to predict heart failure and cardiovascular death after acute myocardial infarction using circulating miR-145 concentration. METHODS: We assessed 246 patients with first ST-segment-elevation myocardial infarction who underwent successful percutaneous coronary intervention. We measured circulating miR-145, N-terminal fragment of the precursor B-type natriuretic peptide, myocardial-band creatine kinase, and cardiac troponin-I concentrations on day 5 after primary percutaneous coronary intervention and assessed their correlations with long-term clinical outcome. RESULTS: During the one-year follow-up period, 72 patients experienced primary composite cardiac events (cardiac death or hospitalization for worsening heart failure). Multivariable Cox proportional hazards analysis indicated that circulating miR-145 (hazard ratio 7.174, 95% confidence interval 4.208-12.229); p < 0.0001) was a significant independent predictor of cardiac events after adjustment for multiple confounders. CONCLUSION: Circulating miR-145 may be a novel biomarker for predicting long-term outcome after acute myocardial infarction.


MicroRNAs/blood , Myocardial Infarction/blood , Aged , Biomarkers/blood , Disease Progression , Female , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Multivariate Analysis , Myocardial Infarction/mortality , Myocardial Infarction/pathology , Myocardial Infarction/therapy , Proportional Hazards Models , Treatment Outcome
5.
Saudi Med J ; 35(9): 945-52, 2014 Sep.
Article En | MEDLINE | ID: mdl-25228175

OBJECTIVES: To investigate the radiosensitizing effects of Radix Angelicae Sinensis-Radix Hedysari (RAS-RH [an ultra-filtration extract]) and its underlying mechanisms in human liver cancer cells H22. METHODS: This study was conducted between September 2010 and August 2012 in the Gansu University of Traditional Chinese Medicine, Lanzhou, China. The groups were assigned as the control group, drug (RAS-RH) group, 12C6+ radiation group, and combination group. The cell counting kit-8 assay, colony formation assay, cell cycle changes, and apoptosis analysis were carried out, and survivin and casepase-9 were evaluated by reverse transcription polymerase chain reaction and Western blot analyses in the 4 groups. RESULTS: The inhibitory effect of RAS-RH on H22 cells was dependent on both concentration and time, RAS-RH was able to enhance the radiosensitivity of H22 cells by increasing cell survival fraction and radiosensitization parameters. Apoptosis and the gap2/mitosis (G2/M) phase transition induced by 12C6+ heavy ion radiation was enhanced by RAS-RH treatment. Irradiation, combined with RAS-RH, decreased survivin expression while increasing casepase-9 expression in H22 cells. CONCLUSION: The RAS-RH increased the radiosensitivity of H22 cells of 12C6+ heavy ion radiation significantly, and its possible mechanism of radiosensitization is to enhance caspase-dependent apoptosis through the down-regulation of survivin, thus, it can be used as an effective radiosensitizer.


Apoptosis/radiation effects , Drugs, Chinese Herbal/therapeutic use , Liver Neoplasms/radiotherapy , Angelica sinensis , Astragalus propinquus , Cell Line, Tumor , Humans , Liver Neoplasms/pathology , Radiation Tolerance
6.
Mol Biol Rep ; 41(8): 4997-5003, 2014 Aug.
Article En | MEDLINE | ID: mdl-24748432

Myocardial infarction (MI) is a serious heart disease. The cardiac cells of patients with MI will die due to lack of blood for a long time. In this study, we aimed to find new targets for MI diagnosis and therapy. We downloaded GSE22229 including 12 blood samples from healthy persons and GSE29111 from Gene Expression Omnibus including 36 blood samples from MI patients. Then we identified differentially expressed genes (DEGs) in patients with MI compared to normal controls with p value < 0.05 and |logFC| > 1. Furthermore, interaction network and sub-network of these of these DEGs were constructed by NetBox. Linker genes were screened in the Global Network database. The degree of linker genes were calculated by igraph package in R language. Gene ontology and kyoto encyclopedia of genes and genomes pathway analysis were performed for DEGs and network modules. A total of 246 DEGs were identified in MI, which were enriched in the immune response. In the interaction network, LCK, CD247, CD3D, FYN, HLA-DRA, IL2, CD8A CD3E, CD4, CD3G had high degree, among which CD3E, CD4, CD3G were DEGs while others were linker genes screened from Global Network database. Genes in the sub-network were also enriched in the immune response pathway. The genes with high degree may be biomarkers for MI diagnosis and therapy.


Biomarkers/metabolism , Gene Expression Regulation/genetics , Myocardial Infarction/genetics , Myocardial Infarction/metabolism , Cluster Analysis , Computational Biology , Gene Expression Profiling , Gene Expression Regulation/immunology , Gene Ontology , Humans , Microarray Analysis , Myocardial Infarction/immunology , Protein Interaction Mapping
7.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 33(2): 220-4, 2013 Feb.
Article Zh | MEDLINE | ID: mdl-23646478

OBJECTIVE: To investigate the effects of the ultra-filtration extract mixture from Hedysarum Polybotrys (UEMHP) on the radiosensitivity of HepG2 cells, and to explore its possible mechanisms. METHODS: The proliferation inhibition effects of UEMHP on HepG2 cells was detected by CCK-8 assay. The colony formation assay was used for the survival fraction (SF) analysis. The distribution of the cell cycle and the apoptosis rate were detected using flow cytometry (FCM). The survivin mRNA expression level was detected using reverse transcription-PCR assay. RESULTS: The inhibition of UEMHP on HepG2 cells was time-and dose-dependent at the concentration ranging between 5 -50 mg/L (P < 0.05). The parameters of the two curve for SF (P < 0.05) showed statistical difference between the irradiation group and the UEMHP irradiation group. UEMHP could inhibit the clone formation of HepG2 cells and enhance the radiosensitivity of HepG2 cells. The results of FCM showed that UEMHP could induce G2/M phase arrest. The apoptosis rate in the UEMHP irradiation group (21.42% +/- 3.74%) was higher than that in the control group (5.35% +/- 0.41%), the only UEMHP group (10.36% +/- 1.75%), or the irradiation group (10.58% +/- 2.01%) (P < 0.01). RT-PCR showed that the survivin mRNA expression level was lower in the UEMHP irradiation group (0.31 +/- 0.02) than in the control group (0.82 +/- 0.06) and the irradiation group (0.58 +/- 0.04) respectively, showing statistical difference (P < 0.01). CONCLUSION: UEMHP can enhance the radiosensitivity of HepG2 cells, and its possible mechanisms might be correlated to down-regulating the survivin mRNA expression and promoting the apoptosis.


Cell Proliferation/drug effects , Cell Proliferation/radiation effects , Drugs, Chinese Herbal/pharmacology , Radiation Tolerance/drug effects , Apoptosis , Hep G2 Cells , Humans , Inhibitor of Apoptosis Proteins/metabolism , Survivin
8.
Acta Pharmacol Sin ; 24(7): 715-8, 2003 Jul.
Article En | MEDLINE | ID: mdl-12852841

AIM: To investigate the pharmacokinetics of loratadine (LOR) and its active metabolite descarboethoxyloratadine (DCL) in healthy Chinese subjects. METHODS: Twenty healthy Chinese male subjects received a single oral dose of LOR 20 mg. A sensitive liquid chromatography-tandem mass spectrometry method (LC/MS/MS) was used for the determination of LOR and DCL in plasma. RESULTS: Mean maximum concentration (C(max)) was found (17+/-14) microg/L for LOR at 1.2 h and (16+/-9) microg/L for DCL at 1.5 h. Mean area under the plasma concentration-time curve from zero to infinity (AUC(0-infinity)) was (47+/-49) microg x h x L(-1) for LOR and (181+/-122) microg x h x L(-1) for DCL, respectively. The apparent elimination half-life (T1/2) of LOR was (6+/-4) h, and that of DCL was (13.4+/-2.6) h. The ratios of AUC(DCL)/AUCLOR ranged from 0.36 to 54.5. CONCLUSION: LOR was rapidly absorbed and transformed to DCL. AUC of the parent drug was extremely variable, while AUC of the active metabolite DCL was moderately variable after an oral dose of LOR to Chinese subjects.


Antipruritics/pharmacokinetics , Loratadine/pharmacokinetics , Piperidines/metabolism , Pyridines/metabolism , Administration, Oral , Adult , Antipruritics/metabolism , Area Under Curve , Asian People , Humans , Loratadine/metabolism , Male
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