1.Analyses of Lp(a) in Serum with Three Methods
Xiaohong CHEN ; Hongying YANG ; Yingfei GAO ; Chengfeng YANG
Journal of Kunming Medical University 1990;0(02):-
Objective To investigate the changes of Lp(a) in serum with three methods.Methods Using three regents to analyze 30 cases Lp(a) in serum.Results The level of 30 cases Lp(a) in serum is different with three methods,P 0.95 and P
2.The elimination of movement artifact in pulse signals.
Yingfei YANG ; Fangming HU ; Weifeng TONG ; Yichu YE
Journal of Biomedical Engineering 2010;27(3):552-555
It is difficult to extract signals under Low Signal Noise Ratio in biomedical signal processing. The elimination of movement artifact is really a bottleneck. A new solution for the movement artifact in pulse signal is proposed in this paper. According to pulse signal features, the signal is decomposed by using wavelet transform firstly. Then empirical mode decomposition (EMD) is applied to the wavelet coefficients in frequency band of useful signals, thus the signal and movement artifact can be distinguished effectively. Furthermore, the effectiveness of the proposed approach is verified by signal-to-noise ratio, energy ratio, cross correlation coefficient and power spectrum. This method can eliminate not only movement artifact, but also baseline wander and high-frequency noise. Thus, it provides an effective approach for the calculation of pulse rate and blood oxygen saturation.
Algorithms
;
Artifacts
;
Humans
;
Pulse
;
Signal Processing, Computer-Assisted
3.To Discuss the Treatment with the Pathogenesis of Weak Yang and Stringy Yin in Golden Chamber in Atherosclerosis
Li MA ; Yingfei YANG ; Xiaoyun TONG
Journal of Zhejiang Chinese Medical University 2017;41(11):855-859
[Objective]To explore the application of the pathogenesis of"weak yang and stringy yin"in the treatment of atherosclerosis. [Methods] Analyze the symptoms and prescriptions of atherosclerosis in the Synopsis of the Golden Chamber, and refer to the literatures on the prescriptions. To describe the concept of atherosclerosis from the "virtual" and "real" two aspects of the pathogenesis of atherosclerosis; access to the literature on the anti-cut Guibao White Liquor Soup, Gualou Xiebai Pinellia Decoction, Guizhi Tang, Guizhi Decoction, Ginseng Decoction, Jizhi Amethyst Decoction, Aconitum Red Stone Pills, Rhubarb Pills and Dazhuai Decoction, and other classic prescriptions of the Golden Chamber. [Results] Although there was no disease of atherosclerosis in Chinese medicine, there were many descriptions of its symptoms and etiology and pathogenesis. "The virtual", "standard" were its main pathogenesis,"Golden Chamber"in the proposed"weak yang and stringy yin" theory, and created a large number of prescriptions, such as Gualou Xiebai white liquor soup, Gualou Xiebai Pinellia Soup, Citrus aurantium Decoction Guizhi Decoction, Guizhi Decoction, Ginseng Decoction, Jizhi Feizhi Decoction, Aconitum Red Stone Pills, Rhubarb Pills and Da Chai Hu Tang. According to the literature, "Golden Chamber" in these prescriptions can be used to treat atherosclerosis. [Conclusion] The general theory of the pathogenesis of"chest palsy"and"weak yang and stringy yin"in the Synopsis of the Golden Chamber is the same as the pathogenesis of atherosclerosis. According to this pathogenesis Zhongjing created a large number of prescriptions, modern pharmacological studies have shown that they can treat atherosclerosis. Therefore, we can extend "weak yang and stringy yin" of the pathogenesis theory to the treatment of atherosclerosis. This treatment is worthy of our further exploration, for the present use, to be effective.
4.An air-liquid interface model of human lung epithelium generated from bronchiolar epithelial cells proliferated using medium containing ROCK kinase inhibitor
Yuanyuan JIA ; Jinxi HE ; Yingfei SUN ; Fei HAN ; Jiali YANG ; Yong LI ; Xiaoming LIU
Chinese Journal of Tissue Engineering Research 2015;(28):4582-4587
BACKGROUND:Primary human lung epithelial cel s are difficult to be isolated and cultured in vitro, which is characterized as limited sources, low cel viability, slow proliferation capacity, and lacking of differentiation capability.
OBJECTIVE:To establish an air-liquid interface model of lung epithelium by in vitro proliferation of human bronchiolar epithelial cel s, which is used for research on function of lung epithelial cel s.
METHODS:Primary human bronchiolar epithelial cel s were isolated using Pronase and DNase I combined digestive methods, and then proliferated using medium containing ROCK kinase inhibitor. The proliferated cel s were used for establishment of the air-liquid interface epithelium model. Cel differentiation was identified using scanning electron microscope, phase contrast microscope and immunofluorescent staining.
RESULTS AND CONCLUSION:The primary human bronchiolar epithelial cel s could be expanded successful y using medium containing ROCK kinase inhibitor, and the basal cel marker Cytokeratin14 was preferential y expressed in the proliferated cel population, indicating that these basal cel s might be the main subpopulation of human lung epithelial stem cel s. Subsequently, the proliferated cel s under the air-liquid interface could differentiate into ciliated cel s and non-ciliated column cel s. The results suggest that the proliferation and differentiation of human bronchiolar epithelial cel s were maintained in the presence of ROCK kinase inhibitor, and the air-liquid interface could promote the differentiation of human bronchiolar epithelial cel s.
5.Identification of novel transcripts and sRNA of Brucella melitensis by RNA-Seq
Yingfei GUO ; Yufei WANG ; Chunli GONG ; Mingjuan YANG ; Jiuyun YUAN ; Yubing ZHUANG ; Yuehua KE ; Xinying DU ; Zhoujia WANG ; Zeliang CHEN
Chinese Journal of Zoonoses 2015;(3):216-221
To identify novel transcripts and sRNA in genome of B .melitensis by transcriptome sequencing ,total RNA were extracted from B .melitensis culture and rRNA were removed .After the addition of adaptor ,RNA was reversely transcribed into cDNA ,which were then subjected to PCR amplification and sequencing .The generated reads were mapped to genome se‐quence of B .melitensis strain 16M .With the mapping results ,novel transcripts and sRNA were identified by bioinformatics methods .Sequencing results analysis showed that genome sequence was covered with the reads with good quality .A total of 773 genes were extended in their 5′and/or 3′ends of their original locations .Sixteen novel transcripts and 241 sRNAs candi‐dates were identified .RT‐PCR showed that some of the sRNAs were differentially expressed under stress conditions .In B . melitensis genome ,there is novel transcript which is not predicted .The sRNA does exist in B .melitensis and were expressed under different conditions .
6.The correlation between the resistance rate of Acinetobacter baumannii and anti-microbial consumption
Jianjun WU ; Yingfei BAO ; Yang ZHAO ; Heping CAI ; Zhangwei YANG ; Jia ZHOU ; Xuebin WANG ; Cuimin CHEN
Journal of Pharmaceutical Practice 2015;(5):467-470
Objective To analyze the relevance between the consumption of various antimicrobials and antimicrobial re-sistance of Acinetobacter baumanni in a grade three hospital during 2007 -2010 .Methods A retrospective analysis was per-formed to count and sort the defined daily doses (DDDs) and the consumption of various antimicrobials in the hospital between 2007 and 2010 .Meanwhile the resistance rates of Acinetobacter baumanni to different antimicrobials were collected in the same period .Data was analyzed by SAS 8 .2 statistical software package using Spearman correlation method .Results The resistance rate of Acinetobacter baumanni to imipenem was significantly positively correlated with the consumption of carbapenems (r=0 .954 6 ,P<0 .01) ,it is positively correlated with the dosage of imipenem (r=0 .849 2 ,P<0 .05) ,it is also significantly posi-tively correlated with the consumption of meropenem (r=0 .999 2 ,P<0 .05) ,and the consumption of amoxicillin/clavulanate potassium ,respectively(r=0 .800 5 ,P<0 .05) .There was no correlation between the resistance rate of Acinetobacter bauman-ni and the dosage of aminoglycosides ,fluoroquinolones ,even β-lactamase inhibitors(P>0 .05) .Conclusion The use of car-bapenems should be correlated with their indications strictly ,only applying to severe infection of Acinetobacter baumanni .The aminoglycosides of amikacin and β-lactamase inhibitors of cefoperazone/sulbactam are the better options to treat A cinetobacter baumanni infection .
7.Efficacy and safety comparison of everolimus and fulvestrant in patients with estrogen receptor-positive advanced breast cancer progressed after endocrine therapy
Yingfei DENG ; Cong XUE ; Xin AN ; Wei YANG ; Yanxia SHI ; Ye CAO
The Journal of Practical Medicine 2018;34(10):1581-1584
Objective To compare the efficacy and safety of everolimus combined with endocrine therapy and fulvestrant in patients with estrogen receptor-positive advanced breast cancer progressed after endocrine thera-py. Methods Ninety-three breast cancer patients were selected from January 2014 to February 2017. The primary end points were progression-free survival and clinical benefit rate and the secondary end points was tolerability. Re-sults The progression-free survival in fulvestrant group was slightly higher than that in the everolimus group(13.4 months vs 12.2 months,P = 0.297). The clinical benefit rates were 46.15% and 31.71% in fulvestrant group and everolimus group,respectively. Patients treated with fewer than 2 lines and endocrine resistant patients benefited more from fulvestrant but without statistical difference. The main adverse events related to everolimus were stomati-tis,with a prevalence rate of about 26% and a localized pneumonia with a prevalence rate of about 10%. The main adverse reaction of fulvestrant was the injection site reaction. Conclusions The efficacy of everolimus in combina-tion with endocrine therapy is not superior to that of fulvestrant for the treatment of advanced breast cancer pro-gressed after endocrine therapy. After weighing the clinical benefits and quality of life,fulvestrant may be better for patients treated with fewer than 2 lines and endocrine resistance.
8.Variation of CYP2D6 genotype between Caucasian and Asian population and inconsistency of serum endox-ifen concentration and phenotype of CYP2D6 in Chinese breast cancer patients
Wei YANG ; Su LI ; Yingfei DENG ; Caiyun HE ; Hai LIAO ; Wenwen WEI ; Yanxia SHI
The Journal of Practical Medicine 2018;34(12):1995-1999,2003
Objective To conduct a prospective phase Ⅱ clinical study to explore the distribution of CYP2D6 gene polymorphism in Chinese population and its relationship with the metabolism of tamoxifen in early-stage hormonal receptor-positive breast cancer. Methods CYP2D6 genotype was tested by Sanger sequencing using the ABI 3500 Genetic Analyzer. Plasma concentrations of tamoxifen and endoxifen were measured using the HPLC-MS/MS(API 2000)assay. We downloaded the data of CYP2D6 allele from the CPIP database. Results In Chi-nese patients,the most common alleles were CYP2D6*1,*2,and *10;the predominant diplotypes were *1/*10 (38.3%)and*10/*10(18.8%). The distribution of metabolic phenotype,plasma concentration of endoxifen,and endoxifen:tamoxifen plasma concentration ratio were inconsistent between the normal metabolic phenotype(EM) and the intermediate phenotype(IM)under different CYP2D6 activity prediction criteria.The differences in the ratios and endoxifen plasma concentrations were statistically significant between the three groups by cluster analysis. Conclusions The CYP2D6 genotype distribution in Chinese population is different from that in the Western popu-lation. There is considerable variation of serum endoxifen concentration in Chinese breast cancer patients possess-ing the phenotype previously known as the intermediate active metabolizers of CYP2D6. Therefore,in the current era of precision medicine,the standard CYP2D6 genotype-phenotype classification system cannot properly stratify the Chinese population with different levels of endoxifen plasma concentration.
9.The effect of total saponins of Panax notoginseng on learning and memory of rats with post stroke depression and its mechanism
Xu HE ; Yan TANG ; Xiaoyu CHEN ; Hong ZHAO ; Hui ZANG ; Yingfei LIU ; Zehua YANG ; Fengjun DENG
Chinese Journal of Behavioral Medicine and Brain Science 2020;29(8):719-724
Objective:To investigate the effect of total saponins of Panax notoginseng (TSPN) on learning and memory of post-stroke depression (PSD) rats and its mechanism.Methods:Four-vessel occlusion method was used to build the rat stroke model and 7 days later these rats were given solitary breeding with chronic unpredictable mild stress (CUMS) to make depression model. Rats were randomly divided into Sham group ( n=10), Model group ( n=10), PSD group ( n=10) and TSPN group ( n=10). The rats in the Model group and PSD group were injected administered with equal volume of 0.9% saline 30 min post-brain ischemia, one injection per day for 30 days. while TSPN group were treated with TSPN. The dose of TSPN (75 mg/kg) was dissolved in 0.9% saline 10 g/L, once per day for 30 days. Then the learning and memory of rats were tested by Morris water maze.The protein levels of DCX and Nestin in the hippocampus were detected by Western blot. Furthermore, the DCX/Ki67 co-labeled cells in the SGZ of hippocampus were observed by the immunofluorescence. Results:The escape latency at the fifth day of PSD group((31.8±3.8)s) was longer than that in the Sham group((10.4±3.2)s) and Model group((19.8±3.7)s) ( t=9.23, 5.15; both P<0.05). The escape latency ((14.2±2.8)s) of TSPN group was shortened significantly than PSD group ( t=8.56, P<0.05). The times across the platform in the Sham group was (10.3±1.7), and the PSD group was (4.1±1.1), difference was statistically significant between two groups( t=11.24, P<0.05). The times across the platform (8.4±1.6) of TSPN group statistically increased compared with PSD group ( t=5.77, P<0.05). The protein levels of DCX and Nestin in the PSD group were (0.60±0.02), (0.58±0.03) respectively, and in the TSPN group were (1.07±0.07), (0.95±0.11) correspondingly, there were significant differences of the DCX, Nestin protein level between the two groups( t=20.22, 7.68, both P<0.01). Moreover, there was significant difference in the number of the DCX/Ki67cells in the hippocampus SGZ between the PSD group((16.2±2.8) /mm 2) and TSPN group ((21.2±3.1) /mm 2)( t=2.42, P<0.05). Conclusion:TSPN could improve the learning and memory of the rats with post-stroke depression through enhancing the hippocampus neurogenesis.
10.Expression of lncRNA LINC01001 in breast cancer and its effect on proliferation of MCF-7 cells
MEI Hong ; LI Changen ; YANG Liang ; GAO Yingfei
Chinese Journal of Cancer Biotherapy 2018;25(2):158-162
[Abstract] Objective: To investigate the expression of long non-coding RNA LINC01001 in breast cancer tissues and its effect on the proliferation of breast cancer MCF-7 cells. Methods: The expression levels of lncRNA LINC01001 were analyzed in 12 cases of cancer and para-cancer tissues from breast cancer patients, who underwent surgical resection in Affiliated People’s Hospital of Hubei University of Medicine from March 2016 to June 2017. The plasmid over-expressing LINC01001 was transfected into human breast cancer MCF-7 cells. The cell cycle distribution and proliferation ability of MCF-7 cells were detected by flow cytometry and MTT assay, respectively. The mRNA expressions of miR-485-5p and CDKN1A mRNA were detected by qRT-PCR, and the protein expressions of CDKN1A, CDK4, CDK6 and Cyclin D1 were detected by Western blotting. Results: The expression level of lncRNA LINC01001 in breast cancer tissues was lower than that in para-cancer tissues (P<0.01). LINC01001 recombinant plasmid transfection significantly inhibited cell cycle progression (P<0.05) and cell proliferation (P<0.05) of MCF-7 cells. qRT-PCR showed that the expression level of miR-485-5p was decreased (P<0.01) and the expression level of CDKN1A mRNA was increased (P<0.01) after over-expressing LINC01001. Western blot results confirmed that over-expression of LINC01001 could promote the expression of CDKN1A protein, but decrease the expressions of CDK4, CDK6 and Cyclin D1 proteins. Conclusion: The expression of LINC01001 in breast cancer tissues was decreased. LINC01001 may down-regulate the expression of miR-485-5p to up-regulate the expression of CDKN1A, and further to inhibit the proliferation of breast cancer MCF-7 cells, providing experimental basis for the clinical application of lncRNA.