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1.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-972466

ABSTRACT

Objective: To investigate the relationship between polymorphisms of rs1532624 and rs289741 loci in cholesteryl ester transfer protein (CETP) genes and atherosclerotic cerebral infarction (ACI). Methods: The CETP gene rs1532624 and rs289741 in 95 patients with ACI and 177 healthy subjects were genotyped by MassARRAY mass spectrometry. Each locus genotype and allele frequency distributions were compared. Results: The difference of allele frequency distribution between the rs1532624 (χ

2.
Article in English | WPRIM (Western Pacific) | ID: wpr-825852

ABSTRACT

Objective:To investigate the relationship between polymorphisms of rs1532624 and rs289741 loci in cholesteryl ester transfer protein (CETP) genes and atherosclerotic cerebral infarction (ACI).Methods:The CETP gene rs1532624 and rs289741 in 95 patients with ACI and 177 healthy subjects were genotyped by MassARRAY mass spectrometry. Each locus genotype and allele frequency distributions were compared.Results:The difference of allele frequency distribution between the rs1532624 (χConclusion:ACI have a positive correlation with rs1532624 polymorphism, and AA genotype may be susceptible factors of ACI.

3.
Article in English | MEDLINE | ID: mdl-24288572

ABSTRACT

Diabetic peripheral neuropathy (DPN) is a common microvascular complication of diabetes associated with high disability rate and low quality of life. Tang-Luo-Ning (TLN) is an effective traditional Chinese medicine for the treatment of DPN. To illustrate the underlying neural protection mechanisms of TLN, the effect of TLN on electrophysiology and sciatic nerve morphology was investigated in a model of streptozotocin-induced DPN, as well as the underlying mechanism. Sciatic motor nerve conduction velocity and digital sensory nerve conduction velocity were reduced in DPN and were significantly improved by TLN or α -lipoic acid at 10 and 20 weeks after streptozotocin injection. It was demonstrated that TLN intervention for 20 weeks significantly alleviated pathological injury as well as increased the phosphorylation of ErbB2, Erk, Bad (Ser112), and the mRNA expression of neuregulin 1 (Nrg1), GRB2-associated binding protein 1 (Gab1), and mammalian target of rapamycin (Mtor) in injured sciatic nerve. These novel therapeutic properties of TLN to promote Schwann cell survival may offer a promising alternative medicine for the patients to delay the progression of DPN. The underlying mechanism may be that TLN exerts neural protection effect after sciatic nerve injury through Nrg1/ErbB2→Erk/Bad Schwann cell survival signaling pathway.

4.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-789258

ABSTRACT

[Objective] To evaluate the effectiveness of AIDS health education for pregnant women in their knowledge ,attitude and behavior on AIDS prevention and mother-to-child transmission , so as to pro-vide scientific basis for health education . [ Methods] From 5 suburban hospitals , a total of 800 preg-nant women investigated accepted AIDS health education intervention study .Interventions included face to face counseling with medical personnel , distribution of publicity materials of basic AIDS prevention , and preventing mother-to-child transmission of AIDS .Through investigation by two questionnaires done before and after intervention , we obtained the changes in pregnant women's knowledge , attitude and behavior on AIDS prevention and mother-to-child transmission , and thus evaluated the efficacy of the intervention . [ Results] Before health education intervention , pregnant women were found to be in lack of knowledge , and had incorrect attitude and behavior on basic AIDS prevention , and mother-to-child transmission of AIDS prevention.After intervention, the situation markedly improved. [Conclusion] AIDS health education intervention increases pregnant women's knowledge on basic AIDS prevention , and mother-to-child transmis-sion of AIDS prevention , changes their wrong attitude and behavior , improves self protection consciousness , and reduces their discrimination against AIDS patients .It is clear that we must continue to carry out health education intervention , so as to control the spread of AIDS effectively .

5.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 32(12): 1675-8, 2012 Dec.
Article in Chinese | MEDLINE | ID: mdl-23469611

ABSTRACT

OBJECTIVE: To study the effects of Qiwei Granule (QWG) on the protein and mRNA expressions of renal tissue transforming growth factor beta1 (TGF-beta1) in KK-Ay mice with spontaneous type 2 diabetes mellitus (T2DM). METHODS: Spontaneous T2DM KK-Ay mice model was adopted. Forty-five male mice were randomly divided into three groups, i. e., the model group, the Chinese medicine group, and the Western medicine group, 15 in each group. Fifteen male C57BL/6J mice were set up as the normal control group. The mice in the Chinese medicine group and the Western medicine group were administered intragastrically with QWG (at the daily dose of 20 g/kg) and valsartan (at the daily dose of 10 mg/kg), and the treatment lasted for 12 successive weeks. The pathological changes of the kidney were observed using HE staining, PAS, and Masson staining. The protein and mRNA expressions of TGF-beta1, were detected using immunohistochemical method and Real-time fluorescent quantitative PCR. RESULTS: The renal pathological changes of mice in the model group showed hypertrophic glomeruli, widened mesenteric matrix, increased mesangial cells, vacuolar renal tubular epithelial cells, tubular ectasia, and foci atrophy. Necrosis was occasionally seen. More protein cast, mesenchymal infiltration of inflammatory cells, and interstitial fibrosis could be seen. The protein and mRNA expressions of TGF-beta1 increased more in the model group than in the normal control group. After treatment by QWG and valsartan, the renal pathological changes were obviously alleviated, and the protein and mRNA expressions of TGF-beta1 were obviously lowered (P<0.05). CONCLUSION: By inhibiting the protein and mRNA expressions of TGF-beta1, QWG could play a role in preventing and curing diabetic nephropathy.


Subject(s)
Diabetes Mellitus, Type 2/metabolism , Drugs, Chinese Herbal/pharmacology , Kidney/metabolism , Transforming Growth Factor beta1/metabolism , Animals , Drugs, Chinese Herbal/therapeutic use , Male , Mice , Mice, Inbred C57BL , RNA, Messenger/metabolism
6.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-336783

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression of Junctophilin 1 (JP1) in cardiogenesis of mammalian.</p><p><b>METHODS</b>Cardiac differentiation of embryonic stem cells (ESCs) was generated by hanging drop method. Fetal heart was obtained from the rats aged d 14-20 of gestation. The expression of JP1 and JP2 during cardiogenesis of ESCs and rat embryos was analyzed by RT-PCR or Western blotting. Immunofluorescence staining was employed to reveal the distribution of JP1 and JP2 in embryoid body (EB), probing for merging of JP1 and JP2 and cardiac sarcomeric α-Actinin or Troponin-T. Percentage of JP1 and JP2-positive staining cells was analyzed quantitatively by FCS on d17.</p><p><b>RESULTS</b>JP1 mRNA was up-regulated at the early stage (d 5-11) and then decreased. The expression of JP1 protein was up-regulated at the early stage (d 7-9), then decreased gradually and disappeared after d 15. While JP2 gene and protein expression increased in a time-dependent manner during cardiogenesis of rat embryos. The results of immunofluorescence staining showed that there was a parallel co-localization of JP2 with Troponin-T or α-Actinin on d17, while JP1 failed to express in the sarcomeric positive area at the same time point. Furthermore, FCS analysis showed that about 16.59% of cells were JP2-positive, while no cells were stained positively for JP1 in d17 EBs.</p><p><b>CONCLUSION</b>JP1 gene is expressed during the whole process of cardiogenesis, while JP1 protein only appears on the early stage. The expression of JP1 in cardiogenesis of ESCs is consistent with that of rat embryos.</p>


Subject(s)
Animals , Mice , Rats , Actinin , Genetics , Metabolism , Cell Differentiation , Cell Line , Embryonic Stem Cells , Cell Biology , Metabolism , Heart , Embryology , Membrane Proteins , Genetics , Metabolism , Mice, Inbred ICR , Myocytes, Cardiac , Cell Biology , Metabolism , RNA, Messenger , Genetics , Troponin T , Genetics , Metabolism
7.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-336782

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression of metabotropic glutamate receptor 4 (mGluR4) in cardiomyocytes differentiated from mouse embryonic stem cells (ES cells).</p><p><b>METHODS</b>ES cells were differentiated into cardiomyocytes with hanging-drop cultures. Retinoic acid (RA) and dimethyl sulfoxide (DMSO) were used as positive and negative controls, respectively. The co-expression of cardiac sarcomeric protein (α-actinin or troponin-T) and mGluR4 were verified by immunocytochemistry and flow cytometry analysis. The mRNA and protein expressions of mGluR4 were verified by RT-PCR and Western blot analysis, respectively. Meanwhile, the expression of mGluR4 in prenatal mouse heart was also examined.</p><p><b>RESULTS</b>mGluR4 was expressed in both mouse ES cells and ES cell-derived cardiomyocytes. The level of mGluR4 protein expression decreased during the maturation of the cardiomyocytes. The co-expression rate of mGluR4 and Troponin T in the beating embryoid bodies (EBs) was only (3.00 ±1.00)%. On the other hand, mGluR4 gene and protein expressions showed remarkable down-regulation in the development of mouse fetal heart, which was not detected in mouse adult heart.</p><p><b>CONCLUSION</b>The expression of mGluR4 is down-regulated in the cardiomyocyte differentiation of ES cells. The trend of expression is consistent with that in the prenatal mouse heart development.</p>


Subject(s)
Animals , Mice , Cell Differentiation , Physiology , Cell Line , Embryonic Stem Cells , Cell Biology , Metabolism , Mice, Inbred ICR , Myocytes, Cardiac , Cell Biology , Metabolism , RNA, Messenger , Genetics , Receptors, Metabotropic Glutamate , Genetics , Metabolism
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