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1.
Journal of Zhejiang University. Science. B ; (12): 990-998, 2020.
Article in English | WPRIM | ID: wpr-880740

ABSTRACT

Disulfide-bond A oxidoreductase-like protein (DsbA-L) is a molecular chaperone involved in the multimerization of adiponectin. Recent studies have found that DsbA-L is related to metabolic diseases including gestational diabetes mellitus (GDM), and can be regulated by peroxisome proliferator-activated receptor γ (PPARγ) agonists; the specific mechanism, however, is uncertain. Furthermore, the relationship between DsbA-L and the novel adipokine chemerin is also unclear. This article aims to investigate the role of DsbA-L in the improvement of insulin resistance by PPARγ agonists in trophoblast cells cultured by the high-glucose simulation of GDM placenta. Immunohistochemistry and western blot were used to detect differences between GDM patients and normal pregnant women in DsbA-L expression in the adipose tissue. The western blot technique was performed to verify the relationship between PPARγ agonists and DsbA-L, and to explore changes in key molecules of the insulin signaling pathway, as well as the effect of chemerin on DsbA-L. Results showed that DsbA-L was significantly downregulated in the adipose tissue of GDM patients. Both PPARγ agonists and chemerin could upregulate the level of DsbA-L. Silencing DsbA-L affected the function of rosiglitazone to promote the phosphatidylinositol 3-kinase (PI3K)-protein kinase B (PKB)/AKT pathway. Therefore, it is plausible to speculate that DsbA-L is essential in the environment of PPARγ agonists for raising insulin sensitivity. Overall, we further clarified the mechanism by which PPARγ agonists improve insulin resistance.

2.
Chinese Journal of Practical Gynecology and Obstetrics ; (12): 145-147, 2019.
Article in Chinese | WPRIM | ID: wpr-816156

ABSTRACT

With the implementation of the two-child policy and the wide application of hysteroscopy and laparoscopy,pregnancy of scarred uterus women is increasing year by year,and most patients still choose cesarean section.Complications of cesarean section has also increased.It is an important task for obstetricians to master the timing and mode of termination of pregnancy and reduce complications.The authors make a comprehensive analysis of the timing and complications of cesarean section for the second pregnancy of scarred uterus.

3.
Journal of Zhejiang University. Science. B ; (12): 93-99, 2008.
Article in English | WPRIM | ID: wpr-277295

ABSTRACT

<p><b>OBJECTIVE</b>To explore the relationship between genetic polymorphisms in methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR), the central enzymes in folate metabolism that affects DNA methylation and synthesis, and the risk of Down syndrome in China.</p><p><b>METHODS</b>Genomic DNA was isolated from the peripheral lymphocytes of 64 mothers of children with Down syndrome and 70 age matched control subjects. Polymerase chain reaction and restriction fragment length polymorphism were used to examine the polymorphisms of MTHFR 677C-->T, MTRR 66A-->G and the relationship between these genotypes and the risk of Down syndrome was analyzed.</p><p><b>RESULTS</b>The results show that the MTHFR 677C-->T polymorphism is more prevalent among mothers of children with Down syndrome than among control mothers, with an odds ratio of 3.78 (95% confidence interval (CI), 1.78 approximately 8.47). In addition, the homozygous MTRR 66A-->G polymorphism was independently associated with a 5.2-fold increase in estimated risk (95% CI, 1.90 approximately 14.22). The combined presence of both polymorphisms was associated with a greater risk of Down syndrome than the presence of either alone, with an odds ratio of 6.0 (95% CI, 2.058 approximately 17.496). The two polymorphisms appear to act without a multiplicative interaction.</p><p><b>CONCLUSION</b>MTHFR and MTRR gene mutation alleles are related to Down syndrome, and CT, TT and GG gene mutation types increase the risk of Down syndrome.</p>


Subject(s)
Female , Humans , Alleles , Case-Control Studies , China , Down Syndrome , Diagnosis , Ethnology , Genetics , Ferredoxin-NADP Reductase , Genetics , Folic Acid , Metabolism , Genetic Predisposition to Disease , Genotype , Homozygote , Lymphocytes , Metabolism , Methylenetetrahydrofolate Reductase (NADPH2) , Genetics , Polymorphism, Genetic , Risk Factors
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