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1.
Front Pharmacol ; 15: 1343582, 2024.
Article in English | MEDLINE | ID: mdl-38803434

ABSTRACT

Background: Evidence indicates that the addition of ezetimibe to statin therapy reduces cardiovascular events. However, the impact of ezetimibe-statin combination therapy on coronary plaque regression, plaque stabilization, and diameter stenosis remains a matter of controversy. Methods: We performed electronic searches in PubMed, Web of Knowledge, and the Cochrane Central Register of Controlled Trials to identify eligible trials assessing the effects of ezetimibe-statin combination therapy versus statin monotherapy reporting at least one outcome among total atheroma volume (TAV), minimum fibrous cap thickness (FCT), lumen volume (LV), and lumen area (LA) derived from intravascular imaging modalities of intravascular ultrasound (IVUS) and optical coherence tomography (OCT). We used the random-effects model and performed trial sequential analysis (TSA) during this meta-analysis. Results: Eleven articles with a total of 926 individuals (460 in the dual-lipid-lowering therapy group and 466 in the statin monotherapy group) were included in the final meta-analysis. Compared to statin monotherapy, ezetimibe-statin combination therapy was associated with significantly decreased TAV [WMD = -3.17, 95% CI (-5.42 to -0.92), and p = 0.006], with no effect on the LV of the coronary artery [WMD = -0.52, 95% CI (-2.24 to 1.21), and p = 0.56], the LA of the coronary artery [WMD = 0.16, 95% CI (-0.10-0.42), and p = 0.22], or minimum FCT thickness [WMD = 19.11, 95%CI (-12.76-50.97)]. Conclusion: In patients with coronary artery disease, ezetimibe-statin combination therapy resulted in a significant regression in TAV compared to statin monotherapy, whereas no overall improvements of minimum FCT or lumenal stenosis were observed.

2.
Calcif Tissue Int ; 103(2): 227-236, 2018 08.
Article in English | MEDLINE | ID: mdl-29523928

ABSTRACT

As a regulator of osteogenesis, microRNA-218 (miR-218) is reported to promote osteogenesis of mesenchymal stem cells (MSCs). However, the in vivo osteogenic effect of miR-218 remains elusive. In this study, miR-218 was confirmed to promote osteogenic differentiation of MSCs by stimulating the alkaline phosphatase activity, calcium nodule formation, and osteogenic marker gene expression. For in vivo study, the miR-218-overexpressing BMSCs were locally administrated into the fracture sites in a femur fracture mouse model. Based on the X-rays, micro-computed tomography, mechanical testing, histology, and immunohistochemistry examinations, miR-218 overexpression improved new bone formation and accelerated fracture healing. These findings suggest that miR-218 may be a promising therapeutic target for bone repair in future clinical applications.


Subject(s)
Bone Marrow Cells/cytology , Bone and Bones/pathology , Fracture Healing , Mesenchymal Stem Cells/cytology , MicroRNAs/physiology , Osteogenesis , Animals , Cell Differentiation , Cell Proliferation , Cells, Cultured , Femoral Fractures/diagnostic imaging , Immunohistochemistry , Male , Mice , Mice, Inbred C57BL , Stress, Mechanical , X-Ray Microtomography
3.
Yi Chuan ; 30(11): 1487-98, 2008 Nov.
Article in Chinese | MEDLINE | ID: mdl-19073559

ABSTRACT

The atp6 and apt9 gene fragments associated with cytoplasmic male sterility (CMS) were cloned from the mitochondrial DNA of a ramie (Boehmeria nivea (L.) Gaud.) cytoplasmic male sterile line and its maintainer and restorer lines using PCR and degenerated primer strategy. The primers were designed according to the reserved sequences in the encoding region of mitochondrial genes atp6 and atp9 of some dicotyledons from GenBank. These fragments did not have complete encoding region but showed the homology of 94% and 85% with atp6 and atp9 genes from the referred dicotyledons in GenBank. The complete atp6 and atp9 genes including the complete open reading frames were cloned by means of amplifying the 3' and 5'end unknown sequences of these gene fragments using DNA Walking method. The atp6 gene showed no difference among ramie male sterile line, maintainer and restorer lines at mtDNA sequence, transcription and translation control and protein level. However, compared to the maintainer and restorer lines, the atp9 gene of the male sterile line was different and deletion in several bases at the 3' end of the encoding region. An abnormally high expression of atp9 gene in the male sterile line at the budding stage and full-bloom stage was analyzed by RT-PCR analysis. These results indicated that the variation in DNA sequence and/or abnormality in expression of atp9 gene in the male sterile line maybe closely related to ramie CMS.


Subject(s)
Boehmeria/genetics , Boehmeria/physiology , Calcium-Transporting ATPases/genetics , Cytoplasm/metabolism , Gene Expression Regulation, Plant , Plant Infertility/genetics , Amino Acid Sequence , Base Sequence , Boehmeria/cytology , Boehmeria/growth & development , Calcium-Transporting ATPases/chemistry , Chromosome Walking , Cloning, Molecular , DNA, Mitochondrial/genetics , Electrophoresis, Agar Gel , Molecular Sequence Data , Open Reading Frames/genetics , Polymerase Chain Reaction , Reproduction/genetics , Sequence Alignment , Sequence Analysis, DNA
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