Dissertation > Excellent graduate degree dissertation topics show

The Expression of Osteopontin in Myocardium of Congenital Heart Disease and Its Related Study

Author: JinZuo
Tutor: XuYi
School: Central South University
Course: Cardiovascular disease
Keywords: Congenital heart disease Cyanotic congenital heart disease Non- cyanotic congenital heart disease Myocardial fibrosis Osteopontin Hypoxia
CLC: R725.4
Type: Master's thesis
Year: 2010
Downloads: 39
Quote: 0
Read: Download Dissertation

Abstract


Objective To detect the expression levels of osteopontin (OPN) in children with congenital heart disease (CHD) myocardial analysis of OPN with CHD types (cyanotic and non-cyanotic), myocardial fibrosis, hypoxia level, age relationship, to explore the role of OPN in the CHD myocardial fibrosis. Method to select patients with congenital heart disease underwent surgery during the same period 45 cases, including 25 cases of non-cyanotic congenital heart disease (non-cyanotic group), 15 males and 10 females, aged 0.5-9.2 years old, with an average of 5.03 ± 1.08 years old ; 20 cases of cyanotic congenital heart disease (cyanotic group), 12 males and 8 females, aged 0.5-8.5 years, an average of 4.53 ± 1.82 years. The intraoperative taken right atrial appendage myocardial tissue 1OOmg, and the two groups of children with myocardial type Ⅰ type III collagen, OPN mRNA expression level was detected by reverse transcription - polymerase chain reaction (RT-PCR). Application SPSS13.0 statistical analysis software were compared between the two groups of children with myocardial type Ⅰ type III collagen, OPN expression levels and the purpose of gene and hypoxia, age, defect size, and OPN mRNA and type Ⅰ, Ⅲ type The relationship of the collagen mRNA. Results (1) cyanotic congenital heart disease group than non-cyanotic congenital heart disease group Ⅰ collagen and type Ⅲ collagen mRNA expression levels were significantly increased (type I collagen p lt; 0.01, type III collagen protein p lt; 0.01); (2) cyanotic congenital heart disease group than in the non-cyanotic congenital heart disease group OPN mRNA expression levels were significantly higher (p lt; 0.05); (3) I type Ⅲ collagen expression in children age positively related (type I collagen and children age r = 0.331, p lt; 0.05; type III collagen and children age r = 0.372, p lt; 0.05), with oxygen saturation a negative correlation (type I collagen, and oxygen saturation r = -0.561, p lt; 0.001; type III collagen and oxygen saturation r = -0.537, p lt; 0.001); (4) OPN mRNA expression level and myocardial collagen protein's expression and defect size as is relevant (OPN and type Ⅰ collagen protein r = 0.625, p-lt; 0.001; OPN and type Ⅲ collagen protein r = 0.287, p-lt; 0.05; OPN and defect size r = 0.524 , p lt; 0.001), and oxygen saturation into a negative correlation (the OPN and blood oxygen saturation r = -0.703, p <0.001). Conclusion (1) cyanotic congenital heart disease than non-cyanotic congenital heart disease myocardial collagen type Ⅰ and Ⅲ collagen expression levels were significantly increased; (2) OPN was significantly higher in cyanotic congenital heart disease myocardial positively correlated with indicators of myocardial fibrosis, OPN may be involved in the process of congenital heart disease, cyanotic congenital heart disease, myocardial fibrosis; (3), congenital heart disease, myocardial fibrosis may be with children age, lack of related to the degree of oxygen; (4) of OPN expression and blood oxygen saturation was negatively related, there is a positive correlation with the defect size, prompted increased hypoxia and volume overload can cause OPN expression was enhanced.

Related Dissertations

  1. Design, Synthesis and Antitumor Activities Study of Quinoxaline-1,4-dioxide Derivatives,R914
  2. The Effects of Atorvastatin on Expression of Osteopontin in Kidney of the Diabetic Rats Its Molecular Mechanism,R587.2
  3. Effect of Hypoxic Postconditioning on Alveolar Epithelial Type Ⅱ Cell Mitochondrial Apoptotic Pathway,R563.8
  4. Right armpit straight incision surgery for congenital heart disease,R654.2
  5. Role of Osteopontin and CD44 in Stone Formation,R691.4
  6. Osteopontin through the MAPK signaling pathway and increased MMP9 expression correlation with embryo implantation,R321
  7. Relationship between Epithelial-mesenchymal Transition Induced by Hypoxia and Invasive Ability in Hepatocellular Carcinoma Cells,R735.7
  8. Effect and Mechanism of Atorvastatin on Myocardial Fibrosis in Rats after Myocardial Infarction,R542.22
  9. Expression Changes of Hypoxia-inducible Factor-1 α and Aquaporin-4 in Brains of Rats after Cardio-pulmonary Resuscitation and the Intervention Effects of β-aescine Sodium,R459.7
  10. The Mechanism of Lethal Effect of High-dose Vitamin C on Renal Cancer Cells,R737.11
  11. Induction of IGF Binding Protein-6 in Vascular Endothelial Cells is a Conserved Negative Feedback Mechanism in Hypoxia-induced Angiogenesis,Q46
  12. The Plasma and Tissue Expression of Osteopontin and CD44v6 in Gastric Carcinoma and Their Significance,R735.2
  13. Insulin Promotes Proliferative Vitality and Invasive Capability of Pancreatic Cancer Cells Via Hypoxia-inducible Factor 1α Pathway,R735.9
  14. The Relationships among Osteopontin, Obesity and Insulin Resistance,R589
  15. Gas6 via PI3K/Akt survival pathway to protect hypoxia -induced cardiomyocyte apoptosis,R363
  16. Waterlogging under anaerobic respiration metabolism of peanut seedlings,S565.2
  17. Expression and Significance of Hypoxia-inducible Factor 1a in Vitreous Body in Patients with Proliferative Vitreo-retinal Diseases,R774.1
  18. The Effect of Chronic Intermittent Hypoxia on Expression of HIF-α, TNF-α, IL-6 in HepG2 Cell,R735.7
  19. Expression of COX-2 and Hif-1α, and Its Correlation with Microvascular Angiogenesis in Cervical Cancer,R737.33
  20. The Effect of Chronic Intermittent Hypoxia on the Oxidative Stress in Corpus Striatum of Parkinson’s Disease Model Mouse,R742.5
  21. The Relationship between Transforming Growth Factor Beta 1 Gene Polymorphism and Serum Concentration and Myocardial Fibrosis in Congenital Heart Disease,R725.4

CLC: > Medicine, health > Pediatrics > Children within the science > Pediatric cardiac and vascular disease
© 2012 www.DissertationTopic.Net  Mobile