AIM: To study the effects of Liquestrazin on succinic dehydrogenase (SDH) and cytochrome oxidase (CCO) in the myocardial mitochondria of the ischemia-reperfusion rats and its mechanism. METHODS:Model of myocardial ischemia-reperfusion injury was produced by coronary artery ligation . The rats were devided into sham operation control (SC), ischemia-reperfusion (IR) and ischemia-reperfusion protected with Liqustrazin (IR+L) group . Activity of SDH,CCO,SOD and GSH?PX and contents of malondialdehyde (MDA),Cyt aa 3,Cyt c and phospholipid(PL) were observed respectively . RESULTS: As compared with ischemia-reperfusion group (IR), IR+L group showed significantly increased activity of SDH, CCO,SOD and GSH?PX (P

Aim To observe the dysfunction of myocardial nuclear calcium transport in rat myocardial injury and effects of taurine on it . Methods The model of myocardial damage was induced by subcutaneous injection of isoproterenol (ISO,5 mg?kg-1?d-1). Myocardial nuclei were purified with Sucrose density centrifugation and identified zymologically. The activity of Ca2+_ATPase was measured zymologically and calcium uptake was assayed with 45Ca2+ isotope.Results Compared with the control, the Ca2+_ATPase activity of myocardial nuclear in ischemia group was decreased by 18.1%(P

The link between nonresolving inflammation and cancer is well documented. On the one hand, epidemiologic evidence supports that approximately 25% of all human cancer worldwide is caused by nonresolving inflammation. On the other hand, inflammatory cells are found in the microenvironment of most, if not all, tumors. In the tumor micro-environment, inflammatory cells and molecules influence almost every aspect of cancer. MicroRNAs (miRNAs) participate in the initiation and progression of nonresolving inflammation-related cancer by regulating the key genes and related signaling pathways. Further investigation into the molecular mechanisms by which miRNAs carry out their functions will be of great value in the prevention, early diagnosis, and treatment of tumors.
Chronic Disease ; Humans ; Inflammation ; complications ; genetics ; immunology ; Inflammation Mediators ; immunology ; MicroRNAs ; genetics ; Neoplasms ; etiology ; genetics ; Tumor Microenvironment

Long non-coding RNAs (lncRNAs) are a group of endogenous RNA molecules which exceed 200 nt in length, lack complete specific open reading frame, and completely lack or possessvery limited protein-coding capacity. Recent studies have revealed that lncRNAs participate in critical processes such as genomic imprinting, cell differentiation, and immune reaction, etc. lncRNAs regulate gene expression at the epigenetic, transcriptional and post-transcriptional levels by modulating chromatin remodeling and histone modifications, interfering the transcription, regulating patterns of alternative splicing, generating small RNAs, and modulating protein activation and localization. Through their numerous functions, lncRNAs play critical roles in the growth, development, senescence, death, and other important physiological and pathological processes. Further investigation into the regulation of gene expression mediated by lncRNAs will be of great value in the thorough understanding of pathogenies and provide new molecular markers and drug targets of diseases.
Alternative Splicing ; Chromatin Assembly and Disassembly ; Gene Expression ; Open Reading Frames ; Proteins ; RNA, Long Noncoding