جستجوی مقالات مرتبط با کلیدواژه "atg7" در نشریات گروه "پزشکی"

Aging is a physiological process that affects heart function. Training is known as a factor accelerating heart output, especially in aged individuals. In the present experimental study, the authors aimed to evaluate how high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) affect autophagy, cardiac remodeling, and cardiac function. 

Twenty-four male Wistar rats, approximately 20 months old, were divided into three groups of control, HIIT, and MICT. The training programs lasted for eight weeks. Aerobic power and training capacity were also assessed. Two-dimensional echocardiography was also applied to assess cardiac indices. At the end of the experiment, tissue sampling of cardiac tissue was applied, and gene expression was assessed using the qRT-PCR technique. Data were analyzed using SPSS software, version 19.

After HIIT and MICT, no significant changes were detected regarding the animal weight. Also, mTORC1, Atg16, and Atg7 gene expression and ejection fraction (EF) and fractional shortening (FS) were accelerated in HIIT and MICT groups compared to control animals. Besides, the collagen type 3 (COLIII) gene expression, left ventricular end-diastolic diameter (LVEDD), and left ventricular end-systolic diameter (LVESD) showed a significant increase (p<0.05) in HIIT and MICT animals than control.

Training can potentially improve cardiac output in older adults. Besides, HIIT seems more effective than MICT.

Autophagy, known as cell death type II, is a housekeeping pathway that currently has been worked on in matters of tumorigenesis and leukemogenesis. Therefore, in this study expression levels of ATG7 and LC3 as two key genes are targeted in AML patients. This study was performed on 55 de novo AML patients against 17 healthy volunteers, acquired samples from bone marrow (BM) and peripheral blood (PB) sources in different ages and gender. The evaluation was executed by mRNA extraction, cDNA synthesis, real-time PCR and data was analyzed by SPSS. Analyzed data indicate a significant decrease between expression of ATG7 and LC3 in AML patients against control (Pv< 0.05). Decrease in both genes expression was detected in most of the patients, 81.81% and 75.55%, respectively. Also LC3 overexpression was detected in 11.33% of AML patients. Moreover, a positive significant correlation between ATG7 and LC3 genes was detected (r= 0.481; Pv= 0.001). This study showed that significant reduction of autophagy genes in de novo AML patients is important to overcome this system and initiate leukomogenesis. It seems a new insight is required for new achievements in diagnosis, prognosis, treatment and monitoring AML patients.