Journal of Basic Research in Medical Sciences
Volume:10 Issue: 4, Autumn 2023

Body defects impact well-being, necessitating efficient prosthetic techniques. This report explores integrating CAD/CAM technology for auricular prostheses, emphasizing a digital approach.

The plan involved irreversible hydrocolloid impressions, generating a digital resin model through an indirect scanner. Traditional molding and 3D printing combined for pattern formation. The mold's investment, fabrication, and coloring used intrinsic and extrinsic painting.

CAD/CAM showcased enhanced compatibility and aesthetics. The digital resin model improved adaptability, streamlining production, and accelerating the wax try-in process. Patient satisfaction during follow-ups validated the prosthesis success.

Exploring auricular prosthesis advancements via digital technology, particularly the digital resin model, demonstrated transformative outcomes. This approach not only enhances adaptability and aesthetics but also expedites production, promising a seamless and time-efficient restoration of ear aesthetics for individuals.

The regenerative potential of cardiac stem and progenitor cells is affected by aging and detraining, with the C-Kit cardiac stem cell expressing the Nkx2.5 transcription factor playing a crucial role. Exercise is known to enhance organ regeneration during aging, but the mechanisms involved in new cardiomyocyte formation during physiological cardiac remodeling remain unclear.

Eighteen aged Wistar rats (~440g) were divided into three groups: Control (CO), aerobic training (AT) (5 days per week, 50-75% of maximum speed) for six weeks, and detraining (DT) for four weeks. RT-PCR analysis determined Nkx2.5 gene expression, while immunohistochemical staining identified C-kit-positive and Ki67-positive cardiac progenitor cells.

In heart tissue, C-Kit and Ki67 values significantly differed between the control–training (P=0.001) and training-detraining (P=0.001) groups but not between the control and detraining groups for C-Kit (P=0.502) and Ki67 (P=0.475). Nkx2.5 exhibited a significant difference between control-training (P=0.001), training-detraining (P=0.001), and control-detraining (P=0.006).

Exercise increased the proliferation of heart stem cells, activating C-Kit differentiation and elevating Nkx2.5 expression, thereby delaying the effects of aging. However, detraining significantly impacted heart stem cell function, emphasizing the importance of sustained exercise for optimal cardiac health.

The combined use of methadone and exercise training holds promise for promoting health. This study investigates the impact of resistance and aerobic training in conjunction with methadone consumption on lipid profiles and C-reactive protein (CRP) levels in addicted men.

Ninety addicted men (mean age 36.82 ± 4.32 years) undergoing prison treatment were randomly assigned to six groups (n=15 each): control, narcotics anonymous (NA), aerobic training + methadone, aerobic training + methadone reduction, resistance training + methadone, resistance training + methadone reduction. The 12-week exercise program, conducted thrice weekly, included aerobic training (4-8 sets, 3 minutes each, at 80-90% maximum heart rate on the ergometer bike) and resistance training (12 repetitions, 3 sets, at 70-85% of one repetition maximum). Blood samples collected pre- and post-intervention measured CRP and blood lipids using specialized kits. Data were analyzed with SPSS software, employing multiple analysis of variance (MANOVA) and Tukey's post hoc test (P<0.05).

High-density lipoprotein (HDL) levels significantly increased in trained groups compared to the control (P<0.001). Moreover, trained groups exhibited significant decreases in low-density lipoprotein (LDL), triglycerides, total cholesterol, and CRP compared to the control group (P<0.05). Importantly, aerobic training was more effective than resistance training in improving the studied variables.

Exercise training, particularly aerobic training with methadone ingestion, yields positive effects, including reduced CRP levels and improved lipid profiles in addicted men. Exercise training with methadone reduction may be considered for empowering individuals with addiction issues.

Multiple sclerosis (MS) is an autoimmune, inflammatory, chronic, and progressive disease targeting neurons in the brain and spinal cord, leading to myelin sheath and axonal damage. Regular physical activity is recognized as a complementary and moderating treatment for MS. Nigella sativa is known for its antioxidant, anti-inflammatory, and anti-apoptotic effects.

Sixty-four adult male C57BL/6 mice (20-26 grams) were randomly divided into eight groups. MS was induced by adding 0.2% cuprizone to rodent food powder. The 8-week training program involved forced treadmill running (15-20 meters/minute), six days a week, twice a day, with 15-minute sessions and a minimum 2-hour interval. Balance was assessed using repeated measurements, BDNF levels through immunohistochemistry, and memory/spatial learning using the Morris blue maze test.

After 8 weeks, BDNF increased in the experimental (37.69±2.04), Nigella sativa (34.96±1.84), and combined groups (43.17±3.2), with a significant difference between the Nigella sativa group and the others (P< 0.05). Clinical examination showed zero scores for sham, NS, EX, and NS+EX groups, indicating no movement disorders or limb weakness. In the Cuprizone group, scores increased, while treatment groups (Cup+NS, Cup+EX, and Cup+NS+EX) demonstrated a significant decrease compared to the Cup group (P< .05).

Nigella sativa and aerobic training appear to delay MS onset, reduce symptom severity, and contribute to the repair of damaged myelin areas, emphasizing their potential as therapeutic interventions. The condensed text is now approximately 249 words.

Angiogenesis, the formation of new capillaries from pre-existing vessels, crucially involves activation of the hypoxia-inducible factor 1 (HIF-1) and vascular endothelial growth factor (VEGF) genes. This study investigates the impact of exercise intensity on the expression of angiogenic genes in the hearts of male rats.

Eighteen male Wistar rats were randomly assigned to three groups: High-Intensity Interval Training (HIIT), Continuous Training (CT), and control (C). Both HIIT and CT groups underwent 8 weeks of training with five sessions per week. Anesthesia and blood sampling occurred 48 hours post final training session. Gene levels of HIF-1 and VEGF were measured in the left ventricle. Data analysis employed ANOVA and LSD post hoc tests (P≤0.05).

VEGF gene expression significantly increased in both HIIT and CT groups compared to the control group (P = 0.001), with a more pronounced elevation in the HIIT group than the CT group (P = 0.004). Furthermore, HIF-1 levels exhibited a significant reduction in both HIIT (P = 0.001) and CT (P = 0.001) groups compared to the control group, with the HIIT-induced decrease surpassing that of the CT group (P = 0.049).

The noteworthy elevation in VEGF and decrease in HIF-1 gene expression levels in trained rats imply that exercise training enhances angiogenesis. Importantly, the extent of this enhancement is contingent upon exercise intensity, with HIIT demonstrating more pronounced positive effects on VEGF levels.

This study investigates the impact of two high-intensity interval training (HIIT) programs on PGC-1α, p53, and citrate synthase (CS) proteins within cardiomyocytes of male type 2 diabetic rats, aiming to discern potential molecular mechanisms influencing cardiac health.

Twenty-four male Wistar rats were randomly assigned to control (NC), diabetic control (DC), diabetic with type 1 HIIT (HIIT-1), and diabetic with type 2 HIIT (HIIT-2) groups. Streptozotocin (STZ) induced type 2 diabetes, excluding the NC group. A four-week HIIT intervention, six sessions per week, preceded the analysis of heart tissue for PGC-1α, p53, and CS protein levels. Statistical analysis employed GraphPad Prism software version 8 and one-way ANOVA (P < 0.05).

Both HIIT-1 (p=0.004) and HIIT-2 (p=0.007) groups exhibited significantly elevated cardiac PGC-1α levels compared to DC. CS levels increased notably in HIIT-1 (p=0.001) and HIIT-2 (p<0.001), with HIIT-2 surpassing HIIT-1 significantly (p=0.010). Concurrently, p53 levels significantly decreased in both HIIT-1 (p=0.005) and HIIT-2 (p=0.001) groups compared to DC.

Exercise training (HIIT) positively influences cardiac metabolism, evident in PGC-1α and CS upregulation and p53 downregulation. While these findings provide valuable insights, further exploration is crucial for a comprehensive understanding of the underlying molecular mechanisms. This study advances our understanding of optimizing exercise interventions for improved cardiac health in type 2 diabetes.

This study explores the combined effects of concurrent training and capecitabine consumption on breast cancer prevention and therapy, focusing on the modulation of BRCA1 gene expression.

In the main study, 12 mice were divided into groups, including Exercise-Tumor-Exercise (ETE), Exercise-Tumor-Exercise+Drug (ETE + D), and various others. Resistance and endurance training were conducted five days a week for 12 weeks before and eight weeks after tumor induction, accompanied by capecitabine administration. BRCA1 gene expression was assessed post-intervention using SPSS 20.

MC4-L2 injection induced tumors. Both pre and post-cancer induction, exercise significantly increased BRCA1 gene expression (p = 0.001, p = 0.001). Exercise combined with post-cancer capecitabine led to increased BRCA1 expression (p = 0.001). Capecitabine alone post-cancer also elevated BRCA1 expression (p = 0.001). Exercise, exercise with capecitabine, and capecitabine alone post-cancer showed significantly higher BRCA1 expression than exercise pre-cancer (p = 0.001). Exercise-tumor-exercise and Exercise-Tumor-Exercise+Drug groups exhibited increased BRCA1 expression compared to exercise-tumor-drug (p = 0.001).

The ETE+D protocol, involving exercise and capecitabine post-cancer, increased BRCA1 expression, suggesting potential roles in tumor prevention and therapy.

Hypertension is a pivotal modifiable risk factor for global cardiovascular diseases and premature mortality, often associated with a high-fat diet. This study aimed to explore the impact of endurance training on selected hemodynamic factors in rats subjected to a high-fat diet.

In this experimental research, 21 male Wistar rats (weighing 200-250 g) were randomly assigned to three groups: high-fat diet (HF), normal diet (C), and high-fat diet with endurance training (HF+T), each comprising seven rats. The HF and HF+T groups were exposed to a high-fat diet (60% calories from fat) for 12 weeks. Subsequently, the HF+T group underwent a six-week, five-sessions-per-week endurance training program. Cardiac parameters were recorded using physiography, and data analysis was performed with SPSS software version 24, utilizing one-way ANOVA.

The one-way ANOVA results showed no significant difference between groups in heart rate (p=0.143). However, systolic blood pressure was significantly higher in the HF+T group compared to C (p=0.001) and HF (p=0.045) groups. The HF group also exhibited significantly elevated systolic blood pressure compared to the C group (p=0.044). Additionally, diastolic blood pressure was significantly higher in both the HF (p=0.021) and HF+T (p=0.009) groups compared to the C group.

This study suggests that a high-fat diet, particularly when combined with endurance training, leads to an increase in blood pressure in rats compared to those fed a normal diet, emphasizing the complex relationship between diet, exercise, and cardiovascular health. The findings underscore the importance of understanding these interactions for comprehensive cardiovascular risk management. The identified hemodynamic changes contribute valuable insights for future interventions aimed at mitigating the impact of high-fat diets on cardiovascular health.