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Background and Objective: New markers of cardiovascular disease have more sensitivity and accuracy in predicting cardiovascular events. Considering the effective role of physical activity in preventing and reducing cardiovascular disease, which will be of great help in improving the health of people in the community. This study was done to determine the effect of diving in different depths on the level of C-reactive protein (CRP) and lipid profiles of diver men.
Methods: This quasi-experimental study was carried out on 6 male diver members of the rescue and rescue team of the Red Crescent Society of Kohkiluyeh and Boyer Ahmad province in Iran. Subjects diverted on the first day at a depth of 1 meter, the second day at a depth of 10 meter, and the third day at a depth of 20 meter for 40 minutes. The subjects were at a depth of 10 and 20 meters at a height of 3 meters to the surface of the water for five-minute steepness. Blood samples were taken before and after diving, and CRP and lipid profiles including triglyceride, total cholesterol, low density lipoprotein and high density lipoprotein were measured.
Results: The increase of environmental stress caused by diving in three depths of 1, 10 and 20 meters of the sea  significantly increased CRP level (P<0.05). No significant changes were observed in the levels of triglyceride, total cholesterol, and low density lipoprotein, but high density lipoprotein level was significantly increased (P<0.05).
Conclusion: Scuba diving, due to the transport of respiratory equipment during activity increases
C-reactive protein and lipid profiles.

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Background and Objective: Oxidative stress plays an important role in the pathogenesis of some diseases such as atherosclerosis and doing high intensity training may enhance oxidative stress. This study was done to evaluate the effect of eight weeks resistance training on malondialdehyd, total, antioxidant capacity, liver enzymes and lipid profile in overweight and obese women.
Methods: In this quasi-experimental study, 16 overweight and obese women were non-randomly divided into intervention (n=9) and control (n=7) groups. The resistance training included the resistance training (with intensity of 50-80% one repetition maximum) that lasted for 8 weeks and 3 sessions per week. Every session lasted for 60 minutes. Malondialdehyd, total antioxidant capacity, liver enzymes and lipid profile for each subject was measured.
Results: The eight weeks resistance training significantly increased total antioxidant capacity high density lipoprotein and triglyceride in interventional group in compared to controls (p<0.05). The eight weeks resistance training significantly reduced alanine aminotransferase in comparison with control group (p<0.05).
Conclusion: Eight weeks resistance training by reducing malondialdehyd and increasing total antioxidant capacity may reduce the risk of atherosclerosis disease and improving cardiovascular health.

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Background and Objective: Sphingosine-1-phosphate (S1P) plays an important role in muscle biology and is involved in hypertrophy and activation of satellite cells. This study was done to determine the effect of eight weeks of concurrent training with different order on S1P in fast and slow muscles in wistar rats.
Methods: In this experimental study, 40 male wistar rats (weight 180-200 gr) were randomly allocated into 5 groups including control, resistance training, endurance training, resistance- endurance training, endurance- resistance training. Resistance training consisted 1-meter ladder climbing with the loading of percent of overloading test (%75 of weight body) in the first week and increased to 30 gr per week. Endurance training consisted of running on treadmill with speed of 12 m/min and 10 minutes in the first week to 30 m/min and 60 minutes in the last week. The resistance- endurance group performed resistance training 5 minutes before endurance training and the endurance- resistance group performed endurance training 5 minutes after resistance training. The protein level of S1P was measured in flexor hallucis longus (FHL) and soleus muscles.
Results: The S1P level in fast and slow twitch muscle increased significantly in endurance- resistance training, resistance- endurance training and resistance training compared to controls (P<0.05). There were no significant differences between concurrent training with differing order.
Conclusion: It seems that exercise order in concurrent training result in no different effect on S1P level in fast and slow twitch muscles in wistar rats.

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Vitamin D deficiency affects a broad range of health-related factors. Both obesity and vitamin D deficiency are associated with the development of oxidative stress and systemic inflammation. Inflammation can culminate in decreased vitamin D levels through the induction of oxidative stress. Evidence suggests that exercise may improve vitamin D status. However, the effects of exercise interventions on inflammation and oxidative stress in the coexistence of vitamin D deficiency and obesity/overweight are not well-established. Therefore, this review aimed to evaluate the effects of exercise on inflammation and oxidative stress in vitamin D deficiency status accompanied by obesity/overweight. A search for articles from 2006 to 2023 was conducted in specialized databases of PubMed, Scopus, and state inpatient database (SID). The searched studies were original research articles, reviews, and clinical trials selected using the keywords of vitamin D deficiency, systemic inflammation, oxidative stress, chemokine, exercise, obesity, and overweight. According to the studies, regular exercise can inhibit the vicious cycle of oxidative stress-inflammation in vitamin D deficiency status accompanied by obesity/overweight by negatively regulating some inflammatory factors and chemokines, reducing lipid peroxidation levels, and increasing antioxidant status. Moreover, the increase in 25-hydroxyvitamin D levels resulting from exercise can be considered another mechanism for reducing oxidative stress-inflammation in vitamin D deficiency status accompanied by obesity/overweight.

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Background and Objective: Docetaxel is an effective chemotherapy drug for treating lung cancer, but its side effects and cytotoxicity limit its use. Natural compounds like carvacrol and thymol, known for their anti-cancer and anti-inflammatory properties, have gained attention as adjunct agents to reduce toxicity and enhance the efficacy of chemotherapy drugs. This study aimed to investigate the impact of carvacrol and thymol on cell viability and function in A549 cancer cells exposed to docetaxel.
Methods: This experimental study was conducted on the epithelial cell line derived from lung cancer tissue (A549), obtained from the Pasteur Institute of Iran at the Faculty of Pharmacy, Mazandaran University of Medical Sciences in the year 1042. In this research, A549 cells were pre-treated with various concentrations of carvacrol and thymol (5, 10, 20, 40, 80, 100, and 200 µg/mL) along with a cytotoxic dose of docetaxel (8.92 µg/mL) over a period of 48 hours. Cytotoxicity was assessed using the MTT assay. Additionally, the levels of reactive oxygen species (ROS) in cells were measured using the DA-DCFH reagent, and malondialdehyde (MDA) levels were determined using the thiobarbituric acid (TBA) reagent.
Results: Carvacrol and thymol significantly reduced the cytotoxic effects of docetaxel at concentrations ranging from 5 to 200 µg/mL (P<0.05). The evaluation of cytotoxicity indicated that at a concentration of 200 µg/mL, carvacrol and thymol exhibited a more pronounced enhancing effect (98.11±1.64%) compared to the concentration of 5 µg/mL (54.64±2.03%). Furthermore, these compounds significantly mitigated the oxidative stress induced by docetaxel by decreasing the production of reactive oxygen species (ROS) and malondialdehyde (MDA) (P<0.05). Specifically, at the concentration of 200 µg/mL, the levels of ROS and MDA were (13.57±0.09%) and (0.55±0.003%), respectively, in contrast to the levels at 5 µg/mL, which were (20.50±0.59%) and (0.98±0.01%). This demonstrates a notable inhibitory effect on the growth of cancer cells by carvacrol and thymol.
Conclusion: Carvacrol and thymol demonstrate high potential as compounds to improve cell function and reduce the cytotoxicity induced by docetaxel in A549 cancer cells. These findings suggest the potential enhancement of chemotherapy regimens for cancer treatment.