Effects of heat exposure and vitamin C intervention on oxidative stress and blood pressure changes in treadmill rats.
10.3760/cma.j.cn121094-20211217-00621
- VernacularTitle:热暴露下跑台大鼠的氧化应激和血压变化及维生素C的干预作用
- Author:
Wei DU
1
;
Yun LI
1
;
Fu Hai SHEN
1
;
Xiao Hua JIANG
2
;
Jing Rui TIAN
2
;
Hong Min FAN
1
Author Information
1. School of Public Health, North China University of Science and Technology, Tangshan 063210, China.
2. School of Basic Medical Sciences, North China University of Science and Technology, Tangshan 063210, China.
- Publication Type:Journal Article
- Keywords:
Heat exposure;
Hypertension;
Oxidative stress;
Vitamin C
- MeSH:
Male;
Animals;
Rats;
Ascorbic Acid;
Antioxidants/pharmacology*;
Blood Pressure;
Hot Temperature;
NF-E2-Related Factor 2;
Oxidative Stress;
Fever
- From:
Chinese Journal of Industrial Hygiene and Occupational Diseases
2023;41(2):112-117
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To investigate the effect of oxidative stress caused by heat exposure on the blood pressure increase of treadmill rats and the intervention of antioxidants. Methods: In June 2021, Twenty-four healthy SD male rats were randomly divided into four groups: normal temperature feeding, normal temperature treadmill, high temperature treadmill and high temperature treadmill supplementation with vitamin C groups, 6 rats in each group. The rats run on the platform in normal temperature or heat exposure environment for 30 min in the morning and in the afternoon daily, 6 days per week. The daily vitamin C supplement dose of high temperature treadmill supplementation with vitamin C group was 10 mg/kg. BP recordings were done at the end of the week. The rat vascular lipofuscin (LF) was detected by ELISA, the rat serum nitric oxide (NO) was detected by nitrate reductase method, the serum malondialdehyde (MDA) was detected by thibabituric acid method, the serum glutathione peroxidase (GPx) and superoxide dismutase (SOD) were detected by chemiluminescence method, and the serum catalase (CAT) was detected by ammonium molybdate method. The total antioxidant capacity (T-AOC) of serum was measured by iron reduction/antioxidant capacity method, and the content of nuclear erythroid 2-related factor 2 (Nrf2) in vascular tissue was measured by Western blot. The intra-group mean was compared by repeated measurement analysis of variance, and the inter-group mean was compared by single-factor analysis of variance and post-event LSD-t test. Results: Compared with the previous time point, the systolic BP and diastolic BP of the high temperature treadmill group were significantly increased at 7, 14 and 21 d, and decreased at 28 d which were higher than the initial level (P<0.05), and the systolic BP and diastolic BP values at each experimental time point were significantly higher than those of normal temperature treadmill group (P<0.001). The changes of thickening of the artery wall, no smoothing of the endodermis and irregular arrangement of muscle cells in high temperature treadmill group were observed. Compared with the normal temperature treadmill group, the content of MDA in serum, and LF in vascular tissue were significantly increased, the activities of SOD, CAT, T-AOC, the content of NO in serum, and the expression of Nrf2 in vascular tissue were significantly decreased in high temperature treadmill group (P<0.05). Compared with the high temperature treadmill group, the systolic BP and diastolic BP values at 7, 14, 21 and 28 d, the content of serum MDA and LF in vascular tissue were significantly decreased, the activities of CAT and T-AOC, and the expression of Nrf2 in vascular tissue significantly increased (P<0.05), the histopathological changes of the artery wall improved in high temperature treadmill supplementation with vitamin C group. Conclusion: Heat exposure has effect on oxidative stress, which may be related to the increase of BP. Vitamin C as an anti-oxidative enhancer can prevent those negative effects, which could alleviate the pathological changes of vessel intima in heat-exposed rats. And the Nrf2 may be a regulated factor to vascular protection.
