Aerobic training prevents the stress-induced endothelial dysfunction in male and female Wistar rats by different pathways.

IF 3.7 3区 医学 Q1 PHYSIOLOGY
Journal of applied physiology Pub Date : 2026-10-01 Epub Date: 2026-09-21 DOI:10.1152/japplphysiol.01061.2025
Bianca Bittencourt Lucchetti, Juliana Arruda de Souza Monnerat, Gabriel Fernandes Teixeira, Juliana Mentzinger, Luiza Rocha, Helena Naly Miguens Rocha, Gabriel Ferreira Lima, Nadia Alice Vieira Motta, Fernanda Carla Ferreira Brito, Priscila Gomes Pereira, Jemima Fuentes Ribeiro da Silva, Natalia Galito Rocha, Antonio Claudio Lucas da Nóbrega, Renata Frauches Medeiros
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引用次数: 0

Abstract

Variable stress contributes to cardiovascular morbidity by impairing endothelial function through oxidative stress, inflammation, and hormonal imbalance. These effects depend on sex-specific physiological responses. Although aerobic exercise is recognized for its vascular benefits, the mechanisms underlying these adaptations may differ between sexes. This study investigated the sex-specific effects of aerobic training on vascular function in Wistar rats subjected to variable stress. For this, male and female Wistar rats (n = 8/group) were assigned to control or stress groups (8 days using four different types of stressor stimuli), with or without aerobic training (treadmill, moderate intensity, 30 min/day for 8 wk). Thoracic aortic endothelial function was evaluated by acetylcholine-induced relaxation and phenylephrine-induced contraction. Antioxidant enzyme activity, nitrite concentration, and protein expression of endothelial nitric oxide synthase (eNOS), phosphorylated eNOS at serine 1177 (p-eNOSser1177), catalase, and superoxide dismutase (SOD) were measured. Stress impaired endothelium-dependent relaxation and increased vascular collagen content in both sexes. In females, stress reduced eNOS phosphorylation and nitrite bioavailability, while increasing antioxidant enzyme activity. In males, no significant changes in the eNOS-nitric oxide (NO) pathway were observed, but SOD activity increased. Aerobic training attenuated stress-induced vascular injury, predominantly through the upregulation of the eNOS-NO signaling pathway in females, whereas in males, possibly through another pathway related to oxidative status. These findings demonstrate the protective effects of aerobic exercise on vascular health in rats subjected to variable stress and underscore the existence of sex-specific mechanisms, with distinct molecular pathways mediating vascular adaptations in males and females. Furthermore, histological analysis revealed that aerobic training reversed collagen deposition and enhanced elastic fiber content.NEW & NOTEWORTHY Variable stress impairs vascular function in male and female rats, reducing endothelium-dependent relaxation and increasing collagen deposition. Aerobic training prevented these stress-induced vascular alterations, acting through nitric oxide upregulation in females and enhanced antioxidant defenses in males. These findings reveal sex-specific mechanisms underlying vascular protection by exercise and highlight aerobic training as an effective strategy to prevent stress-induced endothelial dysfunction and preserve vascular health.

有氧训练通过不同途径预防应激性内皮功能障碍。
可变应激通过氧化应激、炎症和激素失衡损害内皮功能,从而导致心血管疾病的发生。这些影响取决于性别特异性生理反应。虽然有氧运动被认为对血管有益,但这些适应的机制可能因性别而异。本研究探讨了有氧训练对可变应激Wistar大鼠血管功能的性别特异性影响。为此,雄性和雌性Wistar大鼠(n=8/组)被分配到对照组或应激组(8天使用四种不同类型的应激刺激),进行或不进行有氧训练(跑步机,中等强度,每天30分钟,持续8周)。采用乙酰胆碱诱导舒张法和苯肾上腺素诱导收缩法评价胸主动脉内皮功能。测定eNOS、p-eNOSser1177、过氧化氢酶和超氧化物歧化酶的抗氧化酶活性、亚硝酸盐浓度和蛋白表达。应激损害了两性内皮依赖性松弛和血管胶原含量的增加。在雌性中,应激降低eNOS磷酸化和亚硝酸盐的生物利用度,同时增加抗氧化酶活性。在雄性中,eNOS-NO通路未见明显变化,但SOD活性升高。有氧训练减轻应激诱导的血管损伤,主要是通过上调女性的eNOS-NO信号通路,而在男性中,可能通过另一种与氧化状态相关的途径。这些发现证明了有氧运动对可变应激大鼠血管健康的保护作用,并强调了性别特异性机制的存在,在雄性和雌性中存在不同的分子途径介导血管适应。此外,组织学分析显示有氧训练逆转胶原沉积和提高弹性纤维含量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.00
自引率
9.10%
发文量
296
审稿时长
2-4 weeks
期刊介绍: The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.
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