Effects of chronic stress on rat heart function following regional ischemia: a sex-dependent investigation.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American journal of physiology. Heart and circulatory physiology Pub Date : 2024-10-01 Epub Date: 2024-08-23 DOI:10.1152/ajpheart.00424.2024
Megan Cairns, Caitlin Odendaal, Cassidy O'Brien, Erna Marais, Imken Oestlund, Karl-Heinz Storbeck, Balindiwe Sishi, Danzil Joseph, Carine Smith, M Faadiel Essop
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Abstract

Chronic psychological stress is a recognized, yet understudied risk factor for heart disease, with potential sex-specific effects. We investigated whether chronic stress triggers sex-dependent cardiac dysfunction in isolated Wistar rat hearts subjected to ischemia-reperfusion injury. The experimental cohort underwent 1 h of daily restraint stress for 4 wk versus matched controls, followed by euthanasia (sodium pentobarbital) and heart excision for ex vivo perfusion. Blood analysis revealed sex-specific alterations in stress hormones and inflammatory markers. When compared with controls, chronic restraint stress (CRS) males displayed decreased plasma brain-derived neurotrophic factor (BDNF) levels (P < 0.05), whereas CRS females exhibited elevated plasma adrenocorticotropic hormone (ACTH) (P < 0.01) and reduced corticosterone (P < 0.001) alongside lower serum estradiol (P < 0.001) and estradiol/progesterone ratio (P < 0.01). Of note, CRS females showed increased serum cardiac troponin T (P < 0.05) and tumor necrosis factor-α (TNF-α) (P < 0.01) with suppressed interleukin (IL)-1α, IL-1β, IL-6, and IL-10 levels (P < 0.05) when compared with controls. Ex vivo Langendorff perfusions revealed that CRS female hearts displayed impaired postischemic functional recovery for baseline stroke volume (SV, P < 0.01), work performance (P < 0.05), aortic output (AO, P < 0.05), coronary flow (CF, P < 0.01), and overall cardiac output (CO, P < 0.01) when compared with matched controls and CRS males (P < 0.05). Our findings reveal intriguing sex-specific responses at both the systemic and functional levels in stressed hearts. Here, the dysregulation of stress hormones, proinflammatory state, and potential underlying cardiomyopathy in females following the stress protocol renders them more prone to damage following myocardial ischemia. This study emphasizes the importance of incorporating sex as a biological variable in cardiac research focusing on stress-related cardiomyopathy.NEW & NOTEWORTHY Although chronic psychological stress is a risk factor for cardiovascular diseases, the underlying mechanisms remain poorly understood. This study revealed that chronic restraint stress resulted in systemic changes (dysregulated stress hormones, proinflammatory state) and potential cardiomyopathy in females versus controls and their male counterparts. The stressed female hearts also displayed reduced functional recovery following ex vivo ischemia-reperfusion. This highlights the importance of incorporating sex as a biological variable in cardiac research.

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区域性缺血后慢性压力对大鼠心脏功能的影响:一项性别依赖性研究。
慢性社会心理压力是公认的心脏病风险因素,但对它的研究还不够,它可能具有性别特异性影响。我们研究了慢性应激是否会在遭受缺血再灌注损伤的离体 Wistar 大鼠心脏中引发性别依赖性心脏功能障碍。与匹配的对照组相比,实验组大鼠每天接受 1 小时的束缚应激,持续四周,然后安乐死(戊巴比妥钠)并切除心脏进行体外灌注。血液分析显示,应激激素和炎症标志物的变化具有性别特异性。与对照组相比,慢性束缚应激(CRS)男性的血浆脑源性神经营养因子(BDNF)水平降低(p),而慢性束缚应激(CRS)女性的血浆促肾上腺皮质激素(ACTH)升高(p),皮质酮降低(p),同时血清雌二醇(p)和雌二醇/孕酮比值降低(p)。值得注意的是,与对照组相比,CRS 女性的血清心肌肌钙蛋白 T(p)增加,白细胞介素(IL)-1a、IL-1β、IL-6 和 IL-10 水平(p)降低。体外朗根多夫灌流显示,与匹配的对照组和 CRS 男性相比,CRS 女性心脏缺血后的功能恢复受损,包括基线每搏量(p)、工作表现(p)、主动脉输出量(p)、冠状动脉流量(p)和总体心输出量(p)(p)。 我们的研究结果揭示了应激心脏在系统和功能水平上的耐人寻味的性别特异性反应。在这里,女性在应激方案后的应激激素失调、促炎症状态和潜在的潜在心肌病使她们在心肌缺血后更容易受到损伤。这项研究强调了在以应激相关心肌病为重点的心脏研究中将性别作为生物变量的重要性。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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