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慢性应激对大鼠局部缺血后心脏功能的影响:性别依赖性研究。

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

机构信息

Centre for Cardio-metabolic Research in Africa (CARMA), Division of Medical Physiology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

Department of Biochemistry, Faculty of Science, Stellenbosch University, Cape Town, South Africa.

出版信息

Am J Physiol Heart Circ Physiol. 2024 Oct 1;327(4):H880-H895. doi: 10.1152/ajpheart.00424.2024. Epub 2024 Aug 23.

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 ( < 0.05), whereas CRS females exhibited elevated plasma adrenocorticotropic hormone (ACTH) ( < 0.01) and reduced corticosterone ( < 0.001) alongside lower serum estradiol ( < 0.001) and estradiol/progesterone ratio ( < 0.01). Of note, CRS females showed increased serum cardiac troponin T ( < 0.05) and tumor necrosis factor-α (TNF-α) ( < 0.01) with suppressed interleukin (IL)-1α, IL-1β, IL-6, and IL-10 levels ( < 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, < 0.01), work performance ( < 0.05), aortic output (AO, < 0.05), coronary flow (CF, < 0.01), and overall cardiac output (CO, < 0.01) when compared with matched controls and CRS males ( < 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. 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.

摘要

慢性心理应激是一种公认的、但研究不足的心脏病风险因素,可能存在潜在的性别特异性影响。我们研究了慢性应激是否会引发缺血再灌注损伤的 Wistar 大鼠离体心脏的性别依赖性心功能障碍。实验组接受了 4 周每天 1 小时的束缚应激,而匹配的对照组则接受了安乐死(戊巴比妥钠)和心脏切除,以便进行离体灌注。血液分析显示应激激素和炎症标志物存在性别特异性变化。与对照组相比,慢性束缚应激(CRS)雄性大鼠的血浆脑源性神经营养因子(BDNF)水平降低(<0.05),而 CRS 雌性大鼠的血浆促肾上腺皮质激素(ACTH)升高(<0.01),皮质酮降低(<0.001),同时血清雌二醇(<0.001)和雌二醇/孕酮比值降低(<0.01)。值得注意的是,与对照组相比,CRS 雌性大鼠的血清心肌肌钙蛋白 T(<0.05)和肿瘤坏死因子-α(TNF-α)升高(<0.01),同时白细胞介素(IL)-1α、IL-1β、IL-6 和 IL-10 水平降低(<0.05)。离体 Langendorff 灌注显示,与匹配的对照组和 CRS 雄性大鼠相比,CRS 雌性大鼠的缺血后功能恢复受损,基础心排量(SV,<0.01)、做功性能(<0.05)、主动脉输出(AO,<0.05)、冠状血流(CF,<0.01)和整体心排量(CO,<0.01)均降低(<0.05)。我们的研究结果揭示了应激心脏在系统性和功能性水平上的有趣的性别特异性反应。在这里,应激后女性的应激激素失调、促炎状态和潜在的心肌病使她们在心肌缺血后更容易受到损伤。这项研究强调了在关注应激相关心肌病的心脏研究中,将性别作为生物学变量的重要性。尽管慢性心理应激是心血管疾病的一个危险因素,但潜在的机制仍知之甚少。这项研究表明,慢性束缚应激导致雌性而非对照组和雄性大鼠的系统性变化(应激激素失调、促炎状态)和潜在的心肌病。应激后的雌性心脏在离体缺血再灌注后也显示出功能恢复减少。这突出了将性别作为生物学变量纳入心脏研究的重要性。

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