全氟辛烷磺酸暴露诱发雌性大鼠心血管功能障碍:卵巢的作用

Cardiology and cardiovascular medicine Pub Date : 2024-01-01 Epub Date: 2024-06-26 DOI:10.26502/fccm.92920388
Karina Porfirio, Pankaj Yadav, Sri Vidya Dangudubiyyam, Alissa Hofmann, Jay S Mishra, Sathish Kumar
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引用次数: 0

摘要

全氟和多氟烷基物质(PFAS)是一种普遍存在的环境污染物,经常在世界各地的饮用水中检测到。近年来,有关接触 PFAS 与心血管疾病相关的报道大幅增加。此外,女性似乎更容易受到 PFAS 的不良影响。然而,卵巢在女性更易受 PFAS 相关健康影响方面的潜在作用仍然未知。在这项研究中,我们调查了全氟辛烷磺酸(PFOS)(一种主要的全氟辛烷磺酸)对卵巢完好的雌性大鼠和卵巢切除(OVX)雌性大鼠心血管功能的影响。对 8 周大的雌性 SD 大鼠进行双侧卵巢切除或假手术。手术恢复后,给大鼠饮用含有 50 μg/mL 全氟辛烷磺酸的水,持续 3 周。对照组则饮用不含全氟辛烷磺酸的水。接触全氟辛烷磺酸后,完整大鼠和卵巢切除大鼠的体重都明显减轻,但血压却同样升高。超声心动图分析表明,暴露于 PFOS 会降低完整大鼠的心输出量、收缩末期容积和舒张末期容积,但不会降低卵巢切除大鼠的心输出量、收缩末期容积和舒张末期容积。血管功能研究表明,全氟辛烷磺酸同样降低了完整大鼠和卵巢切除大鼠的内皮依赖性和非依赖性松弛反应。完整大鼠和 OVX 大鼠的内皮依赖性收缩反应更为明显。总之,全氟辛烷磺酸通过激素依赖机制影响心脏功能,而血管功能受损与卵巢状态无关,这表明全氟辛烷磺酸暴露、卵巢状态和心血管功能之间存在错综复杂的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perfluorooctane Sulfonate Exposure Induces Cardiovascular Dysfunction in Female Rats: Role of Ovaries.

Per- and polyfluoroalkyl substances (PFAS) are pervasive environmental pollutants frequently detected in drinking water worldwide. Reports linking PFAS exposure to cardiovascular disease have increased significantly in recent years. Furthermore, women appear to be more susceptible to the adverse effects of PFAS. However, the potential role of ovaries in the increased vulnerability of females to PFAS-related health effects remains unknown. In this study, we investigated the impact of perfluorooctane sulfonate (PFOS), a prominent PFAS, on the cardiovascular function in female rats with intact ovaries and ovariectomized (OVX) females. Bilateral OVX or sham surgeries were performed in 8-week-old female SD rats. Following recovery from surgeries, the rats were given drinking water containing 50 μg/mL of PFOS for 3 weeks. Control groups received PFOS-free water. PFOS exposure significantly reduced body weight but increased blood pressure similarly in both intact and OVX rats. Echocardiography analysis revealed that PFOS exposure decreased cardiac output, end-systolic volume, and end-diastolic volume in intact but not OVX rats. Vascular function studies demonstrated that PFOS equally reduced endothelium-dependent and -independent relaxation responses in intact and OVX rats. The endothelium-independent contractile responses were more pronounced in both intact and OVX rats. eNOS protein levels were similarly decreased in both intact and OVX rats. In conclusion, PFOS affects cardiac function through hormone-dependent mechanisms, while vascular function is impaired independent of ovarian status, indicating an intricate interplay between PFOS exposure, ovarian status, and cardiovascular function.

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