Griffin Ashley, Szczepanski Jamie, Spencer Shauna-Kay, Solis Lucia, Bowles Teylor, Robinson Reanna, Williams Jan M, Kyle Patrick B, Wallace Kedra
Program in Neuroscience, University of Mississippi Medical Center, Jackson, MS, United States.
Department of Obstetrics and Gynecology, University of Mississippi Medical Center, Jackson, MS, United States.
Front Physiol. 2024 Nov 25;15:1468793. doi: 10.3389/fphys.2024.1468793. eCollection 2024.
Women with hypertensive disorders of pregnancy such as HELLP (hemolysis, elevated liver enzyme, low platelet) Syndrome are affected by acute kidney injury during pregnancy (PR-AKI) at higher rates than women without hypertension. Both hypertensive disorders of pregnancy and Acute Kidney Injury (AKI) outside the context of pregnancy have been associated with an increased risk of developing Chronic Kidney Disease (CKD) and cognitive impairment. In our current study, we set out to determine if PR-AKI led to the development of CKD and impaired cognition in the postpartum period and if HELLP syndrome exacerbates the impairments.
Using timed-pregnant Sprague Dawley rats, on gestational day (GD) 12, mini-osmotic pumps infusing anti-angiogenic factors were surgically placed in the intraperitoneal cavity to induce HELLP. On GD18, AKI was induced via bilateral renal reperfusion ischemia surgery. Mean arterial pressure and birth outcomes were used to assess the global effects of AKI, and liver enzymes were used to assess HELLP. CKD was assessed by measuring glomerular filtration rate (GFR), urinary output, and renal fibrosis. Anxiety-like behaviors, object recognition memory, spatial memory, and avoidance memory were assessed via behavioral experiments.
HELLP + AKI rats demonstrated more evidence of renal injury, hypertension, and behavioral deficits compared to normal pregnant animals. In addition, AKI had a negative impact on birth outcomes and maternal survival.
HELLP + AKI together led to evidence of persistent hypertension, progressive renal dysfunction, and cognitive impairment, which were exacerbated compared to AKI or HELLP alone. These findings suggest that PR-AKI in the presence of a hypertensive disorder of pregnancy, such as HELLP, leads to the development of CKD, cognitive dysfunction, and hypertension.
患有妊娠期高血压疾病(如 HELLP 综合征,即溶血、肝酶升高、血小板减少综合征)的女性在孕期发生急性肾损伤(PR-AKI)的几率高于非高血压女性。妊娠期高血压疾病和非孕期的急性肾损伤(AKI)均与患慢性肾脏病(CKD)及认知障碍的风险增加有关。在我们当前的研究中,我们着手确定 PR-AKI 是否会导致产后 CKD 的发生和认知功能受损,以及 HELLP 综合征是否会加剧这些损害。
使用定时怀孕的 Sprague Dawley 大鼠,在妊娠第 12 天,通过手术将输注抗血管生成因子的微型渗透泵置于腹腔内以诱导 HELLP。在妊娠第 18 天,通过双侧肾脏再灌注缺血手术诱导 AKI。平均动脉压和出生结局用于评估 AKI 的总体影响,肝酶用于评估 HELLP。通过测量肾小球滤过率(GFR)、尿量和肾纤维化来评估 CKD。通过行为实验评估类似焦虑的行为、物体识别记忆、空间记忆和回避记忆。
与正常怀孕动物相比,HELLP + AKI 大鼠表现出更多肾损伤、高血压和行为缺陷的证据。此外,AKI 对出生结局和母体存活率有负面影响。
HELLP + AKI 共同导致持续性高血压、进行性肾功能障碍和认知障碍的证据,与单独的 AKI 或 HELLP 相比,这些情况更为严重。这些发现表明,在存在妊娠期高血压疾病(如 HELLP)的情况下,PR-AKI 会导致 CKD、认知功能障碍和高血压的发生。