Logistics University of the Chinese People's Armed Police Force, Tianjin, 300309, China; Tianjin Key Laboratory of Cardiovascular Remodeling and Target Organ Injury, Characteristic Medical Center of the Chinese People's Armed Police Force, Tianjin, 300162, China.
Tianjin Economic-Technological Development Area (TEDA) International Cardiovascular Hospital, Tianjin, 300457, China.
Placenta. 2020 Sep 15;99:35-44. doi: 10.1016/j.placenta.2020.06.015. Epub 2020 Jul 20.
Preeclampsia (PE) is a serious maternal inflammatory disease with endothelial cell dysfunction, and there is a lack of effective treatment and prevention. Tadalafil is considered to be a promising drug for PE. This study aimed to determine whether and how tadalafil use during early pregnancy alleviates PE induced by N-nitro-l-arginine-methyl-ester (l-NAME), an antagonist of nitric oxide synthase, in rats.
Twenty-eight Sprague-Dawley (SD) rats were randomly divided into 4 equal groups on gestational day 0 (GD0): a pregnant control group, an l-NAME-treated PE group and two prophylactic low-dose and high-dose tadalafil groups. Blood pressure was measured on GD0, 5, 10, 15 and 20. Proteinuria was assessed on GD0 and 18. Femoral artery ultrasound was performed on GD19. Tissue sampling was performed on GD20. The perinatal outcomes, placenta and kidney tissue morphology, and endothelial and inflammatory markers were examined.
Prophylactic administration of low and high doses of tadalafil improved l-NAME induced hypertension, proteinuria, maternal weight loss during pregnancy, fetal growth restriction and flow-mediated dilatation, balanced endothelial-relative factors, and alleviated inflammation activation in placenta and kidney tissue. What's more, in some results, the HT group performed better than the LT group.
Our results indicate that prophylactic use of tadalafil in l-NAME-induced PE-like rat models alleviates PE symptoms, promotes fetal growth, protects endothelial function and reduces inflammation, suggesting that tadalafil may be a potential drug for the prevention of PE.
子痫前期(PE)是一种严重的母体炎症性疾病,伴有内皮细胞功能障碍,目前缺乏有效的治疗和预防方法。他达拉非被认为是治疗 PE 的一种有前途的药物。本研究旨在确定在妊娠早期使用他达拉非是否以及如何缓解 N-硝基-L-精氨酸甲酯(l-NAME)诱导的大鼠 PE,l-NAME 是一氧化氮合酶的拮抗剂。
28 只 Sprague-Dawley(SD)大鼠在妊娠第 0 天(GD0)随机分为 4 组:妊娠对照组、l-NAME 诱导的 PE 组和两种预防低剂量和高剂量他达拉非组。在 GD0、5、10、15 和 20 测量血压。在 GD0 和 18 评估蛋白尿。在 GD19 进行股动脉超声检查。在 GD20 进行组织取样。检查围产期结局、胎盘和肾脏组织形态以及内皮和炎症标志物。
预防给予低剂量和高剂量他达拉非可改善 l-NAME 诱导的高血压、蛋白尿、妊娠期间母体体重减轻、胎儿生长受限和血流介导的扩张,平衡内皮相关因素,并减轻胎盘和肾脏组织中的炎症激活。更重要的是,在一些结果中,HT 组的表现优于 LT 组。
我们的结果表明,在 l-NAME 诱导的 PE 样大鼠模型中预防性使用他达拉非可缓解 PE 症状、促进胎儿生长、保护内皮功能和减轻炎症,提示他达拉非可能是预防 PE 的一种潜在药物。