Park Mae Ja, Chae Jeong-Pil, Woo Dongju, Kim Ji Yoon, Bae Yong Chul, Lee Ju Yup, Lee Sang Yeon, Nam Eon Jeong, Nam Sung-Wook
Department of Anatomy, School of Medicine, Kyungpook National University, Daegu, 41944, Republic of Korea.
Brain Science and Engineering Institute, Kyungpook National University, Daegu, 41404, Republic of Korea.
Biochem Biophys Res Commun. 2024 Apr 9;703:149565. doi: 10.1016/j.bbrc.2024.149565. Epub 2024 Feb 7.
Ibuprofen, one of the most commonly prescribed nonsteroidal anti-inflammatory drugs, has not been fully assessed for embryonic toxicity in vertebrates. Here, we systematically assessed the embryotoxicity of ibuprofen in Xenopus laevis at various concentrations during embryogenesis. Embryos were treated with different concentrations of ibuprofen, ranging from 8 to 64 mg/L, at 23 °C for 96 h, and examined daily and evaluated at 72 hpf. Lethal or teratogenic effects were documented. For histological analysis, paraffin embedded embryos were transversely sectioned at a thickness of 10-μm and stained with hematoxylin and eosin. Total RNA was isolated from embryos at stages 6, 12, 22 and 36, and real-time quantitative PCR was performed. Ibuprofen-treated embryos showed delayed or failed dorsal lip formation and its closure at the beginning of gastrulation. This resulted in herniation of the endodermal mass after gastrulation under high concentrations of ibuprofen-treated embryos. Underdeveloped intestines with stage and/or intestinal malrotation, distorted microcephaly, and hypoplastic heart, lungs, and pronephric tubules were observed in ibuprofen-treated embryos. Cephalic, cardiac, and truncal edema were also observed in them. The severity of the deformities was observed in a concentration-dependent manner. The teratogenic index was 2.28. These gross and histological disruptions correlated well with the altered expression of each organ marker gene. In conclusion, ibuprofen induced delayed and disrupted gastrulation in the early developmental stage and multiorgan malformation later in the organogenesis stage of Xenopus laevis embryos.
布洛芬是最常用的非甾体抗炎药之一,尚未在脊椎动物中对其胚胎毒性进行全面评估。在此,我们系统地评估了布洛芬在非洲爪蟾胚胎发育过程中不同浓度下的胚胎毒性。将胚胎在23℃下用8至64mg/L的不同浓度布洛芬处理96小时,每天进行检查并在受精后72小时进行评估。记录致死或致畸效应。对于组织学分析,将石蜡包埋的胚胎横向切成10μm厚的切片,并用苏木精和伊红染色。从第6、12、22和36阶段的胚胎中分离总RNA,并进行实时定量PCR。用布洛芬处理的胚胎在原肠胚形成开始时显示背唇形成延迟或失败及其闭合。这导致在高浓度布洛芬处理的胚胎中原肠胚形成后内胚层团块突出。在布洛芬处理的胚胎中观察到肠道发育不全伴阶段和/或肠旋转不良、小头畸形、以及心脏、肺和前肾小管发育不全。在它们中还观察到头、心脏和躯干水肿。畸形的严重程度呈浓度依赖性。致畸指数为2.28。这些大体和组织学破坏与每个器官标记基因表达的改变密切相关。总之,布洛芬在非洲爪蟾胚胎的早期发育阶段诱导原肠胚形成延迟和破坏,并在器官发生阶段后期导致多器官畸形。