Department of Cardiology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China (mainland).
Department of Medicine, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi, China (mainland).
Med Sci Monit. 2020 Jul 7;26:e926441. doi: 10.12659/MSM.926441.
BACKGROUND Hyperbilirubinemia is associated with central nervous system damage in preterm neonates due to the neurotoxicity of bilirubin. This study explored the possible mechanisms of bilirubin's neurotoxicity, and the protective effect of baicalin (BAI) was also investigated. MATERIAL AND METHODS Isolated neonatal rat hippocampal neurons were exposed to free bilirubin (Bf). BAI was used to treat these neurons. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was used to evaluate the cell viability. Terminal deoxynucleotidyl transferase-dUTP nick-end labeling (TUNEL) assay was used to detect apoptosis. Contents of inflammatory cytokines were determined by enzyme-linked immunosorbent assay (ELISA). Protein expression and phosphorylation levels were assessed by Western blotting. Nuclear translocation was observed by immunofluorescent staining. RESULTS Bf incubation significantly induced apoptosis and decreased viabilities of neurons. The phosphorylation levels of MAP kinase kinase (MKK)3, MKK6, p38 mitogen- activated protein kinases (MAPK), nuclear translocation level of p65, and the expression levels of cleaved caspase3 and tumor necrosis factor (TNF)alpha were found to be dramatically higher in Bf-incubated neurons. BAI pre-treatment, however, increased cell viability by reducing cell apoptosis. BAI pre-treatment also reduced phosphorylation levels of MKK3, MKK6, p38 MAPK, and nuclear translocation level of p65, as well as the expression levels of cleaved caspase3 and TNFalpha, in Bf- incubated neurons. CONCLUSIONS BAI suppressed bilirubin-induced neuron apoptosis and inflammation by deactivating p38 MAPK signaling.
胆红素血症可导致早产儿中枢神经系统损伤,这是由于胆红素的神经毒性作用。本研究旨在探讨胆红素神经毒性的可能机制,并研究黄芩苷(BAI)的保护作用。
分离新生大鼠海马神经元,使其暴露于游离胆红素(Bf)中。用 BAI 处理这些神经元。使用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法评估细胞活力。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)测定法用于检测细胞凋亡。酶联免疫吸附测定法(ELISA)用于测定炎症细胞因子的含量。通过 Western blot 评估蛋白表达和磷酸化水平。通过免疫荧光染色观察核转位。
Bf 孵育显著诱导神经元凋亡并降低其活力。Bf 孵育神经元中 MKK3、MKK6、p38 丝裂原激活蛋白激酶(MAPK)的磷酸化水平、p65 的核转位水平以及 cleaved caspase3 和肿瘤坏死因子(TNF)alpha 的表达水平明显升高。然而,BAI 预处理通过减少细胞凋亡来增加细胞活力。BAI 预处理还降低了 Bf 孵育神经元中 MKK3、MKK6、p38 MAPK 的磷酸化水平和 p65 的核转位水平,以及 cleaved caspase3 和 TNFalpha 的表达水平。
BAI 通过抑制 p38 MAPK 信号通路抑制胆红素诱导的神经元凋亡和炎症。