He Cunbao, Yang Shaojie, Zhu Guoqi
Key Laboratory of Molecular Biology (Brain Diseases), Anhui University of Chinese Medicine, Hefei 230012, China.
Second Affiliated Hospital of Anhui University of Chinese Medicine, Hefei 230061, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2025 Apr 20;45(4):765-773. doi: 10.12122/j.issn.1673-4254.2025.04.12.
To observe the effect of 4-(arylethynyl)-pyrrolo[2,3-d] pyrimidine (10b) on post-traumatic stress disorder (PTSD)-like behaviors and ERK1/2-SGK1 signaling pathway in mice.
C57BL/6 mouse models exposed to single prolonged stress (SPS) were treated with daily gavage of saline, 10b at low, moderate and high doses, or paroxetine for 14 days. The changes in PTSD-like behaviors of SPS mice with different treatments were observed using behavioral tests. Western blotting and immunofluorescence assay were used to detect the protein expression levels of mGluR5, p-ERK, and SGK1 in the hippocampus of the mice. Pathological changes in the liver and kidney tissues of the mice were examined using HE staining. Molecular docking and molecular dynamics analyses were employed to evaluate the binding stability between the compound 10b and mGluR5.
Compared to the normal control mice, the SPS mice exhibited obvious PTSD-like behaviors with increased hippocampal expressions of mGluR5 and p-ERK proteins and decreased SGK1 protein expression. Compound 10b significantly ameliorated behavioral abnormalities in SPS mice, inhibited mGluR5 expression, and reversed the dysregulation of p-ERK and SGK1. No obvious liver or kidney toxicity was observed after 10b treatment. Molecular docking and dynamics studies demonstrated a stable interaction between 10b and mGluR5.
The compound 10b ameliorates PTSD-like behaviors induced by SPS in mice possibly by inhibiting mGluR5 expression to modulate the ERK1/2-SGK1 signaling pathway.
观察4-(芳基乙炔基)-吡咯并[2,3-d]嘧啶(10b)对小鼠创伤后应激障碍(PTSD)样行为及细胞外信号调节激酶1/2-血清糖皮质激素激酶1(ERK1/2-SGK1)信号通路的影响。
对遭受单次长时间应激(SPS)的C57BL/6小鼠模型,每日分别灌胃生理盐水、低、中、高剂量的10b或帕罗西汀,持续14天。采用行为学测试观察不同处理的SPS小鼠PTSD样行为的变化。运用蛋白质免疫印迹法和免疫荧光分析法检测小鼠海马中代谢型谷氨酸受体5(mGluR5)、磷酸化细胞外信号调节激酶(p-ERK)和血清糖皮质激素激酶1(SGK1)的蛋白表达水平。采用苏木精-伊红(HE)染色检查小鼠肝、肾组织的病理变化。利用分子对接和分子动力学分析评估化合物10b与mGluR5之间的结合稳定性。
与正常对照小鼠相比,SPS小鼠表现出明显的PTSD样行为,海马中mGluR5和p-ERK蛋白表达增加,SGK1蛋白表达降低。化合物10b显著改善了SPS小鼠的行为异常,抑制了mGluR5表达,并逆转了p-ERK和SGK1的失调。10b处理后未观察到明显的肝或肾毒性。分子对接和动力学研究表明10b与mGluR5之间存在稳定的相互作用。
化合物10b可能通过抑制mGluR5表达来调节ERK1/2-SGK1信号通路,从而改善SPS诱导的小鼠PTSD样行为。