多花蔷薇及其活性化合物鞣花酸通过抑制单胺氧化酶改善小鼠抑郁样行为

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Minji Kim , Dong Wook Lim , Min-Sun Kim , Heejin Nam , Sooim Shin , Changho Lee , Min Young Um
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引用次数: 0

摘要

抑郁症是一项重大的全球健康挑战,造成严重的社会和经济负担。多花蔷薇具有一系列的生物学特性;然而,它在减少压力激素引起的抑郁症中的作用仍不清楚。本研究探讨了多花蔷薇提取物(RMFE)对皮质酮(CORT)诱导的小鼠抑郁样行为的抗抑郁作用,并探讨其分子机制。给予ICR小鼠CORT(40 mg/kg/天,i.p.) 8周,诱导抑郁样行为。然后用RMFE(100或300 mg/kg/day, p.o.)或selegiline(10 mg/kg/day, p.o.)作为阳性对照。通过悬尾和强迫游泳测试评估,RMFE治疗显著缓解了抑郁样行为。RMFE降低海马星形胶质细胞肥大,降低单胺氧化酶A和B (MAOA和MAOB)蛋白和mRNA表达。植物化学分析采用UPLC-MS/MS技术鉴定出5种黄酮类化合物,分别为鞣花酸(EA)、金丝桃苷、异槲皮素、槲皮素和槲皮素-3-葡糖苷。在硅分子对接中发现,这些酚类化合物与MAOA和MAOB相互作用,其中EA表现出最强的结合亲和力。与此一致的是,给药EA有效地缓解了cort治疗小鼠的抑郁样行为,并增加了单胺类神经递质水平。这些结果表明,RMFE通过抑制MAO、恢复单胺水平和调节海马星形细胞肥大来发挥抗抑郁作用,EA被确定为推动其功效的主要生物活性化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rosa multiflora fructus and its active compound ellagic acid improve depressive-like behaviors in mice via monoamine oxidase inhibition
Depression is a significant global health challenge, imposing severe social and economic burdens. Rosa multiflora fructus possesses a range of biological properties; however, its role in reducing stress hormone-induced depression remains unclear. This study examined the antidepressant effects of Rosa multiflora fructus extract (RMFE) on corticosterone (CORT)-induced depressive-like behaviors in mice and explored the underlying molecular mechanisms. ICR mice were administered CORT (40 mg/kg/day, i.p.) for 8 weeks to induce depressive-like behaviors. They were then treated with RMFE (100 or 300 mg/kg/day, p.o.) or selegiline (10 mg/kg/day, p.o.) as a positive control. RMFE treatment significantly alleviated depressive-like behaviors, as evaluated by the tail suspension and forced swimming tests. Furthermore, RMFE reduced hippocampal astrocyte hypertrophy and lowered the protein and mRNA expression of monoamine oxidase A and B (MAOA and MAOB). Phytochemical analysis using UPLC-MS/MS identified five flavonoids in RMFE, including ellagic acid (EA), hyperoside, isoquercetin, quercetin, and quercetin-3-glucuronide. In silico molecular docking revealed that these phenolic compounds interact with MAOA and MAOB, with EA exhibiting the strongest binding affinity. Consistently, EA administration effectively alleviated depressive-like behaviors and increased monoamine neurotransmitter levels in CORT-treated mice. These results suggest that RMFE exerts antidepressant effects by inhibiting MAO, restoring monoamine levels, and modulating hippocampal astrocytic hypertrophy, with EA identified as the primary bioactive compound driving its efficacy.
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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