芙蓉花萼水提物对瑞士雄性小鼠的慢性轻度应激性神经行为障碍和生化扰动具有神经保护作用

Valiant Orodeh Adeoye , Abayomi Mayowa Ajayi , Peter Oghenebrorhie Orodeh , Joseph Chimezie , Love Enebeli , Paul Ademola Adeleke , Olatunde Owoeye , Solomon Umukoro
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引用次数: 0

摘要

芙蓉花茶(俗称玫瑰花茶或中国玫瑰花茶)因其舒缓作用而广为人知,特别是在长时间的压力下。在传统中医(TCM)中,它因其治疗益处而受到重视,包括抗高血压、抗炎和保护肝脏的作用。本研究探讨了沙达尼花萼水提物(AEHS)在缓解不可预测的慢性轻度应激(UCMS)小鼠应激诱导的神经行为和生化变化中的神经保护作用。方法30只雄性瑞士小鼠随机分为5组(n = 6),均给予口服治疗。1组(对照组)和2组(ucms -对照组)给予蒸馏水,3-5组分别给予剂量为50、100和200 mg/kg的AEHS。2 ~ 5组每天进行不可预测的慢性轻度应激(UCMS),持续21 d。在第20天和第21天进行神经行为评估,包括运动活动、记忆、焦虑和抑郁样行为。第22天,分析血糖和血清皮质酮水平以及氧化应激生物标志物、亚硝酸盐、促炎细胞因子(肿瘤坏死因子- α和白细胞介素-6)和前额皮质、杏仁核和海马中的血清素水平。检测脑源性神经营养因子(BDNF)、核因子κB (NF-κB)、环磷酸腺苷(cAMP)反应因子结合蛋白(CREB)、核因子红细胞2相关因子2 (Nrf2)。测定大鼠脑区乙酰胆碱酯酶(AChE)和谷氨酸脱羧酶(GAD)活性及组织形态学变化。结果saehs可有效调节ucms诱导的神经行为障碍,并可提高血糖和血浆皮质酮水平。该提取物减轻了ucms诱导的丙二醛(MDA)、亚硝酸盐、促炎细胞因子、NF-κB和AChE的升高。此外,AEHS恢复了大脑区域内谷胱甘肽、过氧化氢酶、超氧化物歧化酶、CREB、BDNF、Nrf2、血清素和广泛性焦虑症活性的降低水平。此外,AEHS改善了ucms诱导的脑组织形态学改变。讨论/结论本研究表明,AEHS通过增强抗氧化防御和调节BDNF、CREB、Nrf2和NF-κB等关键信号通路,对慢性应激性神经行为障碍、生化和组织形态学改变具有神经保护作用。这些发现强调了AEHS在中医框架内缓解慢性应激相关精神障碍方面的潜在治疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aqueous extract of Hibiscus sabdariffa calyces offers neuroprotection against unpredictable chronic mild stress-induced neurobehavioral disorders and biochemical perturbations in male Swiss mice

Introduction

Hibiscus sabdariffa (commonly known as roselle or Chinese rose tea) is widely known for its soothing effects, particularly during prolonged stress. In Traditional Chinese Medicine (TCM), it is valued for its therapeutic benefits, including antihypertensive, anti-inflammatory, and hepatoprotective effects. This study explores the neuroprotective potential of the aqueous extract of H. sabdariffa calyces (AEHS) in mitigating stress-induced neurobehavioral and biochemical changes in mice subjected to unpredictable chronic mild stress (UCMS).

Methods

Thirty male Swiss mice were randomly assigned to five groups (n = 6) and treated orally. Groups 1 (control) and 2 (UCMS-control) received distilled water, whereas group 3–5 received AEHS at doses of 50, 100, and 200 mg/kg, respectively. Group 2–5 were subjected to unpredictable chronic mild stress (UCMS) daily for 21 days. The neurobehavioral assessments including locomotor activity, memory, anxiety and depressive-like behaviors conducted on days 20 and 21. On day 22, blood glucose and serum corticosterone levels were analyzed alongside oxidative stress biomarkers, nitrites, pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6), and serotonin levels in the prefrontal cortex, amygdala, and hippocampus. The brain-derived neurotrophic factor (BDNF), nuclear factor kappa B (NF-κB), cyclic adenosine monophosphate (cAMP)-response element binding protein (CREB), and nuclear factor erythroid 2-related factor 2 (Nrf2) were evaluated. The enzymatic activities of acetylcholinesterase (AChE) and glutamic acid decarboxylase (GAD) as well as the histomorphological changes in the brain regions were also assessed.

Results

AEHS effectively modulated UCMS-induced neurobehavioral disorders, along with elevated blood glucose and plasma corticosterone levels. The extract mitigated UCMS-induced increases in malondialdehyde (MDA), nitrites, pro-inflammatory cytokines, NF-κB, and AChE. Additionally, AEHS restored the diminished levels of glutathione, catalase, superoxide dismutase, CREB, BDNF, Nrf2, serotonin, and GAD activity within the brain regions. Furthermore, AEHS ameliorated UCMS-induced histomorphological alterations in the brain.

Discussion/Conclusion

This study demonstrated that AEHS confers neuroprotection against chronic stress-induced neurobehavioral disorders, biochemical and histomorphological alterations by enhancing antioxidant defenses and modulating key signaling pathways, including BDNF, CREB, Nrf2 and NF-κB. These findings underscore the potential therapeutic applications of AEHS in mitigating chronic stress-related psychiatric disturbances within the framework of TCM.
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