姜黄素通过上调 BDNF 的表达和成体神经发生,减轻压力诱发的抑郁和海马损伤。

E. U. Wogu, E. I. Edibamode
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摘要

慢性应激被认为是抑郁症的主要诱因,它与各种神经改变有关,包括细胞死亡、神经元萎缩、海马神经发生和可塑性受损。本研究旨在探讨姜黄素对糖皮质激素分泌的影响及其对海马神经元结构完整性和神经发生的影响。研究共使用了 30 只成年白化 Wistar 大鼠,每只体重在 200-250 克之间。除对照组外,这些大鼠都接受了为期 42 天的改良慢性不可预知应激(CUS)治疗,以诱发类似抑郁的状态。诱导 CUS 后,这些大鼠被分为六组,每组接受不同的口服治疗,为期两周。治疗方法包括每公斤体重 30 毫克姜黄素、每公斤体重 20 毫克氟西汀或两者的组合,以及接受蒸馏水的对照组和橄榄油治疗组。使用强迫游泳测试对大鼠进行行为绝望测试,并采集大鼠血液样本进行血清皮质酮测试。随后,对大鼠进行麻醉、经心灌注、解剖海马并准备进行组织病理学研究。这项研究的方法是多方面的,包括行为学、生物化学和组织学评估。与对照组相比(p<0.05),姜黄素治疗大鼠的行为绝望(通过强迫游泳测试)明显减少。此外,姜黄素还能显著降低血清皮质酮水平,使其与对照组水平接近。海马组织形态学分析表明,姜黄素治疗大鼠的神经变性程度大大降低,表现为细胞质空泡减少,神经元结构更加完整。姜黄素治疗大鼠的细胞增殖和 BDNF 水平也有所提高。这项研究阐明了姜黄素缓解海马神经变性的多方面方法,从而显示了姜黄素在改善抑郁症状方面的治疗潜力。
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Curcumin mitigates stress induced depression and hippocampal damage through upregulation of BDNF expression and adult neurogenesis.
Chronic stress, recognized as a major precipitant of depression, has been linked to various neural alterations, including cell death, neuronal atrophy, and compromised hippocampal neurogenesis and plasticity. This study aim to scrutinize curcumin's influence on glucocorticoid hormone secretion and its subsequent effects on the structural integrity and neurogenesis of the hippocampal neurons. A total of 30 adult albino Wistar rats, each weighing between 200-250 g, were utilized for the study. The rats, excluding those in the control group, underwent a 42-day regimen of modified Chronic Unpredictable Stress (CUS) to induce depressive-like states. After inducing CUS, these rats were categorized into six groups, each receiving different oral treatments for two weeks. The treatments included 30 mg/kg body weight of curcumin, 20 mg/kg body weight of fluoxetine, or a combination of both, along with a control group that received distilled water and an olive oil treated group. The rats were tested for behavioural despair using the forced swim test and their blood samples were obtained for serum corticosterone test. Afterwards, the rats were anesthetized, transcardially perfused and the hippocampus dissected and prepared for histopathological study. The study's multi-faceted approach encompassed behavioral, biochemical, and histological evaluations. Behavioral despair, gauged through the forced swimming test, displayed a marked reduction in the curcumin-treated rats compared to controls (p<0.05). Additionally, curcumin significantly lowered serum corticosterone levels, aligning them closely with the control levels. Histomorphological analysis of the hippocampus showed that the curcumin- treated rats exhibited substantially less neurodegeneration, as evidenced by fewer cytoplasmic vacuolations and more intact neuronal structures. Increased cell proliferation and BDNF level were also observed in curcumin treated rats. This study has illuminated a multifaceted approach through which curcumin mitigates hippocampal neurodegeneration, thus showing possible therapeutic potential of curcumin in ameliorating depressive symptoms. 
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