从剂型到功能:γ-谷米醇固体分散体发育及其对抑郁症模型的神经保护作用

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-09-26 DOI:10.1021/acsomega.5c05780
Pichaya Jumnongprakhon, , , Andaman Nitjapol, , , Khwankaew Lonlab, , , Sutisa Nudmamud-Thanoi, , , Pratthana Chomchalao*, , and , Waree Tiyaboonchai*, 
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引用次数: 0

摘要

重度抑郁症(MDD)是一种普遍的精神疾病,与自杀风险和公共卫生影响有关。目前的抗抑郁药通常会产生副作用,而且疗效延迟,这促使人们对具有抗氧化特性的天然化合物作为替代疗法产生了兴趣。γ-稻谷醇(GO)具有抗氧化、神经保护和抗抑郁的特性,值得进一步研究。但由于其不溶于水的性质,口服生物利用度较差,限制了其临床应用。因此,本研究旨在开发γ-稻谷醇固体分散体(GOSD)来提高氧化石墨烯的水溶性。然后,评估其对地塞米松诱导的SK-N-SH细胞毒性的神经保护作用,以在配方和功能之间建立明确的联系。采用溶剂熔融法制备了GOSD。制备的GOSD可使氧化石墨烯的水溶性提高至1.37±0.05 mg/mL,并能在模拟肠道条件下释放氧化石墨烯,表明口服生物利用度提高。此外,在6个月的室温下,GOSD保持了良好的物理和化学稳定性。关于GOSD的神经保护潜力,我们的研究结果表明,所有测试浓度对SK-N-SH细胞无毒。有趣的是,通过增强氧化石墨烯的水溶性,氧化石墨烯预处理在对抗地塞米松诱导的细胞毒性方面表现出优于游离氧化石墨烯的神经保护作用。地塞米松暴露前GOSD预处理通过降低ROS水平和增加SOD活性显著减少异常细胞和凋亡细胞。值得注意的是,GOSD预处理通过降低MAO活性、抑制GR表达、上调synaptophysin表达等多种机制恢复突触可塑性。这些结果有力地支持了GOSD作为治疗抑郁症的一种安全有效的替代治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Formulation to Function: γ-Oryzanol Solid Dispersion Development and Its Neuroprotective Effects on the Depression Model

Major depressive disorder (MDD) is a prevalent psychiatric condition linked to suicide risk and public health impact. Current antidepressants often cause side effects and have delayed efficacy, driving interest in natural compounds with antioxidant properties as alternative treatments. γ-Oryzanol (GO) exhibits antioxidant, neuroprotective, and antidepressant properties that warrant investigation. However, its clinical application is restricted due to its water-insoluble properties, which lead to poor oral bioavailability. Therefore, this study aimed to develop a γ-oryzanol solid dispersion (GOSD) to improve GO water solubility. Then, its neuroprotective effects against dexamethasone-induced toxicity in SK-N-SH cells were evaluated to forge a clear link between the formulation and the function. The GOSD was successfully developed by using a solvent melting method. The developed GOSD could enhance the water solubility of GO up to 1.37 ± 0.05 mg/mL and enabled GO release under simulated intestinal conditions, indicating oral bioavailability improvement. In addition, the GOSD maintained good physical and chemical stability under a 6-month storage period at room temperature. Regarding the neuroprotective potential of the GOSD, our findings indicated that all tested concentrations were nontoxic to SK-N-SH cells. Interestingly, through the enhanced water solubility of GO, GOSD pretreatment demonstrated superior neuroprotective efficacy over free GO against dexamethasone-induced cytotoxicity. GOSD pretreatment prior to dexamethasone exposure significantly decreased abnormal and apoptotic cells by reducing ROS levels and increasing the SOD activity. Remarkably, GOSD pretreatment restored synaptic plasticity through multiple mechanisms: reducing MAO activity, suppressing GR expression, and upregulating synaptophysin expression. These results strongly support the GOSD as a safe and effective alternative therapeutic approach for treating depressive disorders.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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