无环倍半萜类化合物橙花叔醇和法尼醇:从机理上揭示其神经保护潜力。

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacological Reports Pub Date : 2024-10-22 DOI:10.1007/s43440-024-00672-8
Anish Singh, Lovedeep Singh
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引用次数: 0

摘要

倍半萜是一类存在于植物、真菌和一些昆虫中的有机化合物。它们的特点是含有三个异戊二烯单元,分子式通常包含 15 个碳原子(C₁₅H₂₄)。橙花叔醇和法呢醇都是倍半萜醇,存在于许多植物的精油中。它们因其潜在的神经保护特性而备受关注。橙花叔醇和法呢醇是结构异构体,特别是几何异构体,分子式相同(C₁₅H₂₄O),但原子的空间排列不同。这种结构上的差异可能是它们具有不同生物活性的原因。科学证据表明,橙花叔醇和法呢醇具有抗氧化和抗炎特性,这对保护神经至关重要。人们特别注意到,橙花叔醇能够通过调节炎症和氧化应激途径,缓解阿尔茨海默病、帕金森病、脑脊髓炎、抑郁症和焦虑症等疾病。此外,研究表明橙花叔醇和法呢醇都可以调节 Nrf-2/HO-1 抗氧化信号通路,从而减轻氧化应激引起的神经损伤。激活 Nrf-2/HO-1 信号级联可促进细胞存活,增强大脑抵御各种损伤的能力。据报道,橙花叔醇还能通过抑制TLR-4/NF-κB和COX-2/NF-κB炎症信号通路来缓解神经炎症。此外,橙花叔醇还能调节 BDNF/TrkB/CREB 信号通路,从而改善神经元健康。迄今为止,有关法尼醇在神经退行性疾病方面的抗炎特性的研究还很有限。要全面阐明其作用机制以及在神经保护方面的潜在治疗用途,还需要进一步的研究。初步观察表明,法呢醇作为一种天然药物,在保护大脑功能方面具有广阔的前景。因此,本综述借鉴了阐明橙花叔醇和法呢醇神经保护特性的现有文献,试图对它们在神经保护方面的机理基础进行详细分析。
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Acyclic sesquiterpenes nerolidol and farnesol: mechanistic insights into their neuroprotective potential.

Sesquiterpenes are a class of organic compounds found in plants, fungi, and some insects. They are characterized by the presence of three isoprene units, resulting in a molecular formula that typically contains 15 carbon atoms (C₁₅H₂₄). Nerolidol and farnesol are both sesquiterpene alcohols present in the essential oils of numerous plants. They have drawn attention due to their potential neuroprotective properties. Nerolidol and farnesol are structural isomers, specifically geometric isomers, haring the same molecular formula (C₁₅H₂₄O) but differing in the spatial arrangement of their atoms. This variation in structure may contribute to their distinct biological activities. Scientific evidence suggests that nerolidol and farnesol exhibit antioxidant and anti-inflammatory characteristics which are crucial for neuroprotection. Nerolidol has been specifically noted for its ability to alleviate conditions such as Alzheimer's disease, Parkinson's disease, encephalomyelitis, depression, and anxiety by modulating inflammatory and oxidative stress pathways. Moreover, research indicates that both nerolidol and farnesol may modulate the Nrf-2/HO-1 antioxidant signaling pathway to mitigate oxidative stress-induced neurological damage. Activation of Nrf-2/HO-1 signaling cascade promotes cell survival and enhances the brain's ability to resist various insults. Nerolidol has also been reported to alleviate neuroinflammation by inhibiting the TLR-4/NF-κB and COX-2/NF-κB inflammatory signaling pathway. Besides, this nerolidol also modulates BDNF/TrkB/CREB signaling pathway to improve neuronal health. To date, limited research has delved into the anti-inflammatory properties of farnesol concerning neurodegenerative diseases. Further investigation is warranted to comprehensively elucidate the mechanisms underlying its action and potential therapeutic uses in neuroprotection. Initial observations indicate that farnesol exhibits promising prospects as a natural agent for safeguarding brain functions. Henceforth, drawing upon existing literature elucidating the neuroprotective attributes of nerolidol and farnesol, the current review endeavors to provide a detailed analysis of their mechanistic underpinnings in neuroprotection.

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来源期刊
Pharmacological Reports
Pharmacological Reports 医学-药学
CiteScore
8.40
自引率
0.00%
发文量
91
审稿时长
6 months
期刊介绍: Pharmacological Reports publishes articles concerning all aspects of pharmacology, dealing with the action of drugs at a cellular and molecular level, and papers on the relationship between molecular structure and biological activity as well as reports on compounds with well-defined chemical structures. Pharmacological Reports is an open forum to disseminate recent developments in: pharmacology, behavioural brain research, evidence-based complementary biochemical pharmacology, medicinal chemistry and biochemistry, drug discovery, neuro-psychopharmacology and biological psychiatry, neuroscience and neuropharmacology, cellular and molecular neuroscience, molecular biology, cell biology, toxicology. Studies of plant extracts are not suitable for Pharmacological Reports.
期刊最新文献
Retraction Note to: Anti-inflammatory role of leptin in glial cells through p38 MAPK pathway inhibition. Correction: β-Carboline derivatives are potent against acute myeloid leukemia in vitro and in vivo. Special issue: Glutamate- physiology, pathology, therapy. Interactions between metabotropic glutamate and CB1 receptors: implications for mood, cognition, and synaptic signaling based on data from mGluR and CB1R-targeting drugs. Sleep alterations in treatment-resistant depression patients undergoing ketamine treatment.
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