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油桐(Aleurites moluccana (L.) Willd.)叶:一种标准化干燥提取物及其化学标志物的机械性抗伤害作用。

Aleurites moluccana (L.) Willd. Leaves: Mechanical Antinociceptive Properties of a Standardized Dried Extract and Its Chemical Markers.

机构信息

Programa de Mestrado em Ciências Farmacêuticas, Núcleo de Investigações Químico-Farmacêuticas (NIQFAR), Universidade do Vale do Itajaí (UNIVALI), Rua Uruguai 458, 88302-202 Itajaí, SC, Brazil.

出版信息

Evid Based Complement Alternat Med. 2011;2011:179890. doi: 10.1155/2011/179890. Epub 2011 Mar 23.

Abstract

Seeking to develop a new analgesic phytomedicine, a spray-dried extract (SDE) of Aleurites moluccana (L.) Willd. leaves was developed in scale up (5 kg). The SDE was standardized at 3% w/w in relation to the flavonoid 2''-O-rhamnosylswertisin. The SDE batches were evaluated in relation to their physical, physiochemical, and pharmacological characteristics. The results demonstrated the reproducibility of the scale up SDE process which, when dosed orally, reduced carrageenan-induced mechanical hypernociception, with an ID(50)% of 443 mg/kg. Similar results were obtained with animals injected with complete Freund's adjuvant (CFA), in which SDE caused inhibition of 48 ± 4%. SDE was effective in preventing prostaglandin E2 (PGE2)-induced mechanical hypernociception (inhibition of 26 ± 10% and 33 ± 3%, at 250 and 500 mg/kg, respectively). Swertisin and 2''-O-rhamnosylswertisin isolated from the own extract were effective in inhibiting the hypernociceptive response induced by carrageenan (70 ± 2% and 50 ± 5%, resp.). Furthermore, 2''-O-rhamnosylswertisin was capable of significantly inhibiting the mechanical sensitization induced by CFA or PGE2, with inhibitions of 25 ± 3% and 94 ± 6%, respectively. These results suggest that the effects of SDE are related, at least in part, to the presence of these flavonoids.

摘要

为了开发一种新的镇痛植物药,我们对 Aleurites moluccana(L.)Willd. 叶的喷雾干燥提取物(SDE)进行了放大(5kg)。SDE 以 3%w/w 的比例标准化,与黄酮 2''-O-鼠李糖苷 swertisin 相关。对 SDE 批次的物理、物理化学和药理学特性进行了评估。结果表明,放大的 SDE 过程具有重现性,口服给予 SDE 可减轻卡拉胶诱导的机械性痛觉过敏,ID(50)%为 443mg/kg。在注射完全弗氏佐剂(CFA)的动物中也得到了类似的结果,SDE 导致 48±4%的抑制。SDE 可有效预防前列腺素 E2(PGE2)诱导的机械性痛觉过敏(分别在 250 和 500mg/kg 时抑制 26±10%和 33±3%)。从自身提取物中分离出的 swertisin 和 2''-O-鼠李糖苷 swertisin 可有效抑制卡拉胶诱导的痛觉过敏反应(分别为 70±2%和 50±5%)。此外,2''-O-鼠李糖苷 swertisin 能够显著抑制 CFA 或 PGE2 诱导的机械敏感性,抑制率分别为 25±3%和 94±6%。这些结果表明,SDE 的作用至少部分与这些类黄酮的存在有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2bd/3092167/ce5710f6ba54/ECAM2011-179890.001.jpg

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