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肉豆蔻果实中的脱颗粒抑制剂对抗原刺激的大鼠嗜碱性白血病细胞的作用。

Degranulation inhibitors from the arils of Myristica fragrans in antigen-stimulated rat basophilic leukemia cells.

机构信息

Pharmaceutical Research and Technology Institute, Kindai University, 3-4-1 Kowakae, Higashi-osaka, Osaka, 577-8502, Japan.

Antiaging Center, Kindai University, 3-4-1 Kowakae, Higashi-osaka, Osaka, 577-8502, Japan.

出版信息

J Nat Med. 2018 Mar;72(2):464-473. doi: 10.1007/s11418-017-1170-x. Epub 2018 Jan 15.

DOI:10.1007/s11418-017-1170-x
PMID:29336005
Abstract

A methanol extract of mace, the aril of Myristica fragrans (Myristicaceae), was found to inhibit the release of β-hexosaminidase, a marker of antigen-IgE-stimulated degranulation in rat basophilic leukemia cells (RBL-2H3, IC = 45.7 μg/ml). From the extract, three new 8-O-4' type neolignans, maceneolignans I-K (1-3), were isolated, and the stereostructures of 1-3 were elucidated based on spectroscopic and chemical evidence. Among the isolates, maceneolignans A (5), D (6), and H (8), (-)-(8R)-∆-4-hydroxy-3,3',5'-trimethoxy-8-O-4'-neolignan (13), (-)-(8R)-∆-3,4,5,3',5'-pentamethoxy-8-O-4'-neolignan (14), (-)-erythro-(7R,8S)-∆-7-acetoxy-3,4-methylenedioxy-3',5'-dimethoxy-8-O-4'-neolignan (17), (+)-licarin A (20), nectandrin B (24), verrucosin (25), and malabaricone C (29) were investigated as possible degranulation inhibitors (IC = 20.7-63.7 μM). These inhibitory activities were more potent than those of the antiallergic agents tranilast (282 μM) and ketotifen fumalate (158 μM). Compounds 5, 25, and 29 also inhibited antigen-stimulated tumor necrosis factor-α production (IC = 39.5-51.2 μM), an important process in the late phase of type I allergic reactions.

摘要

荜茇中的甲醇提取物,肉豆蔻衣(肉豆蔻科),被发现抑制β-己糖胺酶的释放,β-己糖胺酶是大鼠嗜碱性白血病细胞(RBL-2H3,IC=45.7μg/ml)中抗原-IgE 刺激脱粒的标志物。从提取物中分离出三种新的 8-O-4'型新木脂素,荜茇新木脂素 I-K(1-3),并根据光谱和化学证据阐明了 1-3 的立体结构。在分离出的化合物中,荜茇新木脂素 A(5)、D(6)和 H(8)、(-)-(8R)-∆-4-羟基-3,3',5'-三甲氧基-8-O-4'-新木脂素(13)、(-)-(8R)-∆-3,4,5,3',5'-五甲氧基-8-O-4'-新木脂素(14)、(-)-erythro-(7R,8S)-∆-7-乙酰氧基-3,4-亚甲二氧基-3',5'-二甲氧基-8-O-4'-新木脂素(17)、(+)-licarin A(20)、nectandrin B(24)、verrucosin(25)和 malabaricone C(29)被研究为可能的脱粒抑制剂(IC=20.7-63.7μM)。这些抑制活性比抗过敏药物曲尼司特(282μM)和酮替芬富马酸(158μM)更强。化合物 5、25 和 29 还抑制抗原刺激的肿瘤坏死因子-α产生(IC=39.5-51.2μM),这是 I 型过敏反应晚期的一个重要过程。

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