Inhibitory effects of aloe extracts on antigen- and compound 48/80-induced histamine release from rat peritoneal mast cells

Masatoshi Yamamoto, K. Sugiyama, M. Yokota, Y. Maeda, K. Nakagomi, H. Nakazawa
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引用次数: 2

Abstract

The inhibitory effects of water extracts of five genera of aloe (Aloe arborescens MILLER, A. ferox M., A. barbadensis M., A. africana M., A. saponaria HAWAII) and aloe powder of Japanese Pharmacopoeia (JP Aloe powder) on histamine release from rat peritoneal mast cells induced by antigen and compound 48/80 were investigated in vitro. All the aloe extracts tested inhibited histamine release from mast cells induced by antigen and compound 48/80 in a concentration-dependent manner. The extract of A. ferox M. and JP Aloe powder paticularly strongly inhibited release by either antigen or compound 48/80 at medium inhibitory concentration (IC50) of 0.16 and 0.07 mg/ml, respectively, for antigen and of 0.41 and 0.29 mg/ml for compound 48/80. These results suggest that aloes may be useful in the treatment of type I immediate allergic disorders. Barbaloin, a major constituent of aloes, also exhibited concentration-dependent inhibitory effects on histamine release induced by these two substances, with IC50 being 0.02 and 0.06 mg/ml, respectively. From its yield and inhibitory effects, barbaloin is considered to account for the inhibitory action of the water extracts of A. arborescens M., A. africana M. and JP Aloe powder. Although tranilast, a current antiallergic agent, strongly inhibited antigeninduced histamine release (IC50=0.07 mg/ml), it showed a weak inhibitory effect on compound 48/80-induced histamine release (IC50=0.84 mg/ml). These results suggest that the mechanism of inhibitory action of barbaloin on histamine release differs from that of tranilast.
芦荟提取物对抗原和复方48/80诱导的大鼠腹膜肥大细胞组胺释放的抑制作用
研究了五属芦荟(aloe arborescens MILLER、a.f erox M.、a.b barbadensis M.、a.a africana M.、a.a saponaria HAWAII)水提液和日本药典芦荟粉(JP芦荟粉)对抗原和化合物48/80诱导的大鼠腹膜大细胞组胺释放的体外抑制作用。所有芦荟提取物均能抑制抗原和化合物48/80诱导的肥大细胞释放组胺,且呈浓度依赖性。对抗原和化合物48/80的抑制浓度(IC50)分别为0.16和0.07 mg/ml,对化合物48/80的IC50分别为0.41和0.29 mg/ml,对抗原和化合物48/80的释放具有较强的抑制作用。这些结果表明,芦荟可能是有用的治疗I型直接过敏性疾病。芦荟的主要成分巴巴罗因对两种物质诱导的组胺释放也表现出浓度依赖的抑制作用,IC50分别为0.02和0.06 mg/ml。从其产量和抑制作用来看,巴巴洛因被认为可以解释木叶芦荟、非洲芦荟和JP芦荟粉水提取物的抑制作用。目前常用的抗过敏药物曲尼司特对抗原诱导的组胺释放有较强的抑制作用(IC50=0.07 mg/ml),但对复方48/80诱导的组胺释放有较弱的抑制作用(IC50=0.84 mg/ml)。这些结果表明,巴氏碱对组胺释放的抑制作用机制与曲尼司特不同。
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