Suppr超能文献

酶处理的白花鬼针草对组胺诱导的豚鼠回肠收缩及肥大细胞组胺释放的影响。

Effects of Bidens pilosa L. var. radiata SCHERFF treated with enzyme on histamine-induced contraction of guinea pig ileum and on histamine release from mast cells.

作者信息

Matsumoto Takayuki, Horiuchi Masako, Kamata Katsuo, Seyama Yoshiyuki

机构信息

Department of Physiology and Morphology, Institute of Medicinal Chemistry, Hoshi University, Shinagawa-ku, Tokyo 142-8501, Japan.

出版信息

J Smooth Muscle Res. 2009 Jun;45(2-3):75-86. doi: 10.1540/jsmr.45.75.

Abstract

The medical mechanism against type I allergies is to block the release or production of chemical mediators from mast cells or to block the H(1)-receptor signaling. We previously reported that the anti-allergic action of the dry powder from Bidens pilosa L. var. radiata SCHERFF treated with the enzyme cellulosine (eMMBP) was dependent on the inhibition of histamine release from mast cells. Here, we investigate that the effect of fractions in eMMBP on the histamine-induced contraction in guinea pig ileum and on the release of histamine in rat peritoneal mast cells. The histamine-induced contraction in guinea pig ileum is dose-dependently inhibited by ketotifen, an antagonist of H(1)-receptor. Fractions contained caffeic acid, caffeoylquinic acid and fractions contained flavonoids such as hyperin and isoquercitrin in eMMBP inhibit histamine release from mast cells, but only flavonoids such as hyperin, isoquercitrin and rutin suppress the histamine-induced contraction in guinea pig ileum. Moreover, the histamine-induced contraction was not affected by caffeic acid, however, such contraction was significantly inhibited by rutin. These results suggest that the primary antagonists of H(1)- receptor are different from the components in eMMBP that inhibit histamine release, and that these components participate in the anti-allergic activity of eMMBP.

摘要

针对I型过敏的医学机制是阻止肥大细胞释放或产生化学介质,或阻断H(1)受体信号传导。我们之前报道过,用纤维素酶处理的三叶鬼针草干粉(eMMBP)的抗过敏作用依赖于对肥大细胞组胺释放的抑制。在此,我们研究eMMBP中的组分对组胺诱导的豚鼠回肠收缩以及对大鼠腹膜肥大细胞组胺释放的影响。组胺诱导的豚鼠回肠收缩受到H(1)受体拮抗剂酮替芬的剂量依赖性抑制。eMMBP中含有咖啡酸、咖啡酰奎宁酸的组分以及含有金丝桃苷和异槲皮苷等黄酮类化合物的组分可抑制肥大细胞释放组胺,但只有金丝桃苷、异槲皮苷和芦丁等黄酮类化合物能抑制组胺诱导的豚鼠回肠收缩。此外,组胺诱导的收缩不受咖啡酸影响,然而,这种收缩受到芦丁的显著抑制。这些结果表明,H(1)受体的主要拮抗剂与eMMBP中抑制组胺释放的成分不同,并且这些成分参与了eMMBP的抗过敏活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验