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抗过敏药物和钙通道拮抗剂对大鼠腹膜肥大细胞的作用及交叉反应。药物间作用机制和交叉反应的差异。

Actions and cross-reactivity of antiallergic agents and a calcium channel antagonist on rat peritoneal mast cells. Difference in the action mechanisms and cross-reactivity among the agents.

作者信息

Tanizaki Y, Ohtani J, Kimura I

机构信息

Department of Medicine, Misasa Medical Branch, Okayama University Medical School, Tottori, Japan.

出版信息

Agents Actions. 1992 Sep;37(1-2):8-15. doi: 10.1007/BF01987884.

Abstract

The actions of the antiallergic agents, disodium chromoglycate (DSCG), tranilast and ketotifen, and of a calcium channel antagonist, nicardipine, and cross-reactivity among the agents were examined by observing the inhibition of 45Ca uptake and histamine release in rat mast cells stimulated by antigen and compound 48/80 (comp. 48/80). 1) All agents inhibited 45Ca uptake and histamine release in mast cells stimulated by antigen. The inhibition of 45Ca uptake by the antiallergic agents paralleled the inhibition of histamine release, while nicardipine inhibition of 45Ca uptake was stronger than its inhibition of histamine release. 2) The action of DSCG on 45Ca uptake and histamine release was significantly decreased in cells stimulated with antigen and phosphatidylserine (PS), while tranilast inhibition of histamine release was not affected by the addition of PS despite a significant decrease in the inhibition of 45Ca uptake. 3) The inhibitory effect of DSCG and tranilast was significantly lower in mast cells stimulated by comp. 48/80 than in the cells stimulated by antigen. 4) Tachyphylaxis was observed in cells re-exposed to DSCG and tranilast following previous exposure to the agents. 5) Cross-reactivity was found between DSCG and tranilast.

摘要

通过观察抗原和化合物48/80(48/80复合物)刺激大鼠肥大细胞后45Ca摄取的抑制情况以及组胺释放情况,对抗过敏药色甘酸二钠(DSCG)、曲尼司特和酮替芬,以及钙通道拮抗剂尼卡地平的作用及其之间的交叉反应性进行了研究。1)所有药物均抑制抗原刺激的肥大细胞中45Ca摄取和组胺释放。抗过敏药对45Ca摄取的抑制与组胺释放的抑制平行,而尼卡地平对45Ca摄取的抑制强于其对组胺释放的抑制。2)在抗原和磷脂酰丝氨酸(PS)刺激的细胞中,DSCG对45Ca摄取和组胺释放的作用显著降低,而尽管曲尼司特对45Ca摄取的抑制显著降低,但PS的添加并不影响其对组胺释放的抑制。3)与抗原刺激的细胞相比,48/80复合物刺激的肥大细胞中DSCG和曲尼司特的抑制作用显著降低。4)在先前暴露于DSCG和曲尼司特的细胞再次暴露于这些药物时观察到快速减敏现象。5)发现DSCG和曲尼司特之间存在交叉反应性。

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