大鼠皮肤肥大细胞上组胺H3受体对组胺释放的自动调节。

T Ohkubo, M Shibata, M Inoue, H Kaya, H Takahashi
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引用次数: 0

摘要

在体内和体外研究了外周组织胺H3受体对组胺释放的自调节作用。坐骨神经反向电刺激引起大鼠后爪皮下灌注液中组胺释放显著增加。(R) α -甲基组胺,一种特异性的H3受体激动剂,在静脉注射剂量为0.25- 2mg /kg时,显著且剂量依赖性地抑制组胺释放的增加。硫哌丁胺(2mg /kg,腹腔)是一种特异性H3拮抗剂,可阻止(R) α -甲基组胺的抑制作用。P物质灌注(5-50 μ m)也引起组胺显著升高,(R) α -甲基组胺显著抑制,硫哌丁胺拮抗。(R) α -甲基组胺抑制P物质从体外大鼠腹膜肥大细胞释放组胺,硫哌丁胺降低对(R) α -甲基组胺的反应。这些数据表明肥大细胞可能具有组胺H3受体,并且在神经源性炎症中,组胺可能通过H3受体调节其自身的释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autoregulation of histamine release via the histamine H3 receptor on mast cells in the rat skin.

The autoregulation of the histamine release via the histamine H3 receptor in the periphery was studied in vivo and in vitro. Antidromic electrical stimulation of the sciatic nerve caused a significant increase in histamine release in the subcutaneous perfusate in the rat hindpaw. (R)alpha-methylhistamine, a specific H3 receptor agonist, significantly and dose-dependently inhibited the increase in release of histamine by antidromic stimulation at intravenous doses of 0.25-2 mg/kg. Thioperamide (2 mg/kg, intraperitoneally), a specific H3 antagonist, prevented the inhibitory effect of (R)alpha-methylhistamine. Substance P perfusion (5-50 microM) also elicited a significant increase in histamine, and a significant inhibition by (R)alpha-methylhistamine and the antagonism of thioperamide were observed. (R)alpha-methylhistamine inhibited the histamine release by substance P from rat peritoneal mast cells in vitro, and thioperamide reduced the response to (R)alpha-methylhistamine. These data suggest that mast cells may have histamine H3 receptors, and that histamine probably modulates its own release through the H3 receptor in neurogenic inflammation.

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