Autoregulation of histamine release via the histamine H3 receptor on mast cells in the rat skin.

T Ohkubo, M Shibata, M Inoue, H Kaya, H Takahashi
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Abstract

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.

大鼠皮肤肥大细胞上组胺H3受体对组胺释放的自动调节。
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。
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