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通过给予组氨酸脱羧酶的特异性抑制剂α-氟甲基组氨酸对豚鼠进行组胺的长期耗竭;对组胺受体敏感性的影响。

Long-term depletion of histamine in guinea-pigs by administration of alpha-fluoromethylhistidine, a specific inhibitor of histidine decarboxylase; effect on the sensitivity of histamine receptors.

作者信息

Fukuda H, Maeyama K, Ito Y, Watanabe T, Wada H

机构信息

Department of Pharmacology II, Osaka University School of Medicine, Japan.

出版信息

Agents Actions. 1988 Jun;24(1-2):56-64. doi: 10.1007/BF01968080.

Abstract

The effect of intraperitoneal administration of alpha-fluoromethylhistidine (alpha-FMH), a specific inhibitor of histidine decarboxylase, at a dose of 100 mg/kg twice a day for 6 weeks on the sensitivity of histamine receptors in the guinea-pigs was examined. The histamine contents in the ileum, heart and brain after the treatment decreased to about 54%, 83% and 9-62% (depending on the region), respectively, of those of controls. However, there were no significant difference in the histamine-induced contraction of the ileum and atrium, the maximal binding (Bmax) and the dissociation constant (Kd) of [3H]-mepyramine binding to membrane fractions of the ileum and brain (except the cortex) and the increase of cyclic AMP formation induced by histamine in membranes of the heart and brain (except the cortex) between alpha-FMH-treated- and untreated animals. These results suggest that long-term histamine depletion dose not significantly affect the sensitivity of histamine receptors of guinea-pig except in the brain cortex.

摘要

研究了腹腔注射组氨酸脱羧酶特异性抑制剂α-氟甲基组氨酸(α-FMH),剂量为100mg/kg,每天两次,持续6周,对豚鼠组胺受体敏感性的影响。治疗后,回肠、心脏和大脑中的组胺含量分别降至对照组的约54%、83%和9 - 62%(取决于区域)。然而,α-FMH处理组和未处理组动物在组胺诱导的回肠和心房收缩、[3H]-美吡拉敏与回肠和大脑(皮质除外)膜部分结合的最大结合量(Bmax)和解离常数(Kd)以及组胺诱导的心脏和大脑(皮质除外)膜中环磷酸腺苷形成增加方面没有显著差异。这些结果表明,长期组胺耗竭除了在大脑皮质外,不会显著影响豚鼠组胺受体的敏感性。

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