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前列腺素I2作为大鼠急性炎症的增强剂。

Prostaglandin I2 as a potentiator of acute inflammation in rats.

作者信息

Komoriya K, Ohmori H, Azuma A, Kurozumi S, Hashimoto Y, Nicolaou K C, Barnette W E, Magolda R L

出版信息

Prostaglandins. 1978 Apr;15(4):557-64. doi: 10.1016/0090-6980(78)90052-7.

Abstract

Prostaglandin I2 potentiated the paw swelling induced by carrageenin in rats. Prostaglandin I2 (0.1 microgram) showed similar activity to PGE1 (0.01 microgram). This potentiating property disappeared in 60 minutes and was completely abolished by diphenhydramine (25 mg kg-1, i.p.). In vascular permeability tests, PGI2 itself (2.5 X 10(-10) mol, 88 ng) caused no dye leakage reaction, but PGE1 (2.5 X 10(-10) mol, 88.5 ng) caused a significant dye leakage. This effect of PGE1 was statistically significant compared with vehicle- or PGI2-treated groups (p less than 0.05). Prostaglandin I2 potentiated the increased vascular permeability induced by 5-hydroxytriptamine (2.5 X 10(-10) mol), bradykinin (5 X 10(-10) mol) and histamine (2 X 10(-10) to 2 X 10(-8) mol). The potentiation was the most evident in the case of histamine.

摘要

前列腺素I2增强了角叉菜胶诱导的大鼠爪肿胀。前列腺素I2(0.1微克)显示出与前列腺素E1(0.01微克)相似的活性。这种增强特性在60分钟内消失,并被苯海拉明(25毫克/千克,腹腔注射)完全消除。在血管通透性试验中,前列腺素I2本身(2.5×10⁻¹⁰摩尔,88纳克)未引起染料渗漏反应,但前列腺素E1(2.5×10⁻¹⁰摩尔,88.5纳克)引起了显著的染料渗漏。与溶剂或前列腺素I2处理组相比,前列腺素E1的这种作用具有统计学意义(p<0.05)。前列腺素I2增强了5-羟色胺(2.5×10⁻¹⁰摩尔)、缓激肽(5×10⁻¹⁰摩尔)和组胺(2×10⁻¹⁰至2×10⁻⁸摩尔)诱导的血管通透性增加。在组胺的情况下,增强作用最为明显。

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