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组胺H2受体的刺激与阻断对大鼠消化道及大脑不同部位5-羟色胺周转的影响。

The effect of stimulation and blocking of histamine H2 receptors on the turnover of the serotonin in different parts of the alimentary tract and the brain of the rat.

作者信息

Skrzydło-Radomańska B, Pokora J, Kleinrok Z, Radwan P

出版信息

Agents Actions. 1985 Apr;16(3-4):183-6. doi: 10.1007/BF01983134.

Abstract

In the experiments performed on Wistar rats it was found that histamine (0.05 and 0.5 mg/kg i.p.) caused an acceleration of the turnover of serotonin (5-HT) in the stomach. After the lowest dose of ranitidine (3 mg/kg i.p.) a decrease in the rate of 5-HT turnover in the stomach was observed, whereas the higher doses (15.0 and 30 mg/kg i.p.) accelerated the turnover of this amine. In the duodenum, both doses of histamine accelerated the turnover of 5-HT, however, ranitidine in all doses induced a reduction in the rate of 5-HT turnover in this part of the alimentary tract. In the intestine, both doses of histamine enhanced the turnover of 5-HT but after all doses of ranitidine a decrease of the turnover was observed. The blockade of histamine H2 receptors with ranitidine did not completely abolish the effects of histamine on the 5-HT system, in the parts of the rat digestive system studied which suggests also an indirect activity of other receptors in presented observations. In the rat brain, an acceleration of the turnover of 5-HT after both doses of histamine was found. However, ranitidine only reduced the rate of 5-HT turnover at the lowest dose. In animals treated with ranitidine (15 mg/kg i.p.) for three days, histamine did not produce any change in the turnover of 5-HT in rat brain. These experiments show, that in the alimentary tract a relationship exists between histaminergic and serotoninergic systems.

摘要

在对Wistar大鼠进行的实验中发现,组胺(腹腔注射0.05和0.5毫克/千克)可使胃中5-羟色胺(5-HT)的周转加速。在给予最低剂量的雷尼替丁(腹腔注射3毫克/千克)后,观察到胃中5-HT的周转速率降低,而较高剂量(腹腔注射15.0和30毫克/千克)则加速了这种胺的周转。在十二指肠中,两种剂量的组胺均加速了5-HT的周转,然而,所有剂量的雷尼替丁均导致该消化道部分中5-HT的周转速率降低。在肠道中,两种剂量的组胺均增强了5-HT的周转,但在给予所有剂量的雷尼替丁后,观察到周转减少。雷尼替丁对组胺H2受体的阻断并未完全消除组胺对所研究的大鼠消化系统各部分中5-HT系统的影响,这也表明在这些观察结果中其他受体具有间接活性。在大鼠脑中,发现两种剂量的组胺后5-HT的周转均加速。然而,雷尼替丁仅在最低剂量时降低了5-HT的周转速率。在用雷尼替丁(腹腔注射15毫克/千克)处理三天的动物中,组胺对大鼠脑中5-HT的周转没有产生任何变化。这些实验表明,在消化道中组胺能系统和5-羟色胺能系统之间存在关联。

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