Skrzydło-Radomańska B, Pokora J, Kleinrok Z, Radwan P
Agents Actions. 1985 Apr;16(3-4):183-6. doi: 10.1007/BF01983134.
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.
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。