A Lecklin, L Eriksson, J Leppäluoto, J Tarhanen, L Tuomisto
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引用次数: 11
摘要
在本研究中,研究了有意识大鼠对组胺- n -甲基转移酶抑制剂美托林的肾脏反应。对雄性Wistar大鼠ig给予甲托林(10- 20mg kg(-1))或对照物,并在随后的24小时内观察其效果。发现早在给药后3小时,甲托林20mg kg(-1)的水消耗和尿流量增加了约6-8倍。治疗降低了尿渗透压,增加了游离水清除率,但没有引起血浆肾素活性或血浆加压素浓度的变化。此外,在实验开始的几个小时内,观察到甲托林引起的收缩压升高。在研究的夜间阶段,经甲托林处理的大鼠肾小球滤过率和电解质的排泄没有像对照组大鼠那样增加。心房利钠肽释放的减少也被发现。目前的研究结果表明,甲托宁对组胺分解代谢的抑制可引起肾功能的巨大变化。它似乎促进了肾脏的水分排泄,但另一方面,减少了电解质的排泄。虽然确切的机制,特别是血压升高和夜间抑制房利钠肽的作用,需要进一步澄清,但目前的数据表明肾素-血管紧张素系统和加压素不参与这些对美托林的肾脏反应。
Metoprine-induced thirst and diuresis in Wistar rats.
In the present study, the renal responses to metoprine, a histamine-N-methyltransferase inhibitor, were studied in conscious rats. Metoprine (10-20 mg kg(-1)) or vehicle were administered i.p. to male Wistar rats and the effects were followed for the subsequent 24 h. It was found that as early as 3 h after the drug administration metoprine 20 mg kg(-1) had increased water consumption and urine flow approximately 6-8-fold. The treatment decreased urine osmolality and increased free water clearance, but caused no change in plasma renin activity or plasma vasopressin concentration. In addition, a metoprine-induced elevation in the systolic blood pressure was observed during the first few hours of the experiment. During the nocturnal period of the study, glomerular filtration rate and the excretion of electrolytes did not increase in metoprine-treated rats as they did in control rats. A decrease in the release of atrial natriuretic peptide was also found. The present results show that inhibition of histamine catabolism by metoprine causes massive changes in renal functions. It seems to promote water excretion by the kidneys but, on the other hand, to reduce the excretion of electrolytes. Although the exact mechanisms, especially the role of increased blood pressure and nocturnal suppression of atrial natriuretic peptide, require further clarification, the present data suggest that renin-angiotensin system and vasopressin were not involved in these renal responses to metoprine.