Serros E R, Lowe A G, Kirschenbaum M A
Prostaglandins Med. 1980 Sep;5(3):175-82.
Studies were performed in conscious rats to evaluate the role of renal prostaglandin biosynthesis in demeclocycline-induced polyuria. Three groups of animals were evaluated. Group 1 animals received only the diluents used for both demeclocycline and indomethacin. Group 2 received demeclocycline (20 mg/kg/day) and the indomethacin diluent. Group 3 received both demeclocycline and indomethacin (10 mg/kg/day). After eight days of demeclocycline administration, urine flow rate increased in the group 2 animals from 15.1 +/- 2.1 to 31.1 +/- 5.1 ml/day. Indomethacin failed to alter the magnitude of demeclocycline-induced polyuria despite a 60% reduction in urine prostaglandin E excretion rats. These studies demonstrate that the concentrating defect induced by demeclocycline can occur independent of alterations in praostaglandin biosynthesis and suggest that a change in renal prostaglandin biosynthesis is not an etiologic factor in demeclocycline-induced polyuria.
在清醒大鼠身上进行了研究,以评估肾前列腺素生物合成在去甲金霉素诱导的多尿中的作用。对三组动物进行了评估。第1组动物仅接受用于去甲金霉素和吲哚美辛的稀释剂。第2组接受去甲金霉素(20mg/kg/天)和吲哚美辛稀释剂。第3组接受去甲金霉素和吲哚美辛(10mg/kg/天)。给予去甲金霉素八天后,第2组动物的尿流率从15.1±2.1增加到31.1±5.1ml/天。尽管大鼠尿前列腺素E排泄减少了60%,但吲哚美辛未能改变去甲金霉素诱导的多尿程度。这些研究表明,去甲金霉素诱导的浓缩功能缺陷可独立于前列腺素生物合成的改变而发生,并提示肾前列腺素生物合成的变化不是去甲金霉素诱导多尿的病因学因素。