A lithium chloride (1.1 g/kg) supplemented diet was given to Long Evans (LE) and Brattleboro (DI) rats to investigate its actions in the presence (LE) and absence (DI) of vasopressin. 2. During the first 24 h, Li-supplemented LE rats displayed an initial water deficit (drinking less than renal output), increased plasma antidiuretic (ADH) titres and slightly increased plasma renin activities (PRA) and plasma osmolarities. Such changes were qualitatively similar to those seen in rats fed a normal diet, but deprived of water for 24 hours. After 12 days, the Li-supplemented rats had elevated plasma ADH titres, but reduced pituitary oxytocic and antidiuretic activities. 3. The urinary losses of Na, K and Cl exceeded dietary intakes in LE rats on the introduction of the Li-supplement, and the urinary osmolarity fell by 50%. Electrolyte balances were gradually re-established, although drinking and urine production increased in parallel to reach twice the control values by day 12 of the supplement. 4. Aldosterone and corticosterone secretory rates and their peripheral plasma concentrations were unchanged both after 24 h and 28 days of the Li-supplement. 5. Li elicited no water deficit or saluresis in DI rats, and although the polyuria and polydipsia were exacerbated, urinary osmolarity did not change over the 12 day observation period. 6. Li increased Ca excretion in both rat types; after 12 days the PRA of DI but not LE animals were increased. 7. It is concluded that the overall renal actions of Li are tempered by vasopressin rather than adrenocorticosteroids.
摘要
给长 Evans(LE)大鼠和布拉德福德(DI)大鼠喂食补充了氯化锂(1.1 克/千克)的饮食,以研究其在有(LE)和无(DI)血管加压素情况下的作用。2. 在最初的 24 小时内,补充锂的 LE 大鼠出现初始水 deficit(饮水量少于肾脏排出量),血浆抗利尿激素(ADH)水平升高,血浆肾素活性(PRA)和血浆渗透压略有升高。这些变化在性质上与喂食正常饮食但缺水 24 小时的大鼠所见变化相似。12 天后,补充锂的大鼠血浆 ADH 水平升高,但垂体催产素和抗利尿活性降低。3. 补充锂后,LE 大鼠的钠、钾和氯尿排泄量超过饮食摄入量,尿渗透压下降 50%。电解质平衡逐渐重新建立,尽管饮水量和尿量平行增加,到补充的第 12 天达到对照值的两倍。4. 补充锂 24 小时和 28 天后,醛固酮和皮质酮分泌率及其外周血浆浓度均未改变。5. 锂在 DI 大鼠中未引起水 deficit 或盐利尿,尽管多尿和多饮加剧,但在 12 天观察期内尿渗透压没有变化。6. 锂增加了两种大鼠类型的钙排泄;12 天后,DI 动物的 PRA 增加,而 LE 动物未增加。7. 得出结论,锂的总体肾脏作用受血管加压素而非肾上腺皮质类固醇调节。