Walter S J, Shirley D G, Unwin R J
Department of Physiology, Charing Cross and Westminster Medical School, London, United Kingdom.
Am J Physiol. 1996 Jul;271(1 Pt 2):F223-9. doi: 10.1152/ajprenal.1996.271.1.F223.
Micropuncture techniques were used to investigate the nephron site(s) responsible for the vasopressin-induced reductions in lithium clearance and fractional lithium excretion (FELi) in anesthetized Brattleboro rats lacking endogenous vasopressin. In rats treated intravenously with the vasopressin analogue 1-desamino-8-D-arginine vasopressin (DDAVP; 40 pg/min), FELi was significantly lower than in untreated animals (0.23 +/- 0.01 vs. 0.28 +/- 0.02, P < 0.05). Free-flow micropuncture showed that fractional lithium delivery (FDLi) to late proximal convolutions was identical in the two groups, whereas at the early distal tubule both FDLi (0.28 +/- 0.02 vs. 0.33 +/- 0.01, P < 0.05) and the tubular fluid-to-plasma lithium concentration ratio (1.18 +/- 0.04 vs. 1.36 +/- 0.06, P < 0.05) were lower in the DDAVP-treated group. No differences between the groups with respect to lithium handling beyond the early distal tubule were observed. In rats subjected to in vivo microperfusion of loops of Henle, intravenous infusion of DDAVP (40 pg/min) increased fractional lithium reabsorption in the loop from 0.56 +/- 0.03 to 0.66 +/- 0.04 (P < 0.05) and from 0.39 +/- 0.02 to 0.45 +/- 0.02 (P < 0.05) at perfusion rates of 10 and 15 nl/min, respectively. We conclude that DDAVP stimulates lithium reabsorption in the loop of Henle and suggest that this results from an increased transepithelial potential difference in the thick ascending limb.
采用微穿刺技术,在缺乏内源性血管加压素的麻醉Brattleboro大鼠中,研究负责血管加压素诱导的锂清除率和锂排泄分数(FELi)降低的肾单位部位。用血管加压素类似物1-去氨基-8-D-精氨酸血管加压素(DDAVP;40 pg/min)静脉注射处理的大鼠,其FELi显著低于未处理动物(0.23±0.01对0.28±0.02,P<0.05)。自由流微穿刺显示,两组中晚期近端曲管的锂输送分数(FDLi)相同,而在早期远端小管,DDAVP处理组的FDLi(0.28±0.02对0.33±0.01,P<0.05)和肾小管液与血浆锂浓度比(1.18±0.04对1.36±0.06,P<0.05)均较低。在早期远端小管之后,未观察到两组在锂处理方面的差异。在对Henle袢进行体内微灌注的大鼠中,静脉输注DDAVP(40 pg/min)使Henle袢的锂重吸收分数分别在灌注速率为10和15 nl/min时从0.56±0.03增加到0.66±0.04(P<0.05)以及从0.39±0.02增加到0.45±0.02(P<0.05)。我们得出结论,DDAVP刺激Henle袢中的锂重吸收,并认为这是由于厚壁升支中跨上皮电位差增加所致。