Sharma R, Sharma M, Li J Z, McCarthy E T, Savin V J
Department of Medicine, Froedtert Memorial Lutheran Hospital, Milwaukee, Wisc., USA.
Kidney Blood Press Res. 1997;20(1):25-30. doi: 10.1159/000174107.
Platelet-activating factor (PAF) is an important mediator of injury in acute renal failure and glomerulonephritis. Intrarenal infusion of PAF reduces glomerular filtration rate and renal plasma flow and increases glomerular permselectivity via its renal hemodynamic and/or immunologic effects. Direct effects of PAF on glomerular capillary permeability are not known. We studied the direct effects of PAF on mesangial contraction (a measure of filtration area), glomerular capillary hydraulic conductivity (L[p]) and capillary albumin permeability (P[albumin]). Glomeruli were isolated from Sprague-Dawley rats and incubated with or without various concentrations of PAF (10[-9], 10[-7] and 10[-5] M) for up to 5 h at 37 degrees C. Mesangial contraction (percent change in glomerular volume) was assessed from the gradual decrease in volume of glomeruli during 20 min of incubation with PAF. L(p) was calculated from the rate of change in glomerular volume during the 0.1 s of capillary expansion in response to a transcapillary oncotic gradient. P(albumin) was calculated from a change in relative volume of glomeruli in response to an oncotic gradient. Mesangial contraction was maximal after 20 min of incubation and was concentration dependent (5.2+/-0.9, 7.9+/-1.0 and 10.0+/-1.0%, respectively, with PAF 10(-9), 10(-7) and 10(-5) M). Incubation of glomeruli with PAF 10(-7) M for 60 min at 37 degrees C caused a significant decrease in L(p) (2.25+/-0.30 vs. control 3.12+/-0.28 microl x min(-1) x mm Hg(-1) x cm(-1), n = 5). P(albumin) of glomeruli incubated with PAF was unchanged up to 2 h but increased significantly with the highest concentration of PAF (10(-5) M) after 3 h of incubation (0.60+/-0.18, n=15, vs. control 0.00+/-0.08, n = 20), whereas lower concentrations of PAF (10[-7] or 10[-9] M) required at least 5 h of incubation with glomeruli to cause a significant increase in P(albumin) (0.45+/-0.09 and 0.48+/-0.07, respectively, n=15, vs. control 0.00+/-0.08, n=15). We conclude that PAF has multiple direct effects on glomerular functions, which are time dependent and may contribute to the altered capillary permeability in vivo.
血小板活化因子(PAF)是急性肾衰竭和肾小球肾炎损伤的重要介质。肾内输注PAF可通过其肾血流动力学和/或免疫效应降低肾小球滤过率和肾血浆流量,并增加肾小球通透性。PAF对肾小球毛细血管通透性的直接作用尚不清楚。我们研究了PAF对系膜收缩(滤过面积的一种度量)、肾小球毛细血管水力传导率(L[p])和毛细血管白蛋白通透性(P[白蛋白])的直接作用。从Sprague-Dawley大鼠分离出肾小球,并在37℃下与不同浓度的PAF(10[-9]、10[-7]和10[-5]M)孵育长达5小时,有或无PAF。在与PAF孵育20分钟期间,根据肾小球体积的逐渐减小评估系膜收缩(肾小球体积变化百分比)。L(p)根据对跨毛细血管胶体渗透压梯度的反应,在毛细血管扩张0.1秒期间肾小球体积的变化率计算得出。P(白蛋白)根据对胶体渗透压梯度的反应,肾小球相对体积的变化计算得出。孵育20分钟后系膜收缩最大,且呈浓度依赖性(分别为5.2±0.9、7.9±1.0和10.0±1.0%,PAF浓度分别为10(-9)、10(-7)和10(-5)M)。在37℃下,用10(-7)M的PAF孵育肾小球60分钟导致L(p)显著降低(2.25±0.30对对照组3.12±0.28微升×分钟(-1)×毫米汞柱(-1)×厘米(-1),n = 5)。用PAF孵育的肾小球的P(白蛋白)在长达2小时内未改变,但在孵育3小时后,最高浓度的PAF(10(-5)M)使其显著增加(0.60±0.18,n = 15,对对照组0.00±0.08,n = 20),而较低浓度的PAF(10[-7]或10[-9]M)需要与肾小球孵育至少5小时才能使P(白蛋白)显著增加(分别为0.45±0.09和0.48±0.07,n = 15,对对照组0.00±0.08,n = 15)。我们得出结论,PAF对肾小球功能有多种直接作用,这些作用具有时间依赖性,可能导致体内毛细血管通透性改变。