This study investigated the effects of low dose endotoxin (lipopoly'/> Intrarenal haemodynamics and renal dysfunction in endotoxaemia: effects of nitric oxide synthase inhibition
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Intrarenal haemodynamics and renal dysfunction in endotoxaemia: effects of nitric oxide synthase inhibition

机译:内毒素血症的肾内血流动力学和肾功能不全:一氧化氮合酶抑制作用

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摘要

class="enumerated" style="list-style-type:decimal">This study investigated the effects of low dose endotoxin (lipopolysaccharide, LPS) on (i) systemic haemodynamics, (ii) renal blood flow (RBF), (iii) renal cortical and medullary perfusion and (iv) renal function in the anaesthetized rat. We have also investigated the effects of nitric oxide (NO) synthase (NOS) inhibition with NG-methyl-L-arginine (L-NMMA) on the alterations in systemic and renal haemodynamics and renal function caused by endotoxin.Infusion of low dose LPS (1 mg kg−1 over 30 min, n=6) caused a late fall in mean arterial blood pressure (MAP, at 5 and 6 h after LPS), but did not cause an early (at 1–4 h after LPS) hypotension. The pressor effect of noradrenaline (NA, 1 μg kg−1, i.v.) was significantly reduced at 1 to 6 h after LPS (vascular hyporeactivity). Infusion of L-NMMA (50 μg kg−1 min−1 commencing 60 min before LPS and continued throughout the experiment, n=7) abolished the delayed hypotension and significantly attenuated the vascular hyporeactivity to NA (at 2–6 h).Infusion of LPS (1 mg kg−1 over 30 min, n=6) caused a rapid (within 2 h) decline in renal function (measured by inulin clearance) in the absence of a significant fall in MAP or renal blood flow (RBF). L-NMMA (n=7) attenuated the impairment in renal function caused by LPS so that the inulin clearance in LPS-rats treated with L-NMMA was significantly greater than in LPS-rats treated with vehicle (control) at 3–6 h after infusion of LPS.Endotoxaemia also caused a significant reduction in renal cortical, but not medullary perfusion (measured as Laser Doppler flux). Infusion of L-NMMA caused a significant further fall in cortical perfusion and a significant fall in medullary perfusion in the absence of changes in RBF.Infusion of LPS resulted in a progressive increase in the plasma levels of nitriteitrate (an indicator of the formation of NO), so that the plasma concentration of nitriteitrate was significantly higher than baseline at 150 to 330 min after LPS. Infusion of L-NMMA attenuated the rise in the plasma concentration of nitriteitrate (at 270 and 330 min, P<0.05) caused by LPS.Thus, the renal dysfunction caused by injection of low dose of endotoxin in the rat occurs in the absence of significant falls in blood pressure or total renal blood flow. Inhibition of NOS activity with L-NMMA attenuates the renal dysfunction caused by endotoxin (without improving intrarenal haemodynamics), suggesting that an overproduction of NO may contribute to the development of renal injury and dysfunction by causing direct cytotoxic effects.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 这项研究调查了低剂量内毒素(脂多糖,LPS)对(a)全身麻醉后大鼠的(i)全身血流动力学,(ii)肾血流量(RBF),(iii)肾皮质和髓质灌注以及(iv)肾功能的影响。我们还研究了N G -甲基-L-精氨酸(L-NMMA)对一氧化氮(NO)合酶(NOS)的抑制作用对引起的全身和肾脏血液动力学和肾功能变化的影响 输注低剂量LPS​​(1 mg kg -1 在30 min内,n = 6)导致平均动脉血压(MAP,在5岁时)下降较晚和LPS后6 h),但并未引起早期(LPS后1–4 h)低血压。 LPS(血管反应性低下)后1至6 h,去甲肾上腺素(NA,1,μgkg -1 ,i.v.)的升压作用显着降低。 L-NMMA(LPS前60 min开始输注50μgkg −1 min −1 ,并在整个实验中持续进行,n = 7)消除了延迟的低血压并明显减轻了血压 输注LPS(1 mg kg −1 超过30 min,n = 6)导致快速(在2内) h)在MAP或肾血流量(RBF)没有明显下降的情况下,肾功能下降(通过菊粉清除率衡量)。 L-NMMA(n = 7)减轻了LPS引起的肾功能损害,因此在3–6 h时,L-NMMA治疗的LPS大鼠的菊糖清除率明显高于溶媒治疗的LPS大鼠(对照)中的菊粉清除率输注LPS后。 内毒素血症也引起肾皮质的显着减少,但未引起髓样灌注(以激光多普勒通量测量)。在没有RBF改变的情况下,输注L-NMMA会导致皮质灌注显着进一步下降,而髓质灌注会显着下降。 输注LPS会导致血浆亚硝酸盐/血浆水平逐渐升高硝酸盐(指示NO的形成),因此LPS后150至330 min时,亚硝酸盐/硝酸盐的血浆浓度显着高于基线。输注L-NMMA可以减轻LPS引起的血浆亚硝酸盐/硝酸盐浓度的升高(在270和330 min,P <0.05)。 因此,低剂量注射LPS引起的肾功能不全。内毒素在大鼠中没有明显的血压下降或总肾血流量出现。用L-NMMA抑制NOS活性可减轻由内毒素引起的肾功能不全(而不会改善肾内血流动力学),这表明NO的过量产生可能通过引起直接的细胞毒性作用而导致肾损伤和功能障碍的发展。

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