Ming Zhi, Fan Yi-Jun, Yang Xi, Lautt W Wayne
Department of Pharmacology & Therapeutics, University of Manitoba, Winnipeg, Manitoba, Canada.
Hepatology. 2006 Oct;44(4):813-22. doi: 10.1002/hep.21336.
Acute liver injury is associated with renal insufficiency, whose mechanism may be related to activation of the hepatorenal reflex. We previously showed that intrahepatic adenosine is involved in activation of the hepatorenal reflex to restrict urine production in both healthy rats and in rats with cirrhosis. The aim of the present study was to test the hypothesis that activation of intrahepatic adenosine receptors is involved in the pathogenesis of the renal insufficiency seen in acute liver injury. Acute liver injury was induced by intraperitoneal injection of thioacetamide (TAA, 500 mg/kg) in rats. The animals were instrumented 24 hours later to monitor systemic, hepatic, and renal circulation and urine production. Severe liver injury developed following TAA insult, which was associated with renal insufficiency, as demonstrated by decreased (approximately 25%) renal arterial blood flow, a lower (approximately 30%) glomerular filtration rate, and decreased urine production. Further, the increase in urine production following volume expansion challenge was inhibited. Intraportal, but not intravenous, administration of a nonselective adenosine receptor antagonist, 8-phenyltheophylline, improved urine production. To specify receptor subtype, the effects of 8-cyclopentyl-1,3-dipropylxanthine (DPCPX, an adenosine A(1) receptor antagonist) and 3,7-dimethyl-1-propargylxanthine (DMPX, an adenosine A(2) receptor antagonist) were compared. Intraportal but not intravenous administration of DPCPX greatly improved impaired renal function induced by acute liver injury, and this beneficial effect was blunted in rats with liver denervation. In contrast, neither intraportal nor intravenous administration of DMPX showed significant improvement in renal function. In conclusion, an activated hepatorenal reflex, triggered by intrahepatic adenosine A(1) receptors, contributed to the pathogenesis of the water and sodium retention associated with acute liver injury.
急性肝损伤与肾功能不全相关,其机制可能与肝肾反射的激活有关。我们之前的研究表明,肝内腺苷参与了肝肾反射的激活,从而在健康大鼠和肝硬化大鼠中限制尿液生成。本研究的目的是验证肝内腺苷受体激活参与急性肝损伤中所见肾功能不全发病机制的假说。通过腹腔注射硫代乙酰胺(TAA,500mg/kg)诱导大鼠急性肝损伤。24小时后对动物进行仪器监测,以监测全身、肝脏和肾脏循环及尿液生成。TAA损伤后出现严重肝损伤,并伴有肾功能不全,表现为肾动脉血流减少(约25%)、肾小球滤过率降低(约30%)和尿量减少。此外,容量扩张刺激后尿量的增加受到抑制。门静脉注射而非静脉注射非选择性腺苷受体拮抗剂8-苯基茶碱可改善尿量。为明确受体亚型,比较了8-环戊基-1,3-二丙基黄嘌呤(DPCPX,一种腺苷A(1)受体拮抗剂)和3,7-二甲基-1-丙炔基黄嘌呤(DMPX,一种腺苷A(2)受体拮抗剂)的作用。门静脉注射而非静脉注射DPCPX可显著改善急性肝损伤诱导的肾功能损害,且这种有益作用在去神经肝脏的大鼠中减弱。相比之下,门静脉注射和静脉注射DMPX均未显示肾功能有显著改善。总之,由肝内腺苷A(1)受体触发的激活的肝肾反射促成了与急性肝损伤相关的水钠潴留的发病机制。