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慢性缺氧大鼠中的肾激肽释放酶

Renal kallikrein in chronic hypoxic rats.

作者信息

Chen C F, Chen L W, Chien C T, Wu M S, Tsai T J

机构信息

Department of Physiology, College of Medicine, National Taiwan University, Taipei, ROC.

出版信息

Clin Exp Pharmacol Physiol. 1996 Sep;23(9):819-24. doi: 10.1111/j.1440-1681.1996.tb01186.x.

Abstract
  1. We have studied the role of kallikrein (KK) in the maintenance of renal function in chronic hypoxic rats (high altitude; HA), compared with control rats kept at sea level (SL). Hypoxia was induced by placing female Wistar rats (198-290 g) in an altitude chamber (5500 m) 15 h/day for 4 weeks. Experiments were also conducted to study the interaction of KK with renal nerve activity and endothelin (ET), two parameters previously shown to be altered in this model. 2. It was found that renal cortex tissue KK activity (TKA) was not significantly different in 10 SL and 10 HA rats. However, the urinary KK activity (UKA) was reduced nearly to half (from 35.2 +/- 4.6 to 18.5 +/- 1.7 pkat/min) in HA rats after 4 weeks of chronic hypoxia. 3. Acute renal denervated diuresis was accompanied by a significant increase in UKA (from 9 +/- 2 to 14 +/- 2 pkat/min in HA and denervated HA rats, respectively; P < 0.05) in HA rats. Intrarenal arterial pretreatment of aprotinin reduced the denervated diuresis. 4. Endothelin (600 ng/kg per h) reduced urine flow, sodium and potassium excretion in the ipsilateral kidney in another 10 SL and 10 HA rats. The extent of the drop of these parameters was significantly less in HA rats. Urinary KK activity was correlated significantly with the measured renal functional parameters (r ranging from 0.472 to 0.612) in SL rats, but was insignificant in HA rats (r ranging from 0.032 to 0.192). 5. We have demonstrated that chronic exposure to hypoxia decreases urinary KK excretion and that KK is involved in acute renal denervated diuresis generated in these animals. The present study suggests that KK plays a partial role in the maintenance of renal function in chronic hypoxic rats.
摘要
  1. 我们研究了激肽释放酶(KK)在慢性缺氧大鼠(高海拔;HA)肾功能维持中的作用,并与饲养在海平面(SL)的对照大鼠进行了比较。通过将雌性Wistar大鼠(198 - 290克)置于海拔舱(5500米)中,每天15小时,持续4周来诱导缺氧。还进行了实验以研究KK与肾神经活动和内皮素(ET)的相互作用,这两个参数在该模型中先前已显示发生改变。2. 发现10只SL大鼠和10只HA大鼠的肾皮质组织KK活性(TKA)无显著差异。然而,慢性缺氧4周后,HA大鼠的尿KK活性(UKA)几乎降低了一半(从35.2±4.6降至18.5±1.7皮卡特/分钟)。3. HA大鼠急性肾去神经利尿伴随着UKA的显著增加(HA和去神经HA大鼠分别从9±2增至14±2皮卡特/分钟;P < 0.05)。肾内动脉预先给予抑肽酶可减少去神经利尿。4. 内皮素(每小时600纳克/千克)降低了另外10只SL大鼠和10只HA大鼠同侧肾脏的尿流量、钠和钾排泄。这些参数下降的程度在HA大鼠中明显较小。SL大鼠的尿KK活性与所测肾功能参数显著相关(r范围为0.472至0.612),但在HA大鼠中无显著相关性(r范围为0.032至0.192)。5. 我们已经证明,长期暴露于缺氧会降低尿KK排泄,并且KK参与了这些动物产生的急性肾去神经利尿。本研究表明,KK在慢性缺氧大鼠肾功能维持中起部分作用。

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