Joppich R, Weyer P, Eife R
St. Marien Hospital Amberg, Germany.
Arzneimittelforschung. 1995 Jul;45(7):822-5.
The effects of the diuretic furosemide (CAS 54-31-9) 1 mg/kg bw i.v., of the angiotensin converting enzyme (ACE) inhibitor captopril (CAS 62571-86-2) 1 mg/kg bw p.o. and the prostaglandin synthesis inhibitor indometacin (CAS 53-86-1) 2 mg/kg bw p.o. on kidney function, salt and water excretion, the excretion of renal prostaglandins PGE2, PGF2a, 6-keto-PGF1a, thromboxane B2 (TXB2) and the plasma renin activity (PRA) were investigated on 29 neonatal piglets. Within 1 h, fuorsemide led to pronounced diuresis and natriuresis, to a rise of the glomerular filtration rate (GFR) (which ist low in neonatal pigs) by 1.8 times, increased the excretion of renal prostaglandins (especially the vasoconstrictor, thromboxane B2 (TXB2 and PGF2a) and raised the PRA significantly. Under captopril, the PRA rose significantly, whereas there was no unequivocal change in the excretion of renal prostaglandins. There was a pronounced decline of the sodium and potassium excretion in the urine with a fall in the concentrations of electrolytes in serum and of the hematocrit. Under indometacin, the excretion of all prostaglandins in the urine declined (this decline was most pronounced for PGE2). There was also a decrease in sodium excretion, whereas there was no significant change in PRA. It can be concluded from the results that the effects of the investigated drugs on the pig neonate kidney is at least partially attributable to an influence on hormonal factors.
研究了静脉注射1毫克/千克体重的利尿剂呋塞米(CAS 54-31-9)、口服1毫克/千克体重的血管紧张素转换酶(ACE)抑制剂卡托普利(CAS 62571-86-2)以及口服2毫克/千克体重的前列腺素合成抑制剂吲哚美辛(CAS 53-86-1)对29只新生仔猪肾功能、盐和水排泄、肾前列腺素PGE2、PGF2α、6-酮-PGF1α、血栓素B2(TXB2)排泄以及血浆肾素活性(PRA)的影响。在1小时内,呋塞米导致明显的利尿和利钠作用,使新生仔猪中本来较低的肾小球滤过率(GFR)提高了1.8倍,增加了肾前列腺素的排泄(尤其是血管收缩剂血栓素B2(TXB2和PGF2α)),并显著提高了PRA。在卡托普利作用下,PRA显著升高,而肾前列腺素的排泄没有明确变化。尿液中钠和钾的排泄明显下降,血清中电解质浓度和血细胞比容降低。在吲哚美辛作用下,尿液中所有前列腺素的排泄均下降(PGE2的下降最为明显)。钠排泄也减少,而PRA没有显著变化。从结果可以得出结论,所研究药物对新生仔猪肾脏的影响至少部分归因于对激素因素的影响。