K. Farker et al., DIPYRONE AND DICLOFENAC DO NOT INFLUENCE CREATININE-CLEARANCE, INULIN-CLEARANCE OR PAH-CLEARANCE IN HEALTHY MALE-VOLUNTEERS, International journal of clinical pharmacology and therapeutics, 33(3), 1995, pp. 125-130
The effects of the non-steroidal anti-inflammatory drug diclofenac and
the pyrazolone derivative dipyrone on renal function were compared wi
th those of placebo in 12 healthy male volunteers in a randomized, con
trolled, triple-crossover study with a wash-out period of 4 days betwe
en each of the 3 trial periods (dipyrone, diclofenac and placebo) whic
h lasted three days each. The volunteers received dipyrone(1 g, 3 time
s/day for 2 days, followed by twice 1 g on the main trial day, which w
as day 3 of each study period) or diclofenac (50 mg, 3 times/day for 2
days, followed by twice 50 mg on the main trial day) or placebo orall
y. Standardized meals (50 mEq sodium per day) were given from one week
before the start until the end of the study and on the main trial day
s a protein-rich lunch (2 g protein/kg body weight) was taken. Renal f
unction was assessed in each study period by measurement of creatinine
-clearance, inulin-clearance and p-aminohippurate (PAH)-clearance to c
haracterize glomerular filtration rate and renal plasma flow. High pro
tein intake induced glomerular hyperfiltration (increased creatinine-c
learance, inulin-clearance and PAH-clearance) in all 3 study periods (
dipyrone, diclofenac, placebo). Dipyrone and diclofenac had no effect
on renal clearance of creatinine, inulin or PAH in comparison to place
bo. These results show that dipyrone and diclofenac at therapeutic dos
ages over 3 days do not decrease glomerular filtration and renal plasm
a flow in healthy individuals. Furthermore, it is unlikely that prostg
landins play a major role in protein-induced glomerular hyperfiltratio
n.