Mechanism of attenuated hydrochlorothiazide response during indomethacin administration

Mechanism of attenuated hydrochlorothiazide response during indomethacin administration. Indomethacin antagonizes the natriuretic and chloruretic response to hydrochlorothiazide in most studies. Neither the mechanism nor nephron site of this antagonism has been determined. To identify sites and pote...

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Bibliographic Details
Published in:Kidney international 1987-05, Vol.31 (5), p.1097-1103
Main Authors: Kirchner, Kent A., Brandon, Steven, Mueller, Rebecca A., Smith, Manis J., Bower, John D.
Format: Article
Language:English
Subjects:
Animals
Biological and medical sciences
Chlorides - urine
Diuresis - drug effects
Drug Interactions
Glomerular Filtration Rate - drug effects
Hydrochlorothiazide - pharmacology
Indomethacin - pharmacology
Kidney Tubules, Distal - drug effects
Kidney Tubules, Proximal - drug effects
Male
Medical sciences
Natriuresis - drug effects
Pharmacology. Drug treatments
Prostaglandins - urine
Rats
Rats, Inbred Strains
Urinary system
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Summary:Mechanism of attenuated hydrochlorothiazide response during indomethacin administration. Indomethacin antagonizes the natriuretic and chloruretic response to hydrochlorothiazide in most studies. Neither the mechanism nor nephron site of this antagonism has been determined. To identify sites and potential mechanisms, cortical micropuncture was performed during hydrochlorothiazide treatment in control and indomethacin rats. Indomethacin reduced (P < 0.005) FeCl from 5.20 ± 0.49 % to 2.26 ± 0.49% (mean ±SE). MAP, CIn, and plasma volume were not different between groups. SNGFR and fractional proximal fluid and chloride delivery were not different between groups. Fractional chloride delivery to early distal tubules was 10.8 ± 0.4% in control but 6.2 ± 0.3% in indomethacin rats (P < 0.001). Calculated loop chloride reabsorption was greater in indomethacin than control rats during hydrochlorothiazide administration (41.0 ± 1.6% vs. 34.3 ± 2.3%; P < 0.05). Fractional chloride delivery to late distal tubules was 7.8 ± 0.7% in control and 4.6 ± 0.3% in indomethacin rats (P < 0.005), but distal tubule chloride reabsorption was not different between groups. Papillary tissue chloride was less in control than indomethacin rats during hydrochlorothiazide (P < 0.05). Urinary PGE2 excretion was reduced (P < 0.001) by indomethacin during hydrochlorothiazide. Thus indomethacin induced reductions in hydrochlorothiazide response result in part from increased chloride reabsorption in the loop segment. This suggests indomethacin antagonizes hydrochlorothiazide by reducing chloride delivery to hydrochlorothiazide's site of action in the distal tubule rather than by effects of indomethacin on hydrochlorothiazide pharmacokinetics.
ISSN:0085-2538
1523-1755
DOI:10.1038/ki.1987.114