Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1990 Jan;4(1):44-7.
doi: 10.1007/BF00858438.

Urinary prostaglandins in hyperglycaemic ketoacidosis of type I diabetes mellitus

Affiliations

Urinary prostaglandins in hyperglycaemic ketoacidosis of type I diabetes mellitus

M Miltényi et al. Pediatr Nephrol. 1990 Jan.

Abstract

Urinary excretion of various renal prostaglandins was measured by radioimmunoassay and gas chromatography-mass spectrometry in children who had different degrees of metabolic control. Excretion in PGE2 in diabetic children was twice control values irrespective of the presence or absence of diabetic ketoacidosis (DKA). The urinary excretion of PGF2 alpha was significantly increased in diabetic children with ketoacidosis, but not when diabetes was well controlled. The excretion of 13, 14 dihydro-15-keto PGE2, the major metabolite of circulating PGE2, was increased in all diabetic children, and was most elevated in ketoacidosis when it averaged 10 times basal excretion. Urinary excretion of PGF2 alpha and of 6-keto-PGF1 alpha, the metabolite of PGI2, was approximately doubled in DKA compared with values from healthy subjects. Excretion of PGE2 was twice control values in children with stable diabetes, whereas the equivalent value for TXB2, the metabolite of the active vasoconstrictor TXA2, was reduced by approximately 50%. We suggest that the increased excretion of prostacyclin metabolite may result from a protective biological action on the kidney opposing other vasoconstrictor hormone activity. PGE2 appears not to be involved in this process. The highly elevated excretion of PGE2 metabolite may represent an activation of systemic PGE metabolism during DKA.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Pharmacol Rev. 1978 Sep;30(3):293-331 - PubMed
    1. Arch Dis Child. 1985 Oct;60(10):929-31 - PubMed
    1. Klin Wochenschr. 1979 Oct 1;57(19):1021-9 - PubMed
    1. Am J Med. 1982 Feb;72(2):354-74 - PubMed
    1. Diabetes. 1985 Aug;34(8):761-6 - PubMed

LinkOut - more resources