Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats.
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Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats. / Christensen, P; Holstein-Rathlou, N H.
I: Prostaglandins & Other Lipid Mediators, Bind 22, Nr. 6, 1981, s. 893-902.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats.
AU - Christensen, P
AU - Holstein-Rathlou, N H
N1 - Keywords: Anesthetics; Animals; Chromatography, Gel; Chromatography, Thin Layer; Dinoprost; Dinoprostone; Halothane; Hexobarbital; Male; Nitrous Oxide; Prostaglandins A; Prostaglandins E; Prostaglandins F; Radioimmunoassay; Rats; Rats, Inbred Strains
PY - 1981
Y1 - 1981
N2 - Prostaglandins of the E-type (PGE's) were found to react or combine with a urinary metabolite of Halothane yielding products which were left unrecovered during the purification procedure preceding specific radioimmunoassay of PGE2. The products were retained on sephadex LH-20 columns, and showed on thin layer silica gel plates (TLC) Rf values lower than those of the parent PGE-compounds. The product formation is supposed to involve the beta-hydroxyketone system of PGE, since PG's of the F and A type were unaffected. The product formation could be avoided by inducing anaesthesia with Hexobarbitone and maintaining the anaesthesia with Halothane-nitrous oxide or it could be reversed by adding barbiturates to urine samples obtained from animals anaesthetized with Halothane-nitrous oxide alone. The barbiturates effectively competed with PGE for the metabolite leaving PGE to behave normally on sephadex LH-20 and TLC, thus enabling us to evaluate correctly the PGE2 content by RIA.
AB - Prostaglandins of the E-type (PGE's) were found to react or combine with a urinary metabolite of Halothane yielding products which were left unrecovered during the purification procedure preceding specific radioimmunoassay of PGE2. The products were retained on sephadex LH-20 columns, and showed on thin layer silica gel plates (TLC) Rf values lower than those of the parent PGE-compounds. The product formation is supposed to involve the beta-hydroxyketone system of PGE, since PG's of the F and A type were unaffected. The product formation could be avoided by inducing anaesthesia with Hexobarbitone and maintaining the anaesthesia with Halothane-nitrous oxide or it could be reversed by adding barbiturates to urine samples obtained from animals anaesthetized with Halothane-nitrous oxide alone. The barbiturates effectively competed with PGE for the metabolite leaving PGE to behave normally on sephadex LH-20 and TLC, thus enabling us to evaluate correctly the PGE2 content by RIA.
M3 - Journal article
C2 - 6950460
VL - 22
SP - 893
EP - 902
JO - Prostaglandins and Other Lipid Mediators
JF - Prostaglandins and Other Lipid Mediators
SN - 1098-8823
IS - 6
ER -
ID: 8440591