Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats.

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Standard

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 tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Christensen, P & Holstein-Rathlou, NH 1981, 'Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats.', Prostaglandins & Other Lipid Mediators, bind 22, nr. 6, s. 893-902.

APA

Christensen, P., & Holstein-Rathlou, N. H. (1981). Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats. Prostaglandins & Other Lipid Mediators, 22(6), 893-902.

Vancouver

Christensen P, Holstein-Rathlou NH. Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats. Prostaglandins & Other Lipid Mediators. 1981;22(6):893-902.

Author

Christensen, P ; Holstein-Rathlou, N H. / Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats. I: Prostaglandins & Other Lipid Mediators. 1981 ; Bind 22, Nr. 6. s. 893-902.

Bibtex

@article{ebb6b2b0abf111ddb5e9000ea68e967b,
title = "Interaction between prostaglandins of the E-type with a urinary component from halothane anesthetized rats.",
abstract = "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.",
author = "P Christensen and Holstein-Rathlou, {N H}",
note = "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",
year = "1981",
language = "English",
volume = "22",
pages = "893--902",
journal = "Prostaglandins and Other Lipid Mediators",
issn = "1098-8823",
publisher = "Elsevier",
number = "6",

}

RIS

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