Matches in SemOpenAlex for { <https://semopenalex.org/work/W1969650068> ?p ?o ?g. }
Showing items 1 to 68 of
68
with 100 items per page.
- W1969650068 endingPage "2146" @default.
- W1969650068 startingPage "2139" @default.
- W1969650068 abstract "We studied the effects of continuous administration of recombinant human interleukin-1 beta (IL-1) on pituitary-thyroid function. Rats were equipped with minipumps loaded with either IL-1 (delivery rate, 0.5, 2.0, or 4.0 micrograms/day, ip, for 1 week) or saline. Infusion of 2.0 and 4.0 micrograms IL-1/day caused a significant decrease in plasma free T4 levels during the first 2-4 days, whereas plasma total T4 levels and T4 binding were significantly lowered throughout the week of the study. The infusion of 0.5 micrograms IL-1/day did not significantly change plasma TSH or total and free T4 levels. During the infusion of 2.0 micrograms IL-1/day, the decrease in plasma free T4 levels was paralleled by a significant decline in plasma TSH values and an impaired TSH responsiveness to TRH administration on the second day of infusion. IL-1 (2.0 micrograms/day) treatment significantly lowered plasma levels of T4-binding prealbumin, whereas it did not influence the plasma T3/T4 ratio or hepatic 5'-deiodinase activity. Plasma rT3 levels remained undetectable in both control and IL-1-treated rats. Chronic infusion of rats with 4.0 micrograms IL-1/day induced prolonged fever, whereas at the lower doses of IL-1, temperatures were elevated only on the first 2 days. IL-1 at doses of 2.0 and 4.0 micrograms/day induced a transient decrease in food intake and a suppression of body weight gain. Restriction of food consumption to the level observed in the 2.0 micrograms IL-1 experiment caused small decreases in T3, total and free T4, and TSH levels compared to those in ad libitum fed rats, but had no effects on T4 binding. We conclude that 1) continuous infusion of rats with 2.0 and 4.0 micrograms IL-1/day induces changes in thyroid economy commonly seen during infectious diseases and other systemic illnesses in rats [decreased plasma levels of TSH, T3, and (free) T4; diminished T4 binding; and decreased plasma T4-binding prealbumin levels], 2) the decrease in food intake during IL-1 treatment cannot completely explain the observed changes in thyroid hormone and TSH levels; and 3) it is highly unlikely that the decrease in thyroid hormone binding during chronic IL-1 infusion is caused by decreased food intake. Further studies are needed to clarify whether the observed alterations in thyroid economy during IL-1 infusion reflect direct effects of IL-1 per se or indirect effects caused by the mild illness induced by the cytokine." @default.
- W1969650068 created "2016-06-24" @default.
- W1969650068 creator A5011787323 @default.
- W1969650068 creator A5037020689 @default.
- W1969650068 creator A5038320439 @default.
- W1969650068 creator A5056743984 @default.
- W1969650068 creator A5068183096 @default.
- W1969650068 creator A5076102630 @default.
- W1969650068 creator A5083707441 @default.
- W1969650068 date "1992-11-01" @default.
- W1969650068 modified "2023-09-27" @default.
- W1969650068 title "Continuous infusion of interleukin-1 beta induces a nonthyroidal illness syndrome in the rat." @default.
- W1969650068 doi "https://doi.org/10.1210/endo.131.5.1425414" @default.
- W1969650068 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/1425414" @default.
- W1969650068 hasPublicationYear "1992" @default.
- W1969650068 type Work @default.
- W1969650068 sameAs 1969650068 @default.
- W1969650068 citedByCount "66" @default.
- W1969650068 countsByYear W19696500682012 @default.
- W1969650068 countsByYear W19696500682013 @default.
- W1969650068 countsByYear W19696500682014 @default.
- W1969650068 countsByYear W19696500682015 @default.
- W1969650068 countsByYear W19696500682016 @default.
- W1969650068 countsByYear W19696500682017 @default.
- W1969650068 countsByYear W19696500682019 @default.
- W1969650068 countsByYear W19696500682021 @default.
- W1969650068 countsByYear W19696500682022 @default.
- W1969650068 countsByYear W19696500682023 @default.
- W1969650068 crossrefType "journal-article" @default.
- W1969650068 hasAuthorship W1969650068A5011787323 @default.
- W1969650068 hasAuthorship W1969650068A5037020689 @default.
- W1969650068 hasAuthorship W1969650068A5038320439 @default.
- W1969650068 hasAuthorship W1969650068A5056743984 @default.
- W1969650068 hasAuthorship W1969650068A5068183096 @default.
- W1969650068 hasAuthorship W1969650068A5076102630 @default.
- W1969650068 hasAuthorship W1969650068A5083707441 @default.
- W1969650068 hasConcept C126322002 @default.
- W1969650068 hasConcept C134018914 @default.
- W1969650068 hasConcept C185592680 @default.
- W1969650068 hasConcept C2777397205 @default.
- W1969650068 hasConcept C71924100 @default.
- W1969650068 hasConceptScore W1969650068C126322002 @default.
- W1969650068 hasConceptScore W1969650068C134018914 @default.
- W1969650068 hasConceptScore W1969650068C185592680 @default.
- W1969650068 hasConceptScore W1969650068C2777397205 @default.
- W1969650068 hasConceptScore W1969650068C71924100 @default.
- W1969650068 hasIssue "5" @default.
- W1969650068 hasLocation W19696500681 @default.
- W1969650068 hasLocation W19696500682 @default.
- W1969650068 hasOpenAccess W1969650068 @default.
- W1969650068 hasPrimaryLocation W19696500681 @default.
- W1969650068 hasRelatedWork W1983012135 @default.
- W1969650068 hasRelatedWork W2009877402 @default.
- W1969650068 hasRelatedWork W2014432291 @default.
- W1969650068 hasRelatedWork W2054119993 @default.
- W1969650068 hasRelatedWork W2056503472 @default.
- W1969650068 hasRelatedWork W2071934027 @default.
- W1969650068 hasRelatedWork W2114858141 @default.
- W1969650068 hasRelatedWork W2748952813 @default.
- W1969650068 hasRelatedWork W2899084033 @default.
- W1969650068 hasRelatedWork W2341096078 @default.
- W1969650068 hasVolume "131" @default.
- W1969650068 isParatext "false" @default.
- W1969650068 isRetracted "false" @default.
- W1969650068 magId "1969650068" @default.
- W1969650068 workType "article" @default.