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Anti-inflammatory steroids without pituitary-adrenal suppression.

Abstract
When two new steroids, methyl prednisolonate and methyl 20-dihydroprednisolonate, were applied locally their anti-inflammatory activities were nearly equivalent to those of the parent compound prednisolone in the cotton pellet granuloma bioassay. However, when these two derivatives were administered systemically, their anti-inflammatory activities were weaker than those of the parent compound. Furthermore, unlike the parent compound, these new anti-inflammatory steroids did not suppress pituitary-adrenal function or cause liver glycogen depletion in rats.
AuthorsH J Lee, M R Soliman
JournalScience (New York, N.Y.) (Science) Vol. 215 Issue 4535 Pg. 989-91 (Feb 19 1982) ISSN: 0036-8075 [Print] United States
PMID6296999 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Anti-Inflammatory Agents
  • Liver Glycogen
  • methyl prednisolonate
  • methyl 20-dihydroprednisolonate
  • Adrenocorticotropic Hormone
  • Prednisolone
  • Corticosterone
Topics
  • Administration, Topical
  • Adrenocorticotropic Hormone (blood)
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Corticosterone (blood)
  • Liver Glycogen (biosynthesis)
  • Pituitary-Adrenal System (drug effects)
  • Prednisolone (administration & dosage, analogs & derivatives, pharmacology)
  • Rats

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