Literature DB >> 4051557

Oxidized sterols inhibit the formation of podophyllin-induced metaphase figures in mouse vaginal epithelia.

A A Gaspari, R L Rietschel.   

Abstract

The antimitotic activity of oxidized derivatives of cholesterol was investigated using an assay developed by Van Scott and Bonder. In this assay, a drug that has antimitotic activity and is not a metaphase-blocking agent will inhibit the formation of podophyllin-induced metaphase figures, as counted on histologic specimens. Mouse vaginal epithelia were classified as being estrogen or progesterone predominant on the basis of histologic criteria. Podophyllin-injected mice in the estrogenic phase of the estrus cycle demonstrated high metaphase-figure counts, with an average of 284.86 +/- 132.01. In this group, all intravaginally administered compounds, inhibited the formation of metaphase figures, including a propylene-glycol ethanol vehicle (60% suppression); thus, it is concluded that animals in this phase are not a suitable model for assaying antimitotic activity. Mice in the progesterone-predominant phase of the estrus cycle had lower counts of podophyllin-induced metaphase figures, i.e., 142.13 +/- 39.29. In this group, 25-OH-cholesterol was the most effective inhibitor (59% suppression), followed by 7-ketocholesterol (48% suppression) and methotrexate (40% suppression). Cholesterol (5% suppression) and vehicle (20% suppression) did not have any significant effects. Progesterone-predominant epithelium was only susceptible to methotrexate and oxidized sterols. This suggests that oxidized sterols may have antimitotic activity.

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Year:  1985        PMID: 4051557     DOI: 10.1007/BF00510066

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.017


  18 in total

1.  The site of sterol and squalene synthesis in the human skin.

Authors:  N NICOLAIDES; S ROTHMAN
Journal:  J Invest Dermatol       Date:  1955-02       Impact factor: 8.551

2.  Potent immunosuppression by oxidized cholesterol.

Authors:  G M Humphries; H M McConnell
Journal:  J Immunol       Date:  1979-01       Impact factor: 5.422

3.  Inhibition of sterol synthesis in cultured mouse cells by cholesterol derivatives oxygenated in the side chain.

Authors:  A A Kandutsch; H W Chen
Journal:  J Biol Chem       Date:  1974-10-10       Impact factor: 5.157

4.  A model system for the evaluation of the role of cholesterol -oxide in ultraviolet carcinogenesis.

Authors:  H S Black; D R Douglas
Journal:  Cancer Res       Date:  1972-12       Impact factor: 12.701

5.  Intravaginal and intrarectal screening of antimitotic drugs for topical effectiveness.

Authors:  E J Van Scott; R H Bonder
Journal:  J Invest Dermatol       Date:  1971-02       Impact factor: 8.551

6.  12-O-Tetradecanoylphorbol-13-acetate induced alterations in mouse epidermal 3-hydroxy-3-methylglutaryl CoA reductase.

Authors:  G S Kishore; B C Paton; R K Boutwell; S Goldfarb; T Ramasarma
Journal:  Biochem Biophys Res Commun       Date:  1981-04-30       Impact factor: 3.575

7.  Formation of a carcinogen in human skin irradiated with ultraviolet light.

Authors:  H S Black; W B Lo
Journal:  Nature       Date:  1971-12-03       Impact factor: 49.962

8.  Consequences of blocked sterol synthesis in cultured cells. DNA synthesis and membrane composition.

Authors:  A A Kandutsch; H W Chen
Journal:  J Biol Chem       Date:  1977-01-25       Impact factor: 5.157

9.  Biological activity of some oxygenated sterols.

Authors:  A A Kandutsch; H W Chen; H J Heiniger
Journal:  Science       Date:  1978-08-11       Impact factor: 47.728

10.  Relationship between sterol synthesis and DNA synthesis in phytohemagglutinin-stimulated mouse lymphocytes.

Authors:  H W Chen; H J Heiniger; A A Kandutsch
Journal:  Proc Natl Acad Sci U S A       Date:  1975-05       Impact factor: 11.205

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