Journal of Toxicology and Environmental Health, Part A 1987-01-01

Estrogenic potencies of resorcylic acid lactones and 17 beta-estradiol in female rats.

D J Everett, C J Perry, K A Scott, B W Martin, M K Terry

Index: J. Toxicol. Environ. Health A 20(4) , 435-43, (1987)

Full Text: HTML

Abstract

Uterotrophic response in sexually immature female rats has been used to rank the relative estrogenic potencies of six resorcylic acid lactones (RALs) and to compare their activities with that of 17 beta-estradiol. On oral administration, the estrogenic potency relative to 17 beta-estradiol is as follows: 7 alpha-zearalenol, 10 times less; zeranol, 150 times less; taleranol, 350 times less; zearalanone, 400 times less; zearalenone, 650 times less; 7 beta-zearalenol, 3500 times less. On subcutaneous administration, zeranol is 500 times less estrogenic than 17 beta-estradiol.


Related Compounds

Related Articles:

Determination of resorcylic acid lactones in biological samples by GC-MS. Discrimination between illegal use and contamination with fusarium toxins.

2006-03-01

[Anal. Bioanal. Chem 384(5) , 1221-7, (2006)]

Cytosol protein regulation in H295R steroidogenesis model induced by the zearalenone metabolites, α- and β-zearalenol.

2012-01-01

[Toxicon 59(1) , 17-24, (2012)]

Determination of the cross-reactivities for alpha-zearalenol, beta-zearalenol, zearalanone, alpha-zearalanol, and beta-zearalanol on three commercial immunoaffinity columns targeting zearalenone.

2007-01-01

[J. AOAC Int. 90(4) , 1197-202, (2007)]

The activities of mycotoxins derived from Fusarium and related substances in a short-term transformation assay using v-Ha-ras-transfected BALB/3T3 cells (Bhas 42 cells).

2007-06-15

[Mutat. Res. 630(1-2) , 103-11, (2007)]

Hydroxysteroid dehydrogenases in bovine and porcine granulosa cells convert zearalenone into its hydroxylated metabolites alpha-zearalenol and beta-zearalenol.

2006-05-01

[Vet. Res. Commun. 30(4) , 445-53, (2006)]

More Articles...