Back to Search Start Over

Effect of high doses of synthetic estrogen on lipid metabolism in castrated male rats.

Authors :
Nishikawa M
Seki K
Matsuzawa Y
Minami Y
Kawata S
Miyoshi S
Imai Y
Saitoh R
Noda S
Tamura S
Source :
Lipids [Lipids] 1984 Oct; Vol. 19 (10), pp. 777-83.
Publication Year :
1984

Abstract

The mechanism by which high doses of estrogen influences lipid metabolism was studied with a microtubular blocking agent. Castrated male rats received oral injection daily for 14 days of 3 mg hexestrol in olive oil, or oil alone as controls. About half of the animals in each group were injected intraperitoneally with 4 mg/100 g body weight colchicine 3 hr before they were killed. Hexestrol treatment caused an accumulation of esterified cholesterol in the liver while it decreased those in serum. Triglyceride concentrations slightly decreased in the liver but were unaffected in serum. On polyacrylamide-gel disc electrophoresis, the peaks of high density lipoproteins (HDL) and low density lipoproteins (LDL) were decreased remarkably. Electron microscopic examination of hepatocytes revealed electron-lucent lipid droplets in the cytoplasm. After a colchicine treatment of the control animals, concentrations of esterified cholesterol and triglycerides markedly increased in the liver, while those in serum decreased. Electron microscopic examination of hepatocytes revealed numerous secretory vesicles filled with nascent VLDL. In hexestrol-treated animals, the colchicine treatment was associated with marked decreases in serum-esterified cholesterol and triglyceride as seen in the controls. However, there were no further increases of esterified cholesterol in the liver, and the increase of triglycerides was slight. Electron microscopic examination showed less secretory droplets than in the controls. These data suggest that very low density lipoproteins (VLDL) synthesis in the liver of hexestrol treated rats was inhibited. An accumulation of esterified cholesterol with a marked decrease in serum could not be accounted for by the inhibition of lipoproteins secretion, but rather by their enhanced entry into the liver.

Details

Language :
English
ISSN :
0024-4201
Volume :
19
Issue :
10
Database :
MEDLINE
Journal :
Lipids
Publication Type :
Academic Journal
Accession number :
6094942
Full Text :
https://doi.org/10.1007/BF02534471