Estrogen Replacement Reverses the Hepatic Steatosis Phenotype in the Male Aromatase Knockout Mouse

• Published in: Endocrinology (Philadelphia) 2004-04, Vol.145 (4), p.1842-1848
• Main Authors: Hewitt, Kylie N, Pratis, Kyriakos, Jones, Margaret E. E, Simpson, Evan R
• Format: Article
• Language: English
• Subjects: 17β-Estradiol; Adipose tissue; Adipose tissue (brown); Adipose Tissue - pathology; Animals; Aromatase; Aromatase - deficiency; Aromatase - genetics; Biological and medical sciences; Body Weight; Carrier Proteins - genetics; Cholesterol; Cholesterol - metabolism; Coenzyme A; Disruption; Enzymes - genetics; Enzymes - metabolism; Estradiol - pharmacology; Estrogens; Fatty acids; Fatty Acids - biosynthesis; Fatty Acids - metabolism; Fatty liver; Fatty Liver - enzymology; Fatty Liver - genetics; Fatty Liver - metabolism; Fatty Liver - pathology; Fatty-acid synthase; Fundamental and applied biological sciences. Psychology; Gene Expression; Homeostasis; Hormone replacement therapy; Lipogenesis; Liver - metabolism; Liver - pathology; Male; Males; Mice; Mice, Knockout - genetics; Organ Size; Phenotype; Phenotypes; Protein transport; RNA, Messenger - metabolism; Scavenger receptors; Sex hormones; Sexual dimorphism; Steatosis; Triglycerides; Triglycerides - metabolism; Vertebrates: endocrinology
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.2003-1369

The aromatase knockout (ArKO) mouse cannot synthesize endogenous estrogens due to a disruption to the Cyp19 gene. Previously we have shown both male and female ArKO mice have an age progressive obese phenotype and a sexually dimorphic disruption to hepatic cholesterol and triglyceride homeostasis. Only ArKO males have elevated hepatic triglyceride levels leading to hepatic steatosis partly due to an increase in expression of enzymes involved in de novo lipogenesis and transporters involved in fatty acid uptake. In this study ArKO males were treated with 17β-estradiol (3 μg/ kg·d) at 18 wk old for 6 wk. Wild-type controls were not treated, and ArKO controls received vehicle oil injections. Estrogen replacement reverses the previously reported obese and fatty liver phenotypes; this was achieved by reductions in gonadal, visceral, and brown adipose tissue weights and significantly decreased hepatic triglyceride levels. Estrogen deficiency led to a significant up-regulation of hepatic fatty acid synthase expression, which was reduced with 17β-estradiol replacement, although not quite reaching significance. Acetyl Coenzyme A carboxylase α mRNA expression showed no significant changes. Expression of transcripts encoding adipocyte differentiated regulatory protein, a fatty acid transporter, was significantly elevated in estrogen-deficient males, and 17β-estradiol replacement significantly reduced these levels. Scavenger receptor class b type 1 showed no significantly changes. This study reveals that the previously reported disruption to triglyceride homeostasis in estrogen-deficient males can be reversed with 17β-estradiol treatment, indicating an important role for estrogen in maintaining triglyceride and fatty acid homeostasis in males.