| First Author | Jones ME | Year | 2001 |
| Journal | J Steroid Biochem Mol Biol | Volume | 79 |
| Issue | 1-5 | Pages | 3-9 |
| PubMed ID | 11850201 | Mgi Jnum | J:75652 |
| Mgi Id | MGI:2177331 | Doi | 10.1016/s0960-0760(01)00136-4 |
| Citation | Jones ME, et al. (2001) Aromatase-deficient (ArKO) mice accumulate excess adipose tissue. J Steroid Biochem Mol Biol 79(1-5):3-9 |
| abstractText | Aromatase is the enzyme which catalyses the conversion of C(19) steroids into C(18) estrogens. We have generated a mouse model wherein the Cyp19 gene, which encodes aromatase, has been disrupted, and hence, the aromatase knockout (ArKO) mouse cannot synthesise endogenous estrogens. We examined the consequences of estrogen deficiency on accumulation of adipose depots in male and female ArKO mice, observing that these animals progressively accrue significantly more intra-abdominal adipose tissue than their wildtype (WT) litter mates, reflected in increased adipocyte volume and number. This increased adiposity was not due to hyperphagia or reduced resting energy expenditure, but was associated with reduced spontaneous physical activity levels, reduced glucose oxidation, and a decrease in lean body mass. Elevated circulating levels of leptin and cholesterol were present in 1-year-old ArKO mice compared to WT controls, as were elevated insulin levels, although blood glucose was unchanged. Associated with these changes, the livers of ArKO animals were characterised by a striking accumulation of lipid droplets. Our findings demonstrate an important role for estrogen in the maintenance of lipid homeostasis in both males and females. |
