Atherosclerosis is enhanced by testosterone deficiency and attenuated by CETP expression in transgenic mice

Autor: Patrícia M. Cazita, J.A. Berti, Daniel F. J. Ketelhuth, Magnus Gidlund, A.C. Casquero, Alessandro G. Salerno, E.J.B. Bighetti, Helena C. F. Oliveira
Rok vydání: 2006
Předmět:
Zdroj: Journal of Lipid Research, Vol 47, Iss 7, Pp 1526-1534 (2006)
ISSN: 0022-2275
DOI: 10.1194/jlr.m600135-jlr200
Popis: In this work, we investigated the impact of testosterone deficiency and cholesteryl ester transfer protein (CETP) expression on lipoprotein metabolism and diet-induced atherosclerosis. CETP transgenic mice and nontransgenic (nTg) littermates were studied 4 weeks after bilateral orchidectomy or sham operation. Castrated mice had an increase in the LDL fraction (+36% for CETP and +79% for nTg mice), whereas the HDL fraction was reduced (−30% for CETP and −11% for nTg mice). Castrated mice presented 1.7-fold higher titers of anti-oxidized LDL (Ox-LDL) antibodies than sham-operated controls. Plasma levels of CETP, lipoprotein lipase, and hepatic lipase were not changed by castration. Kinetic studies showed no differences in VLDL secretion rate, VLDL-LDL conversion rate, or number of LDL and HDL receptors. Competition experiments showed lower affinity of LDL from castrated mice for tissue receptors. Diet-induced atherosclerosis studies showed that testosterone deficiency increased by 100%, and CETP expression reduced by 44%, the size of aortic lesion area in castrated mice. In summary, testosterone deficiency increased plasma levels of apolipoprotein B-containing lipoproteins (apoB-LPs) and anti-OxLDL antibodies, decreased LDL receptor affinity, and doubled the size of diet-induced atherosclerotic lesions. The expression of CETP led to a milder increase of apoB-LPs and reduced atherosclerotic lesion size in testosterone-deficient mice.
Databáze: OpenAIRE