Hormone replacement therapy prevents coronary artery disease in ovariectomized cholesterol-fed rabbits
- PMID: 1907151
- DOI: 10.1111/j.1699-0463.1991.tb01250.x
Hormone replacement therapy prevents coronary artery disease in ovariectomized cholesterol-fed rabbits
Abstract
The prevention of coronary artery disease in women is of considerable importance. We have therefore investigated the influence of oestrogen monotherapy and oestrogen-progestogen replacement therapy on coronary artery disease using a simple morphometric method. We studied sixty-three cholesterol-fed rabbits for nineteen weeks. They were randomized to either ovariectomy (51 rabbits) or a sham operation (12 rabbits). The ovariectomized rabbits were randomized to receive either 17 beta-estradiol, 17 beta-estradiol plus norethisterone acetate, 17 beta-estradiol plus levonorgestrel, or placebo. The rabbits with the sham operation received placebo. The hormone therapies reduced the development of coronary artery disease compared to placebo (p less than 0.0001). Furthermore, the coronary artery disease was attended by atherosclerosis in the more distal parts of the coronary arteries (p less than 0.0001), the thoracic aorta (p less than 0.0001) and the abdominal aorta (p less than 0.0001), and by a reduced relative heart weight (p less than 0.05). We conclude that coronary atherosclerosis can be determined quantitatively by morphometry in rabbit arteries. Estradiol monotherapy reduces coronary atherosclerosis in cholesterol-fed rabbits and the addition of norethisterone acetate or levonorgestrel does not attenuate this beneficial effect.
Similar articles
-
Estrogen monotherapy and combined estrogen-progestogen replacement therapy attenuate aortic accumulation of cholesterol in ovariectomized cholesterol-fed rabbits.J Clin Invest. 1991 Apr;87(4):1274-9. doi: 10.1172/JCI115129. J Clin Invest. 1991. PMID: 1901319 Free PMC article.
-
The impact of female sex hormones on secondary prevention of atherosclerosis in ovariectomized cholesterol-fed rabbits.Atherosclerosis. 1996 Jun;123(1-2):139-44. doi: 10.1016/0021-9150(96)05798-x. Atherosclerosis. 1996. PMID: 8782845
-
Progestogens do not affect aortic accumulation of cholesterol in ovariectomized cholesterol-fed rabbits.Circ Res. 1992 Jun;70(6):1198-202. doi: 10.1161/01.res.70.6.1198. Circ Res. 1992. PMID: 1576740
-
Progestins used in hormonal replacement therapy display different effects in coronary arteries from New Zealand white rabbits.Maturitas. 2004 Dec 10;49(4):304-14. doi: 10.1016/j.maturitas.2004.02.007. Maturitas. 2004. PMID: 15531126
-
Estradiol and norgestimate: a review of their combined use as hormone replacement therapy in postmenopausal women.Drugs Aging. 2001;18(11):863-85. doi: 10.2165/00002512-200118110-00007. Drugs Aging. 2001. PMID: 11772126 Review.
Cited by
-
Aging and serum exomiR content in women-effects of estrogenic hormone replacement therapy.Sci Rep. 2017 Feb 14;7:42702. doi: 10.1038/srep42702. Sci Rep. 2017. PMID: 28195143 Free PMC article.
-
A microarray analysis of sexual dimorphism of adipose tissues in high-fat-diet-induced obese mice.Int J Obes (Lond). 2010 Jun;34(6):989-1000. doi: 10.1038/ijo.2010.12. Epub 2010 Feb 16. Int J Obes (Lond). 2010. PMID: 20157318 Free PMC article.
-
Aging and Adiposity-Focus on Biological Females at Midlife and Beyond.Int J Mol Sci. 2024 Mar 4;25(5):2972. doi: 10.3390/ijms25052972. Int J Mol Sci. 2024. PMID: 38474226 Free PMC article. Review.
-
The sexually dimorphic role of adipose and adipocyte estrogen receptors in modulating adipose tissue expansion, inflammation, and fibrosis.Mol Metab. 2013 Jun 4;2(3):227-42. doi: 10.1016/j.molmet.2013.05.006. eCollection 2013. Mol Metab. 2013. PMID: 24049737 Free PMC article.
-
Impaired estrogen receptor action in the pathogenesis of the metabolic syndrome.Mol Cell Endocrinol. 2015 Dec 15;418 Pt 3(Pt 3):306-21. doi: 10.1016/j.mce.2015.05.020. Epub 2015 May 29. Mol Cell Endocrinol. 2015. PMID: 26033249 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical