Esterified estrogens with and without methyltestosterone decrease arterial LDL metabolism in cynomolgus monkeys

被引:35
作者
Wagner, JD [1 ]
Zhang, L [1 ]
Williams, JK [1 ]
Register, TC [1 ]
Ackerman, DM [1 ]
Witta, B [1 ]
Clarkson, TB [1 ]
Adams, MR [1 ]
机构
[1] SOLVAY PHARMACEUT INC,MARIETTA,GA
关键词
estrogen; androgen; women's health; cardiovascular disease; menopause;
D O I
10.1161/01.ATV.16.12.1473
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although both epidemiological and experimental evidence suggests that estrogen replacement therapy reduces the risk of coronary heart disease, the mechanisms for this beneficial effect are largely unknown. Furthermore, the addition of progestins or androgens to estrogen replacement therapy is of concern. The objective of this study was to examine the effects of esterified estrogens alone or in combination with an androgen on arterial LDL metabolism and early atherogenesis in ovariectomized female cynomolgus monkeys. Arterial LDL metabolism was assessed by using dual-labeled LDL that was injected 24 hours before necropsy. Arterial LDL degradation was reduced by 64% to 84% and cholesteryl ester content was decreased by approximate to 50% in the thoracic aorta in both treatment groups compared with controls. In addition, aortic lipid peroxidation products, as assessed by thiobarbituric acid reaction, were significantly lower in animals treated with esterified estrogens, with a similar trend for combined estrogen androgen treatment. Both treatments also reduced plasma concentrations of apoB-containing lipoproteins, reduced LDL particle size, and increased total-body LDL catabolism. The combination of decreased arterial LDL metabolism, decreased arterial lipid peroxidation, and improved plasma lipoprotein metabolism may explain some of the protective effects of estrogens on coronary heart disease and indicate that beneficial actions extend to a combination of estrogen and androgen.
引用
收藏
页码:1473 / 1480
页数:8
相关论文
共 57 条
[1]   INHIBITION OF CORONARY-ARTERY ATHEROSCLEROSIS BY 17-BETA ESTRADIOL IN OVARIECTOMIZED MONKEYS - LACK OF AN EFFECT OF ADDED PROGESTERONE [J].
ADAMS, MR ;
KAPLAN, JR ;
MANUCK, SB ;
KORITNIK, DR ;
PARKS, JS ;
WOLFE, MS ;
CLARKSON, TB .
ARTERIOSCLEROSIS, 1990, 10 (06) :1051-1057
[2]  
ALLAIN CC, 1974, CLIN CHEM, V20, P470
[3]  
AUERBACH BJ, 1990, J LIPID RES, V31, P738
[4]   METABOLIC AND BEHAVIORAL-EFFECTS OF HIGH-DOSE, EXOGENOUS TESTOSTERONE IN HEALTHY-MEN [J].
BAGATELL, CJ ;
HEIMAN, JR ;
MATSUMOTO, AM ;
RIVIER, JE ;
BREMNER, WJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (02) :561-567
[5]   ESTROGEN AND CORONARY HEART-DISEASE IN WOMEN [J].
BARRETTCONNOR, E ;
BUSH, TL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (14) :1861-1867
[6]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[7]   THE MANAGEMENT OF PERSISTENT MENOPAUSAL SYMPTOMS WITH ESTRADIOL TESTOSTERONE IMPLANTS - CLINICAL, LIPID AND HORMONAL RESULTS [J].
BURGER, HG ;
HAILES, J ;
MENELAUS, M ;
NELSON, J ;
HUDSON, B ;
BALAZS, N .
MATURITAS, 1984, 6 (04) :351-358
[8]   DIFFERENCES IN LOW-DENSITY LIPOPROTEIN SUBFRACTIONS AND APOLIPOPROTEINS IN PREMENOPAUSAL AND POSTMENOPAUSAL WOMEN [J].
CAMPOS, H ;
MCNAMARA, JR ;
WILSON, PWF ;
ORDOVAS, JM ;
SCHAEFER, EJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 67 (01) :30-35
[9]   DIFFERENTIAL-EFFECTS OF ESTROGEN ON LOW-DENSITY-LIPOPROTEIN SUBCLASSES IN HEALTHY POSTMENOPAUSAL WOMEN [J].
CAMPOS, H ;
SACKS, FM ;
WALSH, BW ;
SCHIFF, I ;
OHANESIAN, MA ;
KRAUSS, RM .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1993, 42 (09) :1153-1158
[10]   MEASUREMENT INVIVO OF IRREVERSIBLE DEGRADATION OF LOW-DENSITY LIPOPROTEIN IN THE RABBIT AORTA - PREDOMINANCE OF INTIMAL DEGRADATION [J].
CAREW, TE ;
PITTMAN, RC ;
MARCHAND, ER ;
STEINBERG, D .
ARTERIOSCLEROSIS, 1984, 4 (03) :214-224