Activation of cardiac renin-angiotensin system and plasminogen activator inhibitor-1 gene expressions in oral contraceptive-induced cardiometabolic disorder

被引:8
|
作者
Olatunji, Lawrence A. [1 ,2 ]
Usman, Taofeek O. [1 ]
Seok, Young-Mi [2 ,3 ]
Kim, In-Kyeom [2 ,4 ]
机构
[1] Univ Ilorin, Dept Physiol, Cardiovasc & Mol Physiol Unit, Coll Hlth Sci, PMB 1515, Ilorin, Nigeria
[2] Kyungpook Natl Univ, Sch Med, Cardiovasc Res Inst, Daegu, South Korea
[3] Korea Promot Inst Tradit Med Ind, Gyongsan, Gyeongbuk, South Korea
[4] Kyungpook Natl Univ, Sch Med, Dept Pharmacol, Daegu, South Korea
基金
新加坡国家研究基金会;
关键词
Angiotensin-converting enzyme; angiotensin II receptor; cardiac gene expression; oral contraceptive; plasminogen activator inhibitor-1; II TYPE-1 RECEPTOR; METABOLIC SYNDROME; INSULIN-RESISTANCE; MINERALOCORTICOID RECEPTOR; GLUCOSE-TOLERANCE; ETHINYL ESTRADIOL; SKELETAL-MUSCLE; RATS; ALDOSTERONE; DISEASE;
D O I
10.3109/13813455.2016.1160935
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Context: Clinical studies have shown that combined oral contraceptive (COC) use is associated with cardiometabolic disturbances. Elevated renin-angiotensin system (RAS) and plasminogen activator inhibitor-1 (PAI-1) have also been implicated in the development of cardiometabolic events. Objective: To determine the effect of COC treatment on cardiac RAS and PAI-1 gene expressions, and whether the effect is circulating aldosterone or corticosterone dependent. Methods: Female rats were treated (p.o.) with olive oil (vehicle) or COC (1.0 mu g ethinylestradiol and 10.0 mu g norgestrel) daily for six weeks. Results: COC treatment led to increases in blood pressure, HOMA-IR, Ace1 mRNA, Atr1 mRNA, Pai1 mRNA, cardiac PAI-1, plasma PAI-1, C-reactive protein, uric acid, insulin and corticosterone. COC treatment also led to dyslipidemia, decreased glucose tolerance and plasma 17 beta-estradiol. Conclusion: These results demonstrates that hypertension and insulin resistance induced by COC is associated with increased cardiac RAS and PAI-1 gene expression, which is likely to be through corticosterone-dependent but not aldosterone-dependent mechanism.
引用
收藏
页码:1 / 8
页数:8
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