Tkocz R, Hillesheim H G, Schmidt G, Hoffmann H
Central Institute of Microbiology and Experimental Therapy, Academy of Sciences of the GDR, Jena.
Exp Clin Endocrinol. 1988 Sep;92(1):7-12. doi: 10.1055/s-0029-1210774.
The influence of progesterone (P) and synthetic gestagens given alone or in combination with estradiol (E2) on triglyceride (TG) concentration in serum of adult female rats was studied. Norethisterone acetate (NEA), levonorgestrel (LNG), dienogest (DEG), chlormadinone acetate (CMA) and P were administered orally at a dose of 10 mg/kg for three times. E2 was given chronically by s.c. implants. Synthetic gestagens and P were without any effect on the TG serum concentrations but E2 elevated the TG level by 168%. This E2-induced TG increase was not reversed by synthetic gestagens or P given orally but only by P s.c. after combined treatment with E2 plus gestagens. In a second experiment the hepatic TG release into the blood was studied using the model of Triton WR-1339 induced hypertriglyceridemia. E2 as well as the synthetic gestagens stimulated the TG release while the natural P failed to produce this effect. Following treatment with E2 plus gestagens, the E2 stimulated TG release was not significantly influenced by the gestagens. It is concluded that both the hepatic TG release into and the TG removal from the circulation may be stimulated by gestagens.
研究了单独给予孕酮(P)和合成孕激素或与雌二醇(E2)联合使用对成年雌性大鼠血清甘油三酯(TG)浓度的影响。醋酸炔诺酮(NEA)、左炔诺孕酮(LNG)、地诺孕素(DEG)、醋酸氯地孕酮(CMA)和P以10mg/kg的剂量口服给药,共三次。E2通过皮下植入物长期给药。合成孕激素和P对血清TG浓度没有任何影响,但E2使TG水平升高了168%。这种由E2诱导的TG升高不能通过口服合成孕激素或P来逆转,而仅在与E2加孕激素联合治疗后通过皮下注射P来逆转。在第二个实验中,使用Triton WR-1339诱导的高甘油三酯血症模型研究了肝脏TG释放到血液中的情况。E2以及合成孕激素刺激了TG释放,而天然P未能产生这种效果。在用E2加孕激素治疗后,E2刺激的TG释放不受孕激素的显著影响。得出的结论是,孕激素可能刺激肝脏TG释放到循环中以及从循环中清除TG。