阿昔莫克斯对妊娠大鼠血脂和葡萄糖/胰岛素的影响。

I Sánchez-Vera, B Bonet, M Viana, E Herrera, A Indart
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引用次数: 3

摘要

为了确定妊娠后期产妇高甘油三酯血症的降低如何影响葡萄糖/胰岛素关系,怀孕大鼠和未怀孕大鼠口服阿昔莫克斯(一种有效的抗脂药)。在怀孕20天的大鼠中,与用蒸馏水处理的动物相比,服用80mg阿昔莫克斯后不久(长达7小时),血浆甘油三酯(TG)、游离脂肪酸(FFA)和甘油的下降幅度大于未服药的大鼠,而两组大鼠的血浆葡萄糖水平均未受治疗影响。从妊娠第17天至第20天每12小时给予阿昔莫司一次,血浆TG、FFA和甘油水平逐渐升高,而接受相同治疗的处女大鼠的血浆TG、FFA和甘油水平要么降低,要么没有变化,两组的血浆葡萄糖水平都没有影响。妊娠20天大鼠服用阿昔莫司3天后,胎儿体重低于对照组。在妊娠第20天,给予阿匹莫司或蒸馏水后3小时,大鼠口服葡萄糖2 g /kg,发现两组大鼠血浆葡萄糖的变化相似,而给予阿匹莫司的妊娠大鼠血浆胰岛素的增加更大。然而,在接受阿西莫司或蒸馏水的未交配大鼠口服葡萄糖负荷后,两种变量均未发现差异。妊娠大鼠经静脉(i.v)注射胰岛素后,血浆葡萄糖水平未见差异。综上所述,目前的结果表明,在妊娠最后几天服用阿昔莫克斯可以抑制脂肪分解,降低胎儿体重。在短时间内,妊娠大鼠在阿昔莫克斯治疗后血浆FFA和TG的降低改善了葡萄糖诱导的胰岛素释放,但似乎对外周胰岛素抵抗没有任何影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of acipimox on plasma lipids and glucose/insulin in pregnant rats.

To determine how a reduction in maternal hypertriglyceridemia during late pregnancy may affect glucose/insulin relationships, pregnant and virgin rats were orally treated with acipimox, a potent antilipolytic agent. In 20-day pregnant rats receiving 80 mg of acipimox, plasma triglycerides (TG), free fatty acids (FFA), and glycerol decreased more than in virgin rats shortly after the drug (up to 7 hours), when compared with animals treated with distilled water, whereas plasma glucose level was unaffected by the treatment in either group of rats. When acipimox was given every 12 hours from day 17 to day 20 of pregnancy, plasma TG, FFA, and glycerol levels progressively increased, whereas they either decreased or did not change in virgin rats receiving the same treatment, with no effect in plasma glucose levels in either group. Fetal body weight was lower than in controls in 20-day pregnant rats that received acipimox for 3 days. On day 20 of pregnancy, 3 hours after receiving acipimox or distilled water, rats received a 2 g glucose/kg oral load and it was found that the change in plasma glucose was similar in both groups, whereas the increase in plasma insulin was greater in pregnant rats treated with acipimox. However, no difference was found in either variable after the oral glucose load in virgin rats receiving acipimox or distilled water. No differences in plasma glucose levels were found after intravenous (i.v.) administration of insulin in pregnant rats treated or not treated with acipimox. In conclusion, present results show that administration of acipimox during the last days of gestation inhibited lipolysis and decreased fetal weight. Over a short period of time, in pregnant rats, reductions of plasma FFA and TG after acipimox treatment improved the glucose-induced insulin release, but did not seem to have any effect in peripheral insulin resistance.

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