Sharda Daniel R, Miller-Lee Jennifer L, Kanski Gregory M, Hunter J Craig, Lang Charles H, Kennett Mary J, Korzick Donna H
Department of Kinesiology, The Pennsylvania State University, University Park, PA 16802, USA.
J Pharmacol Toxicol Methods. 2012 Nov-Dec;66(3):257-63. doi: 10.1016/j.vascn.2012.08.166. Epub 2012 Aug 23.
Post-menopausal women have a greater risk of developing alcoholic complications compared to age-matched men. Unfortunately, animal models of chronic ethanol consumption with estrogen deficiency are lacking. Here, we characterize the ability of the agar block and Lieber-DeCarli models of chronic ethanol consumption to produce elevated blood alcohol content (BAC) and liver pathology in the F344 postmenopausal animal model of aging.
Adult (3 mo) and aged (18 mo) F344 ovary-intact or ovariectomized rats were administered ethanol for 14-20 weeks as follows: diet 1, standard chow access, 10% ethanol in drinking water, and 40% ethanol in agar blocks; diet 2, diet 1 plus low phytoestrogen chow (known to affect ethanol metabolism) for the final 4 weeks; diet 3, Lieber-DeCarli all liquid diet with 36% kcal ethanol. Control animals were matched isocalorically with dextrin.
For the agar block diet, average BAC was 13±4 mg/dL across groups. BAC was unaffected by reducing dietary phytoestrogen content (12±4 mg/dL), which is known to interfere with ethanol metabolism. Liver pathology was unaffected by the agar block diet. In contrast, the Lieber-DeCarli diet resulted in BAC of 45±5 mg/dL in conjunction with more severe hepatopathology.223
We conclude that the Lieber-DeCarli diet produces greater BAC and hepatopathology to study the effects of chronic ethanol administration in the F344 postmenopausal rodent model of aging when compared to an ethanol agar block diet.
与年龄匹配的男性相比,绝经后女性发生酒精相关并发症的风险更高。遗憾的是,缺乏雌激素缺乏的慢性乙醇摄入动物模型。在此,我们在F344绝经后衰老动物模型中,描述了慢性乙醇摄入的琼脂块模型和Lieber-DeCarli模型产生高血酒精含量(BAC)和肝脏病理变化的能力。
成年(3个月)和老年(18个月)F344卵巢完整或卵巢切除的大鼠接受乙醇处理14 - 20周,如下:饮食1,标准食物,饮用水中含10%乙醇,琼脂块中含40%乙醇;饮食2,饮食1加上低植物雌激素食物(已知会影响乙醇代谢),持续最后4周;饮食3,含36%千卡乙醇的Lieber-DeCarli全液体饮食。对照动物用糊精等热量匹配。
对于琼脂块饮食,各组平均BAC为13±4 mg/dL。降低饮食中植物雌激素含量(已知会干扰乙醇代谢)对BAC无影响(12±4 mg/dL)。琼脂块饮食对肝脏病理无影响。相比之下,Lieber-DeCarli饮食导致BAC为45±5 mg/dL,并伴有更严重的肝脏病理变化。
我们得出结论,与乙醇琼脂块饮食相比,在F344绝经后衰老啮齿动物模型中,Lieber-DeCarli饮食产生更高的BAC和肝脏病理变化,可用于研究慢性乙醇给药的影响。