Cassidy M M, Lightfoot F G, Grau L, Satchitanandum S, Vahouny G V
Dig Dis Sci. 1985 May;30(5):468-76. doi: 10.1007/BF01318181.
The hypolipidemic agent, cholestyramine (Questran), when fed to rats inhibits intestinal absorption of cholesterol and triglycerides and causes significant epithelial cell damage in both small and large intestine. In this study, we report significant accumulation of lipids in the mucosal layer of both jejunum and colon in rats administered 2% cholestyramine for a four-week period, when compared to a control group maintained on regular chow. The total lipid increment with cholestyramine was 4.7-fold in the jejunum and 3.7-fold in the colon. The triglyceride fraction increased substantially in the small but not the large intestine. Relative phospholipid levels decreased in the treated jejunum but not in the colon. The biochemical data were reflected in morphological evidence of lipid-laden enterocytes obtained by light and transmission electron microscopy. Since cholestyramine has been shown to sequester 99.8% of micellar phospholipid in vitro, it is concluded that the presence of cholestyramine in the intestinal lumen may interfere with phospholipid availability for chylomicron synthesis and serosal lipid exit from the epithelium. This unusual deposition of lipid within the mucosal layer may also be correlated with the known cocarcinogenic effect of this resin in experimentally induced intestinal cancer.
降血脂药物消胆胺(考来烯胺,Questran)喂给大鼠时,会抑制肠道对胆固醇和甘油三酯的吸收,并导致小肠和大肠出现明显的上皮细胞损伤。在本研究中,我们报告,与喂食普通食物的对照组相比,给大鼠喂食2%消胆胺四周后,空肠和结肠的黏膜层出现了大量脂质蓄积。消胆胺导致的总脂质增量在空肠中为4.7倍,在结肠中为3.7倍。甘油三酯部分在小肠中大幅增加,但在大肠中没有。处理后的空肠中相对磷脂水平下降,但结肠中没有。生化数据反映在通过光学显微镜和透射电子显微镜获得的充满脂质的肠上皮细胞的形态学证据中。由于已证明消胆胺在体外能螯合99.8%的胶态磷脂,因此得出结论,肠腔内消胆胺的存在可能会干扰乳糜微粒合成中磷脂的可用性以及脂质从上皮细胞向浆膜的排出。黏膜层内这种异常的脂质沉积也可能与这种树脂在实验诱导的肠道癌中的已知促癌作用相关。