Seven groups of female Sprague-Dawley rats (4200 gm initial body weight) were injected i.p. with a single subcarcinogenic dose of diethylnitrosamine (40 mg per kg body weight) between 8 to 10 hr after partial hepatectomy, and after a recovery period of 3 weeks (herein called induction stage) receive
Ezetimibe reverses the inhibitory effects of dietary cholesterol on mammary tumorigenesis in rats
β Scribed by Erin McNamara; Michael C. Archer
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- French
- Weight
- 216 KB
- Volume
- 127
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Abstract
There are concerns regarding increased cancer incidence in patients treated with ezetimibe, an inhibitor of the absorption of dietary cholesterol. Here we tested the hypothesis that ezetimibe will accelerate mammary tumorigenesis in rats. The drug was administered at a dose of 1 ppm in an AINβ93G diet that contained 0.3% cholesterol. This experimental diet and control diets that contained either no additions or cholesterol or ezetimibe only, were fed to groups of 30 SpragueβDawley rats 3 days after they were treated with 50 mg/kg methylnitrosourea (MNU). All rats were euthanized 22 weeks after MNU administration. Tumor multiplicity was significantly smaller in rats fed cholesterol than those fed no cholesterol (1.84 Β± 0.42 vs. 3.86 Β± 0.86 respectively, P < 0.05), but was significantly greater in the cholesterol/ezetimibe group than the group fed only cholesterol (3.48 Β± 0.59 vs. 1.84 Β± 0.42 respectively, P < 0.04). The average weight of tumors/rat was also significantly larger in the cholesterol/ezetimibe group than those fed cholesterol alone (5.67 Β± 1.15 vs. 2.56 Β± 0.71 respectively, P < 0.04). As expected, ezetimibe prevented the cholesterol raising effect of the dietary cholesterol. These results show that ezetimibe reverses the inhibitory effect of dietary cholesterol on the development of rat mammary tumors.
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We have studied the coupling between hepatic uptake of chylomicron remnant cholesteryl ester and biliary excretion of cholesterol and bile acids in rats, after feeding them a cholesterol-free (control) or a high-cholesterol diet ( 1% wt/wt) for 2 wk. We equipped rats with permanent catheters in the
## Abstract Wistar rats received whole body irradiation with 260 cGy gammaβrays at 10 a.m. of individual phases of their estrous cycle and then had diethylstilbestrol pellets implanted for 1 year. When the radiation was given during diβestrus II, the highest incidence (73.3%) of mammary tumorigenes
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