Cholesterol Gallstones In Mice Research Articles

Dissolution of cholesterol gallstones in mice by the oral administration of a fatty acid bile acid conjugate

Gallstones, mostly cholesterol stones, affect some 15% of the population. Oral bile salts dissolve human cholesterol gallstones, but with low efficacy, and surgery remains the main therapeutic option. Fatty acid bile acid conjugates (FABACs) were shown to prevent formation of cholesterol gallstones in experimental animals. The aim of this study was to test whether these compounds could dissolve preexisting cholesterol gallstones via oral administration. Inbred, gallstone-susceptible C57J/L mice were given a lithogenic diet for 2 months, and the presence of gallstones was ascertained. The mice were then switched to a regular diet while part of them were given in addition C20-FABAC, by gavage, at a dose of 0.5 or 3 mg per animal per day. All mice tested had cholesterol gallstones after 2 months on the lithogenic diet. In study I, after 2 months on the regular diet, 3 of 4 (75%) of the controls had gallstones, whereas none of the 6 FABAC-fed animals (3 mg/d) had stones (P = .033). In study II, evaluating 2 FABAC doses, after 2 months on the regular diet, 8 of 8 (100%) of the controls had gallstones, which were found in 2 of 7 (28%) and 1 of 8 (12%) of the mice supplemented with 0.5 mg/d (P = .007) or 3 mg/d (P = .001) FABAC, respectively. On a molar basis, the dose of 0.5 mg FABAC is equivalent to 14 mg/kg/d of a bile acid. In conclusion, FABACs given orally can dissolve preexisting cholesterol gallstones in mice. This was accomplished with a dose of FABAC equivalent to the dose of bile acids used in human gallstone dissolution. (HEPATOLOGY 2002;35:597-600.)

Effect of curcumin and capsaicin on the regression of preestablished cholesterol gallstones in mice

The efficacy of curcumin and capsaicin in causing regression of pre-established cholesterol gallstones (CGS) was investigated in male mice. After confirming the formation of CGS in 100% of the animals, they were fed a diet containing 0.5% curcumin or 5 mg% capsaicin for 5 or 10 weeks. Five weeks feeding of curcumin or capsaicin diet caused a regression of CGS in 45 and 64% of the animals respectively. Ten weeks feeding of these spice principles caused regression of CGS in 80% of the animals. The biliary cholesterol decreased and phospholipids and bile acids increased with increase in the duration of spice principle feeding. Feeding of a control diet to the animals bearing CGS neither caused regression of CGS nor influenced the biliary lipids significantly.

Different susceptibilities to the formation of cholesterol gallstones in mice.

In the search for an animal model of genetic determinants of cholesterol cholelithiasis, we found strain, gender and individual differences in mice. Male black (C57BL6J) mice had a 50% incidence of cholesterol gallstones after they consumed lithogenic food similar to that used by Tepperman et al. for 2 weeks, whereas similarly treated male agouti (CBA/J) mice and females of both strains were free of gallstones. The male and female mice of both strains were fertile at 8 weeks of age, and the male black mice were first susceptible to induction of gallstones at 24 weeks of age. Male agouti mice of the same age did not form gallstones until they had consumed the lithogenic food for 8 weeks. The gallbladder biles of both strains were supersaturated with cholesterol during the lithogenic regimen. The male agouti mice had much higher fractional turnover rates of [24-14C]cholic acid than did the male black mice. In spite of their small total cholate pools, the agouti mice had higher rates of new cholate synthesis than did the black mice. The rate of disappearance of [1,2-3H]cholesterol from the blood was higher in the male agouti than in the black mice. The gallbladders of the agouti mice contained less bile and weighed less empty than gallbladders of the black mice. They also did not increase in volume in response to the lithogenic diet as much as gallbladders of the black mice. The difference in gallstone induction times between male and female black mice was as great as the difference between the two strains.(ABSTRACT TRUNCATED AT 250 WORDS)