IV chenodeoxycholate prevents calcium bilirubinate gallstones during total parenteral nutrition in the prairie dog

被引:8
作者
Broughton, G
Fitzgibbons, RJ
Geiss, RW
Adrian, TE
Anthone, G
机构
[1] CREIGHTON UNIV,SCH MED,DEPT BIOMED SCI,OMAHA,NE 68178
[2] CREIGHTON UNIV,SCH MED,DEPT SURG,OMAHA,NE 68178
[3] CREIGHTON UNIV,SCH MED,DEPT PATHOL,OMAHA,NE 68178
关键词
D O I
10.1177/0148607196020003187
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: The purpose of this study was to determine whether IV chenodeoxycholate (CDC) could prevent total parenteral nutrition (TPN)-associated pigmented gallstones in the prairie dog. Methods: Twelve prairie dogs were divided into two equal groups, each receiving an identical TPN regimen. Each animal received 92 kcal/d with 61% of the calories horn carbohydrate. The total volume of infusate delivered to each animal was 59 mL/d. Animals in one group, termed the TPN + CDC group, received a daily bolus injection of CDC at a dose of 15 mg/kg. Prairie dogs in the second group, termed the TPN group, received water (vehicle carrier) 1 ml/kg/d. The TPN and TPN + CDC groups received TPN for 40.3 +/- 1.3 and 42.5 +/- 0.6 days, respectively. Results: There was no statistical difference in the initial and final weights between the two groups. None of the TPN + CDC-treated animals had gallstones or calcium bilirubinate crystals. In contrast, all of the TPN-treated animals had calcium bilirubinate crystals (p = .002), and five of six had macroscopic black pigmented gallstones (p = .015). Cholesterol crystals were not observed in either group of animals. The amount of biliary bilirubin and ionized calcium was significantly greater in the TPN group (both p < .001); however, both groups had a similar total biliary calcium concentration. Conclusion: IV CDC is effective in preventing TPN-associated gallstones in the prairie dog.
引用
收藏
页码:187 / 193
页数:7
相关论文
共 41 条
  • [1] ADLER RD, 1975, GASTROENTEROLOGY, V68, P326
  • [2] AHLBERG J, 1981, J LIPID RES, V22, P410
  • [3] BILIARY LIPID-COMPOSITION IN PATIENTS WITH PORTAL CIRRHOSIS OF THE LIVER
    ANGELIN, B
    EINARSSON, K
    EWERTH, S
    LEIJD, B
    [J]. SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1980, 15 (07) : 849 - 852
  • [4] BABINSKI ES, 1973, CLIN CHIM ACTA, V46, P55
  • [5] BELL GD, 1972, LANCET, V2, P1213
  • [6] THE QUANTITATIVE AND QUALITATIVE-ANALYSIS FOR BILIARY LIPIDS IN THE PRAIRIE DOG CYNOMYS-LUDOVICIANUS
    BROUGHTON, G
    TSENG, A
    FITZGIBBONS, R
    FISHKIN, AF
    RONGONE, EL
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1990, 97 (03): : 521 - 526
  • [7] HEMATOLOGIC AND BLOOD-CHEMISTRY DATA FOR THE PRAIRIE DOG (CYNOMYS-LUDOVICIANUS)
    BROUGHTON, G
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-PHYSIOLOGY, 1992, 101 (04): : 807 - 812
  • [8] THE PREVENTION OF CHOLELITHIASIS WITH INFUSED SODIUM CHENODEOXYCHOLATE IN THE PRAIRIE DOG (CYNOMYS-LUDOVICIANUS)
    BROUGHTON, G
    TSENG, A
    FITZGIBBONS, R
    TYNDALL, S
    STANISLAV, G
    RONGONE, EL
    [J]. COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-PHYSIOLOGY, 1991, 99 (04): : 609 - 613
  • [9] PHYSICAL-CHEMICAL PATHOGENESIS OF PIGMENT GALLSTONES
    CAHALANE, MJ
    NEUBRAND, MW
    CAREY, MC
    [J]. SEMINARS IN LIVER DISEASE, 1988, 8 (04) : 317 - 328
  • [10] CAMPOS AC, 1990, ARCH SURG-CHICAGO, V125, P447