Orlistat treatment increases fecal bilirubin excretion and decreases plasma bilirubin concentrations in hyperbilirubinemic Gunn rats

被引:36
作者
Nishioka, T [1 ]
Hafkamp, AM [1 ]
Havinga, R [1 ]
Van Lierop, PPE [1 ]
Velvis, H [1 ]
Verkade, HJ [1 ]
机构
[1] Univ Groningen Hosp, Dept Pediat, Ctr Liver Intestine & Metab Dis Pediat Gastroente, NL-9700 RB Groningen, Netherlands
关键词
D O I
10.1067/S0022-3476(03)00298-1
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To determine whether serum levels of unconjugated bilirubin (UCB) can be decreased by enhancing fecal fat excretion. Study design Gunn rats were fed a high-fat diet (control) or the same diet mixed with the lipase inhibitor orlistat. At regular intervals, plasma UCB concentrations were determined and 72-hour fat balances were performed. Results Orlistat treatment decreased plasma UCB concentrations (at 3 weeks; 100 mg/kg, -33% +/- 8%, P < .05; 200 mg/kg, -46% +/- 10%, P < .01). Within days of treatment, orlistat treatment increased fecal excretion of UCB (at day 3; +220%, P < .05). During 24 weeks of orlistat treatment (200 mg/kg diet), the plasma bilirubin concentrations were continuously approximate to35% lower than in control rats. Plasma UCB concentrations were inversely correlated with the amount of fecal fat excretion (n = 12, r = -0.87, P < .001). Conclusions In Gunn rats, orlistat treatment increases the fecal excretion of fat and enhances the disposal of UCB. This approach could lead to novel strategies for prevention and treatment of unconjugated hyperbilirubinemia in patients.
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页码:327 / 334
页数:8
相关论文
共 54 条
  • [1] ENTEROHEPATIC CIRCULATION OF NONCONJUGATED BILIRUBIN IN RATS FED WITH HUMAN-MILK
    ALONSO, EM
    WHITINGTON, PF
    WHITINGTON, SH
    RIVARD, WA
    GIVEN, G
    [J]. JOURNAL OF PEDIATRICS, 1991, 118 (03) : 425 - 430
  • [2] [Anonymous], METABOLIC MOLECULAR
  • [3] BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
  • [5] Role of lipase in the regulation of postprandial gastric acid secretion and emptying of fat in humans: a study with orlistat, a highly specific lipase inhibitor
    Borovicka, J
    Schwizer, W
    Guttmann, G
    Hartmann, D
    Kosinski, M
    Wastiel, C
    Bischof-Delaloye, A
    Fried, M
    [J]. GUT, 2000, 46 (06) : 774 - 781
  • [6] THE GENETIC-BASIS OF THE REDUCED EXPRESSION OF BILIRUBIN UDP-GLUCURONOSYLTRANSFERASE-1 IN GILBERTS-SYNDROME
    BOSMA, PJ
    CHOWDHURY, JR
    BAKKER, C
    GANTLA, S
    DEBOER, A
    OOSTRA, BA
    LINDHOUT, D
    TYTGAT, GNJ
    JANSEN, PLM
    ELFERINK, RPJO
    CHOWDHURY, NR
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (18) : 1171 - 1175
  • [7] Botcher CJF, 1961, ANAL CHIM ACTA, V24, P203
  • [8] Enterohepatic cycling of bilirubin: A putative mechanism for pigment gallstone formation in ileal Crohn's disease
    Brink, MA
    Slors, JFM
    Keulemans, YCA
    Mok, KS
    De Waart, DR
    Carey, MC
    Groen, AK
    Tytgat, GNJ
    [J]. GASTROENTEROLOGY, 1999, 116 (06) : 1420 - 1427
  • [9] Bilirubin cycles enterohepatically after ileal resection in the rat
    Brink, MA
    MendezSanchez, N
    Carey, MC
    [J]. GASTROENTEROLOGY, 1996, 110 (06) : 1945 - 1957
  • [10] BRODERSEN R, 1979, J BIOL CHEM, V254, P2364