Assessment of biliary bicarbonate secretion in humans by positron emission tomography

被引:111
作者
Prieto, J [1 ]
García, N
Martí-Climent, JM
Peñuelas, I
Richter, JA
Medina, JF
机构
[1] Univ Navarra, Sch Med, Clin Univ, Dept Med, E-31008 Pamplona, Spain
[2] Univ Navarra, Sch Med, Clin Univ, Liver Unit, E-31008 Pamplona, Spain
[3] Univ Navarra, Sch Med, Clin Univ, Dept Nucl Med, E-31008 Pamplona, Spain
关键词
D O I
10.1016/S0016-5085(99)70564-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Positron emission tomography (PET) allows imaging and quantitative analysis of organ functions in basal and stimulated conditions. We have applied this method to the study of biliary bicarbonate secretion in humans. Methods: PET was performed in 5 healthy subjects and 13 patients with hepatobiliary disorders after intravenous injection of (NaHCO3)-C-11. In each case the study was performed in basal conditions and after secretin stimulation. Positron emission from the hepatic area was scanned, and normalized uptake values for parenchymal and hilar regions were estimated. Results: In healthy individuals, the injection of (NaHCO3)-C-11 resulted in a peak uptake of the label in parenchymal and hilar regions 2-3 minutes after the injection. In both normal and cirrhotic subjects, secretin administration increased bicarbonate uptake in the parenchymal region, followed by accumulation of the label in the perihilar area. Normal basal uptake with absent response to secretin was registered in extrahepatic biliary obstruction and in untreated primary biliary cirrhosis (PBC). The secretin response was present in patients with PBC undergoing treatment with ursodeoxycholic acid. Conclusions: PET allows investigation of biliary bicarbonate secretion in humans. An impaired response to secretin was observed in cholestatic conditions. Preliminary data suggest that ursodeoxycholic acid might improve the response to secretin in PBC.
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页码:167 / 172
页数:6
相关论文
共 18 条
  • [1] Role of kinases and phosphatases in the regulation of fluid secretion and Cl-/HCO3- exchange in cholangiocytes
    Alvaro, D
    Mennone, A
    Boyer, JL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 273 (02): : G303 - G313
  • [2] LOCALIZATION OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR IN HUMAN BILE-DUCT EPITHELIAL-CELLS
    COHN, JA
    STRONG, TV
    PICCIOTTO, MR
    NAIRN, AC
    COLLINS, FS
    FITZ, JG
    [J]. GASTROENTEROLOGY, 1993, 105 (06) : 1857 - 1864
  • [3] LOCALIZATION AND CHARACTERIZATION OF SECRETIN BINDING-SITES EXPRESSED BY RAT BILE-DUCT EPITHELIUM
    FAROUK, M
    VIGNA, SR
    MCVEY, DC
    MEYERS, WC
    [J]. GASTROENTEROLOGY, 1992, 102 (03) : 963 - 968
  • [4] FUKUMOTO Y, 1989, Gastroenterologia Japonica, V24, P298
  • [5] THE EFFECTS OF SYNTHETIC HUMAN SECRETIN ON CALCIUM-CARBONATE SOLUBILITY IN HUMAN BILE
    KNYRIM, K
    VAKIL, N
    [J]. GASTROENTEROLOGY, 1990, 99 (05) : 1445 - 1451
  • [6] SECRETIN STIMULATES BILE DUCTULAR SECRETORY ACTIVITY THROUGH THE CAMP SYSTEM
    LENZEN, R
    ALPINI, G
    TAVOLONI, N
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (04): : G527 - G532
  • [7] MARTINEZANSO E, 1994, HEPATOLOGY, V19, P1400, DOI 10.1016/0270-9139(94)90234-8
  • [8] SECRETIN ACTIVATES CL- CHANNELS IN BILE-DUCT EPITHELIAL-CELLS THROUGH A CAMP-DEPENDENT MECHANISM
    MCGILL, JM
    BASAVAPPA, S
    GETTYS, TW
    FITZ, JG
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (04): : G731 - G736
  • [9] Decreased anion exchanger 2 immunoreactivity in the liver of patients with primary biliary cirrhosis
    Medina, JF
    MartinezAnso, E
    Vazquez, JJ
    Prieto, J
    [J]. HEPATOLOGY, 1997, 25 (01) : 12 - 17
  • [10] MEDINA JF, 1998, PRIMARY BILIARY CIRR, P35