TY - JOUR
T1 - Physicochemical and physiological properties of 5α-cyprinol sulfate, the toxic bile salt of cyprinid fish
AU - Goto, T.
AU - Holzinger, F.
AU - Hagey, L. R.
AU - Cerrè, C.
AU - Ton-Nu, H. T.
AU - Schteingart, C. D.
AU - Steinbach, J. H.
AU - Shneider, B. L.
AU - Hofmann, A. F.
PY - 2003/9/1
Y1 - 2003/9/1
N2 - 5α-Cyprinol sulfate was isolated form bile of the Asiatic carp, Cyprinus carpio. 5α-Cyprinol sulfate was surface active and formed micelles; its critical micellization concentration (CMC) in 0.15 M Na + using the maximum bubble pressure device was 1.5 mM; by dye solubilization, its CMC was ∼4 mM. At concentrations > 1 mM, 5α-cyprinol sulfate solubilized monooleylglycerol efficiently (2.1 molecules per mol micellar bile salt). When infused intravenously into the anesthetized rat, 5α-cyprinol sulfate was hemolytic, cholestatic, and toxic. In the isolated rat liver, it underwent little biotransformation and was poorly transporled (Tmax ≅ 0.5 μmol/min/kg) as compared with taurocholate. 5α-Cyprinol, its bile alcohol moiety, was oxidized to its corresponding C27 bile acid and to allocholic acid (the latter was then conjugated with taurine); these metabolites were efficiently transported. 5α-Cyprinol sulfate inhibited taurocholate uptake in COS-7 cells transfected with rat asbt, the apical bile salt transporter of the ileal enterocyte. 5α-Cyprinol had limited aqueous solubility (0.3 mM) and was poorly absorbed from the perfused rat jejunum or ileum. Sampling of carp intestinal content indicated that 5α-cyprinol sulfate was present at micellar concentrations, and that it did not undergo hydrolysis during intestinal transit. These studies indicate that 5α-cyprinol sulfate is an excellent digestive detergent and suggest that a micellar phase is present during digestion in cyprinid fish.-Goto, T., F. Holzinger, L. R. Hagey, C. Cerrè, H-T. Ton-Nu, C. D. Schteingart, J. H. Steinbach, B. L. Shneider, and A. F Hofmann. Physicochemical and physiological properties of 5α-cyprinol sulfate, the toxic bile salt of cyprinid fish.
AB - 5α-Cyprinol sulfate was isolated form bile of the Asiatic carp, Cyprinus carpio. 5α-Cyprinol sulfate was surface active and formed micelles; its critical micellization concentration (CMC) in 0.15 M Na + using the maximum bubble pressure device was 1.5 mM; by dye solubilization, its CMC was ∼4 mM. At concentrations > 1 mM, 5α-cyprinol sulfate solubilized monooleylglycerol efficiently (2.1 molecules per mol micellar bile salt). When infused intravenously into the anesthetized rat, 5α-cyprinol sulfate was hemolytic, cholestatic, and toxic. In the isolated rat liver, it underwent little biotransformation and was poorly transporled (Tmax ≅ 0.5 μmol/min/kg) as compared with taurocholate. 5α-Cyprinol, its bile alcohol moiety, was oxidized to its corresponding C27 bile acid and to allocholic acid (the latter was then conjugated with taurine); these metabolites were efficiently transported. 5α-Cyprinol sulfate inhibited taurocholate uptake in COS-7 cells transfected with rat asbt, the apical bile salt transporter of the ileal enterocyte. 5α-Cyprinol had limited aqueous solubility (0.3 mM) and was poorly absorbed from the perfused rat jejunum or ileum. Sampling of carp intestinal content indicated that 5α-cyprinol sulfate was present at micellar concentrations, and that it did not undergo hydrolysis during intestinal transit. These studies indicate that 5α-cyprinol sulfate is an excellent digestive detergent and suggest that a micellar phase is present during digestion in cyprinid fish.-Goto, T., F. Holzinger, L. R. Hagey, C. Cerrè, H-T. Ton-Nu, C. D. Schteingart, J. H. Steinbach, B. L. Shneider, and A. F Hofmann. Physicochemical and physiological properties of 5α-cyprinol sulfate, the toxic bile salt of cyprinid fish.
KW - Bacterial deconjugation
KW - Bile acids
KW - Colestasis
KW - Cyprinus carpio
KW - Fat absorption
KW - Fat digestion
KW - Hepatic transport
KW - Intestinal absorption
KW - Micelles
KW - Solubilization
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U2 - 10.1194/jlr.M300155-JLR200
DO - 10.1194/jlr.M300155-JLR200
M3 - Article
C2 - 12810826
AN - SCOPUS:0141459452
SN - 0022-2275
VL - 44
SP - 1643
EP - 1651
JO - Journal of Lipid Research
JF - Journal of Lipid Research
IS - 9
ER -