scholarly journals Bile Salt Homeostasis in Normal and Bsep Gene Knockout Rats with Single and Repeated Doses of Troglitazone

2017 ◽  
Vol 362 (3) ◽  
pp. 385-394 ◽  
Author(s):  
Yaofeng Cheng ◽  
Shenjue Chen ◽  
Chris Freeden ◽  
Weiqi Chen ◽  
Yueping Zhang ◽  
...  
2009 ◽  
Vol 50 ◽  
pp. S31
Author(s):  
D. Debray ◽  
D. Rainteau ◽  
S. Lerondel ◽  
C. Rey ◽  
L. Humbert ◽  
...  

2017 ◽  
Vol 36 (5) ◽  
pp. 1403-1410 ◽  
Author(s):  
Kiran V.K. Koelfat ◽  
Frank G. Schaap ◽  
Caroline M.J.M. Hodin ◽  
Ruben G.J. Visschers ◽  
Björn I. Svavarsson ◽  
...  

2021 ◽  
Vol 9 (10) ◽  
pp. 2038
Author(s):  
Qiqi Pan ◽  
Xudan Shen ◽  
Leilei Yu ◽  
Fengwei Tian ◽  
Jianxin Zhao ◽  
...  

Lactobacillus salivarius has drawn attention because of its promising probiotic functions. Tolerance to the gastrointestinal tract condition is crucial for orally administrated probiotics to exert their functions. However, previous studies of L. salivarius have only focused on the bile salt resistance of particular strains, without uncovering the common molecular mechanisms of this species. Therefore, in this study, we expanded our research to 90 L. salivarius strains to explore their common functional genes for bile salt resistance. First, the survival rates of the 90 L. salivarius strains in 0.3% bile salt solutions were determined. Comparative genomics analysis was then performed to screen for the potential functional genes related to bile salt tolerance. Next, real-time polymerase chain reaction and gene knockout experiments were conducted to further verify the tolerance-related functional genes. The results indicated that the strain-dependent bile salt tolerance of L. salivarius was mainly associated with four peptidoglycan synthesis-related genes, seven phosphotransferase system-related genes, and one chaperone-encoding gene involved in the stress response. Among them, the GATase1-encoding gene showed the most significant association with bile salt tolerance. In addition, four genes related to DNA damage repair and substance transport were redundant in the strains with high bile salt tolerance. Besides, cluster analysis showed that bile salt hydrolases did not contribute to the bile salt tolerance of L. salivarius. In this study, we determined the global regulatory genes, including LSL_1568, LSL_1716 and LSL_1709, for bile salt tolerance in L. salivarius and provided a potential method for the rapid screening of bile salt-tolerant L. salivarius strains, based on PCR amplification of functional genes.


2009 ◽  
Vol 8 ◽  
pp. S78
Author(s):  
D. Debray ◽  
D. Rainteau ◽  
S. Lerondel ◽  
C. Rey ◽  
L. Humbert ◽  
...  

HPB ◽  
2016 ◽  
Vol 18 ◽  
pp. e163
Author(s):  
K.V.K. Koelfat ◽  
F.G. Schaap ◽  
J.G. Bloemen ◽  
A.K. Groen ◽  
P.L.M. Jansen ◽  
...  

2017 ◽  
Vol 312 (4) ◽  
pp. R477-R484 ◽  
Author(s):  
Dongke Yu ◽  
Han Zhang ◽  
Daniel A. Lionarons ◽  
James L. Boyer ◽  
Shi-Ying Cai

The Na+-dependent taurocholate cotransporting polypeptide (NTCP/SLC10A1) is a hepatocyte-specific solute carrier, which plays an important role in maintaining bile salt homeostasis in mammals. The absence of a hepatic Na+-dependent bile salt transport system in marine skate and rainbow trout raises a question regarding the function of the Slc10a1 gene in these species. Here, we have characterized the Slc10a1 gene in the marine skate, Leucoraja erinacea. The transcript of skate Slc10a1 (skSlc10a1) encodes 319 amino acids and shares 46% identity to human NTCP (hNTCP) with similar topology to mammalian NTCP. SkSlc10a1 mRNA was mostly confined to the brain and testes with minimal expression in the liver. An FXR-bile salt reporter assay indicated that skSlc10a1 transported taurocholic acid (TCA) and scymnol sulfate, but not as effectively as hNTCP. An [3H]TCA uptake assay revealed that skSlc10a1 functioned as a Na+-dependent transporter, but with low affinity for TCA ( Km = 92.4 µM) and scymnol sulfate ( Ki = 31 µM), compared with hNTCP (TCA, Km = 5.4 µM; Scymnol sulfate, Ki = 3.5 µM). In contrast, the bile salt concentration in skate plasma was 2 µM, similar to levels seen in mammals. Interestingly, skSlc10a1 demonstrated transport activity for the neurosteroids dehydroepiandrosterone sulfate and estrone-3-sulfate at physiological concentration, similar to hNTCP. Together, our findings indicate that skSlc10a1 is not a physiological bile salt transporter, providing a molecular explanation for the absence of a hepatic Na+-dependent bile salt uptake system in skate. We speculate that Slc10a1 is a neurosteroid transporter in skate that gained its substrate specificity for bile salts later in vertebrate evolution.


2017 ◽  
Vol 36 ◽  
pp. S31
Author(s):  
A. Huijbers ◽  
K.V. Koelfat ◽  
F.G. Schaap ◽  
M. Lenicek ◽  
G.J. Wanten ◽  
...  

2017 ◽  
Vol 66 (1) ◽  
pp. S558
Author(s):  
K.V. Koelfat ◽  
A. Huijbers ◽  
F.G. Schaap ◽  
M. Lenicek ◽  
G.J. Wanten ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document