Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Bile Acids and Salts/metabolism"'
Autor:
Begoña Porteiro, Reinout L.P. Roscam Abbing, Wietse In het Panhuis, Dirk R. de Waart, Suzanne Duijst, Isabelle Bolt, Esther W. Vogels, Johannes H.M. Levels, Laura A. Bosmans, Winnie G. Vos, Ronald P.J. Oude Elferink, Esther Lutgens, Stan F.J. van de Graaf
Publikováno v:
Journal of Lipid Research, Vol 65, Iss 8, Pp 100594- (2024)
Bile salts can strongly influence energy metabolism through systemic signaling, which can be enhanced by inhibiting the hepatic bile salt transporter Na+ taurocholate cotransporting polypeptide (NTCP), thereby delaying hepatic reuptake of bile salts
Externí odkaz:
https://doaj.org/article/3ec125e1e6b34037b16340136513ac67
Autor:
Samuel A.J. Trammell, Luke F. Gamon, Kamil Gotfryd, Katja Thorøe Michler, Bandar D. Alrehaili, Iben Rix, Filip K. Knop, Pontus Gourdon, Yoon-Kwang Lee, Michael J. Davies, Matthew P. Gillum, Trisha J. Grevengoed
Publikováno v:
Journal of Lipid Research, Vol 64, Iss 9, Pp 100361- (2023)
N-acyl taurines (NATs) are bioactive lipids with emerging roles in glucose homeostasis and lipid metabolism. The acyl chains of hepatic and biliary NATs are enriched in polyunsaturated fatty acids (PUFAs). Dietary supplementation with a class of PUFA
Externí odkaz:
https://doaj.org/article/f84f1e3b40024fd5a3352b3eef7e65dc
Akademický článek
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Publikováno v:
Journal of Lipid Research, Vol 61, Iss 4, Pp 480-491 (2020)
Compared with humans, rodents have higher synthesis of cholesterol and bile acids (BAs) and faster clearance and lower levels of serum LDL-cholesterol. Paradoxically, they increase BA synthesis in response to bile duct ligation (BDL). Another differe
Externí odkaz:
https://doaj.org/article/da249c4ad2704e6e8aa69b69b72474f2
Autor:
Robin van Eenige, Zhixiong Ying, Lauren Tambyrajah, Amanda C.M. Pronk, Niek Blomberg, Martin Giera, Yanan Wang, Tamer Coskun, Mario van der Stelt, Patrick C.N. Rensen, Sander Kooijman
Publikováno v:
Journal of Lipid Research, Vol 62, Iss , Pp 100070- (2021)
Pharmacological blockade of the cannabinoid type 1 receptor, a G protein-coupled receptor expressed in the central nervous system and various peripheral tissues, reverses diet-induced obesity and dyslipidemia through the reduction of food intake and
Externí odkaz:
https://doaj.org/article/9dc750d1ebc14d54b6be276bd11ac14f
Publikováno v:
Journal of Lipid Research, Vol 58, Iss 6, Pp 1143-1152 (2017)
In addition to functioning as detergents that aid digestion of dietary lipids in the intestine, some bile acids have been shown to exhibit antimicrobial activity. However, detailed information on the bactericidal activities of the diverse molecular s
Externí odkaz:
https://doaj.org/article/20c6336b040b48fd8e7e782cf207ac98
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Yared Paalvast, Enchen Zhou, Yvonne J. W. Rozendaal, Yanan Wang, Albert Gerding, Theo H. van Dijk, Jan Freark de Boer, Patrick C. N. Rensen, Ko Willems van Dijk, Jan A. Kuivenhoven, Barbara M. Bakker, Natal A. W. van Riel, Albert K. Groen
Publikováno v:
Nutrients; Volume 14; Issue 22; Pages: 4936
Nutrients, 14(22):4936. MDPI AG
Nutrients, 14(22):4936. Multidisciplinary Digital Publishing Institute (MDPI)
Nutrients, 14(22). MDPI
Nutrients, 14(22):4936. MDPI AG
Nutrients, 14(22):4936. Multidisciplinary Digital Publishing Institute (MDPI)
Nutrients, 14(22). MDPI
Within the human population, considerable variability exists between individuals in their susceptibility to develop obesity and dyslipidemia. In humans, this is thought to be caused by both genetic and environmental variation. APOE*3-Leiden.CETP mice
Publikováno v:
Archives of toxicology, 96(9), 2523-2543. SPRINGER HEIDELBERG
Drugs are often withdrawn from the market due to the manifestation of drug-induced liver injury (DILI) in patients. Drug-induced cholestasis (DIC), defined as obstruction of hepatic bile flow due to medication, is one form of DILI. Because DILI is id
Autor:
Eric J. Niesor, Christine Magg, Naoto Ogawa, Hiroshi Okamoto, Elisabeth von der Mark, Hugues Matile, Georg Schmid, Roger G. Clerc, Evelyne Chaput, Denise Blum-Kaelin, Walter Huber, Ralf Thoma, Philippe Pflieger, Makoto Kakutani, Daisuke Takahashi, Gregor Dernick, Cyrille Maugeais
Publikováno v:
Journal of Lipid Research, Vol 51, Iss 12, Pp 3443-3454 (2010)
The mechanism by which cholesteryl ester transfer protein (CETP) activity affects HDL metabolism was investigated using agents that selectively target CETP (dalcetrapib, torcetrapib, anacetrapib). In contrast with torcetrapib and anacetrapib, dalcetr
Externí odkaz:
https://doaj.org/article/6b0ce888f3634531a2b4ff3ba44e3457