Zobrazeno 1 - 10
of 41
pro vyhledávání: '"CYP2C70"'
Autor:
Kunpeng Huang, Changyan Wang, Bosheng Mei, Jinglei Li, Tianxing Ren, Hanjing Zhan, Yunwei Zhang, Bowen Zhang, Xinyu Lv, Qi Zhang, Yong Guan, Xiaofei Zhang, Guoliang Wang, Wenming Pan, Peng Xu, Hui Wang, Jinxiang Zhang
Publikováno v:
JHEP Reports, Vol 6, Iss 8, Pp 101101- (2024)
Background & Aims: Persistent cholestasis has been associated with poor prognosis after orthotopic liver transplantation. In this study, we aimed to investigate how the accumulation of tauro-beta-muricholic acid (TβMCA), resulting from the reprogram
Externí odkaz:
https://doaj.org/article/24b0a74732b7478aa5c3e5f33c355d5f
Autor:
Mohammad Nazmul Hasan, Jianglei Chen, David Matye, Huaiwen Wang, Wenyi Luo, Lijie Gu, Yung Dai Clayton, Yanhong Du, Tiangang Li
Publikováno v:
Journal of Lipid Research, Vol 64, Iss 3, Pp 100340- (2023)
Therapeutic reduction of hydrophobic bile acids exposure is considered beneficial in cholestasis. The Cyp2c70 KO mice lack hydrophilic muricholic acids and have a human-like hydrophobic bile acid pool resulting in hepatobiliary injury. This study inv
Externí odkaz:
https://doaj.org/article/897440a21bd44797a0f914ca459f29f9
Akademický článek
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Autor:
Mohammad Nazmul Hasan, Jianglei Chen, Huaiwen Wang, Yanhong Du, Yung Dai Clayton, Lijie Gu, Tiangang Li
Publikováno v:
Cells, Vol 12, Iss 10, p 1371 (2023)
Cyp2c70 knockout mice lack the enzyme that produces muricholic acids and show a “human-like” hydrophobic bile acid pool-induced hepatobiliary injury. In this study, we investigated the potential anti-cholestasis effect of glycine-conjugated β mu
Externí odkaz:
https://doaj.org/article/0057211fb2294a19860c3bdebc5e0b6b
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:
Akira Honda, Teruo Miyazaki, Junichi Iwamoto, Takeshi Hirayama, Yukio Morishita, Tadakuni Monma, Hajime Ueda, Seiya Mizuno, Fumihiro Sugiyama, Satoru Takahashi, Tadashi Ikegami
Publikováno v:
Journal of Lipid Research, Vol 61, Iss 1, Pp 54-69 (2020)
The bile acid (BA) composition in mice is substantially different from that in humans. Chenodeoxycholic acid (CDCA) is an end product in the human liver; however, mouse Cyp2c70 metabolizes CDCA to hydrophilic muricholic acids (MCAs). Moreover, in hum
Externí odkaz:
https://doaj.org/article/b6ca2ce2cff4472a9322001da895e681
Autor:
Rumei Li, Anna Palmiotti, Hilde D. de Vries, Milaine V. Hovingh, Martijn Koehorst, Niels L. Mulder, Yue Zhang, Kim Kats, Vincent W. Bloks, Jingyuan Fu, Henkjan J. Verkade, Jan Freark de Boer, Folkert Kuipers
Publikováno v:
Journal of Lipid Research, Vol 62, Iss , Pp 100134- (2021)
Bile acids (BAs) play important roles in lipid homeostasis, and BA signaling pathways serve as therapeutic targets for nonalcoholic fatty liver disease (NAFLD). Recently, we generated cytochrome P450, family 2, subfamily C, polypeptide 70 (Cyp2c70−
Externí odkaz:
https://doaj.org/article/f8cb60c473764338b6419affd52446ef
Publikováno v:
Metabolites; Volume 13; Issue 7; Pages: 824
Taurine, the end product in the sulfur-containing amino acid pathway, is conjugated with bile acids (BAs) in the liver. The rate-limiting enzymes in both taurine synthesis and BA conjugation may be regulated by a nucleus receptor, FXR, that promotes
Cyp2c70 is responsible for the species difference in bile acid metabolism between mice and humans[S]
Autor:
Shogo Takahashi, Tatsuki Fukami, Yusuke Masuo, Chad N. Brocker, Cen Xie, Kristopher W. Krausz, C. Roland Wolf, Colin J. Henderson, Frank J. Gonzalez
Publikováno v:
Journal of Lipid Research, Vol 57, Iss 12, Pp 2130-2137 (2016)
Bile acids are synthesized from cholesterol in the liver and subjected to multiple metabolic biotransformations in hepatocytes, including oxidation by cytochromes P450 (CYPs) and conjugation with taurine, glycine, glucuronic acid, and sulfate. Mice a
Externí odkaz:
https://doaj.org/article/b492e5b921554905ba4d7d1bcb88606c
Akademický článek
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