Diurnal hepatic CYP3A11 contributes to chronotoxicity of the pyrrolizidine alkaloid retrorsine in mice-Reference-Cited by-同舟云学术

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Diurnal hepatic CYP3A11 contributes to chronotoxicity of the pyrrolizidine alkaloid retrorsine in mice

Published:2021-07-26 Issue:9 Volume:51 Page:1019-1028
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Guo Li¹,Zhang Li²,Xu Haiman²,Yu Pei²,Wang Zhigang³,Lu Danyi⁴,Chen Min²,Wu Baojian⁵

Affiliation:

1. Department of Critical Care Medicine, Zhongshan Torch Development Zone Hospital, Zhongshan, China

2. Jinan University, Guangzhou, China

3. Department of Intensive Care Unit, First Affiliated Hospital of Jinan University, Guangzhou, China

4. Jinan University, College of Pharmacy, Guangzhou, China

5. Institute of Molecular Rhythm and Metabolism, Guangzhou University of Chinese Medicine, Guangzhou, China

Funder

Natural Science Foundation of Guangdong Province

Shenzhen Science and Technology Innovation Commission

the Project of Administration of Traditional Chinese Medicine of Guangdong Province of China

Publisher

Informa UK Limited

Subject

Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/00498254.2021.1950867

Reference36 articles.

1. Mechanisms for Pyrrolizidine Alkaloid Activation and Detoxification

2. The Molecular Mechanism Regulating Diurnal Rhythm of Flavin-Containing Monooxygenase 5 in Mouse Liver

3. Identification of rhythmic human CYPs and their circadian regulators using synchronized hepatoma cells

4. Clock gene Bmal1 controls diurnal rhythms in expression and activity of intestinal carboxylesterase 1

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1. The role of the circadian timing system on drug metabolism and detoxification: an update;Expert Opinion on Drug Metabolism & Toxicology;2024-05-20

2. Recent advances in circadian-regulated pharmacokinetics and its implications for chronotherapy;Biochemical Pharmacology;2022-09

3. Pharmacokinetics-based Chronotherapy;Current Drug Metabolism;2022-01

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