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Dynamic changes of cyclophosphamide-induced liver injury in mice
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Can HUANG, Fa-jing HE, Xiao YANG, Li-huan GUAN, Si-min ZHANG, Yan-ying ZHOU, Shi-cheng FAN, Xin-peng YAO, Min HUANG, Hui-chang BI*
Acta Pharmaceutica Sinica | 2019, 54(6) : 1062 - 1068
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Acta Pharmaceutica Sinica | 2019, 54(6): 1062-1068
Original Articles
Dynamic changes of cyclophosphamide-induced liver injury in mice
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Can HUANG, Fa-jing HE, Xiao YANG, Li-huan GUAN, Si-min ZHANG, Yan-ying ZHOU, Shi-cheng FAN, Xin-peng YAO, Min HUANG, Hui-chang BI*
Affiliations
  • Lab of Drug Metabolism and Pharmacokinetics, School of Pharmaceutical Sciences, Guangzhou 510006, China
Published: 2019-06-12 doi: 10.16438/j.0513-4870.2019-0237
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Cyclophosphamide (CPA) is one of the most commonly used alkylating agents in the treatment of malignant cancer. CPA is metabolized by cytochrome P450 enzymes into 4-hydroxycyclophosphamide in vivo which can exhibit anti-tumor activity. Metabolic activation of CPA can cause adverse reactions such as myelosuppression, cystitis, and liver injury. The aim of this study was to evaluate the dynamic changes of hepatic injury induced by CPA in mice. Male BALB/c mice were injected CPA (200 mg·kg-1) intraperitoneally. Both serum and liver samples were collected at 0, 2, 6, 12 and 24 hours after dosing. The animal experiment protocol was approved by the Institutional Animal Care and Use Committee at Sun Yat-sen University. The results showed that hepatotoxicity was observed at 2 hours after CPA dosing, and the most serious liver injury was measured at 12 hours. The level of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and malondialdehyde (MDA) was significantly increased, glutathione (GSH) level was significantly decreased, hepatocyte edema and vacuolar degeneration were widely observed in liver tissue, and began to recover 24 hours after dosing. In addition, due to oxidative stress damage caused by CPA, nuclear factor-erythroid 2-related factor 2 (NRF2) signaling pathway was activated and the mRNA and protein expression of its downstream targets such as quinine oxidoreductase 1 (NQO1), heme oxygenase-1 (HO-1), glutamate-cysteine ligase catalytic subunit (GCLC) and glutamate cysteine modifier subunit (GCLM) were up-regulated, which alleviated oxidative stress injury. In a summary, this study demonstrate the dynamic change of CPA-induced liver injury and the NRF2-mediated protective mechanisms, providing new insights into the CPA-induced liver injury.

cyclophosphamide  /  liver injury  /  oxidative stress  /  nuclear factor-erythroid 2-related factor 2
Can HUANG, Fa-jing HE, Xiao YANG, Li-huan GUAN, Si-min ZHANG, Yan-ying ZHOU, Shi-cheng FAN, Xin-peng YAO, Min HUANG, Hui-chang BI. Dynamic changes of cyclophosphamide-induced liver injury in mice[J]. Acta Pharmaceutica Sinica, 2019 , 54 (6) : 1062 -1068 . DOI: 10.16438/j.0513-4870.2019-0237
Year 2019 volume 54 Issue 6
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Article Info
doi: 10.16438/j.0513-4870.2019-0237
  • Receive Date:2019-04-03
  • Online Date:2026-01-26
  • Published:2019-06-12
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  • Received:2019-04-03
  • Revised:2019-04-25
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    Lab of Drug Metabolism and Pharmacokinetics, School of Pharmaceutical Sciences, Guangzhou 510006, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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