Literature DB >> 34488896

Pharmacokinetic herb-drug interactions between Aidi injection and doxorubicin in rats with diethylnitrosamine-induced hepatocellular carcinoma.

Yuan Lu1,2, Jie Pan2,3, Xiaoqing Zhu2, Shuai Zhang4, Chunhua Liu2,3, Jia Sun1,2, Yueting Li2,3, Siying Chen1,2, Jing Huang2, Chuang Cao2, Yonglin Wang1,2, Yongjun Li5,6, Ting Liu7,8.   

Abstract

BACKGROUND: Aidi Injection (ADI), a Chinese herbal preparation with anti-cancer activity, is used for the treatment of hepatocellular carcinoma (HCC). Several clinical studies have shown that co-administration of ADI with doxorubicin (DOX) is associated with reduced toxicity of chemotherapy, enhanced clinical efficacy and improved quality of life for patients. However, limited information is available about the herb-drug interactions between ADI and DOX. The study aimed to investigate the pharmacokinetic mechanism of herb-drug interactions between ADI and DOX in a rat model of HCC.
METHODS: Experimental HCC was induced in rats by oral administration of diethylnitrosamine. The HCC rats were pretreated with ADI (10 mL/kg, intraperitoneal injection) for 14 consecutive days prior to administration of DOX (7 mg/kg, intravenous injection) to investigate pharmacokinetic interactions. Plasma concentrations of DOX and its major metabolite, doxorubicinol (DOXol), were determined using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).
RESULTS: Preadministration of ADI significantly altered the pharmacokinetics of DOX in HCC rats, leading to increased plasma concentrations of both DOX and DOXol. The area under the plasma drug concentration-time curve (AUCs) of DOX and DOXol in rats pretreated with ADI were 3.79-fold and 2.92-fold higher, respectively, than those in control rats that did not receive ADI.
CONCLUSIONS: Increased levels of DOX and DOXol were found in the plasma of HCC rats pretreated with ADI.
© 2021. The Author(s).

Entities:  

Keywords:  Aidi injection; Doxorubicin; Doxorubicinol; Hepatocellular carcinoma; Pharmacokinetic herb-drug interaction; Rat

Mesh:

Substances:

Year:  2021        PMID: 34488896      PMCID: PMC8419969          DOI: 10.1186/s40360-021-00515-9

Source DB:  PubMed          Journal:  BMC Pharmacol Toxicol        ISSN: 2050-6511            Impact factor:   2.483


  48 in total

1.  Doxorubicin pathways: pharmacodynamics and adverse effects.

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2.  Comparison of Triple-Drug Transcatheter Arterial Chemoembolization (TACE) With Single-Drug TACE Using Doxorubicin-Eluting Beads: Long-Term Survival in 313 Patients.

Authors:  Antoinette S Gomes; Phillip A Monteleone; James W Sayre; Richard S Finn; Saeed Sadeghi; Myron J Tong; Carolyn D Britten; Ronald W Busuttil
Journal:  AJR Am J Roentgenol       Date:  2017-07-13       Impact factor: 3.959

3.  Symptom clusters and symptom interference of HCC patients undergoing TACE: a cross-sectional study in China.

Authors:  Wenting Cao; Juan Li; Chen Hu; Jie Shen; Xiangyan Liu; Yan Xu; Zhixia Ye
Journal:  Support Care Cancer       Date:  2012-07-20       Impact factor: 3.603

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Authors:  Dongwu Liu; Zhiwei Chen
Journal:  Anticancer Agents Med Chem       Date:  2009-05       Impact factor: 2.505

5.  Ginsenoside Rg3 antagonizes adriamycin-induced cardiotoxicity by improving endothelial dysfunction from oxidative stress via upregulating the Nrf2-ARE pathway through the activation of akt.

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Journal:  Phytomedicine       Date:  2015-07-04       Impact factor: 5.340

6.  The natural compound cantharidin induces cancer cell death through inhibition of heat shock protein 70 (HSP70) and Bcl-2-associated athanogene domain 3 (BAG3) expression by blocking heat shock factor 1 (HSF1) binding to promoters.

Authors:  Joo Ae Kim; Youngmi Kim; Byoung-Mog Kwon; Dong Cho Han
Journal:  J Biol Chem       Date:  2013-08-27       Impact factor: 5.157

7.  Neural network assessment of herbal protection against chemotherapeutic-induced reproductive toxicity.

Authors:  Amr Amin; Doaa Mahmoud-Ghoneim; Muhammed I Syam; Sayel Daoud
Journal:  Theor Biol Med Model       Date:  2012-01-24       Impact factor: 2.432

8.  Targeted inhibitors of P-glycoprotein increase chemotherapeutic-induced mortality of multidrug resistant tumor cells.

Authors:  Amila K Nanayakkara; Courtney A Follit; Gang Chen; Noelle S Williams; Pia D Vogel; John G Wise
Journal:  Sci Rep       Date:  2018-01-17       Impact factor: 4.379

Review 9.  Glutathione Transferases: Potential Targets to Overcome Chemoresistance in Solid Tumors.

Authors:  Marija Pljesa-Ercegovac; Ana Savic-Radojevic; Marija Matic; Vesna Coric; Tatjana Djukic; Tanja Radic; Tatjana Simic
Journal:  Int J Mol Sci       Date:  2018-11-28       Impact factor: 5.923

Review 10.  A Review of the Pharmacological Action of Astragalus Polysaccharide.

Authors:  Yijun Zheng; Weiyu Ren; Lina Zhang; Yuemei Zhang; Dongling Liu; Yongqi Liu
Journal:  Front Pharmacol       Date:  2020-03-24       Impact factor: 5.810

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  1 in total

1.  Calotropis gigantea stem bark extracts inhibit liver cancer induced by diethylnitrosamine.

Authors:  Suphunwadee Sawong; Dumrongsak Pekthong; Supawadee Parhira; Piyarat Srisawang; Pennapha Suknoppakit; Thanwarat Winitchaikul; Worasak Kaewkong; Julintorn Somran; Chaidan Intapa
Journal:  Sci Rep       Date:  2022-07-15       Impact factor: 4.996

  1 in total

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