Evaluation of the protective effect of salidroside on arsenic-induced cardiac dysfunction in rats
Author:
Publisher
China Science Publishing & Media Ltd.
Subject
General Medicine,Biochemistry,Biophysics,Molecular Biology
Link
https://engine.scichina.com/doi/pdf/BFC5470C83484500987F3BC367A92A5E
Reference8 articles.
1. Nurchi VM, Buha Djordjevic A, Crisponi G, Alexander J, Bjørklund G, Aaseth J. Arsenic toxicity: molecular targets and therapeutic agents. Biomolecules, 2020, 10:
2. Chen QY, Costa M. Arsenic: a global environmental challenge. Annu Rev Pharmacol Toxicol, 2021, 61: 47-63.
3. Yang Z, Huang X, Lai W, Tang Y, Liu J, Wang Y, Chu K. Synthesis and identification of a novel derivative of salidroside as a selective, competitive inhibitor of monoamine oxidase B with enhanced neuroprotective properties. Eur J Med Chem, 2021, 209:
4. Muthumani M, Prabu SM. Silibinin potentially attenuates arsenic-induced oxidative stress mediated cardiotoxicity and dyslipidemia in rats. Cardiovasc Toxicol, 2014, 14: 83-97.
5. Fallah M, Moghble N, Javadi I, Bahadoran H, Shahriary A. Effect of curcumin and N-acetylcysteine on brain histology and inflammatory factors (MMP-2, 9 and TNF-α) in rats exposed to arsenic. Pharm Sci, 2018, 24: 264-272.
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