ZHANG Ming-liang, CHEN Yu-long, WANG Xiao-yan, CHEN Xiao-fei, ZHANG Hui, WU Ya-li, YANG Liu-qing, ZHANG Shu-qi, NIU Lu, FENG Ke-ran, LI Wei-xia, TANG Jin-fa. Exploring the risk "time interval window" of sequential medication of Reduning injection and penicillin G injection based on the correlation between biochemical indexes and metabolomics characteristicsJ. Acta Pharmaceutica Sinica, 2024, 59(7): 2098-2107. DOI: 10.16438/j.0513-4870.2023-1311
Citation: ZHANG Ming-liang, CHEN Yu-long, WANG Xiao-yan, CHEN Xiao-fei, ZHANG Hui, WU Ya-li, YANG Liu-qing, ZHANG Shu-qi, NIU Lu, FENG Ke-ran, LI Wei-xia, TANG Jin-fa. Exploring the risk "time interval window" of sequential medication of Reduning injection and penicillin G injection based on the correlation between biochemical indexes and metabolomics characteristicsJ. Acta Pharmaceutica Sinica, 2024, 59(7): 2098-2107. DOI: 10.16438/j.0513-4870.2023-1311

Exploring the risk "time interval window" of sequential medication of Reduning injection and penicillin G injection based on the correlation between biochemical indexes and metabolomics characteristics

  • Exploring the risk "time interval window" of sequential medication of Reduning injection (RDN) and penicillin G injection (PG) by detecting the correlation between serum biochemical indexes and plasma metabonomic characteristics, in order to reduce the risk of adverse reactions caused by the combination of RDN and PG. All animal experiments and welfare are in accordance with the requirements of the First Affiliated Experimental Animal Ethics and Animal Welfare Committee of Henan University of Chinese Medicine (approval number: YFYDW2020002). The changes of biochemical indexes in serum of rats were detected by enzyme-linked immunosorbent assay. It was determined that RDN combined with PG could cause pseudo-allergic reactions (PARs) activated by complement pathway. Further investigation was carried out at different time intervals (1.5, 2, 3.5, 4, 6, and 8 h PG+RDN). It was found that sequential administration within 3.5 h could cause significant PARs. However, PARs were significantly reduced after administration interval of more than 4 h. LC-MS was used for plasma metabolomics analysis, and the levels of serum biochemical indicators and plasma metabolic profile characteristics were compared in parallel. 22 differential metabolites showed similar or opposite trends to biochemical indicators before and after 3.5 h. And enriched to 10 PARs-related pathways such as arachidonic acid metabolism, steroid hormone biosynthesis, linoleic acid metabolism, glycerophospholipid metabolism, and tryptophan metabolism. In conclusion, there is a risk "time interval window" phenomenon in the adverse drug reactions caused by the sequential use of RDN and PG, and the interval medication after the "time interval window" can significantly reduce the risk of adverse reactions.
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