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Rhamnetin abrogates polystyrene microplastics prompted hepatic damage by regulating Nrf-2/Keap-1 pathway

Journal of King Saud University - Science 2024 1 citation ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 35 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Saba Yaqoob, Ali Hamza, Saba Yaqoob, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Saba Yaqoob, Saba Yaqoob, Ali Hamza, Moazama Batool, Moazama Batool, Moazama Batool, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Ali Hamza, Moazama Batool, Ali Hamza, Ali Hamza, Ali Hamza, Moazama Batool, Ali Hamza, Aisha Khatoon, Aisha Khatoon, Moazama Batool, Aisha Khatoon, Moazama Batool, Ali Hamza, Moazama Batool, Mian N. Riaz Mian N. Riaz Shaik Althaf Hussain, Shaik Althaf Hussain, Shaik Althaf Hussain, Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz Mian N. Riaz

Summary

Researchers investigated whether rhamnetin, a natural flavonoid, could protect against liver damage induced by polystyrene microplastics in rats administered 0.01 mg/kg PS-MPs for the experimental period. They found that PS-MPs suppressed the Nrf-2/Keap-1 antioxidant pathway, reduced activities of SOD, CAT, GPx, GST, and HO-1 enzymes, elevated ALT, AST, and ALP liver injury markers, and increased apoptotic signaling, while co-administration of 50 mg/kg rhamnetin mitigated all these effects through hepatoprotective, anti-inflammatory, and antioxidant mechanisms.

Polymers
Body Systems
Models

Polystyrene microplastics (PS-MPs) are environmental toxicants that exert adverse effects on organisms. Rhamnetin (RHM) is a natural flavone that shows multiple therapeutic potentials. Therefore, the present study was planned to determine the mitigative effect of RHM against PS-MPs induced liver damage. 48 rats were divided into 4 groups. Control group, PS-MPs (0.01 mg/kg) administered group, PS-MPs (0.01 mg/kg)+ RHM (50 mg/kg) co-administered group and RHM alone (50 mg/kg) administered group. PS-MPs reduced the expressions of Nrf-2 and anti-oxidant gene expressions, while increasing Keap-1 expression. PS-MPs also decreased the activities of catalase (CAT), glutathione reductase (GSR), heme oxygenase-1 (HO-1), glutathione-S-transferase (GST), superoxide dismutase (SOD), glutathione peroxidase (GPx) and glutathione (GSH), besides elevating the levels of MDA and ROS. Additionally, PS-MPs augmented the levels of alanine transaminase (ALT), alkaline phosphatase (ALP) and aspartate aminotransferase (AST). Furthermore, there was an upsurge in the levels of inflammatory indices in PS-MPs treated group. PS-MPs intoxication also increased Bax and Caspase-3 expressions, while lowering the Bcl-2 expression. Nevertheless, RHM mitigated all the damages due to its hepatoprotective, anti-inflammatory, anti-oxidant and anti-apoptotic potentials.

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