# The single and combined effects of deltamethrin and polyethylene microplastics on the development and biochemical responses of Xenopus laevis in early life stages

**Authors:** Duygu Ozhan Turhan, Cihan Anıl Benli, Muhittin Yurekli, Abbas Güngördü

PMC · DOI: 10.1007/s10646-026-03028-5 · Ecotoxicology (London, England) · 2026-01-23

## TL;DR

This study examines how deltamethrin and polyethylene microplastics affect Xenopus laevis embryos and tadpoles, finding combined effects that vary depending on the life stage and biomarker.

## Contribution

The study introduces a detailed assessment of single and combined toxicity of deltamethrin and microplastics in amphibians, highlighting life stage-dependent responses.

## Key findings

- Deltamethrin caused embryotoxicity with LC50 of 68.0 µg/L and EC50 of 7.58 µg/L.
- Combined exposures showed additive and antagonistic effects on enzymatic biomarkers.
- Tadpoles showed inhibited enzyme activity at high microplastic concentrations.

## Abstract

The co-occurrence of microplastics and pesticides in freshwater ecosystems raises concerns for aquatic organisms. However, their combined effects remain poorly understood. In this study, the single and combined effects of deltamethrin (DEL) and polyethylene microplastics (PE-MPs) were investigated in the early life stages of Xenopus laevis. Embryonic developmental toxicity was evaluated under standardized Frog Embryo Teratogenesis Assay–Xenopus (FETAX) conditions in embryos, and sublethal biochemical responses were also assessed in embryos and tadpoles. In the first phase, embryos were exposed for 96 h to a concentration range of DEL (3.125–6,400 µg/L) and PE-MPs (50–1,000 mg/L) to estimate the median lethal concentration (LC50) and the median effective concentration for malformation (EC50), as well as the teratogenic index (TI). In the second phase, assays were performed at DEL 2.72 and 13.6 µg/L (alone or combined with 100 mg/L PE-MPs) and PE-MPs 50 and 250 mg/L alone, assessing malformation and lethality in embryos and enzymatic biomarkers in both embryos and tadpoles. DEL caused significant embryotoxicity, with 96 h LC50 and EC50 values of 68.0 µg/L and 7.58 µg/L, respectively, and a TI of 8.97. PE-MPs alone did not induce lethality or malformations but caused biochemical alterations. Combined exposures produced additive (glutathione S-transferase, GST; carboxylesterase, CaE) and antagonistic (catalase, CAT; acetylcholinesterase, AChE) patterns; notably, CAT showed a synergistic pattern in embryos based on interaction index analysis. In tadpoles, 250 mg/L PE-MP concentration inhibited glutathione reductase (GR) and AChE activity, suggesting life stage–dependent sensitivity. These findings underscore the complexity of mixture toxicity and emphasize the need for combined exposure assessments in amphibian ecotoxicology.

The online version contains supplementary material available at 10.1007/s10646-026-03028-5.

## Linked entities

- **Proteins:** GSTU5 (glutathione S-transferase tau 5), Cat (Catalase), GR (glutathione reductase)
- **Chemicals:** deltamethrin (PubChem CID 40585)
- **Species:** Xenopus laevis (taxon 8355)

## Full-text entities

- **Genes:** Catalase [NCBI Gene 100174793], sod1.S (superoxide dismutase 1 S homeolog) [NCBI Gene 100381040] {aka XSODA, als, als1, ipoa, sod, sod1}, gabpa.S (GA binding protein transcription factor subunit alpha S homeolog) [NCBI Gene 378601] {aka X-alpha1, XrpFI, e4tf1-60, e4tf1a, gabpa-A, nft2}, hpgds.S (hematopoietic prostaglandin D synthase S homeolog) [NCBI Gene 379417] {aka XlGSTS1, gsts, hpgds, hpgds-a, hpgds-b, hpgdsb}, cat.2.L (catalase, gene 2 L homeolog) [NCBI Gene 380236] {aka cat, cat.2}, ache.L (acetylcholinesterase (Cartwright blood group) L homeolog) [NCBI Gene 100158421] {aka ache, arache, n-ache}
- **Diseases:** Malformations (MESH:C564254), Toxicity (MESH:D064420), blister (MESH:D001768), developmental delays (MESH:D002658), neurotoxic (MESH:D020258), developmental abnormalities (MESH:D006130), gut abnormalities (MESH:C536735), abdominal edema (MESH:D000007), developmental (MESH:C567924), endocrine disruption (MESH:D004700), muscle overload (MESH:D019190), paralysis (MESH:D010243), teratogenic (MESH:C535542), Tail malformations (MESH:C562903), neurodevelopmental disruption (MESH:D015451), tail curvature (MESH:D013121), lethality (MESH:C536057), craniofacial edema (MESH:D004487), microcephaly (MESH:D008831), face, head, and eye edema (MESH:D006259), TC (OMIM:275350), microphthalmia (MESH:D008850), intestinal abnormalities (MESH:D007410)
- **Chemicals:** bisphenol A (MESH:C006780), DEL (MESH:C017180), sodium (MESH:D012964), PE (MESH:D020959), polypropylene (MESH:D011126), acetonitrile (MESH:C032159), FETAX (-), ACTI (MESH:C543539), polyvinyl chloride (MESH:D011143), 5,5'-dithio-bis(2-nitrobenzoic acid) (MESH:D004228), salts (MESH:D012492), acetylcholine (MESH:D000109), formalin (MESH:D005557), Pyrethroids (MESH:D011722), GSH (MESH:D005978), GSSG (MESH:D019803), calcium (MESH:D002118), KCl (MESH:D011189), H2O2 (MESH:D006861), water (MESH:D014867), NADPH (MESH:D009249), MS222 (MESH:C003636), DTT (MESH:D004229), nylon (MESH:D009757), GABA (MESH:D005680), MP (MESH:D000080545), EDTA (MESH:D004492), potassium (MESH:D011188), polystyrene (MESH:D011137), PNPA (MESH:C008642), polymer (MESH:D011108), potassium phosphate (MESH:C013216), DMSO (MESH:D004121), ester (MESH:D004952), 1-chloro-2,4-dinitrobenzene (MESH:D004137), plastic (MESH:D010969)
- **Species:** Xenopus laevis (African clawed frog, species) [taxon 8355], Danio rerio (leopard danio, species) [taxon 7955], Rhinella arenarum (Argentine toad, species) [taxon 38577], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]
- **Cell lines:** MLTC-1 — Mus musculus (Mouse), Mouse Leydig cell tumor, Cancer cell line (CVCL_3544)

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## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12827314/full.md

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Source: https://tomesphere.com/paper/PMC12827314