# Evaluation of biochemical, histopathological, hematological, and genotoxic effects of some indigenous weed plant extracts in albino rats toward a natural and safe alternative to synthetic insecticides

**Authors:** Muhammad Asif Zahoor, Muhammad Kashif Zahoor, Hina Rizvi, Zeeshan Nawaz, Aftab Ahmed, Bushra Munir, Mudassir Hassan, Muhammad Zulhussnain

PMC · DOI: 10.3389/fvets.2026.1694297 · Frontiers in Veterinary Science · 2026-02-05

## TL;DR

This study compares the toxicity of two weed plant extracts to a synthetic insecticide in rats, finding the plants to be safer and less harmful.

## Contribution

The study provides new evidence that indigenous weed plant extracts are less toxic than synthetic insecticides in vertebrates.

## Key findings

- Plant extracts showed no significant toxicity in liver, kidney, or blood parameters in rats.
- Cypermethrin caused histopathological damage and genotoxic effects in rats.
- Weed plant extracts are potential candidates for natural, safe biopesticides.

## Abstract

The indiscriminate use of pesticides poses a significant risk to human health and the environment. Plant-based biopesticides offer an alternative to insecticides for integration into insect pest management programs.

The current study assessed the toxicological effects of leaf extracts from indigenous weed plants, Chenopodium murale and Achyranthes aspera, in albino rats, Rattus norvegicus. The extract-mixed diet was fed in three different doses (100 ppm, 150 ppm, and 250 ppm) for 28 days, while the Cypermethrin insecticide was used as a reference insecticide at the same dose levels. Samples from liver and kidney tissues were collected for histopathological study, and the blood serum was obtained for biochemical assay.

Histopathological analysis of cypermethrin revealed congestion in the central vein, hemorrhage in hepatic tissues, and necrosis of liver tissues, while kidney tissues showed necrosis of renal tubules, fibrosis, and swelling in Bowman’s capsule. Moreover, hemorrhage was attenuated by degenerated inflammatory cells, edema, and shrinkage, and the rupturing of glomeruli was also observed. Mortality was also recorded at 28th day. In contrast, no physical signs of toxicity and significant alteration in liver and kidney tissues were shown by both plant extracts. Acetylcholinesterase (AChE) and phosphatase enzymes also showed non-significance with plant extracts and significant results with Cypermethrin. Similarly, genotoxicity through the comet assay revealed no changes for either plant. Hematological parameters showed no significant change with plant extracts. Non-significant results revealed that both plant extracts had no difference when compared to the control for all parameters, which indicates that the weed plants are less toxic as compared to Cypermethrin in vertebrates.

These findings suggest that these weed plants have the potential to be used as biopesticides for future integrated pest management (IPM) programs.

## Linked entities

- **Chemicals:** Cypermethrin (PubChem CID 2912)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Pdlim3 (PDZ and LIM domain 3) [NCBI Gene 114108] {aka Actn2lp, Alp}, Ache (acetylcholinesterase) [NCBI Gene 83817]
- **Diseases:** liver damage (MESH:D056486), paralysis (MESH:D010243), jaundice (MESH:D007565), liver (MESH:D017093), granulomas (MESH:D006099), hemorrhage (MESH:D006470), Glomerular degeneration (MESH:D007674), damage (MESH:D020263), genetic defects (MESH:D030342), insect (MESH:C000719201), necrosis (MESH:D009336), Mortality (MESH:D003643), respiratory diseases (MESH:D012140), carcinogenicity (MESH:D011230), necrosis of renal tubules (MESH:D007673), blood disorders (MESH:D006402), brain and nerve damage (MESH:D001925), granulomatous inflammation (MESH:D007249), anemia (MESH:D000740), birth defects (MESH:D000014), teratological defects (MESH:D000013), fibrosis (MESH:D005355), hepatic fibrosis (MESH:D008103), toxicity (MESH:D064420), impotence (MESH:D007172), emphysema (MESH:D004646), asthma (MESH:D001249), edema (MESH:D004487), infection (MESH:D007239), blood coagulation defects (MESH:D001778), TN (MESH:D007683), fatty lesions (MESH:D065626), cancer (MESH:D009369), infertility (MESH:D007246), bone marrow disorders (MESH:D001855)
- **Chemicals:** Cardiac glycosides (MESH:D002301), petroleum ether (MESH:C004544), terpenoids (MESH:D013729), water (MESH:D014867), E (MESH:D004540), Steroids (MESH:D013256), Flavonoids (MESH:D005419), anthraquinones (MESH:D000880), Creatinine (MESH:D003404), formalin (MESH:D005557), ethanol (MESH:D000431), Saponins (MESH:D012503), p-nitrophenyl phosphate (MESH:C008644), H (MESH:D006859), Alcohol (MESH:D000438), Cypermethrin (MESH:C017160), Alkaloids (MESH:D000470), 5,5'-dithiobis-(2-nitrobenzoic acid) (MESH:D004228), DPX (MESH:C027512), phosphate (MESH:D010710), paraffin (MESH:D010232), Diacetyl Monoxide (-), Tannins (MESH:D013634), ATChI (MESH:C543539), p-nitrophenol (MESH:C024836), bilirubin (MESH:D001663), pyrethroid (MESH:D011722), Xylene (MESH:D014992), carboxylic acids (MESH:D002264), EDTA (MESH:D004492), Uric acid (MESH:D014527), S. urea (MESH:D014508), pNPP (MESH:C068798), xylazine (MESH:D014991)
- **Species:** Muscidae (house flies, family) [taxon 7366], A. aspera [taxon 103516], Achyranthes aspera (species) [taxon 240005], Drosophila melanogaster (fruit fly, species) [taxon 7227], Chenopodiastrum murale (nettle-leaf goosefoot, species) [taxon 46091], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916361/full.md

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Source: https://tomesphere.com/paper/PMC12916361