Skip to content
DraconiticResearch
Search Sources API
190,839 studies31 sourcesUpdated 34 min ago
Peer-reviewedCC BYIPS Journal of Toxicology

Acute Toxicity (LD50) Profile of Ethanol Extracts of Chia Seed (Salvia hispanica), Tiger Nut (Cyperus esculentus), and Their Combination in Wistar Rats

  1. 1Department of Biochemistry, Faculty of Natural Sciences, Chukwuemeka Odumegwu Ojukwu University, Uli, Anambra State, Nigeria

Abstract

Chia seed (Salvia hispanica) and tiger nut (Cyperus esculentus) are increasingly explored as plant-based dietary interventions for the management of diabetes mellitus, but data on the acute safety of their combined use remain scarce. This study evaluated the acute oral toxicity (LD50) of ethanol extracts of chia seed, tiger nut, and their combination in male Wistar rats using Lorke's method. Toxicity testing was conducted in two phases. In Phase I, rats (n = 3 per group) received oral doses of 10, 100, and 1000 mg/kg body weight of each extract and were observed for 24 hours. Since no mortality occurred in Phase I, Phase II was conducted using single rats per group administered higher doses of 1600, 2900, and 5000 mg/kg body weight, with observation extended to 72 hours. No deaths were recorded at any dose level for chia seed extract, tiger nut extract, or their combination, up to the highest tested dose of 5000 mg/kg body weight. Rats administered the highest dose (5000 mg/kg) of the chia seed extract and the combined extract appeared visibly weak, while those given tiger nut extract at the same dose appeared only slightly weak; no other overt behavioural or physical signs of toxicity were observed in any group. Since no lethal dose was established, a definitive LD50 value could not be computed, and the practical LD50 of all three extracts is therefore considered to exceed 5000 mg/kg body weight. These findings suggest that ethanol extracts of chia seed, tiger nut, and their combination are relatively safe for oral consumption at the doses tested and support their classification as practically non-toxic according to the Hodge and Sterner toxicity scale, providing a safety basis for their further pharmacological evaluation in the management of diabetes.

Related

  1. Antimicrobial, Anti-Inflammatory, General Toxicity and Antioxidant Activities of Ultrasound-Assisted Extracts from Prunella vulgaris L.
    Mussa E Zholdasbayev, Roza B Seidakhmetova, Gayane A Atazhanova +9
    Pharmaceuticals (Basel, Switzerland)Peer-reviewedCC BYFull textPlant biologyEurope PMC
  2. Integrative Assessment of Teucrium Extracts: Phytochemical Profile, Nutritional-Mineral Composition, Biological Activities, and Toxicological Assessment In Vitro and In Vivo.
    Kenan Preljević, Ivana Pašić, Milorad Vlaović +11
    Chemistry & biodiversityPeer-reviewedCC BY-NC-NDFull textPlant biologyEurope PMC
  3. Carbon nanoparticles synergistically improve drought tolerance and nutraceutical innovation in okra (Abelmoschus esculentus L.): Antioxidant, antibacterial, and anti-fibrotic activities enhanced via flavonoid accumulation.
    Jiyue Wang, Mingli Yang, Xiuhuan Meng +5
    Food chemistry: XPeer-reviewedCC BY-NC-NDFull textPlant biologyEurope PMC
  4. Elucidating the role of glucose-mediated redox homeostasis, carbohydrate metabolism, and secondary metabolite production in enhancing photosynthetic activity, ionomics, and yield in two okra (Abelmoschus esculentus) varieties
    Yamshi Arif, Saif Ahmad, Priyanka Singh +4
    Frontiers in Plant SciencePeer-reviewedCC BY 4.0Plant biologyFrontiersCrossref
  5. Genetic analysis of earliness and yield traits in intervarietal hybrids of okra [Abelmoschus esculentus (L.)] using multi-environment analysis
    Shweta, Sonia Sood, V. K. Sood +2
    Scientific ReportsPeer-reviewedCC BYFull textPlant biologyDOAJ
BibTeX
@article{nwaka2026acute,
  title = {{Acute Toxicity (LD50) Profile of Ethanol Extracts of Chia Seed (Salvia hispanica), Tiger Nut (Cyperus esculentus), and Their Combination in Wistar Rats}},
  author = {Chinyere Stella Nwaka},
  journal = {IPS Journal of Toxicology},
  year = {2026},
  month = aug,
  doi = {10.54117/00pqy306},
  url = {https://doi.org/10.54117/00pqy306},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Acute Toxicity (LD50) Profile of Ethanol Extracts of Chia Seed (Salvia hispanica), Tiger Nut (Cyperus esculentus), and Their Combination in Wistar Rats
AU  - Chinyere Stella Nwaka
PY  - 2026
DA  - 2026/08/31
JO  - IPS Journal of Toxicology
DO  - 10.54117/00pqy306
UR  - https://doi.org/10.54117/00pqy306
AB  - Chia seed (Salvia hispanica) and tiger nut (Cyperus esculentus) are increasingly explored as plant-based dietary interventions for the management of diabetes mellitus, but data on the acute safety of their combined use remain scarce. This study evaluated the acute oral toxicity (LD50) of ethanol extracts of chia seed, tiger nut, and their combination in male Wistar rats using Lorke's method. Toxicity testing was conducted in two phases. In Phase I, rats (n = 3 per group) received oral doses of 10, 100, and 1000 mg/kg body weight of each extract and were observed for 24 hours. Since no mortality occurred in Phase I, Phase II was conducted using single rats per group administered higher doses of 1600, 2900, and 5000 mg/kg body weight, with observation extended to 72 hours. No deaths were recorded at any dose level for chia seed extract, tiger nut extract, or their combination, up to the highest tested dose of 5000 mg/kg body weight. Rats administered the highest dose (5000 mg/kg) of the chia seed extract and the combined extract appeared visibly weak, while those given tiger nut extract at the same dose appeared only slightly weak; no other overt behavioural or physical signs of toxicity were observed in any group. Since no lethal dose was established, a definitive LD50 value could not be computed, and the practical LD50 of all three extracts is therefore considered to exceed 5000 mg/kg body weight. These findings suggest that ethanol extracts of chia seed, tiger nut, and their combination are relatively safe for oral consumption at the doses tested and support their classification as practically non-toxic according to the Hodge and Sterner toxicity scale, providing a safety basis for their further pharmacological evaluation in the management of diabetes.
SN  - 3115-5413
ER  -