Estimation the Safety of Parenteral Resveratrol in Mice

Authors

  • Rehab AM. Jawad
  • Hayder B Sahib Department of Pharmacology/ College of pharmacy/ Al-Nahrain University

DOI:

https://doi.org/10.31351/vol31iss1pp167-175

Keywords:

Acute toxicity, Intraperitoneally, Histopathology, Resveratrol, LD50, Biochemical assay.

Abstract

   Resveratrol is polyphenolic compound has many biochemical and biological effects on several organs. Therefore, resveratrol can be used to treat many diseases. The aim was to evaluate resveratrol safety when used in a parenteral single bolus dose. This study was conducted on 60 mice (30 males and 30 females). Each male and female mice divided into 6 groups (five mice per group). All mice groups given 1% DMSO and five different doses of resveratrol (5, 2.5, 1.25, 0.625, 0.312) gm/kg intraperitonially given to five groups respectively. The mice were continuously monitored during 14 days. The number of deaths, changes in general behavior, changes in physiological activity, and signs of toxicity were reported. On day 15 blood was collected using a jugular vein puncture to obtain blood samples for hematological and biochemical analysis. All mice were euthanized under anesthesia. The heart, lung, liver, kidney, and gonads were dissected and sent for histopathological study. The result showed that at dose 0.312gm/kg neither signs of toxicity nor death were detected. The LD50 dose was 1.18 g/kg for female and 1.07 g/kg for male mice. The body weight change, biochemical and hematological assay, revealed that at doses 1.25 g/kg,0.625,0.312 g/kg for both sexes no significant changes had reported in comparison with a control group (p?0.05). Histopathological examination revealed that at doses 1.25 g/kg for both sexes no significant tissue changes had reported in comparison with a control group (p?0.05). In conclusion resveratrol has dose-dependent toxicity when used intraperitoneally in Swiss Albino mice and the non-observed adverse effect level at dose 0.312 g/kg.

How to Cite

1.
AM. Jawad R, Sahib HB. Estimation the Safety of Parenteral Resveratrol in Mice. Iraqi Journal of Pharmaceutical Sciences [Internet]. 2022 Jun. 17 [cited 2024 Nov. 21];31(1):167-75. Available from: https://bijps.uobaghdad.edu.iq/index.php/bijps/article/view/1487

Publication Dates

References

Levy E, Delvin E, Marcil V, Spahis S. Can phytotherapy with polyphenols serve as a powerful approach for the prevention and therapy tool of novel coronavirus disease 2019 (COVID-19)? Am J Physiol Endocrinol Metab. 2020;319(4):E689–708.

Salehi B, Mishra AP, Nigam M, Sener B, Kilic M, Sharifi-Rad M, et al. Resveratrol: A double-edged sword in health benefits. Biomedicines. 2018;6(3):1–20.

Rafe T, Shawon PA, Salem L, Chowdhury NI, Kabir F, Bin Zahur SM, et al. Preventive Role of Resveratrol Against Inflammatory Cytokines and Related Diseases. Curr Pharm Des. 2019;25(12):1345–71.

Shaito A, Posadino AM, Younes N, Hasan H, Halabi S, Alhababi D, et al. Potential adverse effects of resveratrol: A literature review. Int J Mol Sci. 2020;21(6): 2084.

Park EJ, Pezzuto JM. The pharmacology of resveratrol in animals and humans. Biochim Biophys Acta - Mol Basis Dis. 2015;1852(6):1071–113.

Fan P, Marston A, Hay AE, Hostettmann K. Rapid separation of three glucosylated resveratrol analogues from the invasive plant Polygonum cuspidatum by high-speed countercurrent chromatography. J Sep Sci. 2009;32(17):2979–84.

Downloads

Published

2022-06-17

Most read articles by the same author(s)