Study of acute, sub-chronic toxicity and anti-hyperuricemic activity of n-hexane fraction of Kaempferia galanga l. on experimental animals

Nguyen Thi Thuý Hang, Nguyen Thi Thanh Binh, Nguyen Thuc Thu Huong, Nguyen Thi Thuy, Phan Hong Minh, Nguyen Thi Mai, Hoang Thu Trang, Mai Phuong Thanh, Nguyen Thi Thanh Ha, Do Thi Hong Khanh

Main Article Content

Abstract

The study evaluates the acute, sub-chronic toxicity and anti-hyperuricemic activity of n-hexane fraction of Kaempferia galanga L. on experimental models. Acute toxicity was assessed using the Litchfield-Wilcoxon method on Swiss albino mice. The sub-chronic toxicity was evaluated following WHO guidelines on Wistar rats at the daily doses of 50 mg/kg/day and 150 mg/kg/day for 4 weeks. The anti-hyperuricemic effect was tested at doses of 100 mg/kg/day and 300 mg/kg/day on Swiss mice, which were intraperitoneally injected with a single dose of potassium oxonate suspension (500 mg/kg). The results showed that n-hexane fraction exhibited acute oral toxicity with an LD50 of 3671.94 mg/kg. In the sub-chronic toxicity study, both dose levels caused no change in general health status, body weight, hematopoietic function, liver and kidney function, or renal structure. However, histopathological changes in the liver were observed at the higher dose, warranting further investigation. Both dose levels demonstrated a blood uric acid-lowering effect.

Article Details

References

1. Singh JA, Gaffo A. Gout epidemiology and comorbidities. Semin Arthritis Rheum. 2020; 50(3): 11-16. doi:10.1016/j.semarthrit.2020.04.008.
2. Mattiuzzi C, Lippi G. Recent updates on worldwide gout epidemiology. Clin Rheumatol. 2020; 39(4): 1061-1063. doi:10.1007/s10067-019-04868-9.
3. Võ Văn Chi. Từ Điển Cây Thuốc Việt Nam. NXB Y học; 2021: 472-473.
4. Wang SY, Zhao H, Xu H, et al. Kaempferia galanga L.: Progresses in Phytochemistry, Pharmacology, Toxicology and Ethnomedicinal Uses. Front Pharmacol. 2021; 12. doi:10.3389/fphar.2021.675350.
5. Kumar A. Phytochemistry, pharmacological activities and uses of traditional medicinal plant Kaempferia galanga L. - An overview. J Ethnopharmacol. 2020; 253: 112667.
6. World Health Organization. General guidelines for methodologies on research and evaluation of traditional medicine. 2000: 28-29.
7. Litchfield JT, Wilcoxon F. A simplified method of evaluating dose-effect experiments. J Pharmacol Exp Ther. 1949; 96(2): 99-113.
8. Etani R, Kataoka T, Kanzaki N, et al. Difference in the action mechanism of radon inhalation and radon hot spring water drinking in suppression of hyperuricemia in mice. J Radiat Res (Tokyo). 2016; 57(3): 250-257. doi:10.1093/jrr/rrw014.
9. Kanjanapothi D, Panthong A, Lertprasertsuke N, et al. Toxicity of crude rhizome extract of Kaempferia galanga L. (Proh Hom). J Ethnopharmacol. 2004; 90(2-3): 359-365. doi:10.1016/j.jep.2003.10.020.
10. Siska S, Bariroh T, Supandi S. Acute Toxicity of Ethyl Acetate Fraction of Kaempferia galanga L. Rhizome. IOP Conf Ser Earth Environ Sci. 2023; 1242:012007. doi:10.1088/1755-1315/1242/1/012007.
11. World Health Organization. WHO Recommended Classification of Pesticides by Hazard and Guidelines to Classification, 2019 Edition. 2020.
12. Bien TT, Trung NQ, Han NV. Extraction of Ethyl-p-methoxycinnamate from Kaempferia galanga L. VNU J Sci Med Pharm Sci. 2020; 36(4).
13. Nurmala S, Zahara I. Acute Toxicity Test Of P-Metoxicynamic Acid Synthetic From Ethyl P-Methysicynamate. J Kim MULAWARMAN. 2022; 19(2): 76-80.
14. Ridtitid W, Sae-wong C, Reanmongkol W, Wongnawa M. Antinociceptive activity of the methanolic extract of Kaempferia galanga Linn. in experimental animals. J Ethnopharmacol. 2008; 118(2): 225-230. doi:10.1016/j.jep.2008.04.002.
15. Samodra G, Febrina D. Anti-Inflammatory Effects of Kaempferia galanga L. Rhizome Extract in Carrageenan-Induced Female Rats. In: Atlantis Press; 2020: 13-17. doi:10.2991/ahsr.k.200204.004.
16. Amuamuta A, Plengsuriyakarn T, Na-Bangchang K. Anticholangiocarcinoma activity and toxicity of the Kaempferia galanga Linn. Rhizome ethanolic extract. BMC Complement Altern Med. 2017; 17(1): 213. doi:10.1186/s12906-017-1713-4.
17. Nguyễn Thế Khánh, Phạm Tử Dương. Xét Nghiệm Sử Dụng Trong Lâm Sàng. Nhà xuất bản Y học; 2015.
18. Tang DH, Ye YS, Wang CY, Li ZL, Zheng H, Ma KL. Potassium oxonate induces acute hyperuricemia in the tree shrew (tupaia belangeri chinensis). Exp Anim. 2017; 66(3): 209-216. doi:10.1538/expanim.16-0096.
19. Zhu JX, Wang Y, Kong LD, Yang C, Zhang X. Effects of Biota orientalis extract and its flavonoid constituents, quercetin and rutin on serum uric acid levels in oxonate-induced mice and xanthine dehydrogenase and xanthine oxidase activities in mouse liver. J Ethnopharmacol. 2004; 93(1): 133-140. doi:10.1016/j.jep.2004.03.037.
20. Mo SF, Zhou F, Lv YZ, Hu QH, Zhang DM, Kong LD. Hypouricemic Action of Selected Flavonoids in Mice: Structure–Activity Relationships. Biol Pharm Bull. 2007; 30(8): 1551-1556. doi:10.1248/bpb.30.1551.