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. 2012:2012:608284.
doi: 10.1155/2012/608284. Epub 2012 Mar 27.

Acute and 28-Day Subchronic Oral Toxicity of an Ethanol Extract of Zingiber zerumbet (L.) Smith in Rodents

Affiliations

Acute and 28-Day Subchronic Oral Toxicity of an Ethanol Extract of Zingiber zerumbet (L.) Smith in Rodents

Chia Ju Chang et al. Evid Based Complement Alternat Med. 2012.

Abstract

The objective of this study was to evaluate the acute and subacute toxicity (28 days) of the ethanol extract of Z. zerumbet rhizomes (EEZZ) via the oral route in Wistar rats of both sexes. In the acute toxicity study, Wistar rats were administered a single dose of 15 g kg(-1) of body weight by gavage, and were monitored for 14 days. EEZZ did not produce any toxic signs or deaths; the 50% lethal dose must be higher than 15 g kg(-1). In the subchronic toxicity study, EEZZ was administered by gavage at doses of 1000, 2000 and 3000 mg/kg daily for 4 weeks to Wistar rats. The subacute treatment with EEZZ did not alter either the body weight gain or the food and water consumption. The hematological and biochemical analysis did not show significant differences in any of the parameters examined in female or male groups. Necropsy and histopathological examination, did not reveal any remarkable and treatment related changes. A no-observed adverse-effect level for EEZZ is 3000 mg kg(-1) for rats under the conditions of this study. Hence, consumption of EEZZ for various medicinal purposes is safe.

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Figures

Figure 1
Figure 1
Photomicrographs of heart of control (a) and 1000, 2000, and 3000 mg kg−1 EEZZ-treated rat (b, c, d), kidney of control (e), and 1000, 2000, and 3000 mg/kg EEZZ-treated rat (f, g, h), and liver of control (i) and 1000, 2000, and 3000 mg/kg EEZZ-treated rat (j, k, l) stained with hematoxyline and eosin (100x).

References

    1. Afzal M, Al-Hadidi D, Menon M, Pesek J, Dhami MSI. Ginger: an ethnomedical, chemical and pharmacological review. Drug Metabolism and Drug Interactions. 2001;18(3-4):159–190. - PubMed
    1. White B. Ginger: an overview. American Family Physician. 2007;75(11):1689–1691. - PubMed
    1. Tushar, Basak S, Sarma GC, Rangan L. Ethnomedical uses of Zingiberaceous plants of Northeast India. Journal of Ethnopharmacology. 2010;132(1):286–296. - PubMed
    1. Nalawade SM, Sagare AP, Lee CY, Kao CL, Tsay HS. Studies on tissue culture of Chinese medicinal plant resources in Taiwan and their sustainable utilization. Botanical Bulletin of Academia Sinica. 2003;44(2):79–98.
    1. Sulaiman MR, Tengku Mohamad TAS, Shaik Mossadeq WM, et al. Antinociceptive activity of the essential oil of zingiber zerumbet. Planta Medica. 2010;76(2):107–112. - PubMed

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