Abstract

Zingiber cassumunar Roxb. has been used for traditional medicine, but few studies have described its potential toxicity. In this study, the acute and chronic oral toxicity of Z. cassumunar extract granules were evaluated in Sprague-Dawley rats. The extract at a single dose of 5000 mg/kg body weight did not produce treatment related signs of toxicity or mortality in any of the animals tested during the 14-day observation period. However, a decrease in body weights was observed in treated males (P < 0.05). The weights of lung and kidney of treated females were increased (P < 0.05). Treated males were increased in spleen and epididymis weights (P < 0.05). In repeated dose 270-day oral toxicity study, the administration of the extracts at concentrations of 0.3, 3, 30, 11.25, 112.5, and 1,125 mg/kg body weight/day revealed no-treatment toxicity. Although certain endpoints among those monitored (i.e., organ weight, hematological parameters, and clinical chemistry) exhibited statistically significant effects, none was adverse. Gross and histological observations revealed no toxicity. Our findings suggest that the Z. cassumunar extract granules are well tolerated for both single and chronic administration. The oral no-observed-adverse-effect level (NOAEL) for the extract was 1,125 mg/kg body weight/day for males and females.

Highlights

  • Zingiber cassumunar Roxb. (Family Zingiberaceae) known locally as “Phlai” in Thai is a perennial herb, consisting of underground rhizomes

  • The separation achieved with thin layer chromatography (TLC) in the present study was consistent with that reported in Thai Herbal Pharmacopoeia [21]

  • Lethal effects were not observed within 14 days after rats were fed with a single dose of Z. cassumunar extract granules (5000 mg/kg bw)

Read more

Summary

Introduction

Zingiber cassumunar Roxb. (Family Zingiberaceae) known locally as “Phlai” in Thai is a perennial herb, consisting of underground rhizomes. Phytochemical investigations of Z. cassumunar rhizomes have revealed the presence of phenylbutanoids, cyclohexene derivatives, naphthoquinones, vanillin, vanillic acid, veratric acid [2,3,4,5], terpenoids, βsitosterol, and curcuminoids [6,7,8,9]. Several isolated compounds have been found to possess anti-inflammatory activity, for example, two phenylbutanoids, (E)-4-(3󸀠, 4󸀠-dimethoxyphenyl) but-3-en-1-ol; compound D (1) and (E)-4-(3󸀠,4󸀠-dimethoxyphenyl) but-3-en-1-yl acetate; compound B󸀠 (2); three cyclohexene derivatives, namely, cis3-(3󸀠, 4󸀠-dimethoxyphenyl)-4-[(E)-3󸀠󸀠󸀠,4󸀠󸀠󸀠-dimethoxystyryl] cyclohex-1-ene; compound B (3), cis-3-(3󸀠,4󸀠-dimethoxyphenyl)-4-[(E)-2󸀠󸀠󸀠,4󸀠󸀠󸀠,5󸀠󸀠󸀠-trimethoxystyryl] cyclohex-1-ene; International Scholarly Research Notices compound C󸀠 (4) and cis-3-(2󸀠,4󸀠,5󸀠-trimethoxyphenyl)4-[(E)-2󸀠󸀠󸀠,4󸀠󸀠󸀠,5󸀠󸀠󸀠-trimethoxystyryl] cyclohex-1-ene; compound C (5) and curcumin (6) [12,13,14,15,16]. Smooth muscle relaxant, uterine relaxant, and antihistaminic activity of compound D [17, 18] and antioxidant activity of curcumin [16] have been reported

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call