%0 Journal Article %J Pharmacognosy Research %D 2016 %T In vivo Toxicity Studies on Gall Extracts of Terminalia chebula (Gaertn.) Retz. (Combretaceae) %A Ravi Shankara Birur Eshwarappa %A Y. L. Ramachandra %A Sundara Rajan Subaramaihha %A Sujan Ganapathy Pasura Subbaiah %A Richard Surendranath Austin %A Bhadrapura Lakkappa Dhananjaya %K Assay %K Brine shrimp assay %K Cytotoxic %K Drug %K Extract %K Galls %K Toxicity %X

The galls of Terminala chebula (Gaertn.) Retz. (Combretaceae) are used for the treatment of various diseases in folk medicine and has been found to posses anti‑inflammatory, anti‑bacterial, anti‑helmintic, anti‑tyrosinase, and anti‑aging activities. Considering the ethano‑botanical and diverse pharmacological applications of galls of T. chebula, in this study, we investigate the possible toxic effects of different gall extracts of T. chebula by Brine shrimp (Artemia salina) toxicity assay. The cytotoxicity test of leaf gall extracts (petroleum ether, chloroform, ethanol, and aqueous) of T. chebula was evaluated by Brine shrimp (A. salina) toxicity assay, which is based on the ability to kill laboratory cultured Artemia nauplii (animals eggs) and also total content of polyphenols, flavonoids with other qualitative phytochemical analysis of the extract were determined. It was observed that the petroleum ether extract was virtually nontoxic on the shrimps, and exhibited very low toxicity with LC50 value of 4356.76 μg/ml. Furthermore, the chloroform extract exhibited very low toxicity, giving LC50 value of 1462.2 μg/ml. On the other hand, the ethanol extract was very toxic to brine shrimps with LC50 value of 68.64 μg/ml. The ethanol extract had the highest total phenolic and flavonoid content of 136 ± 1.5 mg of gallic acid equivalent/g d.w and 113 ± 1.6 mg of quercetin equivalent/g d.w, respectively. The higher toxicity effect was positively correlated to the high content of total polyphenols/flavonoids in the extract. This significant lethality of different extracts to brine shrimp is an indicative of the presence of potent cytotoxic components which warrants further investigation.

%B Pharmacognosy Research %V 8 %P 199-201 %8 May 2016 %G eng %N 3 %9 Original Article %& 199 %R 10.4103/0974-8490.182914