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    Ethanolic leaf extract of Holoptelea integrifolia, Planch. decreases cisplatin-induced pica in rats

    Sharma Shrinivas1, Kale Ravindra1, Mante Aradhana1, Biyani Kailash1 Corresponding author

    1. 1Department of Pharmacology, Anuradha College of Pharmacy, Chikhli – 443201, Maharashtra, India.

    CORRESPONDENCE

    Sharma Shrinivas

    Department of Pharmacology, Anuradha College of Pharmacy, Chikhli – 443201, Maharashtra, India.

    shrinivas.sharma29@gmail.com

    Volume 4, Issue 16 · pp. 293–294 · PUBLISHED 2008 · DOI:

    View on Pharmacogn. Mag. original site ↗

    ABSTRACT

    Treatment of nausea/vomiting caused by cisplatin, a potent chemotherapeutic agent and one of the most emetogenic stimuli, requires a combination of different antiemetic drugs. In this study, we investigated the effects of ethanolic extract of leaves of Holoptelea integrifolia, Planch., an antioxidant herbal medicine, on cisplatin-induced nausea using a rat model. Rats react to emetic/nausea-producing stimuli, such as cisplatin, with altered feeding habits, manifested by pica or increased consumption of kaolin (a type of clay). We measured pica in rats to quantify cisplatin-induced nausea, and to evaluate the antinausea effect of pretreatment with ethanolic extract of Holoptelea integrifolia, Planch (HIE) given orally. Cisplatin at 3 mg/kg (i.p) induced significant pica accompanied by reduced food intake, suggesting the presence of nausea. Hence, this cisplatin dose was selected for testing the antinausea activity of HIE. Cisplatin-induced pica decreased significantly when animals were pretreated with HIE at doses of 250 mg/kg p.o and 500 mg/kg p.o (P<0.01). HIE pretreatment decreased cisplatin-induced kaolin intake in the rat model of simulated nausea, suggesting that HIE and its active constituent(s) may play a therapeutic role in chemotherapy-induced emesis.

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      Shrinivas, S., Ravindra, K., Aradhana, M., & Kailash, B. (2008). Ethanolic leaf extract of Holoptelea integrifolia, Planch. decreases cisplatin-induced pica in rats. Pharmacognosy Magazine, 4(16), 293–294.