» Articles » PMID: 11025170

Preliminary Studies on the Analgesic Activity of Latex of Calotropris Procera

Overview
Date 2000 Oct 12
PMID 11025170
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

In this study we have evaluated the analgesic activity of dry latex (DL) of Calotropis procera. A single oral dose of DL ranging from 165 to 830 mg/kg produced a significant dose dependent analgesic effect against acetic acid induced writhings. The effect of DL at a dose of 415 mg/kg was more pronounced as compared to a 100 mg/kg oral dose of aspirin. On the other hand DL (830 mg/kg) produced marginal analgesia in a tail-flick model which was comparable to aspirin. The analgesic effect of DL was delayed by 1 h by naloxone at a dose of 0. 5 mg/kg, i.p., which completely blocked the analgesic effect of morphine (10 mg/kg, i.p.). However, the effect of aspirin was not blocked by naloxone. The 830 mg/kg oral dose of DL did not produce toxic effects in mice and the LD(50) was found to be 3 g/kg.

Citing Articles

Ethnopharmacological Perspective for Treatment of Epilepsy: An Updated Review.

Kalra S, Bhatia S, Al Harrasi A, Mohan S, Sachdeva H, Sharma D Scientifica (Cairo). 2024; 2024:8052659.

PMID: 39610870 PMC: 11602530. DOI: 10.1155/2024/8052659.


Neuropharmacological Assessment of the Hydroethanolic Leaf Extract of (Ait). R. Br. (Apocynaceae) in Mice.

Obese E, Ameyaw E, Biney R, Adakudugu E, Woode E Scientifica (Cairo). 2021; 2021:5551380.

PMID: 34306795 PMC: 8270701. DOI: 10.1155/2021/5551380.


Anti-inflammatory latex proteins of the medicinal plant Calotropis procera: a promising alternative for oral mucositis treatment.

Ramos M, Freitas A, Leitao R, Costa D, Cerqueira G, Martins D Inflamm Res. 2020; 69(9):951-966.

PMID: 32488316 DOI: 10.1007/s00011-020-01365-7.


Cytotoxicity against tumor cell lines and anti-inflammatory properties of chitinases from Calotropis procera latex.

Viana C, Ramos M, Marinho Filho J, Costa Lotufo L, Figueiredo I, de Oliveira J Naunyn Schmiedebergs Arch Pharmacol. 2017; 390(10):1005-1013.

PMID: 28698893 DOI: 10.1007/s00210-017-1397-9.


Studies on Leaf Extracts as Inhibitors of Key Enzymes Linked to Diabetes Mellitus.

Kazeem M, Mayaki A, Ogungbe B, Ojekale A Iran J Pharm Res. 2017; 15(Suppl):37-44.

PMID: 28228802 PMC: 5242350.