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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/13274
Title: Assessment of acute, sub-acute, chronic and genotoxicity of polyherbal formulation DCD-684 in mice
Authors: Roome, Talat
Qasim, Maha
Aziz, Sabahat
Farooq, Ahsana Dar
Razzaq, Anam
Ali, Syed Farooq
Keywords: Digas colic drops
polyherbal formulation
chronic toxicity
genotoxicity
micronucleus assay
proinflammatory mRNA expression
Issue Date: 20-Jul-2021
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciecnes, University of Karachi
Abstract: Digas colic drops (DCD-684) a polyherbal formulation containing Carum carvi, Foeniculum vulgare, Mentha arvensis, Mentha piperita and Zingiber officinale is widely used in Pakistan against gastrointestinal ailments including infantile colic. The DCD-684 (0.03-3ml/kg.bw) administered orally in acute (7-days) and sub-acute toxicity (14-days) tests, displayed neither mortality nor toxicological changes in physical, behavioral, biochemical and histopathological parameters. In chronic study (90-days), DCD-684 (0.3-12 ml/kg.bw) also revealed no changes. However, at 18 and 36 ml/kg.bw, liver demonstrated mild inflammation correlating with raised aspartate transaminase (AST), alkaline phosphatase (ALP) and alpha fetoprotein (AFP) levels. Increased levels of urea and inflamed renal parenchyma indicated mild nephro-toxicity with high alanine aminotransferase (ALT) at 36 ml/kg.bw. The LD50 of DCD-684 in mice was 27.5 ml/kg.bw. In hepatocytes at 36 ml/kg.bw, elevated mRNA expression of pro-inflammatory chemokines and cytokines were evident. DCD-684 neither damaged DNA nor induced cytotoxicity in micronucleus assay. In conclusion, polyherbal DCD-684 caused neither hepatic, renal, genotoxicity nor any undesirable effect in mice. Higher doses administered for 90 days showed mild toxic effects with no sign of necrosis, fibrosis or genotoxicity. Thus, in mice DCD-684 demonstrated a wide margin of safety to be used for the relief of infantile colic.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/13274
ISSN: 1011-601X
Appears in Collections:Issue No.4 (Supplementary)

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