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Sub-chronic oral toxicity evaluation of herbo-metallic formulation Arshakuthar rasa in rats
Monika Kumari1, Shatrughna Madhukar Bajad2, Shripad Rajendra Kshirsagar2
1Applied Biology Division, CSIR-Indian Institute of Chemical Technology, Tarnaka, Hyderabad, 500 007, Telangana, India.
Ethnopharmacological Relevance:
Arshakuthar rasa (AR) is a mercury based Ayurvedic herbo-metallic formulation. The concerns are being raised about the probable toxicity of mercury after prolonged use of AR. Hence, there is need for a long-term repeated in vivo toxicity study. The study will provide data with scientific evidence to enable safe use of the drug. Moreover, lack of toxicity study with AR incited us to perform sub-chronic study on rats.
Aim Of The Study:
The aim of the study is to generate data by performing a sub-chronic study to assess the toxicity of AR after its prolonged oral intake.
Materials And Methods:
The female and male rats were administered with 30 (low), 300 (medium) and 600 mg/kg BW/day (high) dose of AR for 90 consecutive days. The body weight, feed consumption and water intake were monitored weekly. On 91st day, blood was collected from retro-orbital plexus of rats and then sacrificed to harvest the vital organs for biochemical, haematological, histopathological, genotoxicity along with the expression study of oxidative stress related genes and the biodistribution of elements in the blood.
Results:
Significant alterations in serum biochemical parameters were observed at the medium and high doses. The histopathological changes were in corroboration with biochemical changes at high dose in liver. There was no detectable level of mercury in blood, less to moderate biochemical changes, no haematological changes, moderate regulation of stress-related genes, and low genotoxicity. These results indicated that AR can be considered as moderately toxic above 600 mg/kg BW and mildly toxic at 300 mg/kg BW.
Conclusions:
It may be interpreted that AR may not induce grave toxic response in human after long-duration of oral administration at therapeutic doses.
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