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Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study

OBJECTIVE: To study the analgesic activity of ash of silver used in Indian system of medicine and to explore its safety. MATERIALS AND METHODS: Albino mice of either sex (20-30 gm) were used to investigate the role of ash of silver against noxious stimuli: thermal (Eddy's hot plate and analgesi...

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Autores principales: Inder, Deep, Rehan, Harmeet Singh, Bajaj, Vijay Kumar, Kumar, Pawan, Gupta, Navin, Singh, Jasbir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271539/
https://www.ncbi.nlm.nih.gov/pubmed/22345869
http://dx.doi.org/10.4103/0253-7613.91866
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author Inder, Deep
Rehan, Harmeet Singh
Bajaj, Vijay Kumar
Kumar, Pawan
Gupta, Navin
Singh, Jasbir
author_facet Inder, Deep
Rehan, Harmeet Singh
Bajaj, Vijay Kumar
Kumar, Pawan
Gupta, Navin
Singh, Jasbir
author_sort Inder, Deep
collection PubMed
description OBJECTIVE: To study the analgesic activity of ash of silver used in Indian system of medicine and to explore its safety. MATERIALS AND METHODS: Albino mice of either sex (20-30 gm) were used to investigate the role of ash of silver against noxious stimuli: thermal (Eddy's hot plate and analgesiometer), mechanical (tail clip), and chemical (0.6% acetic acid induced writhing). An effort was made to find nature and site of action of ash of silver following naloxone pre-treatment. Maximum tolerated dose (MTD) and lethal dosage 50 (LD50) were also studied along with toxicological aspects of ash of silver. RESULTS: Test drug (ash of silver) at a dose of 50 mg/kg p.o exhibited analgesic activity against thermal, mechanical, and chemical stimuli. Analgesic effects were compared with the standard drug, morphine, in thermal and mechanical noxious stimuli and to aspirin in chemical stimulus. Analgesic activity of the test drug was reduced following naloxone pre-treatment. MTD was found out to be greater than 1.5 g/kg p.o. LD50 was 2 g/kg p.o. Fraction of mice showed symptoms of argyria as explained by autopsy reports. CONCLUSION: Test drug exhibited moderate analgesic activity at 50 mg/kg p.o against all type of noxious stimuli, also suggesting a role of opioidergic system. The ash of silver was been found to be safe upto a dose of 1.5 g/kg p.o. in mice without any untoward toxicity. Further studies are required to explore the effect of ash of silver on pain mediators and excitatory neurotransmitters like glutamate, aspartate, or N-methyl-D-aspartic acid (NMDA).
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spelling pubmed-32715392012-02-15 Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study Inder, Deep Rehan, Harmeet Singh Bajaj, Vijay Kumar Kumar, Pawan Gupta, Navin Singh, Jasbir Indian J Pharmacol Research Article OBJECTIVE: To study the analgesic activity of ash of silver used in Indian system of medicine and to explore its safety. MATERIALS AND METHODS: Albino mice of either sex (20-30 gm) were used to investigate the role of ash of silver against noxious stimuli: thermal (Eddy's hot plate and analgesiometer), mechanical (tail clip), and chemical (0.6% acetic acid induced writhing). An effort was made to find nature and site of action of ash of silver following naloxone pre-treatment. Maximum tolerated dose (MTD) and lethal dosage 50 (LD50) were also studied along with toxicological aspects of ash of silver. RESULTS: Test drug (ash of silver) at a dose of 50 mg/kg p.o exhibited analgesic activity against thermal, mechanical, and chemical stimuli. Analgesic effects were compared with the standard drug, morphine, in thermal and mechanical noxious stimuli and to aspirin in chemical stimulus. Analgesic activity of the test drug was reduced following naloxone pre-treatment. MTD was found out to be greater than 1.5 g/kg p.o. LD50 was 2 g/kg p.o. Fraction of mice showed symptoms of argyria as explained by autopsy reports. CONCLUSION: Test drug exhibited moderate analgesic activity at 50 mg/kg p.o against all type of noxious stimuli, also suggesting a role of opioidergic system. The ash of silver was been found to be safe upto a dose of 1.5 g/kg p.o. in mice without any untoward toxicity. Further studies are required to explore the effect of ash of silver on pain mediators and excitatory neurotransmitters like glutamate, aspartate, or N-methyl-D-aspartic acid (NMDA). Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3271539/ /pubmed/22345869 http://dx.doi.org/10.4103/0253-7613.91866 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Inder, Deep
Rehan, Harmeet Singh
Bajaj, Vijay Kumar
Kumar, Pawan
Gupta, Navin
Singh, Jasbir
Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study
title Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study
title_full Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study
title_fullStr Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study
title_full_unstemmed Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study
title_short Analgesic activity and safety of ash of silver used in Indian system of medicine in mice: A reverse pharmacological study
title_sort analgesic activity and safety of ash of silver used in indian system of medicine in mice: a reverse pharmacological study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271539/
https://www.ncbi.nlm.nih.gov/pubmed/22345869
http://dx.doi.org/10.4103/0253-7613.91866
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