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In-vivo Anti-inflammatory, Analgesic and Anti-pyretic Activities of Synthetic Indole Derivatives in Mice

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Abstract BackgroundVarious natural compounds have an aromatic heterocyclic compound “Indole” consists of bicyclic structure as a parent constituent in their composition that is used as an important precursor in many pharmaceutical industries and is widely accepted as a substance of fragrance to many novel compositions. In present study some synthetic indole derivatives are used to check their biological potential by performing anti-inflammatory, analgesic and anti-pyretic activity in albino mice.MethodsAlbino mice of either sex of reproductive age were used for each study and number of animals for each group in respective studies was kept 5. In anti-inflammatory activity, the Negative Control (NC) and Positive Control (PC) group animals were treated with normal saline and 10mg/kg of indomethacin respectively. The treated groups received the twenty four different synthetic chemicals, after 30 minutes of sub cutaneous injection of carrageenan. In analgesic activity, hot-plate method is used and for each group the latency period was recorded at zero moment of the provision of required dose and after 30, 60, 90, 120 and 180 minutes. In anti-pyretic activity, Pyrexia was induced by using Brewer's yeast method. Before any treatment and then after duration of 18 hours, the rectal temperatures were recorded. The animals, which showed the abnormally high rectal temperature, were selected for the further chemical investigation. SPSS.20 software is used for statistical analysis.ResultsThis study helped to screen out the most potent indole derivative 3a-II and 4a-II from the 24 synthetic indole derivatives which demonstrated the best anti-inflammatory, analgesic and anti-pyretic potential as compared to remaining ones. ConclusionThe above findings indicate that only two chemicals 3a-II (N-(4´-Chlorophenyl) (4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)methanimine) and 4a-II (N-(4´-Methylphenyl) (4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)methanimine) have given the desired effects like anti-inflammatory, analgesic and anti-pyretic.
Title: In-vivo Anti-inflammatory, Analgesic and Anti-pyretic Activities of Synthetic Indole Derivatives in Mice
Description:
Abstract BackgroundVarious natural compounds have an aromatic heterocyclic compound “Indole” consists of bicyclic structure as a parent constituent in their composition that is used as an important precursor in many pharmaceutical industries and is widely accepted as a substance of fragrance to many novel compositions.
In present study some synthetic indole derivatives are used to check their biological potential by performing anti-inflammatory, analgesic and anti-pyretic activity in albino mice.
MethodsAlbino mice of either sex of reproductive age were used for each study and number of animals for each group in respective studies was kept 5.
In anti-inflammatory activity, the Negative Control (NC) and Positive Control (PC) group animals were treated with normal saline and 10mg/kg of indomethacin respectively.
The treated groups received the twenty four different synthetic chemicals, after 30 minutes of sub cutaneous injection of carrageenan.
In analgesic activity, hot-plate method is used and for each group the latency period was recorded at zero moment of the provision of required dose and after 30, 60, 90, 120 and 180 minutes.
In anti-pyretic activity, Pyrexia was induced by using Brewer's yeast method.
Before any treatment and then after duration of 18 hours, the rectal temperatures were recorded.
The animals, which showed the abnormally high rectal temperature, were selected for the further chemical investigation.
SPSS.
20 software is used for statistical analysis.
ResultsThis study helped to screen out the most potent indole derivative 3a-II and 4a-II from the 24 synthetic indole derivatives which demonstrated the best anti-inflammatory, analgesic and anti-pyretic potential as compared to remaining ones.
ConclusionThe above findings indicate that only two chemicals 3a-II (N-(4´-Chlorophenyl) (4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)methanimine) and 4a-II (N-(4´-Methylphenyl) (4,6-dimethoxy-2,3-diphenyl-1H-indol-7-yl)methanimine) have given the desired effects like anti-inflammatory, analgesic and anti-pyretic.

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