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In Vivo Anti-inflammatory, Analgesic, and Sedative Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon)
[Image: see text] Anti-inflammatory, analgesic, and sedative medicine is used with numerous side effects, including peptic ulcer, headache, addiction, and other complications. In this regard, discovery research is undergoing a process to discover effective, safe, and economical drugs with no side ef...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047645/ https://www.ncbi.nlm.nih.gov/pubmed/33869965 http://dx.doi.org/10.1021/acsomega.1c00537 |
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author | Bawazeer, Saud Rauf, Abdur |
author_facet | Bawazeer, Saud Rauf, Abdur |
author_sort | Bawazeer, Saud |
collection | PubMed |
description | [Image: see text] Anti-inflammatory, analgesic, and sedative medicine is used with numerous side effects, including peptic ulcer, headache, addiction, and other complications. In this regard, discovery research is undergoing a process to discover effective, safe, and economical drugs with no side effects. The aim of this study was to assess chloroform extracts and isolated compounds for anti-inflammatory, analgesic, and sedative activities in animal models. The anti-inflammatory potential was measured by using the carrageenan-induced and histamine-induced paw edema procedure, while the analgesic potential was determined using a hot plate analgesiometer. The sedative effect was observed in an animal model for screening of the locomotor effect of the extract and isolated compound 1. Our data exhibited that the extract and compound 1 attenuated carrageenan-induced and histamine-induced paw edema (93.98 and 89.54%, respectively). Furthermore, compound 1 attenuated biphasic edema associated with histamine and prostaglandins. The chloroform extract showed a moderate analgesic effect; however, compound 1 showed a significant analgesic potential (p < 0.001) by increasing the latency time of the animals in the thermally induced algesia model. Compound 1 exhibited a significant sedative effect and dose-dependent analgesic activity. It is concluded that the chloroform extract and compound 1 showed remarkable anti-inflammatory, analgesic, and sedative activities. This research work strongly rationalizes the folkloric usage of Diospyros kaki in the treatment of inflammation, pain, and insomnia. |
format | Online Article Text |
id | pubmed-8047645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80476452021-04-16 In Vivo Anti-inflammatory, Analgesic, and Sedative Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) Bawazeer, Saud Rauf, Abdur ACS Omega [Image: see text] Anti-inflammatory, analgesic, and sedative medicine is used with numerous side effects, including peptic ulcer, headache, addiction, and other complications. In this regard, discovery research is undergoing a process to discover effective, safe, and economical drugs with no side effects. The aim of this study was to assess chloroform extracts and isolated compounds for anti-inflammatory, analgesic, and sedative activities in animal models. The anti-inflammatory potential was measured by using the carrageenan-induced and histamine-induced paw edema procedure, while the analgesic potential was determined using a hot plate analgesiometer. The sedative effect was observed in an animal model for screening of the locomotor effect of the extract and isolated compound 1. Our data exhibited that the extract and compound 1 attenuated carrageenan-induced and histamine-induced paw edema (93.98 and 89.54%, respectively). Furthermore, compound 1 attenuated biphasic edema associated with histamine and prostaglandins. The chloroform extract showed a moderate analgesic effect; however, compound 1 showed a significant analgesic potential (p < 0.001) by increasing the latency time of the animals in the thermally induced algesia model. Compound 1 exhibited a significant sedative effect and dose-dependent analgesic activity. It is concluded that the chloroform extract and compound 1 showed remarkable anti-inflammatory, analgesic, and sedative activities. This research work strongly rationalizes the folkloric usage of Diospyros kaki in the treatment of inflammation, pain, and insomnia. American Chemical Society 2021-04-01 /pmc/articles/PMC8047645/ /pubmed/33869965 http://dx.doi.org/10.1021/acsomega.1c00537 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Bawazeer, Saud Rauf, Abdur In Vivo Anti-inflammatory, Analgesic, and Sedative Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) |
title | In Vivo Anti-inflammatory, Analgesic, and Sedative
Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) |
title_full | In Vivo Anti-inflammatory, Analgesic, and Sedative
Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) |
title_fullStr | In Vivo Anti-inflammatory, Analgesic, and Sedative
Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) |
title_full_unstemmed | In Vivo Anti-inflammatory, Analgesic, and Sedative
Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) |
title_short | In Vivo Anti-inflammatory, Analgesic, and Sedative
Studies of the Extract and Naphthoquinone Isolated from Diospyros kaki (Persimmon) |
title_sort | in vivo anti-inflammatory, analgesic, and sedative
studies of the extract and naphthoquinone isolated from diospyros kaki (persimmon) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047645/ https://www.ncbi.nlm.nih.gov/pubmed/33869965 http://dx.doi.org/10.1021/acsomega.1c00537 |
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