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The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems
BACKGROUND: Pain is a complex mechanism which involves different systems, including the opioidergic and GABAergic systems. Due to the side effects of chemical analgesic agents, attention toward natural agents have been increased. Artemisinin is an herbal compound with widespread modern and tradition...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pain Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615442/ https://www.ncbi.nlm.nih.gov/pubmed/31257824 http://dx.doi.org/10.3344/kjp.2019.32.3.160 |
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author | Dehkordi, Faraz Mahdian Kaboutari, Jahangir Zendehdel, Morteza Javdani, Moosa |
author_facet | Dehkordi, Faraz Mahdian Kaboutari, Jahangir Zendehdel, Morteza Javdani, Moosa |
author_sort | Dehkordi, Faraz Mahdian |
collection | PubMed |
description | BACKGROUND: Pain is a complex mechanism which involves different systems, including the opioidergic and GABAergic systems. Due to the side effects of chemical analgesic agents, attention toward natural agents have been increased. Artemisinin is an herbal compound with widespread modern and traditional therapeutic indications, which its interaction with the GABAergic system and antinoniceptive effects on neuropathic pain have shown. Therefore, this study was designed to evaluate the antinociceptive effects of artemisinin during inflammatory pain and interaction with the GABAergic and opioidergic systems by using a writhing response test. METHODS: On the whole, 198 adult male albino mice were used in 4 experiments, including 9 groups (n = 6) each with three replicates, by intraperitoneal (i.p.) administration of artemisinin (2.5, 5, and 10 mg/kg), naloxone (2 mg/kg), bicuculline (2 mg/kg), saclofen (2 mg/kg), indomethacin (5 mg/kg), and ethanol (10 mL/kg). Writhing test responses were induced by i.p. injection of 10 mL/kg of 0.6% acetic acid, and the percentage of writhing inhibition was recorded. RESULTS: Results showed significant dose dependent anti-nociceptive effects from artemisinin which, at a 10 mg/kg dose, was statistically similar to indomethacin. Neither saclofen nor naloxone had antinociceptive effects and did not antagonize antinociceptive effects of artemisinin, whereas bicuculline significantly inhibited the antinocicptive effect of artemisinin. CONCLUSIONS: It seems that antinocicptive effects of artemisinin are mediated by GABA(A) receptors. |
format | Online Article Text |
id | pubmed-6615442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66154422019-07-22 The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems Dehkordi, Faraz Mahdian Kaboutari, Jahangir Zendehdel, Morteza Javdani, Moosa Korean J Pain Original Article BACKGROUND: Pain is a complex mechanism which involves different systems, including the opioidergic and GABAergic systems. Due to the side effects of chemical analgesic agents, attention toward natural agents have been increased. Artemisinin is an herbal compound with widespread modern and traditional therapeutic indications, which its interaction with the GABAergic system and antinoniceptive effects on neuropathic pain have shown. Therefore, this study was designed to evaluate the antinociceptive effects of artemisinin during inflammatory pain and interaction with the GABAergic and opioidergic systems by using a writhing response test. METHODS: On the whole, 198 adult male albino mice were used in 4 experiments, including 9 groups (n = 6) each with three replicates, by intraperitoneal (i.p.) administration of artemisinin (2.5, 5, and 10 mg/kg), naloxone (2 mg/kg), bicuculline (2 mg/kg), saclofen (2 mg/kg), indomethacin (5 mg/kg), and ethanol (10 mL/kg). Writhing test responses were induced by i.p. injection of 10 mL/kg of 0.6% acetic acid, and the percentage of writhing inhibition was recorded. RESULTS: Results showed significant dose dependent anti-nociceptive effects from artemisinin which, at a 10 mg/kg dose, was statistically similar to indomethacin. Neither saclofen nor naloxone had antinociceptive effects and did not antagonize antinociceptive effects of artemisinin, whereas bicuculline significantly inhibited the antinocicptive effect of artemisinin. CONCLUSIONS: It seems that antinocicptive effects of artemisinin are mediated by GABA(A) receptors. The Korean Pain Society 2019-07 2019-07-01 /pmc/articles/PMC6615442/ /pubmed/31257824 http://dx.doi.org/10.3344/kjp.2019.32.3.160 Text en © The Korean Pain Society, 2019 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Dehkordi, Faraz Mahdian Kaboutari, Jahangir Zendehdel, Morteza Javdani, Moosa The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems |
title | The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems |
title_full | The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems |
title_fullStr | The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems |
title_full_unstemmed | The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems |
title_short | The antinociceptive effect of artemisinin on the inflammatory pain and role of GABAergic and opioidergic systems |
title_sort | antinociceptive effect of artemisinin on the inflammatory pain and role of gabaergic and opioidergic systems |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615442/ https://www.ncbi.nlm.nih.gov/pubmed/31257824 http://dx.doi.org/10.3344/kjp.2019.32.3.160 |
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