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Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study
Intestinal hypomotility cause health risks and economic losses and is considered as an important digestive disorder that efforts to find prokinetic drugs can solve this major problem. This study investigated the effects of Zingiber officinale aqueous extract (ZOAE) on caecal smooth muscle contractio...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Urmia University Press
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073806/ https://www.ncbi.nlm.nih.gov/pubmed/37033778 http://dx.doi.org/10.30466/vrf.2022.545837.3338 |
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author | Aminfar, Hadi Maham, Masoud Dalir-Naghadeh, Bahram |
author_facet | Aminfar, Hadi Maham, Masoud Dalir-Naghadeh, Bahram |
author_sort | Aminfar, Hadi |
collection | PubMed |
description | Intestinal hypomotility cause health risks and economic losses and is considered as an important digestive disorder that efforts to find prokinetic drugs can solve this major problem. This study investigated the effects of Zingiber officinale aqueous extract (ZOAE) on caecal smooth muscle contractions in healthy cows. To perform in vitro tests, cecum strips connected to the organ bath. Ginger aqueous extract caused concentration-dependent contraction in caecal smooth muscle with an effective threshold concentration of 6.00 mg L(-1). The strongest contraction was caused at a concentration of 100 mg L(-1) with an average contraction of 141%. To evaluate the possible mechanisms underlying the contractile effect on cecum strips, atropine, 1,1-dimethyl-4-diphenylacetoxypiperidinium iodide (4-DAMP) and verapamil completely inhibited aqueous extract induced smooth muscle contractions, while addition of hexamethonium had no effect on the contraction process. The lack of reduction of contractions caused by the extract in the presence of hexamethonium indicates that presence of acetylcholine-like constituents independent of nicotinic receptors. The inhibitory properties of atropine and 4-DAMP indicate that at least part of the prokinetic effect of the extract is due to stimulating the muscarinic receptors, especially M3 receptors. Also, verapamil inhibitory function proves that the extract acting by L-type calcium channels. The results suggest that the ZOAE has a potential prokinetic effect which may provide a pharmacological base to its medicinal or prophylactic use in caecal motility disorders. |
format | Online Article Text |
id | pubmed-10073806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Urmia University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100738062023-04-06 Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study Aminfar, Hadi Maham, Masoud Dalir-Naghadeh, Bahram Vet Res Forum Original Article Intestinal hypomotility cause health risks and economic losses and is considered as an important digestive disorder that efforts to find prokinetic drugs can solve this major problem. This study investigated the effects of Zingiber officinale aqueous extract (ZOAE) on caecal smooth muscle contractions in healthy cows. To perform in vitro tests, cecum strips connected to the organ bath. Ginger aqueous extract caused concentration-dependent contraction in caecal smooth muscle with an effective threshold concentration of 6.00 mg L(-1). The strongest contraction was caused at a concentration of 100 mg L(-1) with an average contraction of 141%. To evaluate the possible mechanisms underlying the contractile effect on cecum strips, atropine, 1,1-dimethyl-4-diphenylacetoxypiperidinium iodide (4-DAMP) and verapamil completely inhibited aqueous extract induced smooth muscle contractions, while addition of hexamethonium had no effect on the contraction process. The lack of reduction of contractions caused by the extract in the presence of hexamethonium indicates that presence of acetylcholine-like constituents independent of nicotinic receptors. The inhibitory properties of atropine and 4-DAMP indicate that at least part of the prokinetic effect of the extract is due to stimulating the muscarinic receptors, especially M3 receptors. Also, verapamil inhibitory function proves that the extract acting by L-type calcium channels. The results suggest that the ZOAE has a potential prokinetic effect which may provide a pharmacological base to its medicinal or prophylactic use in caecal motility disorders. Urmia University Press 2023 2023-03-15 /pmc/articles/PMC10073806/ /pubmed/37033778 http://dx.doi.org/10.30466/vrf.2022.545837.3338 Text en © 2023 Urmia University. All rights reserved https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.https://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Original Article Aminfar, Hadi Maham, Masoud Dalir-Naghadeh, Bahram Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
title | Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
title_full | Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
title_fullStr | Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
title_full_unstemmed | Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
title_short | Effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
title_sort | effects of aqueous ginger extract on smooth muscle contraction in bovine cecum: in vitro study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073806/ https://www.ncbi.nlm.nih.gov/pubmed/37033778 http://dx.doi.org/10.30466/vrf.2022.545837.3338 |
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