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Diclofenac and dexamethasone modulate the effect of cannabidiol on the rat colon motility ex vivo
Due to the growing interest in the use of cannabinoids in supportive therapies, they are increasingly used together with anti-inflammatory drugs. Cannabinoids inhibit gastrointestinal motility, while steroidal and nonsteroidal anti-inflammatory drugs influence motility in other ways. The aim of the...
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Published in: | Journal of veterinary research 2023-06, Vol.67 (2), p.289-295 |
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description | Due to the growing interest in the use of cannabinoids in supportive therapies, they are increasingly used together with anti-inflammatory drugs. Cannabinoids inhibit gastrointestinal motility, while steroidal and nonsteroidal anti-inflammatory drugs influence motility in other ways. The aim of the research was to study the interactions between cannabidiol (CBD) and these two classes of anti-inflammatory drugs in the context of gastrointestinal motility. Dexamethasone (DEX) was selected as a steroidal drug and diclofenac (DCF) as a nonsteroidal counterpart.
The experiments were performed on isolated rat colon strips in isometric conditions. The contractile response to acetylcholine (ACh) (1 μM) was measured with no substance applied as a control value and was measured after application of CBD (80 μM), DEX (100 μM), DCF (100 μM), or a combination of these substances.
Cannabidiol strongly inhibited intestinal motility mediated by ACh application, DCF inhibited it non-significantly, while DEX intensified it. When CBD was co-administered with DEX, the combination inhibited intestinal motility non-significantly relative to the ACh-only control. Co-administration of CBD with DCF inhibited motility more than when these substances were administered separately.
Inhibition of the intestinal response to ACh is likely due to the synergistic effect of CBD and endogenous cannabinoids. Dexamethasone lessened the inhibitory effect of CBD, likely because of diminished availability of the arachidonic acid necessary for endogenous cannabinoid synthesis. However, diclofenac may increase endogenous cannabinoid synthesis, because of the greater availability of arachidonic acid caused by DCF blocking the cyclooxygenation pathway. |
doi_str_mv | 10.2478/jvetres-2023-0029 |
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The experiments were performed on isolated rat colon strips in isometric conditions. The contractile response to acetylcholine (ACh) (1 μM) was measured with no substance applied as a control value and was measured after application of CBD (80 μM), DEX (100 μM), DCF (100 μM), or a combination of these substances.
Cannabidiol strongly inhibited intestinal motility mediated by ACh application, DCF inhibited it non-significantly, while DEX intensified it. When CBD was co-administered with DEX, the combination inhibited intestinal motility non-significantly relative to the ACh-only control. Co-administration of CBD with DCF inhibited motility more than when these substances were administered separately.
Inhibition of the intestinal response to ACh is likely due to the synergistic effect of CBD and endogenous cannabinoids. Dexamethasone lessened the inhibitory effect of CBD, likely because of diminished availability of the arachidonic acid necessary for endogenous cannabinoid synthesis. However, diclofenac may increase endogenous cannabinoid synthesis, because of the greater availability of arachidonic acid caused by DCF blocking the cyclooxygenation pathway.</description><identifier>ISSN: 2450-7393</identifier><identifier>ISSN: 2450-8608</identifier><identifier>EISSN: 2450-8608</identifier><identifier>DOI: 10.2478/jvetres-2023-0029</identifier><identifier>PMID: 38143819</identifier><language>eng</language><publisher>Poland: Sciendo</publisher><subject>additive synergism ; Anti-inflammatory agents ; Arachidonic acid ; Cannabidiol ; Cannabinoids ; Colon ; Contractility ; Dexamethasone ; Diclofenac ; Gastric motility ; Inflammation ; Intestinal motility ; Intestine ; isolated rat colon strips ; Isometric ; Motility ; Nonsteroidal anti-inflammatory drugs ; Steroids</subject><ispartof>Journal of veterinary research, 2023-06, Vol.67 (2), p.289-295</ispartof><rights>2023 Magdalena Chłopecka et al., published by Sciendo.</rights><rights>2023. This work is published under http://creativecommons.org/licenses/by-nc-nd/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-5921eac8051534da3cd142b14f2c08f31d1424981ed69d1a45d512befd3f06443</citedby><cites>FETCH-LOGICAL-c494t-5921eac8051534da3cd142b14f2c08f31d1424981ed69d1a45d512befd3f06443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2826661671?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,36990,44566</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38143819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chłopecka, Magdalena</creatorcontrib><creatorcontrib>Kiraga, Łukasz</creatorcontrib><creatorcontrib>Crowley, Kijan</creatorcontrib><creatorcontrib>Jank, Michał</creatorcontrib><creatorcontrib>Latek, Urszula</creatorcontrib><creatorcontrib>Mendel, Marta</creatorcontrib><creatorcontrib>Karlik, Wojciech</creatorcontrib><title>Diclofenac and dexamethasone modulate the effect of cannabidiol on the rat colon motility ex vivo</title><title>Journal of veterinary research</title><addtitle>J Vet Res</addtitle><description>Due to the growing interest in the use of cannabinoids in supportive therapies, they are increasingly used together with anti-inflammatory drugs. Cannabinoids inhibit gastrointestinal motility, while steroidal and nonsteroidal anti-inflammatory drugs influence motility in other ways. The aim of the research was to study the interactions between cannabidiol (CBD) and these two classes of anti-inflammatory drugs in the context of gastrointestinal motility. Dexamethasone (DEX) was selected as a steroidal drug and diclofenac (DCF) as a nonsteroidal counterpart.
The experiments were performed on isolated rat colon strips in isometric conditions. The contractile response to acetylcholine (ACh) (1 μM) was measured with no substance applied as a control value and was measured after application of CBD (80 μM), DEX (100 μM), DCF (100 μM), or a combination of these substances.
Cannabidiol strongly inhibited intestinal motility mediated by ACh application, DCF inhibited it non-significantly, while DEX intensified it. When CBD was co-administered with DEX, the combination inhibited intestinal motility non-significantly relative to the ACh-only control. Co-administration of CBD with DCF inhibited motility more than when these substances were administered separately.
Inhibition of the intestinal response to ACh is likely due to the synergistic effect of CBD and endogenous cannabinoids. Dexamethasone lessened the inhibitory effect of CBD, likely because of diminished availability of the arachidonic acid necessary for endogenous cannabinoid synthesis. However, diclofenac may increase endogenous cannabinoid synthesis, because of the greater availability of arachidonic acid caused by DCF blocking the cyclooxygenation pathway.</description><subject>additive synergism</subject><subject>Anti-inflammatory agents</subject><subject>Arachidonic acid</subject><subject>Cannabidiol</subject><subject>Cannabinoids</subject><subject>Colon</subject><subject>Contractility</subject><subject>Dexamethasone</subject><subject>Diclofenac</subject><subject>Gastric motility</subject><subject>Inflammation</subject><subject>Intestinal motility</subject><subject>Intestine</subject><subject>isolated rat colon strips</subject><subject>Isometric</subject><subject>Motility</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Steroids</subject><issn>2450-7393</issn><issn>2450-8608</issn><issn>2450-8608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kU1v1DAQhiMEolXpD-CCLHHhEvD3xwmhQkulSlzgbHntcZtVEhfbWbr_Hqe7FAmJg-UZ-51nZvR23WuC31Ou9IftDmqG0lNMWY8xNc-6U8oF7rXE-vkxVsywk-68lC3GmCimDGEvuxOmCW_HnHbu8-DHFGF2Hrk5oAAPboJ650qaAU0pLKOrgOodIIgRfEUpIu_m2W2GMKQRpfnxM7uKfBpbNqU6jEPdI3hAu2GXXnUvohsLnB_vs-7H5ZfvF1_7m29X1xefbnrPDa-9MJSA8xoLIhgPjvlAON0QHqnHOjKyptxoAkGaQBwXQRC6gRhYxJJzdtZdH7ghua29z8Pk8t4mN9jHh5Rvrcu1bQs2ehawlMQEBZwJoTnnhAYjKQQqgDTWuwPrPqefC5Rqp6F4GEc3Q1qKpQYLpZmWqknf_iPdpiXPbVNLNZWti1QrkBxUPqdSMsSnAQm2q532aKdd7bSrna3mzZG8bCYITxV_zGuCjwfBLzdWyAFu87Jvwd8J_guXilJt2G-8J7Bu</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Chłopecka, Magdalena</creator><creator>Kiraga, Łukasz</creator><creator>Crowley, Kijan</creator><creator>Jank, Michał</creator><creator>Latek, Urszula</creator><creator>Mendel, Marta</creator><creator>Karlik, Wojciech</creator><general>Sciendo</general><general>De Gruyter Poland</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20230601</creationdate><title>Diclofenac and dexamethasone modulate the effect of cannabidiol on the rat colon motility ex vivo</title><author>Chłopecka, Magdalena ; 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Cannabinoids inhibit gastrointestinal motility, while steroidal and nonsteroidal anti-inflammatory drugs influence motility in other ways. The aim of the research was to study the interactions between cannabidiol (CBD) and these two classes of anti-inflammatory drugs in the context of gastrointestinal motility. Dexamethasone (DEX) was selected as a steroidal drug and diclofenac (DCF) as a nonsteroidal counterpart.
The experiments were performed on isolated rat colon strips in isometric conditions. The contractile response to acetylcholine (ACh) (1 μM) was measured with no substance applied as a control value and was measured after application of CBD (80 μM), DEX (100 μM), DCF (100 μM), or a combination of these substances.
Cannabidiol strongly inhibited intestinal motility mediated by ACh application, DCF inhibited it non-significantly, while DEX intensified it. When CBD was co-administered with DEX, the combination inhibited intestinal motility non-significantly relative to the ACh-only control. Co-administration of CBD with DCF inhibited motility more than when these substances were administered separately.
Inhibition of the intestinal response to ACh is likely due to the synergistic effect of CBD and endogenous cannabinoids. Dexamethasone lessened the inhibitory effect of CBD, likely because of diminished availability of the arachidonic acid necessary for endogenous cannabinoid synthesis. However, diclofenac may increase endogenous cannabinoid synthesis, because of the greater availability of arachidonic acid caused by DCF blocking the cyclooxygenation pathway.</abstract><cop>Poland</cop><pub>Sciendo</pub><pmid>38143819</pmid><doi>10.2478/jvetres-2023-0029</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | additive synergism Anti-inflammatory agents Arachidonic acid Cannabidiol Cannabinoids Colon Contractility Dexamethasone Diclofenac Gastric motility Inflammation Intestinal motility Intestine isolated rat colon strips Isometric Motility Nonsteroidal anti-inflammatory drugs Steroids |
title | Diclofenac and dexamethasone modulate the effect of cannabidiol on the rat colon motility ex vivo |
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