Publication:
Effect of Nonsteroidal Anti-Inflammatory Drugs on Colorectal Distension-Induced Visceral Pain

dc.authorscopusid57188639438
dc.authorscopusid6701590971
dc.authorscopusid35561472800
dc.authorscopusid56146605500
dc.authorscopusid56386156400
dc.authorscopusid55623179000
dc.authorscopusid55623179000
dc.contributor.authorBaskin, V.
dc.contributor.authorBilge, S.S.
dc.contributor.authorBozkurt, A.
dc.contributor.authorAkyüz, B.
dc.contributor.authorAğrı, A.E.
dc.contributor.authorGüzel, H.
dc.contributor.authorİlkaya, F.
dc.date.accessioned2020-06-21T13:34:09Z
dc.date.available2020-06-21T13:34:09Z
dc.date.issued2016
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Baskin] Veysel, Department of Pharmacology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Bilge] Süleyman Sirri, Department of Pharmacology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Bozkurt] Ayhan, Department of Physiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Akyüz] Bahar, Department of Pharmacology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ağrı] Arzu Erdal, Department of Pharmacology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Güzel] Hasan, Department of Pharmacology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [İlkaya] Fatih, Department of Pharmacology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractObjectives: To investigate nonsteroidal anti-inflammatory drugs effectiveness in colorectal distension (CRD)-induced visceral pain model. Materials and Methods: Male Sprague-Dawley (250-300 g) rats were anesthetized with ketamine (50 mg/kg, intraperitoneally [i.p.]) and chlorpromazine (25 mg/kg, i.p.). Two bipolar Teflon-coated Ni/Cr wire electrodes (80-M diameter) were placed in the abdominal external oblique muscle for the recording of electromyography. Jugular vein catheter was placed for the administration of drugs. CRD method was applied to evaluate of visceral pain. All drugs (paracetamol, meloxicam, metamizole, and dexketoprofen) administered intravenously. Results: Paracetamol 200, 400, and 600 mg/kg did not change the visceromotor response (VMR) when compare with the control group. Meloxicam 2 and 4 mg/kg showed no effect but at doses of 6 mg/kg meloxicam significantly ([51.9 ± 6.4%] [P < 0.001]) decreased VMR compared with the control group. Metamizole 200 mg/kg did not change responses but dose of 400 and 600 mg/kg metamizole reduced VMR. Dexketoprofen 2 and 4 mg/kg did not cause a change in VMR but 6 mg/kg dose significantly reduced response compared with the control group ([43.9 ± 3.9%, 36.8 ± 2.8%, 34.8 ± 2.5%, 42.1 ± 4.8%, 40.7 ± 3.5%, 36.4 ± 2.7%, and 26.1 ± 2.2%]; from 10 min to 70 min, respectively, [P < 0.05]). Conclusion: Metamizole, dexketoprofen and meloxicam show antinociceptive effect with different duration of action on CRD-induced visceral pain model. This condition can be explained due to different chemical structures and different mechanisms which play a role in modulation of pain. © 2016 Indian Journal of Pharmacology Published by Wolters Kluwer - Medknow.en_US
dc.identifier.doi10.4103/0253-7613.178830
dc.identifier.endpage154en_US
dc.identifier.issn0253-7613
dc.identifier.issn1998-3751
dc.identifier.issue2en_US
dc.identifier.pmid27114637
dc.identifier.scopus2-s2.0-84962013982
dc.identifier.scopusqualityQ3
dc.identifier.startpage150en_US
dc.identifier.urihttps://doi.org/10.4103/0253-7613.178830
dc.identifier.volume48en_US
dc.identifier.wosWOS:000373479600008
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherMedknow Publications B9, Kanara Business Centre, off Link Road, Ghatkopar (E) Mumbai 400 075en_US
dc.relation.ispartofIndian Journal of Pharmacologyen_US
dc.relation.journalIndian Journal of Pharmacologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAnti-Inflammatoryen_US
dc.subjectRaten_US
dc.subjectVisceral Painen_US
dc.titleEffect of Nonsteroidal Anti-Inflammatory Drugs on Colorectal Distension-Induced Visceral Painen_US
dc.typeArticleen_US
dspace.entity.typePublication

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