In vitro and in vivo modulation of LPS and carrageenan-induced expression of inflammatory genes by amitriptyline

(2017) In vitro and in vivo modulation of LPS and carrageenan-induced expression of inflammatory genes by amitriptyline. Journal of Pharmacy & Pharmacognosy Research. pp. 144-155. ISSN 0719-4250

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Abstract

Context: Amitriptyline, a tricyclic antidepressant is used for the management of psychological disorders and various types of pain. In the previous work, it is founded that amitriptyline inhibited the migration of polymorphonuclear (PMN) into the site of inflammation. Aims: To evaluate the effect of amitriptyline on the expression of some inflammatory mediators such as intercellular adhesion molecule (ICAM-1), vascular cell adhesion molecule (VCAM-1), cyclooxygenase 2 (COX2) and inducible nitric oxide synthase (iNOS). Methods: An in vitro model system of LPS-stimulated human endothelial cells and U-937 macrophages and also in vivo model of carrageenan-induced paw edema in rat were used. The expression of inflammatory mediator genes was determined by qRT-Real-time PCR. In endothelial cells, soluble forms of ICAM-1 and VCAM-1 were quantified by ELISA. Results: The expression of ICAM-1, VCAM-1, COX2, iNOS, sICAM-1 and sVCAM-1 significantly decreased by amitriptyline. The finding of this study also confirmed that intraperitoneal (i.p.) injection of amitriptyline inhibited carrageenan-induced inflammation in rat paw edema. Conclusions: The results of the present study provide further evidence for the anti-inflammatory effect of amitriptyline. This effect appears to be mediated by down-regulation of inflammatory genes.

Item Type: Article
Keywords: amitriptyline cyclooxygenase 2 inducible nitric oxide synthase inflammation intercellular adhesion molecule-1 vascular cell adhesion molecule-1 induced paw edema human endothelial-cells adhesion molecules interferon-gamma nitric-oxide signaling pathway major depression epithelial-cells antidepressants fluoxetine
Divisions: Cardiovascular Research Institute > Applied Physiology Research Center
Faculty of Medicine > Department of Basic Science > Department of Physiology
Faculty of Pharmacy and Pharmaceutical Sciences > Department of Toxicology and Pharmacology
Page Range: pp. 144-155
Journal or Publication Title: Journal of Pharmacy & Pharmacognosy Research
Journal Index: ISI
Volume: 5
Number: 3
ISSN: 0719-4250
Depositing User: مهندس مهدی شریفی
URI: http://eprints.mui.ac.ir/id/eprint/587

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