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Antifibrotic potential of a selective Cox-2 inhibitor (celecoxib) and a synthetic PPAR gamma ligand (pioglitazone) on liver fibrosis in rats

Thesis

Last updated: 06 Feb 2023

Subjects

-

Tags

Pharmacology

Advisors

Galal, Ahmad H. , El-Battrawi, Fattma A. , El-Alqami, Essam F.

Authors

Abdel-Lattif, Nuha Samir

Accessioned

2017-07-12 06:40:11

Available

2017-07-12 06:40:11

type

M.Sc. Thesis

Abstract

Chronic liver injury, independent of the cause, is generally associated with the accumulation of matrix proteins, a process referred to as fibrosis. Over the last decade liver fibrosis is no longer viewed as either passive or permanent but as a dynamic process and potential therapies continue to be identified. Hepatic stellate cells (HSCs) play a critical role in the fibrogenesis of liver, so they are the target cells of antifibrotic therapy. Activated HSCs but not quiescent HSCs express cyclooxygenase-2 (COX-2). Peroxisome proliferator activated receptor gamma (PPAR gamma) has been shown to be expressed in quiescent HSCs in the normal liver and decreased PPARγ expression has been associated with activation of HSC. The present study was designed to investigate the possible prophylactic and therapeutic effects of a selective COX-2 inhibitor (celecoxib) and a synthetic PPAR gamma ligand (pioglitazone) on liver fibrosis induced by thioacetamide (TAA) in rats.

Issued

1 Jan 2011

DOI

http://dx.doi.org/10.21473/iknito-space/35139

Details

Type

Thesis

Created At

28 Jan 2023