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The effects of peroxisome proliferator-activated receptor-gamma (PPARy) agonists on monocytic cell activation and endothelial function in diabetes

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posted on 2022-10-17, 16:17 authored by Maninder Ahluwalia

 

 Peroxisome Proliferator-activated Receptor-y (PPARy) is a ligand-activated transcription factor responsible for controlling genes involved in lipid and glucose metabolism. The thiazolidinediones (TZDs) are a class of synthetic PPARy ligands used as anti-hyperglycaemic agents in the treatment of type 2 diabetes. Recently it hasbeen shown that these agonists have additional anti-inflammatory properties beyondtheir metabolic functions. This study evaluated the role of TZDs in monocytic cell activation and endothelial function. Human monocytic cell lines and peripheralmonocytes were stimulated with various advanced glycation end-products (AGEs) tomimic the chronic inflammatory hlperglycaemic state typical of diabetes. Release ofcytokines, such as TNF-o, was determined as indicators of inflammation. Endothelialfunction was studied using rabbit aortic rings and primary human aortic cellsPPARy agonists, GW7845 and rosiglitazone, were obseryed to significantly reduceAGE-induced TNF-cr expression and release. It was demonstrated that this reduction was not completely dependent on PPARy transcriptional activity, as PPARyantagonists did not negate the actions of the agonist. The anti-inflammatory propertiesof PPARy agonists appeared to be (i). time-dependent, (ii) dose-dependent (iii) celltype specific and (iv) involve two distinct pathways: PPARy-dependent and PPART-independent. To elucidate the molecular mechanisms controlling the observed inhibition of TNF-cr release the effect of PPARy agonists on the activation of ERKand NF-rB was investigated. It was found that rosiglitazone reduced gBSA-inducedERK activity, although basal levels remained unaffected. Surprisingly, rosiglitazonedid not appear to modulate glycated BSA-stimulated NF-rB DNA binding activity.Conversely, rosiglitazone increase basal levels of NF-rB DNA binding activity but this did not result in NF-rB-dependent TNF-cr gene expression. It was postulated thatthis up regulation of NF-rB might interfere with signalling processes necessary forinfl ammatory responses.The effect of PPARy agonist on receptor of AGE (RAGE) expression was studied atboth transcriptional and translational level. PPARy agonist did not increase mRNA expression for RAGE, however the protein expression was increased in the presenceof the agonist after 241'rs, indicating that the regulation of RAGE by the agonist maybe at the post-transcriptional and./or post-translational levels.PPARy is also expressed in endothelium and vascular smooth muscle cells. Therefore this study also investigated the role of agonists on the vascular tone of the vessel wallin rabbit aortic rings. It was determined that GW7845 (>20¡tM) inhibited bothphenylephrine-induced contraction and acetylcholine-induced relaxation, whereas sodium nitroprusside (SNP)-induced relaxation was slightly improved. This enhancement of SNP induced relaxation may indicate an increased sensitivity ofVSMCs to the exogenous nitric oxide. GV/7845 did not influence the NO release and eNOS expression in human primary endothelial cells. It was postulated that these direct vasomodulatory effects involve cGMP signalling and calcium trafficking in smooth muscle cells.Taken together these findings indicate that PPARy agonists can reduce the inflammatory processes of monocytic cells. However the mechanisms involved appear to be influenced by both PPRE-dependent and PPRE-independent pathwaysand the net anti-inflammatory and anti-atherogenic clinical benefits of TZD therapy are likely to be governed by the interactions and balance between these two pathways. 

History

School

  • School of Sport and Health Sciences

Qualification level

  • Doctoral

Qualification name

  • PhD

Publication year

2005

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