The functional link between microsomal prostaglandin E synthase-1 (mPGES-1) and peroxisome proliferator-activated receptor γ (PPARγ) in the onset of inflammation
Autor: | Asif J. Iqbal, Gian Marco Casillo, Nicola Mascolo, Francesco Maione, Federica Raucci |
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Přispěvatelé: | Maione, Francesco, Casillo, Gian Marco, Raucci, Federica, Iqbal, Asif J, Mascolo, Nicola |
Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
TXA(2) (CID:5280497) PPARγ medicine.medical_treatment 13-HODE (CID:6443013) Anti-Inflammatory Agents Peroxisome proliferator-activated receptor 12-HETE (CID:5283154) Pharmacology chemistry.chemical_compound 0302 clinical medicine PGE(2) Receptor PGD(2) (CID:448457) Prostaglandin-E Synthases chemistry.chemical_classification PGF(2α) (CID:5280363) Peroxisome 9-oxoODE (CID:9839084) 030220 oncology & carcinogenesis Arachidonic acid (CID:444899) lipids (amino acids peptides and proteins) 9-HODE (CID:5282945) Inflammation Mediators medicine.symptom 15-HETE (CID:5280724) LTB4 (CID:5280492) Signal Transduction Prostaglandin E 13-oxoODE (CID:6446027) Prostaglandin Inflammation 5-HETE (CID:5353349) 8-HETE (CID:5283154) 03 medical and health sciences LTE4 (CID:5280879) medicine Animals Humans PGI(2) (CID:5282411) PGE(2) (CID:5280360) Lipid signaling mPGES-1 PPAR gamma 030104 developmental biology Enzyme LTC4 (CID:5280493) chemistry |
Popis: | Many years have elapsed since the discovery of anti-inflammatories as effective therapeutics for the treatment of inflammatory-related diseases, but we are still uncovering their various mechanisms of action. Recent biochemical and pharmacological studies have shown that in different tissues and cell types lipid mediators from thearachidonic acid cascade, play a crucial role in the initiation and resolution of inflammation by shifting from pro-inflammatory prostaglandin (PG)E2 to anti-inflammatory PGD2 and PGJ2. Considering that until now very little is known about the biological effects evoked by microsomal prostaglandin E synthase-1 (mPGES-1) and contextually by peroxisome proliferator-activated receptor γ (PPARγ) modulation (key enzymes involved in PGE2 and PGD2/PGJ2metabolism), in this opinion paper we sought to define the coordinate functional regulation between these two enzymes at the "crossroads of phlogistic pathway" involved in the induction and resolution of inflammation. |
Databáze: | OpenAIRE |
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