The functional link between microsomal prostaglandin E synthase-1 (mPGES-1) and peroxisome proliferator-activated receptor γ (PPARγ) in the onset of inflammation.
Pharmacol Res
; 157: 104807, 2020 07.
Article
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| MEDLINE
| ID: mdl-32330552
ABSTRACT
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.
Palabras clave
12-HETE, (CID:5283154); 13-HODE, (CID:6443013); 13-oxoODE, (CID:6446027); 15-HETE, (CID:5280724); 5-HETE, (CID:5353349); 8-HETE, (CID:5283154); 9-HODE, (CID:5282945); 9-oxoODE, (CID:9839084); Arachidonic acid (CID:444899); Inflammation; LTB4, (CID:5280492); LTC4, (CID:5280493); LTE4, (CID:5280879); PGD(2), (CID:448457); PGE(2); PGE(2), (CID:5280360); PGF(2α), (CID:5280363); PGI(2), (CID:5282411); PPARγ; TXA(2), (CID:5280497); mPGES-1
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Transducción de Señal
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Mediadores de Inflamación
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PPAR gamma
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Prostaglandina-E Sintasas
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Inflamación
Límite:
Animals
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Humans
Idioma:
En
Revista:
Pharmacol Res
Asunto de la revista:
FARMACOLOGIA
Año:
2020
Tipo del documento:
Article