The endogenous ligands for the leukotriene, lipoxin and oxoeicosanoid receptors are bioactive products produced by the action of the lipoxygenase family of enzymes, as depicted in Fig 1 [2,4]. The formation of leukotrienes by 5-lipoxygenase from acid arachidonic acid starts with the epoxide intermediate LTA4, which serves as precursor for leukotriene synthesis (Fig. 1). Subsequent metabolism through the enzyme LTA4 hydrolase leads to the formation of LTB4, which is the ligand for the BLT receptors. Alternatively, the conjugation of LTA4 with glutathione yields the cysteinyl-leukotrienes (Fig 1) acting on CysLT receptors (Fig 1). The leukotriene receptor class also includes receptors for other mediators derived from arachidonic acid through lipoxygenase metabolism, namely the ALX/FPR2 receptor for lipoxin A4 [10], and the OXE receptor for 5-Oxo-ETE [1].

Leukotriene receptors [Interactive Resource] / M. Bäck, T. Shimizu, T. Yokomizo, G.E. Rovati, C.N. Serhan, S.E. Dahlén, J. Drazen, J.F. Evans, M. Nakamura, W. Powell, J. Rokach, N. Chiang, C. Brink, D.W.P. Hay. - [s.l], 2013.

Leukotriene receptors

G.E. Rovati;
2013

Abstract

The endogenous ligands for the leukotriene, lipoxin and oxoeicosanoid receptors are bioactive products produced by the action of the lipoxygenase family of enzymes, as depicted in Fig 1 [2,4]. The formation of leukotrienes by 5-lipoxygenase from acid arachidonic acid starts with the epoxide intermediate LTA4, which serves as precursor for leukotriene synthesis (Fig. 1). Subsequent metabolism through the enzyme LTA4 hydrolase leads to the formation of LTB4, which is the ligand for the BLT receptors. Alternatively, the conjugation of LTA4 with glutathione yields the cysteinyl-leukotrienes (Fig 1) acting on CysLT receptors (Fig 1). The leukotriene receptor class also includes receptors for other mediators derived from arachidonic acid through lipoxygenase metabolism, namely the ALX/FPR2 receptor for lipoxin A4 [10], and the OXE receptor for 5-Oxo-ETE [1].
2013
Leukotriene ; GPCR
Settore BIO/14 - Farmacologia
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/230536
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact