000 nab a22 7a 4500
999 _c16376
_d16376
003 PC16376
005 20210625062821.0
008 210429b xxu||||| |||| 00| 0 eng d
040 _cH12O
041 _aeng
100 _92408
_aCuartero, María Isabel
_eInstituto de Investigación i+12
100 _92407
_aBallesteros, Iván
_eInstituto de Investigación i+12
100 _92410
_aLizasoain, Ignacio
_eInstituto de Investigación i+12
100 _92826
_aDe la Parra, Juan
_eInstituto de Investigación i+12
245 0 0 _a L-kynurenine/aryl hydrocarbon receptor pathway mediates brain damage after experimental stroke.
_h[artículo]
260 _bCiruculation,
_c2014
300 _a130(23):2040-51.
500 _aFormato Vancouver: Cuartero MI, Ballesteros I, de la Parra J, Harkin AL, Abautret-Daly A, Sherwin et al. L-kynurenine/aryl hydrocarbon receptor pathway mediates brain damage after experimental stroke. Circulation. 2014 Dec 2;130(23):2040-51.
501 _aPMID: 25359166
504 _aContiene 44 referencias
520 _aBackground: Aryl hydrocarbon receptor (AhR) is a transcription factor that belongs to the basic helix-loop-helix PAS (Per-Arnt-Sim homology domain) family known to mediate the toxic and carcinogenic effects of xenobiotics. Interestingly, AhR is widely expressed in the central nervous system, but its physiological and pathological roles are still unclear. Methods and results: To define the role of AhR in stroke, we used middle cerebral artery occlusion in mice and oxygen-glucose deprivation in rat cortical neurons. The results presented here show that the ischemic insult increases total and nuclear AhR levels and AhR transcriptional activity in neurons in vivo and in vitro. We also show that AhR has a causal role in acute ischemic damage because pharmacological or genetic loss-of-function approaches result in neuroprotection. Inhibition of cAMP response element-binding protein-dependent signaling may participate in the deleterious actions of AhR. Finally, we have also found that L-kynurenine, a tryptophan metabolite with AhR agonistic properties, is an endogenous ligand that mediates AhR activation in the brain after middle cerebral artery occlusion. Conclusions: Our data demonstrate that an L-kynurenine/AhR pathway mediates acute brain damage after stroke and open new possibilities for the diagnosis and treatment of this pathology.
710 _9625
_aInstituto de Investigación imas12
856 _uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/1/pc16376.pdf
_ySolicitar documento
942 _2ddc
_cART
_n0