L-Kynurenine/Aryl Hydrocarbon Receptor Pathway Mediates Brain Damage After Experimental Stroke

@article{Cuartero2014LKynurenineArylHR,
  title={L-Kynurenine/Aryl Hydrocarbon Receptor Pathway Mediates Brain Damage After Experimental Stroke},
  author={Mar{\'i}a I Cuartero and Iv{\'a}n Ballesteros and Juan de la Parra and Andrew Harkin and A. Abautret-daly and Eoin Sherwin and Pedro M. Fern{\'a}ndez-Salguero and {\'A}ngel L. Corb{\'i} and Ignacio Lizasoain and Mar{\'i}a Angeles Moro},
  journal={Circulation},
  year={2014},
  volume={130},
  pages={2040–2051}
}
Background— 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… 
Aryl hydrocarbon receptor modulates stroke-induced astrogliosis and neurogenesis in the adult mouse brain
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Selective Aryl Hydrocarbon Receptor Modulator 3,3′-Diindolylmethane Impairs AhR and ARNT Signaling and Protects Mouse Neuronal Cells Against Hypoxia
TLDR
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TLDR
It is found that AhR protein levels decrease with age in this brain structure, strongly suggesting a link between AhR and aging.
Aryl Hydrocarbon Receptor: A New Player of Pathogenesis and Therapy in Cardiovascular Diseases
TLDR
The structure, distribution, and ligands of AhR and the AhR signaling pathway are described and the impact ofAhR on cardiovascular physiology is reviewed and the potential contribution of Ahr as a new potential factor in the targeted treatment of cardiovascular diseases is discussed.
The Aryl Hydrocarbon Receptor and the Nervous System
TLDR
This review presents how the AhR regulates neural functions in both invertebrates and vertebrates as deduced mainly from the effects of xenobiotics, and some of the molecular mechanisms triggered by the well-known AhR ligand, 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), which impact on neuronal proliferation, differentiation, and survival.
Uremic Toxic Blood-Brain Barrier Disruption Mediated by AhR Activation Leads to Cognitive Impairment during Experimental Renal Dysfunction.
TLDR
Cognitive impairment in CKD rats and an increase of blood-brain barrier permeability associated with renal dysfunction are found and a significant correlation between 99mTc-DTPA content in brain and both the discrimination index in the novel object recognition test and indoxyl sulfate concentrations in serum is found.
The Role of AhR in the Hallmarks of Brain Aging: Friend and Foe
TLDR
An overview of the impact of AhR pathways on various aging hallmarks in the brain and the implications for AhR signaling as a mechanism in regulating aging-related diseases of the brain is provided.
The aryl hydrocarbon receptor promotes aging phenotypes across species
TLDR
The data from human subjects suggest that AhR expression levels could serve as an additional, new predictor of vessel aging, as well as regulators of cell growth, differentiation and apoptosis.
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TLDR
Granule neuroblasts are direct targets for developmental AhR-mediated TCDD neurotoxicity and TCDd exposure may disrupt granule cell neurogenesis, according to a concentration-dependent manner.
An Interaction between Kynurenine and the Aryl Hydrocarbon Receptor Can Generate Regulatory T Cells
TLDR
It is demonstrated that kynurenine, the first breakdown product in the IDO-dependent tryptophan degradation pathway, activates the aryl hydrocarbon receptor and this activation leads to AHR-dependent Treg generation, which shed light on the relationship of IDO to the generation of Tregs.
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TLDR
Evidence is provided for a previously unidentified pathophysiological function of the AHR that is constitutively generated by human tumours via tryptophan-2,3-dioxygenase (TDO), a liver- and neuron-derived Trp-degrading enzyme not yet implicated in cancer biology.
Transcriptional Factor Aryl Hydrocarbon Receptor (Ahr) Controls Cardiovascular and Respiratory Functions by Regulating the Expression of the Vav3 Proto-oncogene*
TLDR
It is shown that Ahr is important for Vav3 expression in kidney, lung, heart, liver, and brainstem regions, and the presence of sympathoexcitation and new cardiorespiratory defects in Ahr−/− mice is revealed.
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TLDR
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TLDR
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Neuronal activity enhances aryl hydrocarbon receptor‐mediated gene expression and dioxin neurotoxicity in cortical neurons
TLDR
Activation of AhR by the selective agonist 2,3,7,8‐tetrachlorodibenzo‐p‐dioxin induced dioxin‐responsive gene expression and calcium entry, which were attenuated by AhR small interfering RNA, the NMDA receptor channel blocker MK801, and the action potential blocker tetrodotoxin (TTX).
CH223191 is a ligand-selective antagonist of the Ah (Dioxin) receptor.
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A novel ligand-selective antagonist is identified that preferentially inhibits the ability of some classes of AhR agonists, but not others, to bind to and/or activate the AhR and AhR signal transduction.
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