Implication of the Kallikrein-Kinin system in neurological disorders: Quest for potential biomarkers and mechanisms

dc.contributor.authorNokkari, Amaly
dc.contributor.authorAbou-El-Hassan, Hadi
dc.contributor.authorMechref, Yehia S.
dc.contributor.authorMondello, Stefania
dc.contributor.authorKindy, Mark Stephen
dc.contributor.authorJaffa, Ayad A.
dc.contributor.authorKobeissy, Firas H.
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:59Z
dc.date.available2025-01-24T11:37:59Z
dc.date.issued2018
dc.description.abstractNeurological disorders represent major health concerns in terms of comorbidity and mortality worldwide. Despite a tremendous increase in our understanding of the pathophysiological processes involved in disease progression and prevention, the accumulated knowledge so far resulted in relatively moderate translational benefits in terms of therapeutic interventions and enhanced clinical outcomes. Aiming at specific neural molecular pathways, different strategies have been geared to target the development and progression of such disorders. The kallikrein-kinin system (KKS) is among the most delineated candidate systems due to its ubiquitous roles mediating several of the pathophysiological features of these neurological disorders as well as being implicated in regulating various brain functions. Several experimental KKS models revealed that the inhibition or stimulation of the two receptors of the KKS system (B1R and B2R) can exhibit neuroprotective and/or adverse pathological outcomes. This updated review provides background details of the KKS components and their functions in different neurological disorders including temporal lobe epilepsy, traumatic brain injury, stroke, spinal cord injury, Alzheimer's disease, multiple sclerosis and glioma. Finally, this work will highlight the putative roles of the KKS components as potential neurotherapeutic targets and provide future perspectives on the possibility of translating these findings into potential clinical biomarkers in neurological disease. © 2018 Elsevier Ltd
dc.identifier.doihttps://doi.org/10.1016/j.pneurobio.2018.01.003
dc.identifier.eid2-s2.0-85040911893
dc.identifier.pmid29355711
dc.identifier.urihttp://hdl.handle.net/10938/28944
dc.language.isoen
dc.publisherElsevier Ltd
dc.relation.ispartofProgress in Neurobiology
dc.sourceScopus
dc.subjectBiomarkers
dc.subjectBradykinin
dc.subjectBrain injury
dc.subjectKallikrein-kinin system
dc.subjectKinin
dc.subjectNeurological disorders
dc.subjectAnimals
dc.subjectHumans
dc.subjectKinins
dc.subjectNervous system diseases
dc.subjectReceptors, bradykinin
dc.subjectSignal transduction
dc.subjectBiological marker
dc.subjectKinin 1 receptor
dc.subjectKinin 2 receptor
dc.subjectReceptor
dc.subjectUnclassified drug
dc.subjectBradykinin receptor
dc.subjectAlzheimer disease
dc.subjectCerebrovascular accident
dc.subjectGlioma
dc.subjectHuman
dc.subjectKallikrein kinin system
dc.subjectMultiple sclerosis
dc.subjectNervous system inflammation
dc.subjectNeurologic disease
dc.subjectNeuropathology
dc.subjectNonhuman
dc.subjectPriority journal
dc.subjectProtein function
dc.subjectProtein targeting
dc.subjectReview
dc.subjectSpinal cord injury
dc.subjectSystems biology
dc.subjectTemporal lobe epilepsy
dc.subjectTraumatic brain injury
dc.subjectAnimal
dc.subjectMetabolism
dc.subjectPhysiology
dc.titleImplication of the Kallikrein-Kinin system in neurological disorders: Quest for potential biomarkers and mechanisms
dc.typeReview

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