grant

Neurobehavioral and pathophysiological effects of traumatic brain injury in spontaneously hypertensive rats

Organization UNIVERSITY OF PITTSBURGH AT PITTSBURGHLocation PITTSBURGH, UNITED STATESPosted 16 Apr 2024Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY202514 year old14 years of age21+ years oldAdultAdult HumanAdult femalesAdult womenAffectAgeAmerican Heart AssociationAmmon HornAnimal ModelAnimal Models and Related StudiesAnxietyApoplexyAreaArteriesAstrocytesAstrocytusAstrogliaAstroproteinAttentionBed SoresBedsoreBehavior assessmentBehavioral AssayBlood flowBody TissuesBrain TraumaBrain Vascular AccidentBrain regionCardiac ChronotropismCardiac infarctionCardiovascular DiseasesCerebral StrokeCerebrovascular ApoplexyCerebrovascular StrokeCessation of lifeChildhoodChildhood InjuryChronicCirculatory CollapseClinicClinicalCognitiveCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalCommon Rat StrainsComplexContralateralCornu AmmonisCorpus StriatumCorpus striatum structureDeathDevelopmentDiagnosisDifferences between sexesDiffers between sexesDisturbance in cognitionED visitER visitEmergency care visitEmergency department visitEmergency hospital visitEmergency room visitEmotionalEquilibriumExhibitsFemaleFemales in adulthoodFundingFutureGFA-ProteinGFAPGlial Fibrillary Acid ProteinGlial Fibrillary Acidic ProteinGlial Intermediate Filament ProteinHeart RateHippocampusHistologicHistologicallyHumanHypertensionImmunohistochemistryImmunohistochemistry Cell/TissueImmunohistochemistry Staining MethodImpaired cognitionImpairmentImpulsivityInbred SHR RatsInbred WKY RatsInjuryIpsilateralKnowledgeLearningLesionLocationMedicalMedical RehabilitationMenstrual cycleModalityModern ManMotorMuscleMuscle TissueMyocardial InfarctMyocardial InfarctionNational Institutes of HealthNeurocognitiveNeurologicNeurologicalOutcomeParietalPatientsPersonsPhasePhenotypePhysiologicPhysiologicalPopulationPre-Clinical ModelPreclinical ModelsPressure SorePressure UlcerQOLQuality of lifeR-Series Research ProjectsR01 MechanismR01 ProgramRatRats MammalsRattusReaction TimeRehabilitationRehabilitation therapyResearchResearch GrantsResearch Project GrantsResearch ProjectsResponse RTResponse TimeRotarod AssayRotarod MethodRotarod Performance TestRotarod TestSHR RatsSchoolsSeveritiesSex DifferencesSexual differencesShockSpontaneously Hypertensive RatsStriate BodyStriatumStrokeSurvivorsSymptomsTBI recoveryTestingThalamic structureThalamusTherapeuticTimeTissuesTraumatic Brain InjuryTraumatic Brain Injury recoveryUnited StatesUnited States Department of Veterans AffairsUnited States National Institutes of HealthUnited States Veterans AdministrationVascular Hypertensive DiseaseVascular Hypertensive DisorderVeterans AdministrationVeterans AffairsWKY RatsWalkingWistar Kyoto RatsWomanWomen in adulthoodadult youthadulthoodage 14 yearsagesastrocytic gliabalancebalance functionbehavioral assessmentbench bed sidebench bedsidebench to bed sidebench to bedsidebench to clinicbench to clinical practicebrain attackcardiac infarctcardiovascular disordercerebral vascular accidentcerebrovascular accidentcirculatory shockclinical relevanceclinically relevantco-morbidco-morbiditycognitive dysfunctioncognitive losscomorbiditycontrolled cortical impactcoronary attackcoronary infarctcoronary infarctiondecrease disabilitydecrease in disabilitydecubitus ulcerdesigndesigningdevelopmentaldisability reductionexperimentexperimental researchexperimental studyexperimentsflexibilityflexiblefourteen year oldfourteen years of ageheart attackheart infarctheart infarctionhigh blood pressurehippocampalhyperpiesiahyperpiesishypertensivehypertensive diseasehypertensive disorderinjuredinjured childinjured childreninjuriesinjury in childrenlessen disabilitymaleminimize disabilitymitigate disabilitymodel of animalmuscularneural inflammationneurobehavioralneuroinflammationneuroinflammatoryneuronal survivalnormotensivenovelpediatricpediatric injurypre-clinicalpre-clinical researchpre-clinical studypreclinicalpreclinical researchpreclinical studyprematureprematuritypressure injurypsychomotor reaction timepsychosocialrecovery after TBIrecovery after traumatic brain injuryreduction in disabilityrehab therapyrehabilitativerehabilitative therapyresponsesex based differencessex-dependent differencessex-related differencessex-specific differencesshocksslow disabilityspontaneous hypertensive ratstriatalstrokedstrokessustained attentionthalamictraumatic brain damageyoung adultyoung adult ageyoung adulthood
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Full Description

ABSTRACT
Approximately 2.8 million people sustain a traumatic brain injury (TBI) yearly in the United States, with over

500,000 emergency room visits being attributed to childhood-acquired brain trauma (<14 years of age).

Survivors often endure long-term cognitive and emotional disabilities that reduce quality of life and the ability to

return to school/workforce. Current and past research has largely overlooked complex attention impairments

post-TBI, especially in conjunction with overlapping clinical comorbidities, which may exacerbate injury effects.

We aim to remedy the paucity of studies examining comorbidities of TBI by exploring how hypertension/high

blood pressure, a common underlying condition, can affect TBI-related neurological, physiological, and

cognitive impairments. An estimated 50% of the adult population is diagnosed with hypertension, which can

lead to heart attacks, blocked or damaged arteries, reduced blood flow to the muscles, strokes, and premature

death. Thus, there is a critical need to investigate preclinical models of TBI that are also affected by

hypertension (i.e., hypertensive rats) to better characterize neurological, physiological, and cognitive

impairments, in an effort to enhance bench-to-bedside translatability by more closely reflecting the existing

clinical landscape. This study explores the effects of TBI on Spontaneously Hypertensive Rats (SHR), a widely

used animal model of hypertension, by administering a battery of behavioral assays across different modalities,

such as motor coordination/balance, higher-order sustained and flexible attention, and anxiety-like symptoms.

Moreover, it is important to determine whether being subjected to TBI during pediatric (i.e., prior to

developing stable hypertension at 16 weeks of age) or adult age (i.e., after hypertension onset) alters

physiological, emotional, and cognitive outcomes long term. The aims are designed to 1) determine

interactions of moderate parietal TBI and age-at-impact (pediatric versus adulthood) on motor function (rotarod

test), sustained attention and impulsivity (3-choice serial reaction time task), cognitive flexibility (attentional set-

shifting test), and anxiety-like responses (elevated plus-maze test, shock-probe defensive burying) in SHR

versus normotensive male and female adult rats, and 2) evaluate TBI-induced and sex-related differences in

histological assessments of lesion volumes, neuronal survival, and neuroinflammation markers in SHR versus

normotensive rats. Studies will be conducted in both male and normal cycling female rats, an approach that is

clinically relevant. Women represent up to 45% of the TBI cases, thus evaluating normal cycling female rats

parallels the real world, where injuries occur independent of menstrual cycles. The findings from this R21

Exploratory/Developmental Research Grant will serve as proof-of-concept for significant future funding support

from the National Institutes of Health, the American Heart Association, or the US Department of Veterans

Affairs, as dissecting the impact that underlying conditions such as hypertension may have on TBI preclinically

is critical to further developing clinically-relevant therapies.

Grant Number: 5R21NS137253-02
NIH Institute/Center: NIH

Principal Investigator: Corina Bondi

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