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BrainSci. 2016,6, 16
Table3.BodyWeight.
Group %Difference
Con/Con(n=10) +1.0%˘1.4%†
Con/EtOH(n=11) ´6.6%˘2.1%*
EtOH/EtOH(n=8) ´8.7%˘1.7%*
Adlibitum (n=4) +25.2%˘1.7%
*p<0.05vs.Con/Conandad libitum; † p<0.05vs. ad libitumonly.
3.2.OX-42 Immunoreactivity IncreasedbyEtOHExposure
OX-42expressionwasexaminedtodeterminewhethermicrogliawere furtherordifferentially
activated following a secondbinge exposure. OX-42positive cellswere apparent in all treatment
groups,which is consistentwith its constitutive expression inall typesofmicroglia [59]; however,
therewas avisiblydistinct increase in immunoreactivity in ethanol treated animals accompanied
byanapparentmorphological change. Microglia inethanol animals appeared tohave shorterbut
thickenedramificationscomparedwiththecontrolanimals(Figures1B,Cand2B,C).One-wayANOVAs
indicatedasignificanteffectoftreatmentintheCA1(F(3,29)=16.81,p<0.0001),CA2/3(F(3,29)=18.34,
p<0.0001), andDG(F(3,29)=14.43,p<0.0001)fields (Figure1), aswell as in theentorhinal cortex
(F(3,28)=19.01,p<0.0001) (Figure2).Asexpectedbasedonpreviousdata [22],post-hocTukey’s tests
indicatedasignificant increase inOX-42density inall ethanol treatedgroups inall subregionsof the
hippocampuscomparedwith thecontrolorad libitumgroups. Importantly, theEtOH/EtOHgroup
showedgreater immunoreactivity thanCon/EtOHinall regionsanalyzedexcept theDG.Moreover,
nodifference inOX-42wasobservedbetweenad libitumanimalsandtheCon/Congroup.Correlations
betweenbingemodelparameters (intoxicationbehavior,doseperday, totaldose,BEC,percentweight
loss)andOX-42 immunoreactivitywererunwithintheEtOH/EtOHandCon/EtOHgroup,butno
significantcorrelationswereobserved(Table4).
Figure1.PotentiatedMicroglialActivationintheHippocampusbyRepeatedEthanolExposure.OX-42
(CD11b/c) is upregulated in thehippocampusof ethanol-exposed rats as shown in representative
photomicrographsof the (A–C)hippocampaldentategyrus for (B)Con/EtOHand(C)EtOH/EtOH
groupscomparedto (A) controls.AnalysisofOX-42 immunoreactivity indicatedthat theEtOH/EtOH
grouphadsignificantlymorestaining than theCon/EtOHgroup in the: (D) cornuamonis1 (CA1)
and(E) cornuamonis2/3 (CA2/3) regionsbutnot the (F)dentategyrus (DG).Dataexpressedasa
percentageofad libitumcontrol (notshown). Imageswere takenat50ˆmagnificationwith insetsat
600ˆmagnification. Scalebar=200μm;inset30μm. *p<0.05comparedtoad libitumandCon/Con
groups;#p<0.05comparedtoCon/EtOH.
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Buch Advances in Neuroimmunology"
Advances in Neuroimmunology
- Titel
- Advances in Neuroimmunology
- Autor
- Donna Gruol
- Herausgeber
- MDPI
- Ort
- Basel
- Datum
- 2017
- Sprache
- englisch
- Lizenz
- CC BY-NC-ND 4.0
- ISBN
- 978-3-03842-571-7
- Abmessungen
- 17.0 x 24.0 cm
- Seiten
- 164
- Schlagwörter
- neuroimmune, cytokine, chemokine, glia cel, neuron, neurodevelopment, neuroimmune disorder, neurologic disease, psychiatric disease, neuronal injury
- Kategorie
- Medizin