دورية أكاديمية

Deformation-based Morphometry MRI Reveals Brain Structural Modifications in Living Mu Opioid Receptor Knockout Mice.

التفاصيل البيبلوغرافية
العنوان: Deformation-based Morphometry MRI Reveals Brain Structural Modifications in Living Mu Opioid Receptor Knockout Mice.
المؤلفون: Nasseef MT; Department of Psychiatry, School of Medicine, Douglas Hospital Research Center, McGill University, Montreal, QC, Canada., Devenyi GA; Department of Psychiatry, School of Medicine, Douglas Hospital Research Center, McGill University, Montreal, QC, Canada., Mechling AE; Engineering Science, Computer Science and Imaging Laboratory (ICube), Integrative Multimodal Imaging in Healthcare, CNRS, University of Strasbourg, Strasbourg, France.; Department of Radiology, Medical Physics, Faculty of Medicine, Medical Center University of Freiburg, University of Freiburg, Freiburg, Germany., Harsan LA; Engineering Science, Computer Science and Imaging Laboratory (ICube), Integrative Multimodal Imaging in Healthcare, CNRS, University of Strasbourg, Strasbourg, France.; Department of Radiology, Medical Physics, Faculty of Medicine, Medical Center University of Freiburg, University of Freiburg, Freiburg, Germany., Chakravarty MM; Department of Psychiatry, School of Medicine, Douglas Hospital Research Center, McGill University, Montreal, QC, Canada.; Department of Biological and Biomedical Engineering, McGill University, Montreal, QC, Canada., Kieffer BL; Department of Psychiatry, School of Medicine, Douglas Hospital Research Center, McGill University, Montreal, QC, Canada., Darcq E; Department of Psychiatry, School of Medicine, Douglas Hospital Research Center, McGill University, Montreal, QC, Canada.
المصدر: Frontiers in psychiatry [Front Psychiatry] 2018 Dec 03; Vol. 9, pp. 643. Date of Electronic Publication: 2018 Dec 03 (Print Publication: 2018).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101545006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-0640 (Print) Linking ISSN: 16640640 NLM ISO Abbreviation: Front Psychiatry Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Switzerland : Frontiers Research Foundation, 2010-
مستخلص: Mu opioid receptor (MOR) activation facilitates reward processing and reduces pain, and brain networks underlying these effects are under intense investigation. Mice lacking the MOR gene (MOR KO mice) show lower drug and social reward, enhanced pain sensitivity and altered emotional responses. Our previous neuroimaging analysis using Resting-state (Rs) functional Magnetic Resonance Imaging (fMRI) showed significant alterations of functional connectivity (FC) within reward/aversion networks in these mice, in agreement with their behavioral deficits. Here we further used a structural MRI approach to determine whether volumetric alterations also occur in MOR KO mice. We acquired anatomical images using a 7-Tesla MRI scanner and measured deformation-based morphometry (DBM) for each voxel in subjects from MOR KO and control groups. Our analysis shows marked anatomical differences in mutant animals. We observed both local volumetric contraction (striatum, nucleus accumbens, bed nucleus of the stria terminalis, hippocampus, hypothalamus and periacqueducal gray) and expansion (prefrontal cortex, amygdala, habenula, and periacqueducal gray) at voxel level. Volumetric modifications occurred mainly in MOR-enriched regions and across reward/aversion centers, consistent with our prior FC findings. Specifically, several regions with volume differences corresponded to components showing highest FC changes in our previous Rs-fMRI study, suggesting a possible function-structure relationship in MOR KO-related brain differences. In conclusion, both Rs-fMRI and volumetric MRI in live MOR KO mice concur to disclose functional and structural whole-brain level mechanisms that likely drive MOR-controlled behaviors in animals, and may translate to MOR-associated endophenotypes or disease in humans.
References: Nat Rev Neurosci. 2000 Dec;1(3):199-207. (PMID: 11257908)
Curr Opin Neurobiol. 2004 Jun;14(3):370-8. (PMID: 15194118)
Science. 2004 Jun 25;304(5679):1983-6. (PMID: 15218152)
Nat Rev Neurosci. 2008 Apr;9(4):314-20. (PMID: 18354400)
Brain Res. 2009 Oct 13;1293:61-75. (PMID: 19332030)
Mol Psychiatry. 2011 Aug;16(8):809-17. (PMID: 20479755)
Methods Mol Biol. 2011;711:349-61. (PMID: 21279611)
Nat Rev Neurosci. 2012 May 03;13(6):421-34. (PMID: 22551663)
Trends Neurosci. 2013 Mar;36(3):195-206. (PMID: 23219016)
J Neurosci. 2013 Jan 30;33(5):1797-803a. (PMID: 23365219)
J Pharmacol Exp Ther. 2013 Apr;345(1):41-51. (PMID: 23370795)
Prog Neurobiol. 2013 May;104:93-105. (PMID: 23499729)
PLoS One. 2013 Aug 13;8(8):e71027. (PMID: 23967148)
Neuropharmacology. 2014 Jan;76 Pt B:204-17. (PMID: 24035914)
Neuropsychopharmacology. 2014 Aug;39(9):2049-60. (PMID: 24619243)
Brain Struct Funct. 2015 Mar;220(2):677-702. (PMID: 24623156)
Br J Pharmacol. 2015 Jan;172(2):654-67. (PMID: 24913308)
Front Neuroinform. 2014 Jul 30;8:67. (PMID: 25126069)
Mol Psychiatry. 2015 Feb;20(1):118-25. (PMID: 25199916)
Annu Rev Med. 2016;67:433-51. (PMID: 26332001)
N Engl J Med. 2016 Jan 14;374(2):154-63. (PMID: 26760086)
Nat Neurosci. 2016 Feb;19(2):198-205. (PMID: 26814589)
Mol Psychiatry. 2016 Apr;21(4):450-63. (PMID: 26878891)
Proc Natl Acad Sci U S A. 2016 Oct 11;113(41):11603-11608. (PMID: 27671662)
Int J Neuropsychopharmacol. 2017 May 1;20(5):403-409. (PMID: 28031268)
Biol Psychiatry. 2017 May 1;81(9):778-788. (PMID: 28185645)
Nat Neurosci. 2017 Feb 23;20(3):314-326. (PMID: 28230838)
Neurosci Lett. 2017 Nov 30;:. (PMID: 29195911)
Mol Autism. 2018 Apr 10;9:24. (PMID: 29651330)
Neuroimage. 2018 Aug 1;176:226-238. (PMID: 29704613)
Annu Rev Neurosci. 2018 Jul 8;41:453-473. (PMID: 29852083)
Nat Rev Neurosci. 2018 Aug;19(8):499-514. (PMID: 29934561)
Front Psychiatry. 2018 Sep 19;9:441. (PMID: 30283366)
Prog Neurobiol. 1995 Aug;46(6):575-605. (PMID: 8545545)
Nature. 1996 Oct 31;383(6603):819-23. (PMID: 8893006)
معلومات مُعتمدة: P50 DA005010 United States DA NIDA NIH HHS
فهرسة مساهمة: Keywords: MRI; anatomical; in-vivo; mice; mu opioid receptor; structural change
تواريخ الأحداث: Date Created: 20181219 Latest Revision: 20200929
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC6287113
DOI: 10.3389/fpsyt.2018.00643
PMID: 30559685
قاعدة البيانات: MEDLINE
الوصف
تدمد:1664-0640
DOI:10.3389/fpsyt.2018.00643