Specific Metabolomics Adaptations Define a Differential Regional Vulnerability in the Adult Human Cerebral Cortex

被引:19
作者
Cabre, Rosanna [1 ]
Jove, Mariona [1 ]
Naudi, Alba [1 ]
Ayala, Victoria [1 ]
Pinol-Ripoll, Gerard [2 ]
Gil-Villar, Maria P. [2 ]
Dominguez-Gonzalez, Mayelin [3 ]
Obis, Elia [1 ]
Berdun, Rebeca [1 ]
Mota-Martorell, Natalia [1 ]
Portero-Otin, Manuel [1 ]
Ferrer, Isidre [3 ,4 ]
Pamplona, Reinald [1 ]
机构
[1] Univ Lleida, Dept Expt Med, Inst Res Biomed Lleida UdL IRBLleida, Lleida, Spain
[2] Hosp Santa Maria Lleida, Div Neurol, Lleida, Spain
[3] Univ Barcelona, Inst Neuropathol, Barcelona, Spain
[4] Inst Salud Carlos III ISCIII, Ctr Biomed Res Neurodegenerat Dis, Barcelona, Spain
来源
FRONTIERS IN MOLECULAR NEUROSCIENCE | 2016年 / 9卷
关键词
energy metabolism; mammalian target of rapamycin (mTOR); metabolomics; methionine cycle; mitochondrial stress; nucleotide metabolism; one-carbon metabolism; selective neuronal vulnerability; NEURODEGENERATIVE DISEASES; METHIONINE RESTRICTION; ALZHEIMERS-DISEASE; POSTMORTEM CHANGES; STRESS RESISTANCE; OXIDATIVE STRESS; RAT-BRAIN; EVOLUTION; AGE; METABOLISM;
D O I
10.3389/fnmol.2016.00138
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain neurons offer diverse responses to stresses and detrimental factors during development and aging, and as a result of both neurodegenerative and neuropsychiatric disorders. This multiplicity of responses can be ascribed to the great diversity among neuronal populations. Here we have determined the metabolomic profile of three healthy adult human brain regions-entorhinal cortex, hippocampus, and frontal cortex using mass spectrometry based technologies. Our results show the existence of a lessened energy demand, mitochondria' stress, and lower one-carbon metabolism (particularly restricted to the methionine cycle) specifically in frontal cortex. These findings, along with the better antioxidant capacity and lower mTOR signaling also seen in frontal cortex, suggest that this brain region is especially resistant to stress compared to the entorhinal cortex and hippocampus, which are more vulnerable regions. Globally, our results show the presence of specific metabolomics adaptations in three mature, healthy human brain regions, confirming the existence of cross-regional differences in cell vulnerability in the human cerebral cortex.
引用
收藏
页数:13
相关论文
共 32 条
  • [1] mTOR IN BRAIN PHYSIOLOGY AND PATHOLOGIES
    Bockaert, Joel
    Marin, Philippe
    [J]. PHYSIOLOGICAL REVIEWS, 2015, 95 (04) : 1157 - 1187
  • [2] Elevated gene expression levels distinguish human from non-human primate brains
    Cáceres, M
    Lachuer, J
    Zapala, MA
    Redmond, JC
    Kudo, L
    Geschwind, DH
    Lockhart, DJ
    Preuss, TM
    Barlow, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (22) : 13030 - 13035
  • [3] A quantitative GC-MS method for three major polyamines in postmortem brain cortex
    Chen, Gary G.
    Turecki, Gustavo
    Mamer, Orval A.
    [J]. JOURNAL OF MASS SPECTROMETRY, 2009, 44 (08): : 1203 - 1210
  • [4] Redox proteomic profiling of neuroketal-adducted proteins in human brain: Regional vulnerability at middle age increases in the elderly
    Dominguez, Mayelin
    de Oliveira, Eliandre
    Antonia Odena, Maria
    Portero, Manuel
    Pamplona, Reinald
    Ferrer, Isidro
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2016, 95 : 1 - 15
  • [5] Selection of controls in the study of human neurodegenerative diseases in old age
    Ferrer, I.
    [J]. JOURNAL OF NEURAL TRANSMISSION, 2015, 122 (07) : 941 - 947
  • [6] Brain banks: benefits, limitations and cautions concerning the use of post-mortem brain tissue for molecular studies
    Ferrer, Isidre
    Martinez, Anna
    Boluda, Susana
    Parchi, Piero
    Barrachina, Marta
    [J]. CELL AND TISSUE BANKING, 2008, 9 (03) : 181 - 194
  • [7] Rapid metabolic evolution in human prefrontal cortex
    Fu, Xing
    Giavalisco, Patrick
    Liu, Xiling
    Catchpole, Gareth
    Fu, Ning
    Ning, Zhi-Bin
    Guo, Song
    Yan, Zheng
    Somel, Mehmet
    Paeaebo, Svante
    Zeng, Rong
    Willmitzer, Lothar
    Khaitovich, Philipp
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (15) : 6181 - 6186
  • [8] TOR on the brain
    Garelick, Michael G.
    Kennedy, Brian K.
    [J]. EXPERIMENTAL GERONTOLOGY, 2011, 46 (2-3) : 155 - 163
  • [9] An anatomically comprehensive atlas of the adult human brain transcriptome
    Hawrylycz, Michael J.
    Lein, Ed S.
    Guillozet-Bongaarts, Angela L.
    Shen, Elaine H.
    Ng, Lydia
    Miller, Jeremy A.
    van de lagemaat, Louie N.
    Smith, Kimberly A.
    Ebbert, Amanda
    Riley, Zackery L.
    Abajian, Chris
    Beckmann, Christian F.
    Bernard, Amy
    Bertagnolli, Darren
    Boe, Andrew F.
    Cartagena, Preston M.
    Chakravarty, M. Mallar
    Chapin, Mike
    Chong, Jimmy
    Dalley, Rachel A.
    Daly, Barry David
    Dang, Chinh
    Datta, Suvro
    Dee, Nick
    Dolbeare, Tim A.
    Faber, Vance
    Feng, David
    Fowler, David R.
    Goldy, Jeff
    Gregor, Benjamin W.
    Haradon, Zeb
    Haynor, David R.
    Hohmann, John G.
    Horvath, Steve
    Howard, Robert E.
    Jeromin, Andreas
    Jochim, Jayson M.
    Kinnunen, Marty
    Lau, Christopher
    Lazarz, Evan T.
    Lee, Changkyu
    Lemon, Tracy A.
    Li, Ling
    Li, Yang
    Morris, John A.
    Overly, Caroline C.
    Parker, Patrick D.
    Parry, Sheana E.
    Reding, Melissa
    Royall, Joshua J.
    [J]. NATURE, 2012, 489 (7416) : 391 - 399
  • [10] Metabolomics of Human Brain Aging and Age-Related Neurodegenerative Diseases
    Jove, Mariona
    Portero-Otin, Manuel
    Naudi, Alba
    Ferrer, Isidre
    Pamplona, Reinald
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2014, 73 (07) : 640 - 657