-
Je něco špatně v tomto záznamu ?
Microbiome: A Potential Component in the Origin of Mental Disorders
GB. Stefano, R. Ptacek, J. Raboch, RM. Kream,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, přehledy
NLK
PubMed Central
od 2011
Europe PubMed Central
od 2011
Open Access Digital Library
od 2011-01-01
Medline Complete (EBSCOhost)
od 2017-01-01
PubMed
28636585
DOI
10.12659/msm.905425
Knihovny.cz E-zdroje
- MeSH
- antibakteriální látky farmakologie terapeutické užití MeSH
- chování účinky léků MeSH
- duševní poruchy mikrobiologie MeSH
- lidé MeSH
- mikrobiota * účinky léků MeSH
- morfin terapeutické užití MeSH
- probiotika farmakologie terapeutické užití MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
It is not surprising to find microbiome abnormalities present in psychiatric disorders such as depressive disorders, bipolar disorders, etc. Evolutionary pressure may provide an existential advantage to the host eukaryotic cells in that it survives in an extracellular environment containing non-self cells (e.g., bacteria). This phenomenon is both positive and negative, as with other intercellular processes. In this specific case, the phenomenal amount of information gained from combined bacterial genome could enhance communication between self and non-self cells. This can be coupled to both pathological processes and healthy ones. In this review, we chose to examine potential associated disorders that may be coupled to the microbiome, from the perspective of their bidirectional communication with eukaryotic cells in the gut. Cognition, being the newest neural networking functionality to evolve, consumes a good amount of organismic energy, 30% of which arises from the gut flora. Furthermore, the mammalian gut is highly innervated and has a highly developed immune component, reflecting brain complexity. The brain-gut axis uses similar molecular messengers as the brain, which affects bacterial processes as well. Thus, any modification of normal bacterial processes may manifest itself in altered behavior/cognition, originating from the gut. The origin of some disorders associated with this bidirectional communication may be harnessed to restore normal functioning.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18010464
- 003
- CZ-PrNML
- 005
- 20180419142231.0
- 007
- ta
- 008
- 180404s2017 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.12659/msm.905425 $2 doi
- 035 __
- $a (PubMed)28636585
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Stefano, George B $u Department of Psychiatry, Charles University First Faculty of Medicine and General Teaching Hospital, Center for Cognitive Molecular Neuroscience, Prague, Czech Republic.
- 245 10
- $a Microbiome: A Potential Component in the Origin of Mental Disorders / $c GB. Stefano, R. Ptacek, J. Raboch, RM. Kream,
- 520 9_
- $a It is not surprising to find microbiome abnormalities present in psychiatric disorders such as depressive disorders, bipolar disorders, etc. Evolutionary pressure may provide an existential advantage to the host eukaryotic cells in that it survives in an extracellular environment containing non-self cells (e.g., bacteria). This phenomenon is both positive and negative, as with other intercellular processes. In this specific case, the phenomenal amount of information gained from combined bacterial genome could enhance communication between self and non-self cells. This can be coupled to both pathological processes and healthy ones. In this review, we chose to examine potential associated disorders that may be coupled to the microbiome, from the perspective of their bidirectional communication with eukaryotic cells in the gut. Cognition, being the newest neural networking functionality to evolve, consumes a good amount of organismic energy, 30% of which arises from the gut flora. Furthermore, the mammalian gut is highly innervated and has a highly developed immune component, reflecting brain complexity. The brain-gut axis uses similar molecular messengers as the brain, which affects bacterial processes as well. Thus, any modification of normal bacterial processes may manifest itself in altered behavior/cognition, originating from the gut. The origin of some disorders associated with this bidirectional communication may be harnessed to restore normal functioning.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antibakteriální látky $x farmakologie $x terapeutické užití $7 D000900
- 650 _2
- $a chování $x účinky léků $7 D001519
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a duševní poruchy $x mikrobiologie $7 D001523
- 650 12
- $a mikrobiota $x účinky léků $7 D064307
- 650 _2
- $a morfin $x terapeutické užití $7 D009020
- 650 _2
- $a probiotika $x farmakologie $x terapeutické užití $7 D019936
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Ptacek, Radek $u Department of Psychiatry, Charles University First Faculty of Medicine and General Teaching Hospital, Center for Cognitive Molecular Neuroscience, Prague, Czech Republic.
- 700 1_
- $a Raboch, Jiri $u Department of Psychiatry, Charles University First Faculty of Medicine and General Teaching Hospital, Center for Cognitive Molecular Neuroscience, Prague, Czech Republic.
- 700 1_
- $a Kream, Richard M $u Department of Psychiatry, Charles University First Faculty of Medicine and General Teaching Hospital, Center for Cognitive Molecular Neuroscience, Prague, Czech Republic.
- 773 0_
- $w MED00003251 $t Medical science monitor international medical journal of experimental and clinical research $x 1643-3750 $g Roč. 23, č. - (2017), s. 3039-3043
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28636585 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180404 $b ABA008
- 991 __
- $a 20180419142332 $b ABA008
- 999 __
- $a ok $b bmc $g 1287949 $s 1007276
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 23 $c - $d 3039-3043 $e 20170621 $i 1643-3750 $m Medical Science Monitor $n Med Sci Monit $x MED00003251
- LZP __
- $a Pubmed-20180404