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1.
Eur Neuropsychopharmacol ; 45: 15-28, 2021 04.
Article de Anglais | MEDLINE | ID: mdl-33730683

RÉSUMÉ

Physical inactivity, the fourth leading mortality risk factor worldwide, is associated with chronic mental illness. Identifying the mechanisms underlying different levels of baseline physical activity and the effects of these levels on the susceptibility to stress is very important. However, whether different levels of baseline physical activity influence the susceptibility and resilience to chronic social defeat stress (CSDS), and the underlying mechanisms in the brain remain unclear. The present study segregated wild-type mice into low baseline physical activity (LBPA) and high baseline physical activity (HBPA) groups based on short term voluntary wheel running (VWR). LBPA mice showed obvious susceptibility to CSDS, while HBPA mice were resilient to CSDS. In addition, the expression of tyrosine hydroxylase (TH) in the ventral tegmental area (VTA) was lower in LBPA mice than in HBPA mice. Furthermore, activation of TH neurons in the VTA of LBPA mice by chemogenetic methods increased the levels of VWR and resilience to CSDS. In contrast, inhibiting TH neurons in the VTA of HBPA mice lowered the levels of VWR and increased their susceptibility to CSDS. Thus, this study suggests that different baseline physical activities might be mediated by the dopamine system. This system also affects the susceptibility and resilience to CSDS, possibly via alteration of the baseline physical activity. This perspective on the neural control and impacts on VWR may aid the development of strategies to motivate and sustain voluntary physical activity. Furthermore, this can maximize the impacts of regular physical activity toward stress-reduction and health promotion.


Sujet(s)
Neurones dopaminergiques , Défaite sociale , Animaux , Souris , Souris de lignée C57BL , Activité motrice , Stress psychologique , Tyrosine 3-monooxygenase , Aire tegmentale ventrale
2.
Psychoneuroendocrinology ; 119: 104767, 2020 09.
Article de Anglais | MEDLINE | ID: mdl-32563935

RÉSUMÉ

Major depressive disorder (MDD) is a common mental disorder characterized by a persistent feeling of sadness, slow thought, impaired focus and loss of interest but the underlying mechanisms are largely unknown. Dendritic spines play an important role in the formation and maintenance of emotional circuits in the brain. Abnormalities in this process can lead to psychiatric diseases. 7,8-Dihydroxy-4-methylcoumarin (Dhmc), a precursor in the synthesis of derivatives of 4-methyl coumarin, plays an important role in protecting the nervous system from developing diseases and its most distinctive feature is safety. The aim of this study was to investigate whether Dhmc alleviates chronic unpredictable mild stress (CUMS)-induced depression-like behaviors and reverses CUMS-induced alterations in dendritic spines of principal neurons in brain areas of the emotional circuits including the hippocampus, medial prefrontal cortex (mPFC), nucleus accumbens (NAc) and basolateral amygdala (BLA) in male rats. Our results showed that CUMS-induced depression-like behaviors were accompanied by a decrease in spine density in pyramidal neurons of both the hippocampal CA3 area and the mPFC, and an increase in spine density in both the neurons of BLA and the medium spiny neurons (MSNs) of the NAc, as well as a decrease in the levels of the AMPA receptor subunit GluA1 and Kalirin-7 in the hippocampus compared with the control group. Intraperitoneal injection (i.p.) of Dhmc to the CUMS-exposed rats ameliorated CUMS-induced depression-like behaviors and reversed CUMS-mediated alterations in spine density and the levels of both GluA1 and Kalirin-7. Our results show an important role of Dhmc in reversing CUMS-induced depression-like behaviors and CUMS-mediated alterations in spine density.


Sujet(s)
Affect/effets des médicaments et des substances chimiques , Coumarines/usage thérapeutique , Épines dendritiques/effets des médicaments et des substances chimiques , Dépression/traitement médicamenteux , Animaux , Comportement animal/effets des médicaments et des substances chimiques , Coumarines/pharmacologie , Épines dendritiques/anatomopathologie , Épines dendritiques/physiologie , Dépression/anatomopathologie , Dépression/psychologie , Modèles animaux de maladie humaine , Mâle , Réseau nerveux/effets des médicaments et des substances chimiques , Réseau nerveux/anatomopathologie , Réseau nerveux/physiologie , Rats , Rat Sprague-Dawley , Stress psychologique/traitement médicamenteux , Stress psychologique/anatomopathologie , Stress psychologique/physiopathologie , Stress psychologique/psychologie
3.
Arch Virol ; 160(1): 365-9, 2015 Jan.
Article de Anglais | MEDLINE | ID: mdl-25287130

RÉSUMÉ

The complete genome sequence of a novel duck orthoreovirus, designated DRV strain TH11(DRV-TH11), was determined and characterized. The DRV-TH11 genome is comprised of 23,417 bp and its genome organization is more similar to that of avian orthoreoviruses (ARVs) of chicken origin than other reoviruses. The results of comparative sequence analysis and dendrograms based on the µB- and σC-encoding genes indicated that TH11 may be derived from the reassortment of ARVs and classic Muscovy duck reovirus (MDRV). A possible recombinant event was identified using the SimPlot program, and it occurred in the M2 segment. The results indicated that reassortment and mutation play a role in the evolution of duck reovirus.


Sujet(s)
Canards , Orthoréovirus aviaire/isolement et purification , Maladies de la volaille/virologie , Infections à Reoviridae/médecine vétérinaire , Animaux , Chine/épidémiologie , Orthoréovirus aviaire/génétique , Phylogenèse , Maladies de la volaille/épidémiologie , Infections à Reoviridae/épidémiologie , Infections à Reoviridae/virologie
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