scholarly journals Effects of Curcumin (Curcuma longa) on Learning and Spatial Memory as Well as Cell Proliferation and Neuroblast Differentiation in Adult and Aged Mice by Upregulating Brain-Derived Neurotrophic Factor and CREB Signaling

2014 ◽  
Vol 17 (6) ◽  
pp. 641-649 ◽  
Author(s):  
Sung Min Nam ◽  
Jung Hoon Choi ◽  
Dae Young Yoo ◽  
Woosuk Kim ◽  
Hyo Young Jung ◽  
...  
Cells ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 360
Author(s):  
Giulia Federica Mancini ◽  
Enrico Marchetta ◽  
Irene Pignani ◽  
Viviana Trezza ◽  
Patrizia Campolongo

Early-life adverse experiences (first hit) lead to coping strategies that may confer resilience or vulnerability to later experienced stressful events (second hit) and the subsequent development of stress-related psychopathologies. Here, we investigated whether exposure to two stressors at different stages in life has long-term effects on emotional and cognitive capabilities, and whether the interaction between the two stressors influences stress resilience. Male rats were subjected to social defeat stress (SDS, first hit) in adolescence and to a single episode of prolonged stress (SPS, second hit) in adulthood. Behavioral outcomes, hippocampal expression of brain-derived neurotrophic factor, and plasma corticosterone levels were tested in adulthood. Rats exposed to both stressors exhibited resilience against the development of stress-induced alterations in emotional behaviors and spatial memory, but vulnerability to cued fear memory dysfunction. Rats subjected to both stressors demonstrated resilience against the SDS-induced alterations in hippocampal brain-derived neurotrophic factor expression and plasma corticosterone levels. SPS alone altered locomotion and spatial memory retention; these effects were absent in SDS-exposed rats later exposed to SPS. Our findings reveal that exposure to social stress during early adolescence influences the ability to cope with a second challenge experienced later in life.


PLoS ONE ◽  
2013 ◽  
Vol 8 (5) ◽  
pp. e63535 ◽  
Author(s):  
Catarina Rendeiro ◽  
David Vauzour ◽  
Marcus Rattray ◽  
Pierre Waffo-Téguo ◽  
Jean Michel Mérillon ◽  
...  

Cancer ◽  
2010 ◽  
Vol 117 (6) ◽  
pp. 1321-1391 ◽  
Author(s):  
Peter E. Zage ◽  
Timothy C. Graham ◽  
Lizhi Zeng ◽  
Wendy Fang ◽  
Christine Pien ◽  
...  

2011 ◽  
Vol 14 (3) ◽  
pp. 195-200 ◽  
Author(s):  
In Koo Hwang ◽  
Ki-Yeon Yoo ◽  
Dae Young Yoo ◽  
Jung Hoon Choi ◽  
Choong Hyun Lee ◽  
...  

2019 ◽  
Vol 39 (6) ◽  
Author(s):  
Yu-Hui You ◽  
Zhi-Qiang Qin ◽  
Huan-Li Zhang ◽  
Zhao-Hong Yuan ◽  
Xin Yu

AbstractAutism is known as a severe neurobehavioral syndrome, with males affected more often than females. Previous studies have revealed that microRNAs (miRNAs) play a critical role in the search for novel therapeutic strategies for autism. Therefore, we evaluate the ability of miR-153 to influence brain-derived neurotrophic factor (BDNF) of autism as well as proliferation and apoptosis of hippocampal neuron through the janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling pathway by targeting leptin receptor (LEPR). Firstly, the autistic mice models were established and Morris water maze was employed for the analysis of the learning ability and memory of the mice. Besides, in vitro experiments were conducted with the transfection of different mimic, inhibitor, or siRNA into the hippocampal neuron cells, after which the effect of miR-153 on LEPR and the JAK-STAT signaling pathway-related factors was investigated. Next, 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide assay and flow cytometry assay were conducted to evaluate cell proliferation, cell cycle, and apoptosis respectively following transfection. The results revealed that there was a significant decrease in learning ability and memory in the autistic mice along with a reduction in the positive expression rate of BDNF and serious inflammatory reaction. LEPR was confirmed as a target gene of miR-153 by the dual luciferase reporter gene assay. After transfection of overexpressed miR-153, LEPR and the JAK-STAT signaling pathway were inhibited followed by an increase in BDNF and enhancement of cell proliferation. In conclusion, the high expression of miR-153 can inhibit activation of JAK-STAT signaling pathway by LEPR, thus improving BDNF expression and the proliferative ability of hippocampal neurons.


2012 ◽  
Vol 226 (2) ◽  
pp. 357-369 ◽  
Author(s):  
Santoshkumar Tota ◽  
Ruby Goel ◽  
Shakti Deep Pachauri ◽  
Rajasekar N. ◽  
Abul Kalam Najmi ◽  
...  

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