Early-life chronic di(2-ethylhexyl)phthalate exposure worsens age-related long-term associative memory decline associated with insulin/IGF-1 signaling and CRH-1/CREB in Caenorhabditis elegans

2021 ◽  
pp. 126044
Author(s):  
Chun Ming How ◽  
Ting-An Lin ◽  
Vivian Hsiu-Chuan Liao
2017 ◽  
Vol 42 ◽  
pp. 86-92 ◽  
Author(s):  
Ning Wei ◽  
Xiaoyan Feng ◽  
Zhiqin Xie ◽  
Yanan Zhang ◽  
Ying Feng

2021 ◽  
Author(s):  
Alexandra O Cohen ◽  
Morgan M Glover ◽  
Xinxu Shen ◽  
Camille V Phaneuf ◽  
Kristen N Avallone ◽  
...  

Reward motivation enhances memory through interactions between mesolimbic, hippocampal, and cortical systems - both during and after encoding. Developmental changes in these distributed neural circuits may lead to age-related differences in reward-motivated memory and the underlying neural mechanisms. Converging evidence from cross-species studies suggests that subcortical dopamine signaling is increased during adolescence, which may lead to stronger memory representations of rewarding, relative to mundane, events and changes in the contributions of underlying subcortical and cortical brain mechanisms across age. Here, we used fMRI to examine how reward motivation influences the "online" encoding and "offline" post-encoding brain mechanisms that support long-term associative memory from childhood to adulthood. We found that reward motivation led to both age-invariant as well as adolescent-specific enhancements in associative memory after 24 hours. Furthermore, reward-related memory benefits were linked to age-varying neural mechanisms. During encoding, interactions between the prefrontal cortex and ventral tegmental area (VTA) were associated with better high-reward memory to a greater degree with increasing age. Pre- to post-encoding changes in functional connectivity between the anterior hippocampus and VTA were also associated with better high-reward memory, but more so at younger ages. Our findings suggest that there may be developmental shifts - from offline subcortical to online cortical processes - in the brain mechanisms supporting reward-motivated memory.


2015 ◽  
Vol 1622 ◽  
pp. 137-148 ◽  
Author(s):  
E. Bauer ◽  
M. Toepper ◽  
H. Gebhardt ◽  
B. Gallhofer ◽  
G. Sammer

2018 ◽  
Vol 4 (10) ◽  
pp. eaat6994 ◽  
Author(s):  
Birgit Michels ◽  
Hanna Zwaka ◽  
Ruth Bartels ◽  
Oleh Lushchak ◽  
Katrin Franke ◽  
...  

Cognitive impairments can be devastating for quality of life, and thus, preventing or counteracting them is of great value. To this end, the present study exploits the potential of the plantRhodiola roseaand identifies the constituent ferulic acid eicosyl ester [icosyl-(2E)-3-(4-hydroxy-3-methoxyphenyl)-prop-2-enoate (FAE-20)] as a memory enhancer. We show that food supplementation with dried root material fromR. roseadose-dependently improves odor-taste reward associative memory scores in larvalDrosophilaand prevents the age-related decline of this appetitive memory in adult flies. Task-relevant sensorimotor faculties remain unaltered. From a parallel approach, a list of candidate compounds has been derived, includingR. rosea–derived FAE-20. Here, we show that bothR. rosea–derived FAE-20 and synthetic FAE-20 are effective as memory enhancers in larvalDrosophila. Synthetic FAE-20 also partially compensates for age-related memory decline in adult flies, as well as genetically induced early-onset loss of memory function in young flies. Furthermore, it increases excitability in mouse hippocampal CA1 neurons, leads to more stable context-shock aversive associative memory in young adult (3-month-old) mice, and increases memory scores in old (>2-year-old) mice. Given these effects, and given the utility ofR. rosea—the plant from which we discovered FAE-20—as a memory enhancer, these results may hold potential for clinical applications.


2021 ◽  
Author(s):  
Annalise Aleta LaPlume ◽  
Larissa Mcketton ◽  
Brian Levine ◽  
Nicole Anderson ◽  
Angela K. Troyer

INTRODUCTION: More women than men develop Alzheimer’s disease, yet women show less age-related episodic memory decline, a contradiction that may be accounted for by modifiable risk factors for dementia. METHODS: Associations between sex, modifiable dementia risk factors, and cognition were measured in a cross-sectional online sample (n = 21,840, ages 18-89). RESULTS: Across four tests of associative memory and executive functions, only a Face-Name Association task revealed sex differences in age-related decline. Men had worse associative memory than women (the equivalent of four years of aging). Each additional risk factor had the equivalent of three and a half years of aging. Men had greater age-related decline in associative memory than women among those with no to one risk factors, but multiple risk factors eliminated the female advantage. DISCUSSION: Because the relationship between dementia risk factors and age-related memory decline differs for men and women, sex-specific dementia prevention approaches are warranted.


2018 ◽  
Author(s):  
Jimmy Y. Zhong

Memory decline in old age is highly noticeable based on tasks assessing episodic memory, which require remembering information about events at specific times and places. The exact cognitive mechanism that accounts for this prominent age-related decline in episodic memory has not been well-understood, and the multitude of mechanisms that were proposed have drawn a credible amount of research and discussions. The current review focuses on the associative deficit hypothesis (ADH) - originally proposed by Naveh-Benjamin and colleagues - that was suggested to form the basis of age-related declines in episodic memories. According to the ADH, older adults’ poorer episodic memory is attributed to the difficulties they experience in formulating relations or links between single units of information (i.e., items or contextual elements), binding them together into a coherent distinctive unit, and retrieving the links between the component features/units whenever necessary [COPYRIGHT CC-BY-NC-ND 4.0 J. Y. ZHONG, 2018].


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