Behavioral response of a chimpanzee mother toward her dead infant

2011 ◽  
Vol 73 (5) ◽  
pp. 415-421 ◽  
Author(s):  
Katherine A. Cronin ◽  
Edwin J.C. van Leeuwen ◽  
Innocent Chitalu Mulenga ◽  
Mark D. Bodamer
Keyword(s):  
Behavioral Response ◽  
Dead Infant

Biological and Behavioral Response Studies of Marine Mammals in Southern California, 2010 (SOCAL-10")"

2011 ◽  
Author(s):  
B. Southall ◽  
J. Calambokidis ◽  
P. Tyack ◽  
D. Moretti ◽  
J. Hildebrand ◽  
...  
Keyword(s):  
Behavioral Response ◽  
Marine Mammals ◽  
Southern California

Short- and long-term dynamics of the physiological and behavioral response to heat stress and thymol supplementation in Japanese quail

2021 ◽  
pp. 102876
Author(s):  
Maria Emilia Fernandez ◽  
Maria Carla Labaque ◽  
Gabriel Orso ◽  
Raúl Hector Marin ◽  
Jackelyn Melissa Kembro
Keyword(s):  
Heat Stress ◽  
Japanese Quail ◽  
Behavioral Response ◽  
Short And Long Term

scholarly journals Activation of the p11/SMARCA3/Neurensin-2 pathway in parvalbumin interneurons mediates the response to chronic antidepressants

2021 ◽  
Author(s):  
Gali Umschweif ◽  
Lucian Medrihan ◽  
Kathryn A. McCabe ◽  
Yotam Sagi ◽  
Paul Greengard
Keyword(s):  
Chromatin Remodeling ◽  
Behavioral Response ◽  
Hippocampal Neurons ◽  
Selective Serotonin Reuptake Inhibitors ◽  
Chronic Treatment ◽  
Target Genes ◽  
Delayed Response ◽  
Dynamic Changes ◽  
Parvalbumin Interneurons ◽  
Transcriptional Changes

AbstractThe delayed behavioral response to chronic antidepressants depends on dynamic changes in the hippocampus. It was suggested that the antidepressant protein p11 and the chromatin remodeling factor SMARCA3 mediate this delayed response by inducing transcriptional changes in hippocampal neurons. However, what target genes are regulated by the p11/SMARCA3 complex to mediate the behavioral response to antidepressants, and what cell type mediates these molecular changes remain unknown. Here we report that the p11/SMARCA3 complex represses Neurensin-2 transcription in hippocampal parvalbumin-expressing interneurons after chronic treatment with Selective Serotonin Reuptake Inhibitors (SSRI). The behavioral response to antidepressants requires upregulation of p11, accumulation of SMARCA3 in the cell nucleus, and a consequent repression of Neurensin-2 transcription in these interneurons. We elucidate a functional role for p11/SMARCA3/Neurensin-2 pathway in regulating AMPA-receptor signaling in parvalbumin-expressing interneurons, a function that is enhanced by chronic treatment with SSRIs. These results link SSRIs to dynamic glutamatergic changes and implicate p11/SMARCA3/Neurensin-2 pathway in the development of more specific and efficient therapeutic strategies for neuropsychiatric disorders.

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