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Published on: June 12, 2017
Regulation of AKT activity prevents autonomic nervous system imbalance
Tsubasa Furuhashi1, Kazuichi Sakamoto1
1Graduate School of Life and Environmental Sciences, University of Tsukuba, Japan.
Abstract:
Autonomic nervous system (ANS) imbalances are involved in the etiology of cancer, allergy, and collagen diseases. Previously, we hypothesized that FoxO and HSF-1 limit autonomic stress responses via negative feedback on the ANS. Here, we evaluated the role of AKT, a negative regulator of FoxO, during activation of the ANS by loneliness stress in mice. Spontaneous motility was increased during loneliness stress and decreased after release from stress. The AKT activator SC79 attenuated stress-induced spontaneous motility, whereas the AKT inhibitor API-2 prevented decreases in motility after stress release. Our results show that AKT activity regulates ANS responses to loneliness stress.
Insights
Autonomic nervous system (ANS) imbalances are linked to diseases. AKT activity regulates ANS stress responses, specifically during loneliness, impacting spontaneous motility in mice.
Area of Science:
- Neuroscience
- Physiology
- Molecular Biology
Background:
- Autonomic nervous system (ANS) imbalances are implicated in various diseases, including cancer, allergies, and collagen disorders.
- Previous research suggested FoxO and HSF-1 proteins limit autonomic stress responses through negative feedback.
- The role of AKT, a known negative regulator of FoxO, in stress responses was not fully understood.
Purpose of the Study:
- To investigate the role of AKT in regulating autonomic nervous system (ANS) responses to loneliness stress in a mouse model.
- To determine how AKT activity influences behavioral changes associated with stress and stress recovery.
Main Methods:
- Mice were subjected to loneliness stress to activate the ANS.
- Changes in spontaneous motility were monitored as an indicator of ANS activity.
- The AKT activator SC79 and the AKT inhibitor API-2 were administered to assess their effects on stress responses and motility.
Main Results:
- Loneliness stress increased spontaneous motility in mice, indicating ANS activation.
- The AKT activator SC79 reduced stress-induced spontaneous motility.
- The AKT inhibitor API-2 blocked the decrease in motility observed after stress release, suggesting a role in stress recovery.
Conclusions:
- AKT activity plays a significant role in modulating autonomic nervous system (ANS) responses to loneliness stress.
- AKT signaling influences both the immediate reaction to stress and the recovery process.
- These findings contribute to understanding the physiological mechanisms underlying stress-related disorders.
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