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Odor blocking of stress hormone responses
Eun Jeong Lee1,2, Luis R Saraiva1,3, Naresh K Hanchate1,4
1Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, A3-020, Seattle, WA, 98109, USA.
Scientific Reports
|May 24, 2022
Summary
Aromas can reduce stress hormone release in mice by impacting brain pathways. These findings reveal scent
Area of Science:
- Neuroscience
- Olfactory system research
- Stress response mechanisms
Background:
- The use of scents to alleviate stress is ancient, yet the underlying biological mechanisms remain largely unelucidated.
- Stress and fear trigger hormonal responses mediated by specific neural circuits, including corticotropin-releasing hormone neurons (CRHNs).
Purpose of the Study:
- To investigate the neurobiological mechanisms by which common odorants can mitigate stress responses in a mammalian model.
- To identify the specific neural pathways and neuronal populations involved in scent-mediated stress reduction.
Main Methods:
- Utilized mouse models exposed to common odorants and potent stressors (physical restraint, predator odor, social confrontation).
- Measured stress hormone levels and monitored neuronal activity in key brain regions, including the bed nucleus of the stria terminalis (BNSTa) and the ventromedial hypothalamus (VMH).
- Employed optogenetic techniques to selectively silence inhibitory neurons in the VMH to assess their role.
Main Results:
- Two common odorants significantly blocked stress hormone increases induced by physical restraint, predator odor, and social confrontation.
- One odorant inhibited the activation of excitatory neurons in the BNSTa that project to CRHNs.
- Both odorants activated inhibitory neurons in the VMH, and silencing these neurons impaired the stress-blocking effect of odors.
Conclusions:
- Odorants can attenuate stress hormone responses through at least two distinct neural mechanisms.
- Mechanism 1: Inhibition of excitatory stress-transmitting neurons upstream of CRHNs (e.g., in BNSTa).
- Mechanism 2: Activation of inhibitory neurons (e.g., in VMH) that suppress CRHN activation, either directly or indirectly.
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