# The early and lasting mechanisms underlying predator odor stressor-induced adaptations to alcohol interoceptive sensitivity > **NIH NIH F31** · UNIV OF NORTH CAROLINA CHAPEL HILL · 2022 · $38,259 ## Abstract PROJECT SUMMARY/ABSTRACT Post-traumatic stress disorder (PTSD) can be precipitated by a traumatic stressor and is an enduring and debilitating disorder for which only limited treatment options exist. Furthermore, PTSD increases an individual’s likelihood to develop a co-morbid alcohol use disorder (AUD), demonstrating the importance of understanding the brain mechanisms underlying the relationship between stress and alcohol sensitivity. Alcohol interoceptive sensitivity refers to the subjective stimulus effects of alcohol on an organism. As such, interoceptive sensitivity has the potential to inform alcohol intake (i.e., signal satiety or drive more drinking). However, due to clinical limitations, little is known about brain mechanisms that underlie stressor-induced diminished sensitivity to alcohol. Therefore, we propose to use a well-established predator odor exposure (2,5‐dihydro‐2,4,5‐ trimethylthiazoline (TMT)) stressor model in rats that has demonstrated lasting behavioral consequences relevant to PTSD. Stress is associated with dysregulated cortical glutamate function. In agreement with the clinical stress literature, I find altered expression of mGlu receptor gene expression in the rat cortex following TMT exposure. Specifically, Grm3 (mGlu3) was downregulated in the prelimbic cortex (PrL) two days after TMT exposure. Additionally, several NMDA receptor gene transcripts (GriN2A, GriN2B, GriN2C, GriN2D, GriN3A, and GriN3B) were upregulated in the insular cortex (IC) 2 weeks after the TMT exposure. This is important as NMDA receptors modulate expression of the interoceptive effects of alcohol, and my preliminary data demonstrate diminished interoceptive sensitivity to alcohol in rats previously exposed to TMT at the same time point (2 weeks after TMT). Because the IC is involved in alcohol interoceptive processing and is one of the major outputs of the PrL, I hypothesize that plasticity induced by stress between PrL (mGlu3)IC circuitry triggers the NMDA-related brain changes in the IC that may underlie the blunted sensitivity to the interoceptive effects of alcohol. Aim 1 investigates the potential mechanisms that occur during the TMT stressor to promote the changes to alcohol interoceptive sensitivity. Exp 1.1 uses an mGlu3 negative allosteric modulator (NAM) to block mGlu3 receptor signaling in the PrL immediately prior to TMT exposure, and to determine if this treatment prevents the attenuated sensitivity to alcohol 2 weeks later. Exp. 1.2 uses a chemogenetic approach to silence glutamatergic projections from the PrL to the IC prior to TMT exposure, to assess if this treatment will prevent the blunted alcohol interoceptive sensitivity. Aim 2 investigates whether the NMDA receptor adaptations in the IC underlie the attenuated sensitivity to alcohol. Exp. 2.1 determines if TMT exposure produces NMDA receptor adaptation in optically evoked EPSC’s from IC neurons receiving projections from the PrL. Exp. 2.2 investigates the functional adapt... ## Key facts - **NIH application ID:** 10465305 - **Project number:** 1F31AA029946-01A1 - **Recipient organization:** UNIV OF NORTH CAROLINA CHAPEL HILL - **Principal Investigator:** Ryan Edward Tyler - **Activity code:** F31 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2022 - **Award amount:** $38,259 - **Award type:** 1 - **Project period:** 2022-02-01 → 2023-10-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10465305 ## Citation > US National Institutes of Health, RePORTER application 10465305, The early and lasting mechanisms underlying predator odor stressor-induced adaptations to alcohol interoceptive sensitivity (1F31AA029946-01A1). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10465305. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*