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        <datestamp>2025-12-01T00:00:00Z</datestamp>
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          <dc:title>Role of Rostromedial Tegmental Nucleus Afferents in Symptoms of Withdrawal from Chronic Ethanol Exposure</dc:title>
          <dc:creator>Hyerim Yang (23292139)</dc:creator>
          <dc:subject>Withdrawal symptoms</dc:subject>
          <dc:subject>Alcohol use disorder</dc:subject>
          <dc:description>A significant number of individuals with alcohol use disorder struggle to maintain sobriety as a result of withdrawal symptoms including heightened pain sensitivity. Although common, the precise neural mechanisms underlying nociceptive symptoms of withdrawal are not well understood. The rostromedial tegmental nucleus (RMTg) is a GABAergic region that plays a critical role in avoidance behavior, aversive signaling, and pain modulation. Accumulating data provides evidence of RMTg hyperactivity during acute withdrawal and points to a role for the RMTg in regulating withdrawal symptoms. Yet, the role of this region in withdrawal-induced changes in pain sensitivity and the afferents that promote RMTg activity during acute withdrawal are unknown. In this thesis, I examined the role of RMTg afferents in regulating hyperalgesia during acute withdrawal. I found that thermal hyperalgesia emerged early after the cessation of ethanol exposure and persisted into protracted withdrawal. cFos expression, a marker of recent neuronal activity, was significantly increased in both the RMTg and RMTg-projecting lateral habenula (LHb) neurons during acute withdrawal. In vivo chemogenetic inhibition of this circuit attenuated withdrawal-induced thermal hyperalgesia in a sex-dependent manner. Collectively, these data suggest that RMTg-projecting LHb neurons play an important role in nociceptive symptoms of withdrawal from chronic ethanol exposure.</dc:description>
          <dc:date>2025-12-01T00:00:00Z</dc:date>
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          <dc:identifier>10.25417/uic.31451890.v1</dc:identifier>
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          <dc:rights>In Copyright</dc:rights>
          <dc:rights>Open Access after 2028-01-01</dc:rights>
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