Sex Differences in Central Amygdala Glutamate Responses to Calcitonin Gene-Related Peptide

Women are disproportionately affected by chronic pain compared with men. While societal and environmental factors contribute to this disparity, sex-based biological differences in the processing of pain are also believed to play significant roles. The central lateral nucleus of the amygdala (CeLC) is a key region for the emotional-affective dimension of pain, and a prime target for exploring sex differences in pain processing since a recent study demonstrated sex differences in CGRP actions in this region. Inputs to CeLC from the parabrachial nucleus (PB) play a causal role in aversive processing and release both glutamate and calcitonin gene-related peptide (CGRP). CGRP is thought to play a crucial role in chronic pain by potentiating glutamatergic signaling in CeLC. However, it is not known if this CGRP-mediated synaptic plasticity occurs similarly in males and females. Here, we tested the hypothesis that female CeLC neurons experience greater potentiation of glutamatergic signaling than males following endogenous CGRP exposure. Using trains of optical stimuli to evoke transient CGRP release from PB terminals in CeLC, we find that subsequent glutamatergic responses are preferentially potentiated in CeLC neurons from female mice. This potentiation was CGRP dependent and involved a postsynaptic mechanism. This sex difference in CGRP sensitivity may explain sex differences in affective pain processing.

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Publication Details

Journal
Journal of Neuroscience
Published
2024-12-11
DOI
https://doi.org/10.1523/jneurosci.1898-24.2024
Citations
7
Primary Topic
Pain Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
2.29

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article

Sex Differences in Central Amygdala Glutamate Responses to Calcitonin Gene-Related Peptide

Jason Bondoc Alipio, Yadong Ji, Asaf Keller, Sung Han et al.
7 citations
Journal of Neuroscience
Pain Mechanisms and Treatments
2.29
article

Sex Differences in Central Amygdala Glutamate Responses to Calcitonin Gene-Related Peptide

Jason Bondoc Alipio, Yadong Ji, Asaf Keller, Sung Han, Rebecca M. Lorsung, Radi Masri, Nathan Cramer
article en
7 citations

Abstract

Women are disproportionately affected by chronic pain compared with men. While societal and environmental factors contribute to this disparity, sex-based biological differences in the processing of pain are also believed to play significant roles. The central lateral nucleus of the amygdala (CeLC) is a key region for the emotional-affective dimension of pain, and a prime target for exploring sex differences in pain processing since a recent study demonstrated sex differences in CGRP actions in this region. Inputs to CeLC from the parabrachial nucleus (PB) play a causal role in aversive processing and release both glutamate and calcitonin gene-related peptide (CGRP). CGRP is thought to play a crucial role in chronic pain by potentiating glutamatergic signaling in CeLC. However, it is not known if this CGRP-mediated synaptic plasticity occurs similarly in males and females. Here, we tested the hypothesis that female CeLC neurons experience greater potentiation of glutamatergic signaling than males following endogenous CGRP exposure. Using trains of optical stimuli to evoke transient CGRP release from PB terminals in CeLC, we find that subsequent glutamatergic responses are preferentially potentiated in CeLC neurons from female mice. This potentiation was CGRP dependent and involved a postsynaptic mechanism. This sex difference in CGRP sensitivity may explain sex differences in affective pain processing.

Journal of NeuroscienceVol. 45(2)
University of Jordan (JO), University of Maryland, Baltimore (US), Salk Institute for Biological Studies (US)
National Institutes of Health, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 11%
Pain Mechanisms and Treatments
2.29
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