CGRP as a potential mediator for the sexually dimorphic responses to traumatic brain injury

• Published in: Biology of sex differences Vol. 15; no. 1; pp. 44 - 18
• Main Authors: Li, Chunyan, Ajmal, Erum, Alok, Khaled, Powell, Keren, Wadolowski, Steven, Tambo, Willians, Turpin, Justin, Barthélemy, Ernest, Al-Abed, Yousef, LeDoux, David
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 30.05.2024; BioMed Central; BMC
• Subjects: Animals; Anxiety; Brain; Brain - metabolism; Brain Injuries, Traumatic - metabolism; Calcitonin; Calcitonin gene-related peptide; Calcitonin Gene-Related Peptide - metabolism; Depression, Mental; Endothelium; Estrogen; Estrogens; Female; Females; Gender differences; Hormones; Injuries; Male; Males; Microvascular dysfunction; Microvasculature; Neuroprotection; NF-E2-Related Factor 2 - metabolism; Nitric oxide; Nitric Oxide Synthase Type III - metabolism; Nitric-oxide synthase; Oxidative Stress; Peptides; Progesterone; Rats; Rats, Sprague-Dawley; Scientific equipment and supplies industry; Sex Characteristics; Sex differences; Sex hormones; Sexual dimorphism; Spatial memory; Structure-function relationships; Substantia alba; Traumatic brain injury; United States; United States > US; Calcitonin gene-related peptide; Oxidative stress; Sex hormones; Traumatic brain injury; Memory; Microvascular dysfunction; Depression; Anxiety; Sexual dimorphism
• ISSN: 2042-6410; 2042-6410
• DOI: 10.1186/s13293-024-00619-x

The outcomes of traumatic brain injury (TBI) exhibit variance contingent upon biological sex. Although female sex hormones exert neuroprotective effects, the administration of estrogen and progesterone has not yielded conclusive results. Hence, it is conceivable that additional mediators, distinct from female sex hormones, merit consideration due to their potential differential impact on TBI outcomes. Calcitonin gene-related peptide (CGRP) exhibits sexually dimorphic expression and demonstrates neuroprotective effects in acute brain injuries. In this study, we aimed to examine sex-based variations in TBI structural and functional outcomes with respect to CGRP expression. Male and female Sprague Dawley rats were exposed to controlled cortical impact to induce severe TBI, followed by interventions with and without CGRP inhibition. In the acute phase of TBI, the study centered on elucidating the influence of CGRP on oxidative stress, nuclear factor erythroid 2-related factor 2 (Nrf2) and endothelial nitric oxide synthase (eNOS) signaling in the peri-impact tissue. Subsequently, during the chronic phase of TBI, the investigation expanded to evaluate CGRP expression in relation to lesion volume, microvascular dysfunction, and white matter injury, as well as working and spatial memory, anxiety-like, and depression-like behaviors in subjects of both sexes. Female rats exhibited elevated levels of CGRP in the peri-impact brain tissue during both baseline conditions and in the acute and chronic phases of TBI, in comparison to age-matched male counterparts. Enhanced CGRP levels in specific brain sub-regions among female rats correlated with superior structural and functional outcomes following TBI compared to their male counterparts. CGRP inhibition induced heightened oxidative stress and a reduction in the expression of Nrf2 and eNOS in both male and female rats, with the observed alteration being more pronounced in females than in males. This study marks the inaugural identification of CGRP as a downstream mediator contributing to the sexually dimorphic response observed in TBI outcomes.