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Sex-Specific Effects of Buprenorphine on Endoplasmic Reticulum Stress, Abnormal Protein Accumulation, and Cell Loss
Megan B Faulkner1, Mariam Rizk1, Zahraa Bazzi1
1Department of Natural Sciences, University of Michigan-Dearborn, Dearborn, Michigan, USA.
Insights
Buprenorphine (BPN) shows sex-specific effects on endoplasmic reticulum (ER) stress after pediatric traumatic brain injury (TBI). While BPN helps reduce protein buildup and cell loss in both sexes, it only lessens ER stress in males.
Area of Science:
- Neuroscience
- Pediatric Medicine
- Pharmacology
Background:
- Traumatic brain injury (TBI) in children can cause long-term developmental issues due to secondary injuries like endoplasmic reticulum (ER) stress.
- Buprenorphine (BPN) is a common pain reliever for children, but its impact on ER stress in pediatric TBI is not fully understood.
Purpose of the Study:
- To investigate the sex-specific effects of BPN on ER stress, protein accumulation, and cell loss in a pediatric TBI mouse model.
- To determine if BPN's effects differ between male and female mice following TBI.
Main Methods:
- A mouse model of pediatric TBI using the impact acceleration method was employed.
- Male and female mice were treated with saline or BPN after TBI, with evaluations at 1, 3, and 7 days post-injury.
- Key indicators assessed included ER stress pathway activation, abnormal protein accumulation, and cell loss.
Main Results:
- TBI induced greater ER stress in males than females at early time points (1-3 days).
- Females experienced more severe abnormal protein accumulation and cell loss by day 7 post-TBI.
- BPN reduced protein accumulation and cell loss in both sexes but only decreased ER stress in males.
Conclusions:
- Buprenorphine exhibits sex-specific and time-dependent effects on ER stress and cellular damage in the acute phase after pediatric TBI.
- These findings highlight the need to consider sex when evaluating BPN's potential therapeutic role in pediatric TBI recovery.
Abstract:
Traumatic brain injury (TBI) in children often leads to poor developmental outcomes attributable to progressive cell loss caused by secondary injuries, including endoplasmic reticulum (ER) stress. Buprenorphine (BPN) is commonly used in children for pain management; however, the effects of BPN on ER stress in the pediatric population are still inconclusive. This study investigated the sex-specific effects of BPN on ER stress, abnormal protein accumulation, and cell loss in a mouse impact acceleration model of pediatric TBI. On post-natal day 20-21 (P20-21), male and female littermates were randomized into sham, TBI + saline and TBI + BPN groups. BPN (0.075 mg/kg) was administered to TBI + BPN mice at 30 min after injury and then every 6-12 h for 2 days. The impact of BPN was evaluated at 1, 3, and 7 days post-injury. We found that TBI induced more prominent ER stress pathway activation at 1 and 3 days post-injury in males, compared to females, whereas abnormal protein accumulation and cell loss were more severe in females at 7 days post-injury, compared with males. Although BPN partially ameliorated abnormal protein accumulation and cell loss in both males and females, BPN only decreased ER stress pathway activation in males, not in females. In conclusion, BPN exhibits sex-specific effects on ER stress, abnormal protein accumulation, and cell loss in a time-dependent manner at the acute phase after pediatric TBI, which provides the rationale to assess the potential effects of BPN on long-term outcomes after pediatric TBI in both males and females.
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