Sex Dimorphism in Pain Threshold and Neuroinflammatory Response: The Protective Effect of Female Sexual Hormones on Behavior and Seizures in an Allergic Rhinitis Model.
Mohammad ElahiZahra Ebrahim SoltaniArya AfroogheElham AhmadiAhmad Reza DehpourPublished in: Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology (2024)
Our previous research demonstrated that allergic rhinitis could impact behavior and seizure threshold in male mice. However, due to the complex hormonal cycles and hormonal influences on behavior in female mice, male mice are more commonly used for behavioral tests. In this study, we aimed to determine whether these findings were replicable in female mice and to explore the potential involvement of sexual hormones in regulating neuroinflammation in an allergic model. Our results indicate that pain threshold was decreased in female mice with allergic rhinitis and the levels of IL-23/IL-17A/IL-17R were increased in their Dorsal root ganglia. However, unlike males, female mice with AR did not display neuropsychological symptoms such as learning and memory deficits, depression, and anxiety-like behavior. This was along with decreased levels of DNA methyl transferase 1 (DNMT1) and inflammatory cytokines in their hippocampus. Ovariectomized mice were used to mitigate hormonal effects, and the results showed that they had behavioral changes and neuroinflammation in their hippocampus similar to male mice, as well as increased levels of DNMT1. These findings demonstrate sex differences in how allergic rhinitis affects behavior, pain sensitivity, and seizure thresholds. Furthermore, our data suggest that DNMT1 may be influenced by sexual hormones, which could play a role in modulating inflammation in allergic conditions.
Keyphrases
- allergic rhinitis
- high fat diet induced
- chronic pain
- dna methylation
- neuropathic pain
- traumatic brain injury
- pain management
- mental health
- oxidative stress
- cognitive impairment
- polycystic ovary syndrome
- spinal cord
- lipopolysaccharide induced
- cerebral ischemia
- machine learning
- wild type
- mild cognitive impairment
- lps induced
- gene expression
- insulin resistance
- adipose tissue
- brain injury
- artificial intelligence
- cell free
- big data
- electronic health record
- sleep quality
- nucleic acid