Lab study, 2023
How does allopregnanolone help with PMDD symptoms?
In rats with PMDD-like symptoms, allopregnanolone reduced anxiety and improved how brain receptors work in areas that control emotions.
What they did
Researchers created rats with PMDD symptoms using a resident-intruder stress test. They measured progesterone and allopregnanolone levels in different brain areas and studied how brain receptors responded.
What they found
Allopregnanolone reduced anxiety in the rats. It adjusted how a brain receptor (GABAA-Rα4) was expressed in the amygdala and hippocampus. When allopregnanolone was added to brain cells, it improved electrical signals that help control emotions.
What it means for you
This suggests allopregnanolone might help PMDD by changing how brain receptors work. The main limit is that this is an animal study, not human research, so we don't know if it works the same way in women.
About the study
- Original title
- Allopregnanolone-mediated GABAA-Rα4 function in amygdala and hippocampus of PMDD liver qi-invasion syndrome model rats
- Authors
- Sun Y, Gao M, Gao D et al.
- Journal
- Aging
- Year
- 2023
- Study design
- Lab study
- What was tested
- Treatment with allopregnanolone
- Open access
- Yes
- Read the paper
- doi.org/10.18632/aging.204541
Original abstract
Background: Premenstrual dysphoric disorder (PMDD) is a common mental health challenge among women of reproductive age. Allopregnanolone (3α, 5α-THP; ALLO) mediated functional alterations of GABAA receptors (GABAA-R) are involved in PMDD pathogenesis, however, the specific mechanism remains unknown. Therefore, we investigated the role of ALLO mediated GABAA-Rα4 in the pathophysiology of PMDD. Purpose: We determined whether the pathogenesis of PMDD is associated with ALLO mediated GABAA-Rα4 expression changes in different brain regions. Methods: Rat models of PMDD liver-qi invasion syndrome (PMDD-LIS) were established via the resident intruder paradigm. Behavioral changes of rats were assessed by aggressive behavior tests, EPM and OFT. The levels of progesterone and ALLO in serum as well as brain areas were determined by ELISA. Variations in GABAA-Rα4 levels in brain regions were assessed by immunofluorescence and RT-PCR. Medicated serum was used to interfere with rat hippocampal neurons, and changes in Cl - current were recorded through electrophysiology. Results: Premenstrual anxiety and irritability of PMDD-LIS patients can be simulated in PMDD-LIS rat models. Exogenous ALLO significantly improved the anxiety behaviors of PMDD-LIS rats. Changes in ALLO among different brain regions varied. GABAA-Rα4 expressions were low in the amygdala and abnormally high in the hippocampus, however, ALLO alleviated these deviations. Whole-cell patch clamp recording technique showed a weaker Cl - current intensity of PMDD-LIS rats, reduced neuroinhibitory functions and increased Cl - current intensity in the ALLO group drug serum intervention and enhanced emotional inhibition function. Conclusion: We established that ALLO regulation of the GABAA-Rα4 subunit in the amygdala and hippocampus is involved in PMDD-LIS pathogenesis.
Reproduced under CC-BY.
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