Dysregulation of miR‑24‑3p and miR‑186‑5p and GABA<sub>A</sub> receptor expression in focal cortical dysplasia

Spontaneous synaptic activity mediated by GABAA receptor is associated with epileptogenicity in focal cortical dysplasia (FCD). miRNAs are potentially involved in the regulation of GABAA receptor subunit expression and activity. This study aimed to determine the expression of miRNAs in FCD and correlate their expression level with mRNA levels of GABAA receptor subunits. Expression of GABAA receptor subunits (α1 and α4) and miRNAs (miR‑155‑5p, miR‑186‑5p, and miR‑24‑3p) were evaluated using real‑time PCR in resected brain samples from FCD patients. miRNA levels were also determined in the serum of FCD patients. Spontaneous GABAA receptor‑mediated synaptic activity was measured using patch clamp technique. Significant increase in α1 and α4 subunit expression and miR‑155‑5p levels, while decrease in miR‑24‑3p and miR‑186‑5p levels, was observed in the brain samples of FCD. In the serum of FCD patients, miR‑155‑5p levels were increased, whereas miR‑24‑3p and miR‑186‑5p levels remained unaltered. Increased α4 subunit expression in FCD might be due to reduced levels of miR‑24‑3p and miR‑186‑5p. In addition, reduced miR‑186‑5p levels might be responsible for increased expression of α1 subunit. We also observed an increase in the spontaneous GABAA receptor‑mediated synaptic transmission in FCD. In conclusion, dysregulation of miRNAs and GABAA receptor expression suggest that these miRNAs may contribute to altered GABAA receptor‑mediated synaptic activity in FCD.

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Journal
Acta Neurobiologiae Experimentalis
Published
2025-03-07
DOI
https://doi.org/10.55782/ane-2024-2656
Primary Topic
MicroRNA in disease regulation
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article
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0.00

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article

Dysregulation of miR‑24‑3p and miR‑186‑5p and GABAA receptor expression in focal cortical dysplasia

Sanjeev Lalwani, Manjari Tripathi, Jyotirmoy Banerjee, Ramesh Doddamani et al.
Acta Neurobiologiae Experimentalis
MicroRNA in disease regulation
article

Dysregulation of miR‑24‑3p and miR‑186‑5p and GABAA receptor expression in focal cortical dysplasia

Sanjeev Lalwani, Manjari Tripathi, Jyotirmoy Banerjee, Ramesh Doddamani, Mehar Chand Sharma, P. Sarat Chandra, Soumil Dey, Aparna Banerjee Dixit, Yashaswini Agarwal, Arpna Srivastava
article en

Abstract

Spontaneous synaptic activity mediated by GABAA receptor is associated with epileptogenicity in focal cortical dysplasia (FCD). miRNAs are potentially involved in the regulation of GABAA receptor subunit expression and activity. This study aimed to determine the expression of miRNAs in FCD and correlate their expression level with mRNA levels of GABAA receptor subunits. Expression of GABAA receptor subunits (α1 and α4) and miRNAs (miR‑155‑5p, miR‑186‑5p, and miR‑24‑3p) were evaluated using real‑time PCR in resected brain samples from FCD patients. miRNA levels were also determined in the serum of FCD patients. Spontaneous GABAA receptor‑mediated synaptic activity was measured using patch clamp technique. Significant increase in α1 and α4 subunit expression and miR‑155‑5p levels, while decrease in miR‑24‑3p and miR‑186‑5p levels, was observed in the brain samples of FCD. In the serum of FCD patients, miR‑155‑5p levels were increased, whereas miR‑24‑3p and miR‑186‑5p levels remained unaltered. Increased α4 subunit expression in FCD might be due to reduced levels of miR‑24‑3p and miR‑186‑5p. In addition, reduced miR‑186‑5p levels might be responsible for increased expression of α1 subunit. We also observed an increase in the spontaneous GABAA receptor‑mediated synaptic transmission in FCD. In conclusion, dysregulation of miRNAs and GABAA receptor expression suggest that these miRNAs may contribute to altered GABAA receptor‑mediated synaptic activity in FCD.

Acta Neurobiologiae ExperimentalisVol. 85(1)
All India Institute of Medical Sciences Raipur (IN), Ambedkar University Delhi (IN), All India Institute of Medical Sciences Bhopal (IN), All India Institute of Medical Sciences (IN)
All-India Institute of Medical Sciences
Openalex Percentile: Top 91%
MicroRNA in disease regulation
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