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Updated: Jan 22, 2026

An Ultrasonic Tool for Nerve Conduction Block in Diabetic Rat Models
Published on: October 20, 2017
MicroRNA-155 mimics ameliorates nerve conduction velocities and suppresses hyperglycemia-induced pro-inflammatory
Ji Chen1, Wenjie Liu2, Han Yi2
1Department of Endocrinology, The First Affiliated Hospital of University of South China Hunan Province 421001, China.
Background:
MicroRNA-155 (miR-155) regulates inflammatory cytokines, however its role in Diabetic neuropathy (DN) remains unexplored.
Methods:
A strain of mice (db/db) having type II diabetes were studied for expression of miR-155 in plasma and in sciatic nerves. The miR-155 mimic treated mice were studied for effect on motor and sensory nerve conduction velocities along with blood perfusion in sciatic nerves and response to thermal stimuli test. The mice were evaluated for density of blood vessels, quantity of intra-epidermal nerve fibers (IENF), diameters of axons & thickness of myelin sheath of sciatic nerves. Bioinformatics analysis was done to confirm target genes of miR-155.
Results:
The db/db mice showed significant suppression of miR-155 in sciatic nerves. The treatment of miR-155 mimic elevated levels of miR-155 in both sciatic nerves and plasma; it also enhanced the blood flow in sciatic nerves and velocities of conduction for both sensory and motor nerves. The treatment showed significant decrease in the threshold to thermal stimuli in db/db mice. A significant improvement in density of perfused blood vessels was observed, along with elevation of IENF and thickness of myelin and axon diameters of sciatic nerves. The treatment attenuated levels of TNF-α, iNOS, IL1-β and Ym1. Microarray analysis showed that the treatment decreased the expression of proinflammatory genes TRAF2 and Notch2, SORT1 and were identified as target by in silico studies.
Conclusion:
Treatment of miR-155 mimic in db/db mice attenuated DN, suppressed diabetic associated proinflammatory genes and confirmed miR-155 mimic as therapeutic strategy for treating DN.
Insights
MicroRNA-155 (miR-155) mimic treatment improved nerve function and blood flow in diabetic neuropathy (DN) mice. This suggests miR-155 mimic is a potential therapeutic strategy for treating DN.
Area of Science:
- Endocrinology
- Neuroscience
- Molecular Biology
Background:
- MicroRNA-155 (miR-155) is known to regulate inflammatory cytokines.
- The specific role of miR-155 in the development of diabetic neuropathy (DN) has not been previously investigated.
Purpose of the Study:
- To investigate the role of miR-155 in diabetic neuropathy.
- To evaluate the therapeutic potential of miR-155 mimic in a mouse model of type 2 diabetes.
Main Methods:
- Expression of miR-155 was analyzed in plasma and sciatic nerves of type 2 diabetic mice (db/db).
- db/db mice were treated with miR-155 mimic to assess effects on nerve conduction, blood perfusion, and thermal sensitivity.
- Histological analyses evaluated blood vessel density, intra-epidermal nerve fiber (IENF) count, axon diameter, and myelin sheath thickness.
- Bioinformatics and microarray analyses identified miR-155 target genes.
Main Results:
- Diabetic mice exhibited significantly reduced miR-155 levels in sciatic nerves.
- miR-155 mimic treatment increased miR-155 levels, enhanced sciatic nerve blood flow, and improved motor and sensory nerve conduction velocities.
- Treatment led to decreased thermal sensitivity threshold, increased blood vessel density, IENF count, axon diameter, and myelin sheath thickness.
- miR-155 mimic attenuated pro-inflammatory markers (TNF-α, iNOS, IL1-β, Ym1) and decreased expression of TRAF2 and Notch2.
Conclusions:
- miR-155 mimic treatment demonstrated a therapeutic effect in attenuating diabetic neuropathy in mice.
- The study identified miR-155 mimic as a potential therapeutic strategy for DN by suppressing associated pro-inflammatory genes.
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