Oscillating field stimulation promotes axon regeneration and locomotor recovery after spinal cord injury.

Oscillating field stimulation (OFS) is a potential method for treating spinal cord injury. Although it has been used in spinal cord injury (SCI) therapy in basic and clinical studies, its underlying mechanism and the correlation between its duration and nerve injury repair remain poorly understood. In this study, we established rat models of spinal cord contusion at T10 and then administered 12 weeks of OFS.

Early electrical field stimulation prevents the loss of spinal cord anterior horn motoneurons and muscle atrophy following spinal cord injury.

Our previous study revealed that early application of electrical field stimulation (EFS) with the anode at the lesion and the cathode distal to the lesion reduced injury potential, inhibited secondary injury and was neuroprotective in the dorsal corticospinal tract after spinal cord injury (SCI). The objective of this study was to further evaluate the effect of EFS on protection of anterior horn motoneurons and their target musculature after SCI and its mechanism. Rats were randomized into three equal groups.

Injury potentials of spinal cord in ex vivo compression injury model.

The effect of applied electric field on neuroprotection and axonal regeneration has been studied in previous studies of acute spinal cord injury (SCI). However, due to the complexity of the microenvironment of the lesion site, the underlying mechanism of applied electric field is not yet fully understood. Thus, the injury potential, a significant index of the microenvironment change, was investigated in ex vivo spinal cords compression injury.

The effects of chronic repetitive transcranial magnetic stimulation on glutamate and gamma-aminobutyric acid in rat brain.

Recent studies have shown that repetitive transcranial magnetic stimulation (rTMS) has therapeutic potential for some neurological and psychiatric disorders. However, the neurobiological effects of this tool are not sufficiently explained so far, previous research reported that rTMS can change dopamine release, there have been few studies to examine a possible effect of rTMS on amino acid neurotransmitter. This study aimed to determine the effects of chronic rTMS on glutamate and gamma-aminobutyric acid concentration in the rat brain.

[The effect of low frequency transcranial magnetic stimulation on neuropeptide-Y expression and apoptosis of hippocampus neurons in epilepsy rats induced by pilocarpine].

Objective: To analyze the effect of low frequency transcranial magnetic stimulation (LF-TMS) on changing neuropeptide-Y (NPY) expression and apoptosis of hippocampus neurons in epilepsy rats induced by pilocarpine (PLO).

Methods: Thirty male Sprague Dawley rats (240 g +/- 20 g) were randomly divided into 2 groups. I group simply celiac injected pilocarpine.

[Effects of extremely low frequency pulsed electromagnetic field on different-derived osteoblast-like cells].

Objective: To investigate the effect of the extremely low frequency pulsed electromagnetic field (PEMF) on the proliferation and differentiation of osteoblast-like cells.

Methods: The MC3T3-E1 cell and the primary osteoblast cell derived from 2-day-old Sprague Dawley (SD) rat calvaria were exposed to PEMF with a magnetic flux density of 1.55 mT at 48 Hz for 24 or 48 h.

[The design of a transcranial magnetic stimulation (TMS) system and its implementation].

Transcranial magnetic stimulation (TMS) is a non-invasive diagnostic and therapeutic technigue. This paper expounds the design and manufacture of the TMS system, which meets all the requirements of the TMS study and clinical diagnosis and treatments.

[Effect of extremely low frequency magnetic fields on intracellular free calcium in HepG2 cells].

Objective: To study the effect of extremely low frequency magnetic fields on intracellular calcium concentration ([Ca(2+)]i).

Methods: Fura-2 loaded HepG2 cells were exposed to 1.55 mT (average value), 16 Hz pulsed magnetic fields for 60 min and to 300 mT, 2 Hz rotating magnetic fields for 5 min, and then [Ca(2+)]i was measured by fluorescence spectrophotometer.

[Effects of low frequency pulsed magnetic field on the proliferation and differentiation of HepG2 cells].

Objective: To study the effects of low frequency pulsed magnetic field on the proliferation and differentiation of HepG2 cells.

Methods: 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) colorimetry method and ELISA assay of alpha-fetoprotein (AFP) were used to determine the cell proliferation and differentiation after the cells were exposed to pulsed magnetic fields with different frequency but the same field intensity.

Results: There were no significant differences in cell proliferation between sham and treated groups exposed to the field of 80 Hz, 1.