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1.
Chinese Journal of Surgery ; (12): 1685-1687, 2007.
Article in Chinese | WPRIM | ID: wpr-338088

ABSTRACT

<p><b>OBJECTIVE</b>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).</p><p><b>METHODS</b>Thirty male Sprague Dawley rats (240 g +/- 20 g) were randomly divided into 2 groups. I group simply celiac injected pilocarpine. II group celiac injected PLO after LF-TMS. Pathological item included HE staining, NPY immunohistochemical staining and apoptosis staining.</p><p><b>RESULTS</b>HE staining revealed neurons of hippocampus were obviously death and cell's structure was destroyed in PLO group. The PLO + LF-TMS group was less injured and destroyed. Using One-Way ANOVA, NPY immunohistochemical staining shown the positive cell number was increased at all areas of hippocampus in PLO group contrasting with the low positive cell number in the PLO + LF-TMS group. In PLO group the number of apoptosis cell at hippocampus areas was significant higher than the PLO + LF-TMS group.</p><p><b>CONCLUSIONS</b>Using the PLO evoked epilepsy model, LF-TMS alleviated neurons injury at hippocampus area, so LF-TMS might playing an important role in resisting the progressing of epilepsy. The positive cell number of NPY increased at all areas of hippocampus, which indicated the close relation between NPY and epilepsy. NPY might have some function on resisting epilepsy.</p>


Subject(s)
Animals , Male , Rats , Apoptosis , Disease Models, Animal , Epilepsy, Temporal Lobe , Metabolism , Pathology , Therapeutics , Hippocampus , Metabolism , Pathology , Neurons , Metabolism , Pathology , Neuropeptide Y , Metabolism , Pilocarpine , Toxicity , Random Allocation , Rats, Sprague-Dawley , Transcranial Magnetic Stimulation , Methods
2.
Chinese Journal of Industrial Hygiene and Occupational Diseases ; (12): 710-713, 2007.
Article in Chinese | WPRIM | ID: wpr-338935

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of the extremely low frequency pulsed electromagnetic field (PEMF) on the proliferation and differentiation of osteoblast-like cells.</p><p><b>METHODS</b>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. MTS was applied to analyze cell proliferation and flow cytometry to detect cell cycle. The intracellular alkaline phosphatase (ALP) activity was measured by colorimetry.</p><p><b>RESULTS</b>PEMF of 1.55 mT at 48 Hz decreased significantly the cell percentage of S or G(2)M phase (P < 0.05), but did not affect cell number of MC3T3-E1 cells. Although the number of the primary osteoblast cells did not alter by MTS assay after exposure to PEMF for 24 h continuously, the cell percentage of G(2)M phase increased significantly (P < 0.01). When the culture time extended to 48 h, the cell number increased greatly (P < 0.01) and the cell percentage of G(2)M phase decreased significantly despite of the exposure type (P < 0.01). After the primary osteoblast cells were exposed to PEMF for 24 h continuously, the ALP activity decreased significantly (P < 0.05), whereas it increased significantly after exposure to PEMF for 48 h continuously (P < 0.05).</p><p><b>CONCLUSION</b>PEMF of 1.55 mT at 48 Hz does not affect proliferation and differentiation of MC3T3-E1 cell, but it promotes proliferation of primary osteoblast cell, inhibits differentiation at proliferation stage and promotes differentiation at differentiation stage of primary osteoblast cell.</p>


Subject(s)
Animals , Mice , Rats , Cell Differentiation , Radiation Effects , Cell Proliferation , Radiation Effects , Cells, Cultured , Dose-Response Relationship, Radiation , Electromagnetic Fields , Osteoblasts , Cell Biology , Metabolism , Radiation Effects , Rats, Sprague-Dawley
3.
Chinese Journal of Medical Instrumentation ; (6): 17-18, 2005.
Article in Chinese | WPRIM | ID: wpr-241112

ABSTRACT

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.


Subject(s)
Humans , Cerebral Cortex , Physiology , Electric Stimulation , Electromagnetic Fields , Equipment Design , Transcranial Magnetic Stimulation
4.
Chinese Journal of Industrial Hygiene and Occupational Diseases ; (12): 326-328, 2003.
Article in Chinese | WPRIM | ID: wpr-340047

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of low frequency pulsed magnetic field on the proliferation and differentiation of HepG2 cells.</p><p><b>METHODS</b>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.</p><p><b>RESULTS</b>There were no significant differences in cell proliferation between sham and treated groups exposed to the field of 80 Hz, 1.55 mT for 1, 4, 8, 12, 24 h (P > 0.05). There were also no significant differences in cell proliferation and AFP secretion between sham and treated groups exposed to 16 Hz, 1.55 mT pulsed magnetic fields for 1, 4, 8, 24 h (P > 0.05).</p><p><b>CONCLUSION</b>There were no "window effects" found in HepG2 cells proliferation or AFP secretion at 16 Hz and 80 Hz pulsed magnetic fields.</p>


Subject(s)
Humans , Cell Differentiation , Radiation Effects , Cell Division , Radiation Effects , Cell Line, Tumor , Cell Biology , Metabolism , Radiation Effects , Electromagnetic Fields , alpha-Fetoproteins
5.
Chinese Journal of Industrial Hygiene and Occupational Diseases ; (12): 332-334, 2003.
Article in Chinese | WPRIM | ID: wpr-340045

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of extremely low frequency magnetic fields on intracellular calcium concentration ([Ca(2+)]i).</p><p><b>METHODS</b>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. [Ca(2+)]i of HepG2 cells was also measured when they were exposed to 0.9 mT [root mean square (rms)], 16 Hz sinusoidal magnetic fields in real time.</p><p><b>RESULTS</b>The R values (F(340) nm/F(380) nm) of the control and the exposed group were 2.4519 +/- 0.2378 and 2.5266 +/- 0.2915 respectively after HepG2 cells were exposed to 1.55 mT, 16 Hz magnetic fields, 1.365 0 +/- 0.0626 and 1.3602 +/- 0.0771 respectively to 300 mT, 2 Hz rotating magnetic fields. The ratios of the trendline slope [r((501 - 1,000)) / r((0 - 500))] from the data of R values were 1.1213 +/- 0.4559 and 1.0727 +/- 0.1971 respectively (P > 0.05), and the ratios of the intercept [b((501 - 1,000)) / b((0 - 500))] from the trendline were 0.9912 +/- 0.0098 and 0.9979 +/- 0.0060 (P > 0.05) when HepG2 cells were exposed to the 0.9 mT, 16 Hz sinusoidal magnetic fields.</p><p><b>CONCLUSION</b>The effect of extremely low frequency magnetic fields on [Ca(2+)]i of HepG2 cells under the experimental condition has not been found.</p>


Subject(s)
Humans , Calcium , Metabolism , Cell Line, Tumor , Metabolism , Radiation Effects , Chelating Agents , Pharmacology , Egtazic Acid , Pharmacology , Electromagnetic Fields , Ion Transport , Radiation Effects , Octoxynol , Pharmacology , Spectrometry, Fluorescence , Time Factors
6.
Chinese Journal of Physical Medicine and Rehabilitation ; (12)2003.
Article in Chinese | WPRIM | ID: wpr-683183

ABSTRACT

Objective To observe the effects of low frequency transcranial magnetic stimulation (LF-TMS) on the electroencephalogram (EEG),expression of NPY in hippocampus in pilocarpine (PLO)-induced epileptic rats. Methods Forty male Sprague-Dawley rats (240-260 g) were used to establish a model of epilepsy by in- tradominal injection of pilocarpine,and then randomized into 2 groups:a control group and an intervention group. The control group was treated by sham LF-TMS,while the intervention group was treated by LF-TMS once daily for 7 days.Ⅰgroup simply celiac inject pilocarpine.Ⅱgroup celiac inject PLO after LF-TMS.The EEG was recorded in both groups and the checked pathology.Pathological item include HE staining,NPY immunohisto chemical staining. Results The latency for seizure attack was significantly lengthened,while the frequency of seizure attack and times of major seizure attack were significantly decreased in the intervention group.The HE staining revealed significant de- generation and necrosis of neurons in the hippocampus,especially in the CA3 region,in rats in the control group. The pathologic changes were significantly less severe in the intervention,Immunohistochemical staining showed a sig- nificantly higher expression of NPY in the hippocampus as compared with the intervention group. Conclusion U- sing the PLO-induced epilepsy model,LF-TMS could not only postpone the generation of kindling but also inhibit the progress of epilepsy.The increased NPY expression in the hippocampusin the intervention group implied a close rela- tionship between NPY and epilepsy attack.

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