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1.
Chinese Journal of Applied Physiology ; (6): 407-413, 2005.
Article in Chinese | WPRIM | ID: wpr-254646

ABSTRACT

<p><b>AIM</b>To investigate the regulatory network of hippocampal-systemic arterial blood pressure during epileptic network reestablishment.</p><p><b>METHODS</b>7.2 microg picrotoxin (PTX) was microinjected into the right HPC (RHPC) to induce rat epilepsy. Contralateral hippocampal EEG, single unit discharges, femoral artery blood pressure and ECG were recorded simultaneously.</p><p><b>RESULTS</b>PTX might induce: (1) A resemblance interspike intervals (ISI) spot distribution of long duration neuronal burst and unit after discharges in contralateral HPC. (2) Delayed the initiation time of hippocampal neuronal bursts coupled with arterial blood pressure depression. (3) Hippocampal neuronal burst or unit after discharges coupled complexly with arterial blood pressure depression. (4) Resemblance hippocampal EEG interpeak intervals (IPI) and neuronal firing ISI spot distribution coupled with arterial blood pressure depression.</p><p><b>CONCLUSION</b>During contralateral hippocampal epileptic network reestablishment after microinjection of PTX to the RHPC, the function of the hippocampal-arterial blood pressure regulatory network could be modulated by characteristic network and neuronal temporal code patterning.</p>


Subject(s)
Animals , Male , Rats , Blood Pressure , Physiology , Electrocardiography , Electroencephalography , Epilepsy , Hippocampus , Physiology , Rats, Sprague-Dawley
2.
Journal of Experimental Hematology ; (6): 261-264, 2004.
Article in Chinese | WPRIM | ID: wpr-352086

ABSTRACT

To study and compare the immunomodulatory functions of human bone marrow mesenchymal stem cell (MSC) and cord blood mononuclear cell (CBMNC) in vitro, human bone marrow MSC were separated with Percoll (1.073 g/L) and cultured in low-glucose DMEM, and cord blood mononuclear cells were isolated with Ficoll (1.077 g/L). These two kinds of cells were added to mixed lymphocyte cultures and PHA induction transformation cultures with various concentrations. The proliferation of lymphocytes was measured by MTT method, effects of MSC and CBMNC on mixed lymphocyte response and PHA-induced lymphocyte transformation were investigated. The results showed that both 5 x 10(4), 1 x 10(4) MSC and 2 x 10(5) CBMNC could inhibit the mixed lymphocyte response (MLR) and PHA induced transformation. But with lower concentrations (MSC < or = 1 x 10(3), CBMNC < or = 1 x 10(5)), the inhibition effects of MSC and CBMNC were less consistent. 1 x 10(2) MSC and 1 x 10(4) CBMNC mainly increased the lymphocyte activation. In addition, the inhibition ratio of 5 x 10(4) MSC (MLC 65.3%, PHA 79.1%) was higher than that of 2 x 10(5) CBMNC (MLC 8.6%, PHA 37.3%). It is concluded that larger numbers of both MSC and CBMNC showed negative immunomodulatory functions and inhibited the mixed lymphocyte response and induction of transformation in vitro. Moreover, the inhibitory effect of MSC was much stronger than that of CBMNC.


Subject(s)
Humans , Bone Marrow Cells , Fetal Blood , Cell Biology , Leukocytes, Mononuclear , Physiology , Lymphocyte Activation , Lymphocyte Culture Test, Mixed , Mesenchymal Stem Cells , Physiology , Phytohemagglutinins , Pharmacology
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