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1.
Journal of Southern Medical University ; (12): 1696-1699, 2008.
Article in Chinese | WPRIM | ID: wpr-340745

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the changes in stress hormones in neurogenic pulmonary edema (NPE) and explore the clinical value of mild hypothermia therapy for treatment of NPE.</p><p><b>METHODS</b>Fifty-two patients with cerebral hemorrhage patients and concomitant NPE were randomly divided into two groups for local mild hypothermia therapy (23 cases, LMH group) or routine treatment (29 cases, RT group). In the former group, local mild hypothermia therapy was applied in addition to the routine treatment. The changes of serum corticotrophin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH), corticosteroid (Cor), arginine vasopressin (AVP) and blood sugar were observed before and 7 days after the treatment, and compared with those of 58 NPE-free patients with cerebral hemorrhage and 40 healthy individuals.</p><p><b>RESULTS</b>Serum CRH, ACTH, Cor, and AVP levels and blood sugar in NPE patients and the NPE-free patients were all significantly higher than those in the healthy individuals (P<0.01), and the levels were significantly higher in NPE patients than in the NPE-free patients (P<0.05). In the NPE patients, the mortality rate and NIHSS score were significantly lower in RT group (P<0.01); after 7 days of treatment, both LMH and RT groups showed significant reduction in serum CRH, ACTH, Cor, and AVP levels (P<0.05), and the reduction was more conspicuous in LMH group (P<0.05).</p><p><b>CONCLUSION</b>The occurrence of NPE is closely associated with stress reactions, which might be the basis of NPE. Local mild hypothermia therapy improves of the quality of life of NPE patients and also decreases the mortality of NPE possibly by inhibiting the secretion of stress hormones and stabilizing the hypothalamic-pituitary-adrenal axis.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Adrenocorticotropic Hormone , Blood , Arginine Vasopressin , Blood , Corticotropin-Releasing Hormone , Blood , Head , Hypothermia, Induced , Methods , Intracranial Hemorrhages , Blood , Therapeutics , Pulmonary Edema , Blood , Therapeutics , Treatment Outcome
2.
Chinese Journal of Traumatology ; (6): 3-6, 2004.
Article in English | WPRIM | ID: wpr-270290

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of GM1 on inducing adult rat bone marrow stromal cells (MSCs) to form neural progenitor cells and their differentiation.</p><p><b>METHODS</b>Purified MSCs were induced by different components of basic fibroblast growth factor (bFGF) alone, GM1 alone or combination of bFGF with GM1. After 3 days' incubation, fibronectin and collagen I were detected with immunocytochemistry, and nestin was detected with immunofluorescence. Neuron-specific enolase (NSE), glial fibrillary acidic protein (GFAP) and galactose cerebroside (GalC) were detected with immunocytochemistry after 7 days' incubation.</p><p><b>RESULTS</b>After induction with bFGF alone or combination of bFGF and GM1, some MSCs exhibited the phenotypes of neural progenitor cells, and then neurons and astrocytes. In these two groups, the positive cells for fibronectin and collagen I decreased markedly after 3 days' induction. At the same time, the positive cells for nestin increased markedly. After 7 days' induction, NSE and GFAP-positive cells increased significantly. Furthermore, the addition of bFGF and GM1 caused the maximal variation. However, addition of GM1 alone had no inductive effects.</p><p><b>CONCLUSIONS</b>Combination of bFGF with GM1 may synergistically promote the transformation of MSCs and differentiation into neurons and astrocyte-like cells. The results suggest a promising route for the application of MSCs.</p>


Subject(s)
Animals , Rats , Analysis of Variance , Bone Marrow Cells , Cell Differentiation , Physiology , Cells, Cultured , Drug Synergism , Fibroblast Growth Factor 2 , Pharmacology , Fluorescent Antibody Technique , G(M1) Ganglioside , Pharmacology , Immunohistochemistry , Probability , Rats, Wistar , Sensitivity and Specificity , Stem Cells , Pathology , Physiology , Stromal Cells , Physiology
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