Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
Add filters








Year range
1.
China Journal of Chinese Materia Medica ; (24): 3630-3635, 2015.
Article in Chinese | WPRIM | ID: wpr-320895

ABSTRACT

To explore the antagonistic effect of gingerols against the inflammation induced by lectin from Pinellia ternata. In this study, ELISA method was used to determine the effect of different extracts from gingerols on the release of inflammatory factor TNF-α from macrophages induced by lectin from P. ternata. The fluorescence probe was used to determine the effect of gingerols on the changes in ROS of macrophages induced by lectin from P. ternata. The western-blot method was applied to study the effect of gingerols on the increase in expression of cell receptor interacting protein RIP3 in macrophages induced by lectin from P. ternata. The scanning electron microscope (SEM) was used to study the effect of gingerols on morphological changes in macrophages induced by lectin from P. ternata. According to the results, gingerols can significantly inhibit the release of inflammatory factor from macrophages induced by lectin from P. ternata, ROS overproduction and increase in RIP3 expression. SEM results showed that gingerols can inhibit the cytomorphosis and necrocytosis induced by lectin from P. ternata. Fresh ginger's detoxication may be related to gingerols' effects in inhibiing release of inflammatory factor, ROS overproduction and increase in RIP3 expression caused by macrophages induced by lectin from P. ternata, which are mainly inflammatory development.


Subject(s)
Animals , Male , Mice , Catechols , Pharmacology , Cells, Cultured , Drug Antagonism , Fatty Alcohols , Pharmacology , Zingiber officinale , Chemistry , Lectins , Toxicity , Macrophages , Metabolism , Mice, Inbred ICR , Pinellia , Chemistry , Toxicity , Reactive Oxygen Species , Metabolism , Receptor-Interacting Protein Serine-Threonine Kinases , Genetics , Metabolism , Tumor Necrosis Factor-alpha , Genetics , Metabolism
2.
China Journal of Chinese Materia Medica ; (24): 3893-3897, 2013.
Article in Chinese | WPRIM | ID: wpr-319683

ABSTRACT

<p><b>OBJECTIVE</b>To explore the pro-inflammatory toxicity of Pinellia pedatiecta, as well as the alum processing method on its pro-inflammatory effect.</p><p><b>METHOD</b>Raphide and agglutinin (PPA) proteins were isolated from fresh P. pedatiecta. The overall animal and cellular level models were applied to investigate the pro-inflammatory effect of raphide and PPA in P. pedatiecta, as well as the impact of the alum processing method on the pro-inflammatory effect, with inflammatory mediators as the index.</p><p><b>RESULT</b>Intraperitoneal injection with P. pedatiecta raphide suspension could significantly increase the content of inflammatory mediators PGE2 and NO. After the alum processing method was adopted, fresh P. pedatiecta and raphide-induced PGE2 and NO release significantly reduced. The stimulation of mice macrophages with P. pedatiecta agglutinin protein could cause the content of dose-dependent inflammatory mediators TNF-alpha and IL-6. After the alum processing method was adopted, PGE2 content in P. pedatiecta agglutinin protein-induced mice peritoneal exudate notably decreased.</p><p><b>CONCLUSION</b>The irritation and toxicity of P. pedatiecta were inflammatory responses in organisms. Its raphide and agglutinin proteins were toxic components, both could cause significant the release of inflammatory medium. The alum processing method could help significantly reduce the pro-inflammatory toxicity of P. pedatiecta.</p>


Subject(s)
Animals , Female , Male , Alum Compounds , Chemistry , Drug Compounding , Methods , Drugs, Chinese Herbal , Chemistry , Toxicity , Inflammation Mediators , Chemistry , Toxicity , Interleukin-6 , Allergy and Immunology , Macrophages , Allergy and Immunology , Mice, Inbred ICR , Pinellia , Chemistry , Tumor Necrosis Factor-alpha , Allergy and Immunology
3.
China Journal of Chinese Materia Medica ; (24): 1041-1045, 2013.
Article in Chinese | WPRIM | ID: wpr-350664

ABSTRACT

<p><b>OBJECTIVE</b>To study the toxic mechanism of toxic raphides from Pinellia ternata.</p><p><b>METHOD</b>Mouse peritoneal macrophage in vitro culture model was adopted to study dose-dependent and time-dependent curves of toxic raphides, with TNF-alpha, IL-1beta and IL-6 in supernatant as indexes. Scanning electron microscopy was used to observe the changes in surface morphology of raphides-treated macrophages. Macrophages-neutrophils co-cultured the transport model to study the effect of toxic raphides' stimulation of macrophages on neutrophils migration.</p><p><b>RESULT</b>Toxic raphides' stimulation of macrophages could cause the increase in the levels of TNF-alpha, IL-1beta and IL-6 released, and showed dose dependence and time dependence. Scanning electron microscopy showed that toxic raphides were swallowed by macrophages, with notable cell membrane creases, increase in the number of pseudopods and decrease in integrity of cell membranes, and could significantly induce migration of neutrophils.</p><p><b>CONCLUSION</b>The inflammatory process induced by toxic raphides is mainly mediated by macrophages. The toxic mechanism of toxic raphides from P. ternata is that toxic raphides penetrate into tissues to activate resident macrophages, release phagocytic and inflammatory cytokines, and cause migration of neutrophils, which finally results in acute inflammatory response.</p>


Subject(s)
Animals , Male , Mice , Drugs, Chinese Herbal , Toxicity , Inflammation Mediators , Toxicity , Interleukin-1beta , Allergy and Immunology , Interleukin-6 , Allergy and Immunology , Macrophages, Peritoneal , Allergy and Immunology , Mice, Inbred ICR , Pinellia , Chemistry , Tumor Necrosis Factor-alpha , Allergy and Immunology
4.
China Journal of Chinese Materia Medica ; (24): 1610-1613, 2013.
Article in Chinese | WPRIM | ID: wpr-294058

ABSTRACT

<p><b>OBJECTIVE</b>To extract and separate toxic components from Phytolaccae Radix, and to comare the changes in toxicity of Phytolaccae Radix before and after being processed with vinegar.</p><p><b>METHOD</b>The mucous membrane irritation response, mouse peritoneal inflammation model and in vitro macrophages release NO model were applied to compared the changes in inflammatory toxicity of toxic components from Phytolaccae Radix before and after being processed with vinegar.</p><p><b>RESULT</b>Toxic components of Phytolacca Radix had significant inflammatory toxicity, which could cause conjunctival edema in rabbits, and increase of PGE2 and macrophages release NO content in peritoneal exudate in mice. After being processed with vinegar, they showed reduced irritation, which resulted in decrease of PGE2 and macrophages release NO content in peritoneal exudate in mice.</p><p><b>CONCLUSION</b>After being processed with vinegar, the toxicity of toxic components from Phytolacca Radix decreased obviously.</p>


Subject(s)
Animals , Male , Mice , Rabbits , Acetic Acid , Chemistry , Chemistry, Pharmaceutical , Methods , Drugs, Chinese Herbal , Toxicity , Eye , Allergy and Immunology , Mice, Inbred ICR , Phytolacca , Chemistry
5.
Chinese Medical Journal ; (24): 367-372, 2012.
Article in English | WPRIM | ID: wpr-262610

ABSTRACT

<p><b>OBJECTIVE</b>To assess the experimental and clinical data regarding the effects of electromagnetic fields (EMFs) on fracture non-union.</p><p><b>DATA SOURCES</b>The English language literature regarding EMFs on fracture non-union were searched using MEDLINE, Web of Science and Embase, for the period January 2006 to June 2011. The search terms were electromagnetic fields and non-union/bone marrow stem cells (BMSCs)/bone.</p><p><b>STUDY SELECTION</b>Articles were included in the review if they were related to the use of EMFs on BMSCs or bone tissue. Papers without full manuscripts available were excluded.</p><p><b>RESULTS</b>The basic and clinical research in this field, while somewhat limited, supports the insightful application of EMFs to ameliorate disability due to fracture non-union.</p><p><b>CONCLUSIONS</b>Further basic and clinical research to validate the use of EMFs in facilitating function and bone reparative processes in fracture non-union is required.</p>


Subject(s)
Animals , Humans , Bone Regeneration , Physiology , Electromagnetic Fields
6.
Chinese Medical Journal ; (24): 4031-4036, 2012.
Article in English | WPRIM | ID: wpr-339905

ABSTRACT

<p><b>BACKGROUND</b>Repair of large bone defects remains a challenge for clinicians. The present study investigated the ability of mesenchymal stem cells (MSCs) and/or periosteum-loaded poly (lactic-co-glycolic acid) (PLGA) to promote new bone formation within rabbit ulnar segmental bone defects.</p><p><b>METHODS</b>Rabbit bone marrow-derived MSCs (passage 3) were seeded onto porous PLGA scaffolds. Forty segmental bone defects, each 15 mm in length, were created in the rabbit ulna, from which periosteum was obtained. Bone defects were treated with either PLGA alone (group A), PLGA + MSCs (group B), periosteum-wrapped PLGA (group C) or periosteum-wrapped PLGA/MSCs (group D). At 6 and 12 weeks post-surgery, samples were detected by gross observation, radiological examination (X-ray and micro-CT) and histological analyses.</p><p><b>RESULTS</b>Group D, comprising both periosteum and MSCs, showed better bone quality, higher X-ray scores and a greater amount of bone volume compared with the other three groups at each time point (P < 0.05). No significant differences in radiological scores and amount of bone volume were found between groups B and C (P > 0.05), both of which were significantly higher than group A (P < 0.05).</p><p><b>CONCLUSIONS</b>Implanted MSCs combined with periosteum have a synergistic effect on segmental bone regeneration and that periosteum plays a critical role in the process. Fabrication of angiogenic and osteogenic cellular constructs or tissue-engineered periosteum will have broad applications in bone tissue engineering.</p>


Subject(s)
Animals , Rabbits , Bone Regeneration , Physiology , Cells, Cultured , Lactic Acid , Chemistry , Mesenchymal Stem Cells , Cell Biology , Periosteum , Cell Biology , Polyglycolic Acid , Chemistry , Tissue Engineering , Methods , Tissue Scaffolds , Chemistry
SELECTION OF CITATIONS
SEARCH DETAIL