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1.
Chinese Acupuncture & Moxibustion ; (12): 609-613, 2013.
Article in Chinese | WPRIM | ID: wpr-253940

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effect difference of behavior training with head needling retention and behavior training after acupuncture for autism children.</p><p><b>METHODS</b>Sixty qualified autism children were divided randomly into simultaneous head needling retention and behavior training group (trial group) and behavior training after acupuncture treatment group (control group) with 30 case in each group. Retention needles on the head with simultaneous behavior training was applied for the trial group. The main acupoints included Sishen Xue, Dingshen Sanxue (3 points for mental tranquilization), Nao Sanxue (3 points for the function of brain), Shou Zhisanxue (3 points for mental activities on hand) and Zozhi Sonxue (3 points for mental activities on foot). Other points were combined according to conditions of patients. Needles on the 4 extremities were withdrawn first after 30 minutes, needles on head were remained during behavior training. While behavior training was applied to the control group when acupuncture treatment was completely accomplished. Treatments were applied once a day to both groups. And 3 months was taken as one observation cycle. Estimation was made on therapeutic effect and developing level of autism children with CARS and PEP.</p><p><b>RESULTS</b>The total effective rate of the trial group was 83.3% (25/30), better than 66.7% (20/30) of the control group (P < 0.05). The CARS scores of both groups declined after the treatment. And the score of trail group was lower than the control group (all P < 0.05). While the PEP scores of both groups increased, and the score of trail group was higher than the control group (all P < 0.05). The increasing level of scores of cognitive understanding and cognitive expression were all better than the control group (all P < 0.05).</p><p><b>CONCLUSION</b>The effect of behavior training with head needle retention on autism children is better than behavior training after acupuncture treatment, especially in enhancing cognition understanding and cognition expression.</p>


Subject(s)
Child , Child, Preschool , Female , Humans , Male , Acupuncture Points , Acupuncture Therapy , Autistic Disorder , Psychology , Therapeutics , Behavior Therapy
2.
Chinese journal of integrative medicine ; (12): 529-533, 2012.
Article in English | WPRIM | ID: wpr-347167

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the protective effects of the natural medicinal monomer isopsoralen (ISR) with estrogenic activity against oxidative damage in human lens epithelial cells B3 (HLE-B3) caused by hydrogen peroxide (H(2)O(2)) and to pursue the possible mitochondrial proteomic regularity of the protective effects.</p><p><b>METHODS</b>HLE-B3 cells were treated with H(2)O(2) (300 μ mol/L), β-estradiol (E(2): 10(-8) mol/L) and H(2)O(2), ISR (10(-5) mol/L) and H(2)O(2), or left untreated. Altered expressions of all mitochondrial proteins were analyzed by protein array and surfaceenhanced laser desorption ionization time of flight mass spectrometry (SELDI-TOF-MS). The mass/charge (m/z) ratios of each peak were tested by the Kruskal-Wallis rank sum test, and the protein peak value of the m/z ratio for each treatment by pair comparison was analyzed with the Nemenyi test.</p><p><b>RESULTS</b>H(2)O(2) up-regulated the expressions of two protein spots (with m/z of 6532 and 6809). E(2) mitigated the oxidative damage, and the expression of one protein spot (m/z 6532) was down-regulated. In contrast, ISR down-regulated both of protein spots (m/z 6532 and 6809).</p><p><b>CONCLUSIONS</b>ISR could effectively inhibit H(2)O(2)-induced oxidative damage in HLE-B3 cells. The protein spot at m/z of 6532 might be the target spot of ISR against oxidative damage induced by H(2)O(2).</p>


Subject(s)
Humans , Cell Line , Epithelial Cells , Metabolism , Pathology , Estradiol , Pharmacology , Furocoumarins , Pharmacology , Hydrogen Peroxide , Toxicity , Lens, Crystalline , Pathology , Mitochondria , Metabolism , Oxidation-Reduction , Oxidative Stress , Protective Agents , Pharmacology , Proteome , Metabolism , Proteomics , Methods
3.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 76-79, 2012.
Article in Chinese | WPRIM | ID: wpr-326611

ABSTRACT

<p><b>OBJECTIVE</b>To study the effects of ecdysterone (ECR) on the expression of nuclear factor (NF)-kappaB in H2O2 induced oxidative damage of human lens epithelial cells (HLECs).</p><p><b>METHODS</b>The cultured HLECs were divided into 5 groups, i.e., the control group, the H2O2 group, the beta-estradiol (E2) group, the ECR group, and the pyrrolidine dithiocarbamate group (PDTC) group. The expression rate of NF-kappaB p65 in the HLECs were detected by flow cytometer (FCM).</p><p><b>RESULTS</b>The expression of NF-kappaB p65 occurred in normal HLECs (9. 53%). The expression rate of NF-kappaB p65 in the H2O2 group obviously increased (39.87%, P < 0.01). The expression rate of NF-kappaB p65 in the PDTC group obviously decreased (5.90%, P < 0.01). The expression rates of NF-kappaB p65 in the ECR group (13.99%) and the E2 group (25.18%) ranged between the control group and the H2O2 group, but still lower than that of the H2O2 group (P < 0.01).</p><p><b>CONCLUSIONS</b>The activation of NF-kappaB in the HLECs could be induced by H2O2 ECR with the estrogenic activity could effectively inhibit the activation of NF-kappaB.</p>


Subject(s)
Humans , Cells, Cultured , Ecdysterone , Pharmacology , Epithelial Cells , Metabolism , Hydrogen Peroxide , Lens, Crystalline , Cell Biology , Oxidative Stress , Transcription Factor RelA , Metabolism
4.
China Journal of Chinese Materia Medica ; (24): 725-728, 2007.
Article in Chinese | WPRIM | ID: wpr-283396

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of Rhizoma Curcumae (RC), arsenite trioxide (As2O3) on proliferation ana signal transduction molecule in lens epithelial cell (LEC), in order to provide experiment evidence for prevention and treatment of after cataract.</p><p><b>METHOD</b>Proliferation of cultured bovine LEC were induced by induced by recombinant human basic fibroblast growth factor (rhbFGF); Inhibitory rates of LEC proliferation induced by RC, As2O3 were detected by methyl thiazolyl tetrazolium (MTT); Inhibitory effects of expression of proliferating cell nuclear antigen (PCNA) induced by RC, As2O3 in LEC were assayed via flow cytometer (FCM); Concentrations of LEC calcium ([Ca2+]i) were determined by spectrofluoremeter, intracellular concentrations of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) of LEC were measured by radioimmunoassay.</p><p><b>RESULT</b>Inhibitory rates of RC, As2O3 on LEC proliferation induced by rhbFGF increased significantly, showing dose-dependent (P < 0.01). PCNA expression of LEC proliferation induced by rhbFGF were down regulated obviously by RC, As2O3, showing dose-dependent (P < 0.01). Concentrations of [Ca2+]and cAMP increased and cGMP decreased significantly in LEC of proliferation inhibited by RC, As2O3 (P < 0.01).</p><p><b>CONCLUSION</b>RC, As2O3 can inhibit LEC proliferation obviously. Signal transductions of [Ca2+]i, cAMP, cGMP may be the important molecular mechanism. There are broad prospect for RC, As2O3 on prevention and treatment of after cataract.</p>


Subject(s)
Animals , Cattle , Arsenicals , Pharmacology , Calcium , Metabolism , Cell Proliferation , Cells, Cultured , Curcuma , Chemistry , Cyclic AMP , Metabolism , Cyclic GMP , Metabolism , Dose-Response Relationship, Drug , Drugs, Chinese Herbal , Pharmacology , Epithelial Cells , Cell Biology , Metabolism , Fibroblast Growth Factor 2 , Genetics , Pharmacology , Flow Cytometry , Growth Inhibitors , Pharmacology , Lens, Crystalline , Cell Biology , Metabolism , Oxides , Pharmacology , Proliferating Cell Nuclear Antigen , Metabolism , Radioimmunoassay , Recombinant Proteins , Pharmacology , Rhizome , Chemistry , Signal Transduction
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