RESUMEN
BACKGROUND: Bone marrow mesenchymal stem cells (BMMSCs) and bone marrow mononuclear cells (BMMNCs) are both used to treat spastic cerebral palsy. However, the differences in therapeutic effect remain unknown. METHODS: A total of 105 patients with spastic cerebral palsy were enrolled and randomly assigned to three groups: the BMMSC group, the BMMNC group and the control group. Patients in both transplantation groups received four intrathecal cell injections. Patients in the control group received Bobath therapy. The gross motor function measure (GMFM) and the fine motor function measure (FMFM) were used to evaluate the therapeutic efficacy before transplantation and 3, 6, and 12 months after transplantation. RESULTS: Three months after cell transplantation, scores in the A dimension of GMFM and the A and C dimensions of FMFM scores in the BMMSC group are all higher than those of the BMMNC and the control groups (P < 0.05). Six months after cell transplantation, scores in the A, B dimensions of GMFM and the A, B, C, D, and E dimensions of FMFM scores in the BMMSC group are higher than those of the BMMNC and the control groups (P < 0.05). Twelve months after cell transplantation, scores in the A, B, and C dimensions of GMFM and the A, B, C, D, and E dimensions of FMFM scores in the BMMSC group are all higher than those of the BMMNC and the control groups (P < 0.05). No obvious adverse effects were investigated during follow-up. CONCLUSIONS: BMMSC transplantation for the treatment of cerebral palsy is safe and feasible, and can improve gross motor and fine motor function significantly. In addition, compared with BMMNC, the motor function of children improved significantly in terms of gross motor and fine motor functions.
Asunto(s)
Parálisis Cerebral/terapia , Leucocitos Mononucleares/trasplante , Trasplante de Células Madre Mesenquimatosas , Células Madre Mesenquimatosas/citología , Parálisis Cerebral/fisiopatología , Niño , Preescolar , Femenino , Humanos , Lactante , Masculino , Trasplante de Células Madre Mesenquimatosas/efectos adversos , Actividad MotoraRESUMEN
BACKGROUND: Tetranychus cinnabarinus (Boisduval) is one of the most important, highly polyphagous pests of a wide range of field and greenhouse crops throughout the world. The control of this mite is still based primarily on the use of synthetic chemical pesticides. In this study, we screened eight plant extracts from China and evaluated the natural compounds showing acaricidal properties from the plant extract, considering their potential use as an alternative to synthetic pesticides. RESULTS: In bioassay screening assays, the Cinnamomum camphora (L.) Presl extract showed significantly greater acaricidal activity against T. cinnabarinus than the other seven plant extracts tested. Five compounds were identified from the C. camphora extract via repeated column chromatography and gas chromatography-mass spectrometry analysis. All the compounds presented acaricidal activity, with 2,4-di-tert-butylphenol and ethyl oleate exhibiting the greatest activity. At 7 days after treatment in a potted seedling experiment, the LC50 values of 2,4-di-tert-butylphenol and ethyl oleate were found to be 1850.94 and 2481.65 mg kg(-1) respectively. Microscopic observations showed that the mites displayed the symptomology of poisoning. CONCLUSION: These results demonstrated that the C. camphora extract and its two active components show the potential to be developed as new natural acaricides for controlling carmine spider mites.
Asunto(s)
Acaricidas/farmacología , Cinnamomum camphora/química , Ácidos Oléicos/farmacología , Fenoles/farmacología , Tetranychidae/efectos de los fármacos , Animales , Bioensayo , China , Extractos Vegetales/farmacología , Vicia fabaRESUMEN
BACKGROUND: Colletotrichum lagenarium is an important plant-pathogenic fungus that causes anthracnose of cucumber, a disease that is widespread under both greenhouse and field cultivation. To find a promising method for the control of this disease, extracts of eight plants from China were screened in the study presented here. RESULTS: The results showed that the extract of Cinnamomum camphora (L.) Presl had significantly greater inhibitory activity against C. lagenarium than the other seven plant extracts tested in vitro. At 5 days after inoculation in a potted seedling experiment, C. camphora extract demonstrated 95% control of C. lagenarium at a concentration of 16 mg mL⻹, and the MIC50 was 2.596 mg mL⻹. Microscopic observation showed that this extract had a significant impact on the morphology of the fungus, leading to shorter hyphae that were more branched; this observation was associated with the inhibition of mycelial growth. Stability assays revealed that the extract was relatively stable at 80 °C, under acidic conditions and when exposed to light and short periods of UV radiation. CONCLUSION: These results demonstrated that the extract from C. camphora could be used as a potent phytochemical fungicide.
Asunto(s)
Antifúngicos/farmacología , Cinnamomum , Colletotrichum/efectos de los fármacos , Cucumis sativus/microbiología , Enfermedades de las Plantas/prevención & control , Extractos Vegetales/farmacología , China , Colletotrichum/crecimiento & desarrollo , Estabilidad de Medicamentos , Calor , Concentración de Iones de Hidrógeno , Luz , Micelio/efectos de los fármacos , Micelio/crecimiento & desarrollo , Enfermedades de las Plantas/microbiología , Rayos UltravioletaRESUMEN
Ten new triterpenoids, named meliasenins I-R (1-10), one new steroid (11), and 11 related known compounds (12-22) were isolated from fruits of Melia toosendan. The structures of the new compounds were established on the basis of spectroscopic methods, including 2D NMR techniques and mass spectrometry. The relative configuration of 1, (20R*,23E)-25-hydroperoxyeupha-7,23-diene-3ß,16ß-diol (meliasenin I), was confirmed by single-crystal X-ray diffraction analysis. All isolated triterpenoids (1-10, 12-15) and two steroids (11, 20) were tested for their cytotoxicity against U20S human osteosarcoma and MCF-7 human breast cancer cells using the MTT assay, and some of them were significantly cytotoxic (IC(50) <10 µg/mL). The insecticidal properties of compounds 1-15 and 20 were also briefly evaluated.