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Objective: To investigate the potential toxic effects and mechanisms of Tris(1; 3-dichloro-2-propyl) phosphate (TDCIPP) on thyroid in female SD rats.Methods: Thirty-two 3-weeks-old female SD rats were randomly divided into normal group(treated with corn oil ), and low/moderate/high-dose group treated with TDCIPP (dissolved in corn oil )(n=8). All rats were treated with corn oil or TDCIPP (50, 100, 250 mg/(kg·d)) once a day during a 21-day period. All rats were sacrificed after the last administration. Serum thyroid stimulating hormone (TSH), 3,3',5-triiodothyronine (T3), 3,3',5,5'-tetraiodothyronine (T4), free 3,3',5,5'-tetraiodothyronine (FT4) were detected with ELISA kit. Morphology of thyroid was observed with hematoxylin and eosin (HE) staining. Expressions of genes and proteins correlate with thyroid were measured respectively by real-time fluorescence quantitative PCR and Western blot. Results: Compared with control group, morphology of thyroid showed follicles irregular arrangement, hypocolloid, and follicular hyperplasia in TDCIPP treatment groups. The levels of serum TSH in low-dose TDCIPP group and T3 in high-dose TDCIPP group were significantly higher than those in control group(Pï¼0.05). Thyroid stimulating hormone receptor (TSHR) mRNA expression was decreased distinctly in low-dose TDCIPP group, while the expression of thyroperoxidase (TPO) mRNA was increased notably in moderate and high-dose TDCIPP groups(Pï¼0.05,Pï¼0.01). Compared with control group, the level of TRß protein was decreased significantly in moderate and high-dose TDCIPP groups, while the expressions of udp-glucuronosyl-transferases (UGTs) and cytochrome-p450-3A1 (CYP3A1) proteins were upregulated notably in TDCIPP treatment groups(Pï¼0.05). Conclusion: Treated with 50 mg/(kg·d) TDCIPP can cause thyroid hyperplasia, change the levels of thyroid hormones, and disturb thyroid function, therefore, it has toxic effects on the thyroid.
Asunto(s)
Organofosfatos , Glándula Tiroides , Hormonas Tiroideas , Animales , Femenino , Organofosfatos/toxicidad , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Disgenesias Tiroideas/inducido químicamente , Glándula Tiroides/efectos de los fármacos , Hormonas Tiroideas/sangreRESUMEN
OBJECTIVES: Gingival recession and alveolar bone loss are common manifestations of periodontitis. Periodontal regeneration is the ideal strategy for rehabilitating periodontal tissue defects and preventing tooth loss. The present study examined whether localized, topical application of gingival overgrowth-inducing drugs, phenytoin, nifedipine or cyclosporine, induces periodontal regeneration. METHODS: Polylactic-co-glycolic acid (PLGA) was used as the carrier for preparation of phenytoin, nifedipine or cyclosporine-loaded PLGA microspheres, using an oil-in-water emulsification technique. The drug-loaded microspheres were delivered to periodontal defects created on alveolar ridges mesial to the first maxillary molars of Sprague-Dawley rats. After eight weeks, the operation area in each rat, including the maxillary molars and periodontal tissues, was harvested and evaluated by micro-computed tomography, histochemical and immunohistochemical analyses. RESULTS: Physical parameters representative of periodontal regeneration, including the length of new alveolar bone (p < 0.01) and the area of new alveolar bone (p < 0.01) were significantly improved in the phenytoin group. Compared to other groups, the phenytoin group demonstrated increased expression of COL-1, VEGF-A, osteoblast and osteoclast markers (BMP-2, TGF-ß1, OCN and TRAP staining), as well as decreased expression of MMP-8. CONCLUSIONS: Results of the present study provided new evidence that localized, controlled release of phenytoin confers therapeutic benefits toward gingival recession and alveolar bone loss. Phenytoin appears to be a promising drug that promotes periodontal regeneration.
Asunto(s)
Pérdida de Hueso Alveolar , Portadores de Fármacos , Recesión Gingival , Microesferas , Nifedipino , Fenitoína , Poliésteres , Animales , Masculino , Ratas , Administración Tópica , Pérdida de Hueso Alveolar/tratamiento farmacológico , Biomarcadores/análisis , Ciclosporina/administración & dosificación , Portadores de Fármacos/administración & dosificación , Recesión Gingival/tratamiento farmacológico , Inmunohistoquímica , Nifedipino/administración & dosificación , Fenitoína/administración & dosificación , Poliésteres/administración & dosificación , Distribución Aleatoria , Ratas Sprague-Dawley , Método Simple Ciego , Microtomografía por Rayos XRESUMEN
The harm assessment and responsibility of marine mineral oil pollution require the content of mineral oil to be obtained by real-time online monitoring. In the present paper, the method of online monitoring of the oil content in water is presented, a creative technology based on optical scattering theory was proposed. Firstly the particle distribution of oil drops was scanned by Marvin laser particle meter, then with the help of the scattering signal, the crude, diesel of different concentrations from 0 to 30 mg x L(-1) was measured in experiment, the linearity is more than 0.99. This paper presents a feasible setup for the online monitoring of the content of mineral oil.
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People have paid a more attention to the pesticides residues, so the rapid detection method is required. In this paper the application of molecular imprinting technique on the detection of pesticides residues was reviewed, including recognition principles, preparation, current applications, problems and its future.