ABSTRACT
Exposure to solar ultraviolet B (UV-B) is a known causative factor for many skin complications such as wrinkles, black spots, shedding and inflammation. Within the wavelengths 280320 nm, UV-B can penetrate to the epidermal level. This investigation aimed to test whether extracts from the tropical abalone [Haliotis asinina (H. asinina)] mucus-secreting tissues, the hypobranchial gland (HBG) and gills, were able to attenuate the inflammatory process, using the human keratinocyte HaCaT cell line. Cytotoxicity of abalone tissue extracts was determined using an AlamarBlue viability assay. Results showed that HaCaT cells could survive when incubated in crude HBG and gill extracts at concentrations between <11.8 and <16.9 µg/ml, respectively. Subsequently, cell viability was compared between cultured HaCaT cells exposed to serial doses of UV-B from 1 to 11 (x10) mJ/cm2 and containing 4 different concentrations of abalone extract from both the HBG and gill (0, 0.1, 2.5, 5 µg/ml). A significant increase in cell viability was observed (P<0.001) following treatment with 2.5 and 5 µg/ml extract. Without extract, cell viability was significantly reduced upon exposure to UV-B at 4 mJ/cm2. Three morphological changes were observed in HaCaT cells following UV-B exposure, including i) condensation of cytoplasm; ii) shrunken cells and plasma membrane bubbling; and iii) condensation of chromatin material. A calcein AMpropidium iodide livedead assay showed that cells could survive cytoplasmic condensation, yet cell death occurred when damage also included membrane bubbling and chromatin changes. Western blot analysis of HaCaT cell COX2, p38, phosphop38, SPK/JNK and phosphoSPK/JNK following exposure to >2.5 µg/ml extract showed a significant decrease in intensity for COX2, phosphop38 and phosphoSPK/JNK. The present study demonstrated that abalone extracts from the HGB and gill can attenuate inflammatory proteins triggered by UV-B. Hence, the contents of abalone extract, including cellmetabolites and peptides, may provide new agents for skin antiinflammation, preventing damage due to UV-B.
Subject(s)
Biological Products/pharmacology , Gills/chemistry , Inflammation/etiology , Inflammation/metabolism , Ultraviolet Rays/adverse effects , Animals , Biomarkers , Cell Line , Cell Survival/drug effects , Cells, Cultured , Female , Gills/metabolism , Humans , Inflammation Mediators/metabolism , Keratinocytes/drug effects , Keratinocytes/metabolism , Male , Signal TransductionABSTRACT
INTRODUCTION: In this preliminary study, we investigated early histologic changes of paradental tissues in response to a clear plastic appliance in rats. METHODS: Fifteen rats were divided into 3 groups. Group I was the untreated controls; group II received a clear plastic appliance made from a model, with the maxillary left first molar repositioned mesially 0.5 mm from the origin; and group III had a closed-coil spring to move the molar mesially. Specimens were prepared in parasagittal sections, and changes in paradental tissues were evaluated on days 1, 4, and 7 by light microscopy. RESULTS: In group II, the periodontal ligament (PDL) was compressed in the bifurcation and apical areas of the roots of the molar. On day 7, the PDL of the apical and distal aspects of the roots and the bifurcation area showed further compression, with the PDL of the roots stretched along the mesial side. In group III, a disorganized and compressed PDL in the mesial cervical half and interradicular septum was observed, and the stretched fibers were at the distal aspects of the roots after days 4 to 7. CONCLUSIONS: Early histologic changes in response to the clear plastic appliance were intrusion and distal tipping despite the intended mesial movement. In this rat model, the observed histologic changes were subject to the direction and magnitude of forces generated by the clear aligner.