RESUMEN
OBJECTIVE: Osteonecrosis of the femoral head (ONFH) is a common orthopedic disease with a high disability rate. The clinical effect of BuShenHuoXue decoction (BSHX) for ONFH is satisfactory. We aimed to elucidate the potential angiogenic mechanisms of BSHX in a rat femoral osteonecrosis model and bone marrow mesenchymal stem cells (BMSCs). METHODS: With in vivo experiments, we established the steroid-induced osteonecrosis of the femoral head (SONFH) model using Sprague-Dawley (SD) rats (8-week-old). The rats were randomly divided into five group of 12 rats each and given the corresponding interventions: control, model (gavaged with 0.9% saline), BSHX low-, medium- and high-dose groups (0.132 3, 0.264 6, and 0.529 2 g/mL BSHX solution by gavage). After 12 weeks, haematoxylin and eosin (H&E) staining was preformed to evaluate rat osteonecrosis. the expression of angiogenic factors (CD31, VEGFA, KDR, VWF) in rat femoral head was detected by immunohistochemistry, qPCR and western blotting. In cell experiment, BMSCs were isolated and cultured in the femoral bone marrow cavity of 4-week-old SD rats. BMSCs were randomly divided into eight groups and intervened with different doses of BSHX-containing serum and glucocorticoids: control group (CG); BSHX low-, medium-, and high-dose groups (CG + 0.661 5, 1.323, and 2.646 g/kg BSHX gavage rat serum); dexamethasone (Dex) group; and Dex + BSHX low-, medium-, and high-dose groups (Dex + 0.661 5, 1.323, and 2.646 g/kg BSHX gavaged rat serum), the effects of BSHX-containing serum on the angiogenic capacity of BMSCs were examined by qPCR and Western blotting. A co-culture system of rat aortic endothelial cells (RAOECs) and BMSCs was then established. Migration and angiogenesis of RAOECs were observed using angiogenesis and transwell assay. Identification of potential targets of BSHX against ONFH was obtained using network pharmacology. RESULTS: BSHX upregulated the expression of CD31, VEGFA, KDR, and VWF in rat femoral head samples and BMSCs (p < 0.05, vs. control group or model group). Different concentrations of BSHX-containing serum significantly ameliorated the inhibition of CD31, VEGFA, KDR and VWF expression by high concentrations of Dex. BSHX-containing serum-induced BMSCs promoted the migration and angiogenesis of RAOECs, reversed to some extent the adverse effect of Dex on microangiogenesis in RAOECs, and increased the number of microangiogenic vessels. Furthermore, we identified VEGFA, COL1A1, COL3A1, and SPP1 as important targets of BSHX against ONFH. CONCLUSION: BSHX upregulated the expression of angiogenic factors in the femoral head tissue of ONFH model rats and promoted the angiogenic capacity of rat RAOECs and BMSCs. This study provides an important basis for the use of BSHX for ONFH prevention and treatment.
Asunto(s)
Necrosis de la Cabeza Femoral , Osteonecrosis , Ratas , Animales , Cabeza Femoral , Necrosis de la Cabeza Femoral/inducido químicamente , Necrosis de la Cabeza Femoral/tratamiento farmacológico , Necrosis de la Cabeza Femoral/metabolismo , Células Endoteliales/metabolismo , Farmacología en Red , Factor de von Willebrand/efectos adversos , Ratas Sprague-Dawley , OsteogénesisRESUMEN
Surface water samples of Yincungang and Chendonggang Rivers were collected from September 2012 to August 2013 in Lake Taihu. Water temperature, Chlorophyll a and bacterial abundance were analyzed, as well as dissolved organic carbon (DOC) concentrations, stable carbon isotope of DOC (Δ13C(DOC)), specific UV absorbance (SUVA254 ) and dissolved carbohydrates concentrations. Δ13C(DOC) ranged from -27.03% per thousand ± 0.30% per thousand to -23.38%per thousand ± 0.20% per thousand, indicating a terrestrial source. Both the autochthonous and allochthonous sources contributed to the carbohydrates pool in the tributaries. Significant differences in PCHO (polysaccharides) and MCHO (monosaccharides) concentrations were observed between spring-summer and autumn-winter (P < 0.01, n = 12; P < 0.01, n = 12), which might be caused by the variation in the sources and bioavailability of carbohydrates. PCHO contributed a major fraction to TCHO (total dissolved carbohydrates) in autumn and winter, which could be explained by the accumulation of undegradable PCHO limited by the low water temperature; MCHO contributed a major fraction to TCHO in spring and summer, which might be caused by the transformation from PCHO by microbes at high water temperature.
Asunto(s)
Carbohidratos/análisis , Carbono/análisis , Ríos/química , Disponibilidad Biológica , Isótopos de Carbono/análisis , China , Lagos , Estaciones del AñoRESUMEN
To study the temporal and spatial distribution of dissolved organic matter (DOM) and the related influencing factors of Lake Chaohu, surface water samples were collected at seventeen sites in three different regions of the Lake from April 2013 to April 2014. The concentration of dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) were then analyzed. A significance difference in DON concentration was observed among the sampling sites (P <0. 01, n = 13), which was caused by the terrestrial input from the western rivers and the bioavailability of DON. The ratio of total nitrogen to total phosphorus, total dissolved nitrogen to total dissolved phosphorus, and dissolved inorganic nitrogen to soluble reactive phosphorus (DIN/SRP) declined gradually during the phytoplankton bloom period, especially the ratio of DIN/SRP dropped to 5 ± 7 in August 2013, indicating the nitrogen was limited in lake water. Moreover, the concentration of DON was decreased and a significant negative correlation was observed between DON and Chl-a (r = - 0. 265, P < 0. 05, n = 91), suggesting that DON is bioavailable, and can be utilized by phytoplankton directly or indirectly during nitrogen limitation. No significant difference in DOC concentration was observed and water temperature was the major factor related to the variation of DOC. Chl-a and nitrate concentrations can also affect the dynamics of DOC. In addition, the ratio of DOC/DON was considerably varied, the concentration of DON contributed to the variation of DOC/DON, and DON was the major component contributed to the bioavailability of DOM.