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1.
Chinese Journal of Experimental Traditional Medical Formulae ; (24): 37-45, 2022.
Artículo en Chino | WPRIM | ID: wpr-940384

RESUMEN

ObjectiveTo study the effect of Jinlida granules on visceral fat accumulation and its induced inflammatory response in prediabetic rats. MethodMale SD rats were randomly divided into normal group, model group, Jinlida low-dose group (1.5 g·kg-1), Jinlida high-dose group (3.0 g·kg-1) and atorvastatin group (10 mg·kg-1). Prediabetic rat model was established using high-carbohydrate, high-fat diet combined with low-dose streptozotocin (STZ) by multiple small-dose intraperitoneal injections. After 8 weeks of modeling and drug intervention for 13 consecutive weeks, body weight, oral glucose tolerance test(OGTT), fasting blood glucose (FBG), fasting insulin (FINS), insulin resistance index (HOMA-IR), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C) were measured in each group of rats. The content of visceral fat was quantified by micro-computed tomography (Micro-CT). Hematoxylin-eosin staining (HE) was used to observe the pathological changes of fat cells. The levels of tumor necrosis factor-α (TNF-α) and interleukin- 6 (IL-6) in rat visceral fat and serum were determined by enzyme linked immunosorbent assay (ELISA). The expression of macrophage marker CD68 in visceral fat was detected by immunofluorescence and Western blot. ResultCompared with normal group, model group had increased oral glucose tolerance, FBG, FINS, HOMA-IR, TC, LDL-C (P<0.01), elevated body weight and visceral fat accumulation (P<0.05, P<0.01), enhanced CD68 protein expression and TNF-α and IL-6 levels (P<0.01), decreased HDL-C (P<0.01), and abnormal hypertrophy of adipocytes. Compared with model group, Jinlida high- and low-dose groups lowered oral glucose tolerance, HOMA-IR, TC and LDL-C (P<0.05, P<0.01), body weight and visceral fat accumulation (P<0.05), and CD68 protein expression and TNF-α and IL-6 levels (P<0.05, P<0.01) and lessened hypertrophy of fat cells. ConclusionJinlida can improve the insulin resistance in prediabetic rats by reducing visceral fat accumulation and its induced inflammatory response, which provides a new pharmacological basis for clinical treatment of prediabetes by Jinlida granules.

2.
Artículo | IMSEAR | ID: sea-203603

RESUMEN

Aim: To evaluate the internal adaptation of some dental adhesive restorative material (Nano-composite resin /Biodentine,Nanocomposite resin / Nano- resin-modified glass ionomer and Nano-composite resin) to the primary dentinal surface usingmicro-computed tomography (Micro-CT) Materials and methods: Forty-five extracted primary molars, due to caries ororthodontic reasons, were collected provided that it has an intact buccal/ lingual surface(s) and one half to two-thirds ofroot length. The selected teeth were disinfected and stored in normal saline at room temperature. The teeth were randomlyassigned to one of the three experimental restorative groups according to the restoration type (15 per group): group A:Nanocomposite resin / Biodentine, group B: Nanocomposite resin / Nano-resin-modified glass ionomer and group C:restored totally with Nanocomposite resin. A high- resolution desktop micro-CT (Model 1172, Skyscan, Belgium) was usedto image the samples. Results: The mean rank of volumetric dimension values of the total gap at the restorative material –dentine interface demonstrated significant difference among the three groups (P= 0.003). Moreover, there was a significantdifference in the mean rank of the ratio of total gap volume/cavity volume among the three restorative groups (P=0.015).The data demonstrate that group A showed the lowest in total gap volume and mean ratio of total gap volume /cavity volumewhile group C recorded the highest value. Conclusion: Biodentine exhibited a higher internal adaptation to a dentinalsurface which is comparable to Nano resin-modified glass ionomer. The study results potentiate the importance of usingBiodentine liners under Nano-composite (sandwich technique) in terms of excellent internal adaptation, in addition to itshigh biocompatibility and easy handling as well.

3.
Oral Science International ; : 27-35, 2009.
Artículo en Inglés | WPRIM | ID: wpr-362791

RESUMEN

The objective of this study was to assess the possibility of developing a clinical minimally invasive and standardized method to evaluate the relationship between the microstructure of the jaw bone and systemic bone turnover. For this purpose, we performed standardized bone biopsy of the alveolar bone, and compared the 3D bone microstructure using micro-computed tomography (micro-CT) with bone mineral density (BMD) of the lumbar spine and biochemical markers of bone turnover. We evaluated a total of 9 samples taken from 6 patients by standardized biopsy using a trephine bur. BMD was evaluated using dual energy X-ray absorptiometry (DXA). Regarding the biochemical markers of bone turnover, serum bone-specific alkaline phosphatase (BAP) and serum osteocalcin (OC) were used as bone formation markers, and urinary cross-linked N-telopeptides of type I collagen (NTx) and urinary deoxypyridinoline (DPD) were selected as bone resorption markers. We scanned micro-CT images of these samples. Bone volume fraction (BV/TV), trabecular thickness (Tb.Th), trabecular number (Tb.N), trabecular spacing (Tb.Spac), fractal dimension, trabecular bone pattern factor (TBPf) and node-strut (Nd.Nd/TV, TSL/TV) were measured. Regarding the correlations between the parameters of bone microstructures, TB/TV, Tb.N, fractal dimension, and node-strut seemed to be positively correlated and Tb.Spac and TBPf seemed to be negatively correlated with each other, but Tb.Th seemed to have a low correlation with other parameters. OC and/or BAP showed a significantly high correlation with many structural parameters (p<0.05%). In conclusion, some microstructural parameters may change according to the systemic bone turnover.

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