Autologous chondrocyte-seeded scaffolds have proved to be one of the most promising alternative therapies for articular cartilage defects. However, the chondrocytes have specific nutritional requirements and risk of dedifferentiation during in vitro expansion. Stichopus chloronotus aqueous extract (SCAE) was investigated as a medium supplement for threedimensional (3D) collagen type I hydrogel scaffold seeded with chondrocytes to determine whether SCAE is capable of maintaining phenotype and sustaining extracellular matrix synthesis and deposition. Human osteoarthritis articular chondrocytes were isolated from the knee joint cartilage of patients underwent total knee replacement surgery. Human osteoarthritis articular chondrocytes were encapsulated in collagen type I hydrogel and cultured in basic medium with 0, 0.1 and 0.2% of SCAE. The chondrocytes in 3D culture were evaluated by means cell morphology and proliferation, quantitative phenotypic expression of collagen type I, II, aggrecan core protein and sox-9. H&E, toluidine blue staining and sulfated glycosaminoglycan (sGAG) production were analyzed after 7 days in culture. Chondrocytes cultured in 3D with various SCAE concentration appeared with polygonal morphology maintaining their chondrocytes characteristic. SCAE supplementation promoted chondrocytes proliferation and the ability of the cells to express gene encoding collagen type I decreased, whereas their ability to express collagen type II, aggrecan core protein and sox9 increased as compared to control. The cartilaginous matrices were positively stained toluidine blue concomitant with higher sGAG accumulation in SCAE-supplemented culture medium. This study shown that SCAE may be beneficial for in vitro development of 3D chondrocytes culture for use in cartilage tissue engineering therapies.

Chlorella vulgaris, a coccoid green eukaryotic microalga, is a popular food supplement and has been marketed as a nutritional supplement in Asia. Despite numerous reports on the antioxidant property of this species, its toxic effect has not been extensively studied. The aim of this study was to determine the acute oral toxic effect of C. vulgaris on female Sprague Dawley (SD) rats. An acute oral toxicity assessment of C. vulgaris was performed based on the Organization for Economic Cooperation and Development (OECD) Guideline 420. These guidelines are divided into a sighting study and a main study. In the sighting study, C. vulgaris extract was administered orally in sequential doses of 5, 50, 300 and 2000 mg kg−1 body weight (BW) with one rat used for each dosage. Clinical observation and mortality were observed for each rat to monitor signs of toxicity for 14 days. BW and relative organ weight (ROW) were recorded. Blood was collected for liver function test (LFT). Gross pathological evaluations were performed after euthanasia of rats. Haematoxylin and eosin (H&E) staining of the liver and kidney was also performed. The main study was performed based on the highest dose in the sighting study that did not exhibit any signs of toxicity and mortality. For 14 days, clinical observations, BW, and ROW were recorded. Blood from rats in the main study was also measured for LFT, and gross pathological evaluations and H&E staining of the liver and kidney were also performed. The highest dose of 2000 mg kg−1 BW C. vulgaris was used in the main study. No toxicity and mortality were observed in both the sighting study and the main study. Increases in BW were observed in both studies. Gross pathological evaluations showed no signs of organ abnormalities on each organ in the sighting and main studies. The ROW also showed no differences. The values of biochemical parameters in the liver function test showed no differences in the sighting study. However, in the main study, significant decreases in alkaline phosphatase (ALP) and aspartate aminotransferase (AST) were observed on day 14 compared with day 0 (p < 0.05). Chlorella vulgaris showed no toxicity at the dose of 2000 mg kg−1 BW. In conclusion, C. vulgaris can be categorized as unclassified according to the Globally Harmonised Classification System (GHS) for chemical substances and mixtures.

The present study aims to examine the effects of a palm-oil-derived vitamin E mixture containing tocotrienol (~70%) and tocopherol (~30%) on plasma lipids and on the formation of atherosclerotic plaques in rabbits given a 2% cholesterol diet. Eighteen New Zealand White rabbits (2.2-2.8 kg) were divided into three groups; group 1 (control) was fed a normal diet, group 2 (AT) was fed a 2% cholesterol diet and group 3 (PV) was fed a 2% cholesterol diet with oral palm vitamin E (60 mg/kg body weight) given daily for 10 weeks. There were no differences in the total cholesterol and triacylglycerol levels between the AT and PV groups. The PV group had a significantly higher concentrations of HDL-c and a lower TC/HDL-c ratio compared to the AT group (P < 0.003). The aortic tissue content of cholesterol and atherosclerotic lesions were comparable in both the AT and PV groups. However, the PV group had a lower content of plasma and aortic tissue malondialdehyde (P < 0.005). Our findings suggest that despite a highly atherogenic diet, palm vitamin E improved some important plasma lipid parameters, reduced lipid peroxidation but did not have an effect on the atherosclerotic plaque formation.

ABSTRAKPeriodontitis adalah penyakit kronik yang melibatkan kehilangan tulang dan inflamasi pada tisu periodontium. , respectively. However, there was no significant difference in plasma level of Periodontitis is a chronic disease which results in alveolar bone loss and inflammation at the periodontal gingival tissue. Interleukin-6 (IL-6) and Tumor Necrosis Factor-α (TNF-α) are the crucial pro-inflammatory markers in periodontitis. Twenty Sprague-Dawley rats were divided into four groups: which was control group (CS); control treated with Gelam honey (3 g/mL) (CH); periodontitis group (TS); and periodontitis treated with Gelam honey (3 g/mL) (TH