[Effects of Loquat-Branch Dust Substitution on Ganoderma lucidum Cultivation in Its Main Active Components].

OBJECTIVE: To select the best Ganoderma lucidum cultivation medium of replacing sawdust into loquat-branch dust, in order to realize high output and high quality production of Ganoderma lucidum. METHODS: Loquat-branch dust was added as substitution in Ganoderma lucidum cultivation, its effects on the biomass and the content of Ganoderma polysaccharides, triterpenoids and flavonoids were analyzed. RESULTS: By using loquat-branch dust in culture, Ganoderma lucidum grew well with normal fruiting body obtained and spores released. Compared with control group, the biological efficiency was increased by 11.34%, when the addition of the loquat-branch dust was 80%, while the amount of spore had little difference. When the addition of the loquat-branch dust was 90%, the content of Ganoderma polysaccharides and triterpenoids was increased by 32.29% and 30.58% respectively, while the efficiency of flavonoids had little difference. CONCLUSION: Using loquat-branch dust cultivation can improve the quality of Ganoderma lucidum. According to the comprehensive score, 80% loquat-branch dust is the most suitable cultivation medium.

Raman spectroscopic study on the structure in the surface and the bulk shell of Ce(x)Pr(1-x)O(2-delta) mixed oxides.

The difference between the surface and the bulk shell of Ce(x)Pr(1-x)O(2-delta) mixed oxides was studied by Raman spectroscopy with four different excitation lasers. Two Raman peaks appear at 465 and 570 cm(-1) under all of the four lasers. The former is attributed to the Raman active F(2g) mode of CeO2, while the latter is attributed to oxygen vacancy. On the basis of the fact that the laser with shorter wavelength is closer to the electronic adsorption of samples, it is found that the Raman information detected by excitation laser with shorter wavelength is more sensitive to the surface region of samples. An inflection is observed in the relationship of the value I570/I465 to the Ce content in Ce(x)Pr(1-x)O(2-delta). With the increase in the wavelength of excitation laser, the Ce content corresponding to the inflection decreases. Combined with the surface concentration obtained by XPS, it can be deduced that the composition of Ce(x)Pr(1-x)O(2-delta) mixed oxide particles in the surface region and the bulk shell are different, the former is enrichment of Pr component and the latter is enrichment of Ce component. The thickness of the surface layer with rich Pr component decreases with the increase in the Ce content.

[Role of TNF-alpha in vascular endothelial cells injury mediated by frozen/thawed PMN].

AIM: To investigate the role of TNF-alpha in vascular endothelial cells injury mediated by freezing/thaw ing PMN. METHODS: Freezing/thawing cell model was founded using rat PMN isolated by dextran sedimentation technique and VEC cultured in vitro. The injury level of VEC was indicated by measuring activity of LDH in medium. The number of frozen/thawed PMN adhering to VEC was counted with Phagocytizing reactive dyes the degree of frozen/thawed PMN and VEC adhesion. Expression of LFA-1 on the surface of frozen/thawed PMN was analyzed with flow cytometry. RESULTS: TNF-alpha could obviously upregulate expression of LFA-1 on surfaced of frozen/thawed PMN. Upregulation of LFA-1 expression promoted adhesion of frozen/thawed PMN and normal VEC,and aggravated VEC injury. Monoclonal antibody against LFA-1 could partly block adhesion of frozen/thawed PMN and normal VEC,and attenuate VEC injury. CONCLUSION: TNF-alpha can promote expression of LFA-1 on surface of frozen/thawed PMN adhering of frozen/thawed PMN to normal VEC and VEC injury increase, monoclonal antibody against LFA-1 could partly block PMN-VEC adhesion and attenuate VEC injury.

Initiation of cartilage cell culture from skate (Raja porasa Günther).

Cartilage tissues from the proboscis of skate (Raja porasa Günther) were used to initiate primary cultures of cartilage cells. Aseptically dissected cartilage tissues were immersed in MEM medium free of fetal bovine serum (FBS), pH 7.6, and minced into small pieces (1 mm3 on average). After hydrolysis with collagenase II, hyaluronidase, and trypsin for 2 hours at room temperature, the acquired cartilage cells were rinsed twice with 20% FBS-supplemented MEM medium and then inoculated into 25-cm3 cell culture flasks, and incubated at 24 degrees C. The primary cultures were initiated successfully, and the cartilage cells grew gradually into a confluent monolayer at day 10. Effects of growth factors were also tested in this study, and it was found that 20 ng/ml of basic fibroblast growth factor and 100 ng/ml of insulin-like growth factor II together had the most prominent stimulating effect on the growth and division of cartilage cells in the series of concentration combinations employed. The induced cartilage cells cultured formed a confluent monolayer at day 7.