[Clinical Observation of Recombinant Bovine Basic Fibroblast Growth Factor as an Adjuvant Therapy for Patients with Atrophic Acne Scar].

Objective To study the influence of recombinant bovine basic fibroblast growth factor as an adjuvant therapy on scar alleviation and inflammatory cytokines in patients with atrophic acne scar. Methods The random number table was employed to randomly assign 120 patients with atrophic acne scar into a test group and a control group.Both groups of patients were treated with CO2 lattice laser.After the operation,the control group was routinely smeared with erythromycin ointment and the test group was coated with recombinant bovine basic fibroblast growth factor gel.The clinical efficacy,clinical indicators,scar alleviation,and inflammatory cytokine levels before and after treatment were compared,and adverse reactions were counted. Results The test group had higher total effective rate(P=0.040) and lower total incidence of adverse reactions(P=0.028) than the control group.Compared with the control group,the test group showcased short erythema duration after treatment(P=0.025),early scab forming(P=0.002),and early edema regression(P<0.001).After treatment,the proportion of grade 1 scars graded by Goodman and Baron's acne scar grading system in the test group and control group increased(P=0.001,P=0.027),and the proportion of grade 4 scars decreased(P<0.001,P=0.034).Moreover,the proportion of grade 1 scars in the test group was higher than that in the control group(P=0.031) after treatment,and the proportion of grade 4 scars presented an opposite trend(P=0.031).After treatment,the levels of tumor necrosis factor-α(TNF-α) and interleukin-1ß(IL-1ß) in both groups declined(all P<0.001),and the test group had lower TNF-α and IL-1ß levels than the control group(all P<0.001). Conclusion The recombinant bovine basic fibroblast growth factor gel as an adjuvant therapy of CO2 lattice laser can effectively alleviate the atrophic acne scar,relieve local inflammatory reaction,and has good curative effect and less adverse reactions.

[New effect of G-protein coupled receptors on blood pressure regulation].

Hypertension is a clinical syndrome characterized by elevated systemic arterial blood pressure, which may be accompanied by functional or organic damage of heart, brain, kidney and other organs. The pathogenesis and development of hypertension are affected by genetic, environmental, epigenetic, intestinal microbiota and other factors. They are the result of multiple factors that promote the change of blood pressure level and vascular resistance. G protein coupled receptors(GPCRs) are the largest and most diverse superfamily of transmembrane receptors that transmit signals across cell membranes and mediate a large number of cellular responses required by human physiology. A variety of GPCRs are involved in the control of blood pressure and the maintenance of normal function of cardiovascular system. Hypertension contributes to the damages of heart, brain, kidney, intestine and other organs. Many GPCRs are expressed in various organs to regulate blood pressure. Although many GPCRs have been used as therapeutic targets for hypertension, their efficacy has not been fully studied. The purpose of this paper is to elucidate the role of GPCRs in blood pressure regulation and its distribution in target organs. The relationship between GPCRs related to intestinal microorganisms and blood pressure is emphasized. It is proposed that traditional Chinese medicine may be a new way to treat hypertension by regulating the related GPCRs via intestinal microbial metabolites.

Comparative proteomes change and possible role in different pathways of microRNA-21a-5p in a mouse model of spinal cord injury.

Our previous study found that microRNA-21a-5p (miR-21a-5p) knockdown could improve the recovery of motor function after spinal cord injury in a mouse model, but the precise molecular mechanism remains poorly understood. In this study, a modified Allen's weight drop was used to establish a mouse model of spinal cord injury. A proteomics approach was used to understand the role of differential protein expression with miR-21a-5p knockdown, using a mouse model of spinal cord injury without gene knockout as a negative control group. We found that after introducing miR-21a-5p knockdown, proteins that played an essential role in the regulation of inflammatory processes, cell protection against oxidative stress, cell redox homeostasis, and cell maintenance were upregulated compared with the negative control group. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis identified enriched pathways in both groups, such as the oxidative phosphorylation pathway, which is relevant to Parkinson's disease, Huntington's disease, Alzheimer's disease, and cardiac muscle contraction. We also found that miR-21a-5p could be a potential biomarker for amyotrophic lateral sclerosis, as miR-21a-5p becomes deregulated in this pathway. These results indicate successful detection of some important proteins that play potential roles in spinal cord injury. Elucidating the relationship between these proteins and the recovery of spinal cord injury will provide a reference for future research of spinal cord injury biomarkers. All experimental procedures and protocols were approved by the Experimental Animal Ethics Committee of Shandong University of China on March 5, 2014.

[The changes of extracellular matrix in adult degenerative nucleus pulposus cells with stiring microcarrier culture system in vitro].

OBJECTIVE: To evaluate the biological effect on the synthesis of the extracellular matrix (ECM) in the cultivation of adult degenerative nucleus pulposus cells using the stiring microcarrier system in vitro. METHODS: Thirty-four specimens were collected after intervertebral fusion operations of the patients with intervertebral disc herniation diseases from September 2005 to May 2009. The specimens were then randomly allocated into 2 groups for in vitro cultivation: monolayer culture group and microcarrier culture group. On the exponential phase, SP-ABC immunohistochemical staining and Western blot quantitative analysis were conducted in the two groups to detect the collagen type I and II. Proteoglycan contents of two groups in different growth phases were detected with (35)S-sulfate incorporation assay. RESULT: The expressions of collagen type I and II in microcarrier culture group were significantly higher than those in monolayer culture group: SP-ABC immunohistochemical staining (collagen type I: 32.5 ± 4.4 vs. 15.2 ± 1.2, t = 2.871, P < 0.01; collagen type II: 43.6 ± 4.1 vs. 23.1 ± 2.2, t = 2.375, P < 0.05); Western blot quantitative analysis (collagen type I: 0.62 ± 0.08 vs. 0.50 ± 0.06, t = 3.327, P < 0.01; collagen type II: 1.46 ± 0.08 vs. 0.86 ± 0.04, t = 2.453, P < 0.05). Nucleus pulposus cells cultivated in stiring microcarrier system showed significantly increased proteoglycan synthesis than monolayer culture group does on both exponential phase and stationary phase (exponential phase: 34 821 ± 312 vs. 21 046 ± 673, t = 2.134, P < 0.05; stationary phase: 45 134 ± 175 vs. 32 193 ± 713, t = 2.801, P < 0.01). CONCLUSIONS: The expression of collagen type I, II and proteoglycan of adult degenerative nucleus pulposus cells are positive regulated by the stiring microcarrier system, which can be used in the mass amplification of the adult degenerative nucleus pulposus cells.

[Study on the interaction of cobalt (II) polyamidomine dendrimer with DNA by spectrometry techniques].

Cobalt (II) polyamidomine dendrimer was prepared by the reaction of cobalt chloride, glyoxal and polyamidomine dendrimer of 5.0 generation. The interaction of cobalt (II) polyamidomine dendrimer complex with herring sperm (hsDNA) was carried out using methylene blue (MB) as the probe molecule by absorption and fluorescence spectroscopy and synchronous fluorescence spectroscopy. The results showed that the intensity of absorption peaks and fluorescence peaks increased when the complex interacted with hsDNA. The effect of sodium chloride showed that sodium ion can significantly constrain the interaction of cobalt(II) polyamidomine dendrimer with hsDNA. The curves indicated the competitive inhibition of MB binding to hsDNA in the presence of cobalt (II) polyamidomine dendrimer complexes, also MB could insert into interior of cobalt (II) polyamidomine dendrimer complexes. The results suggested that the complex mainly interacted with negatively charged phosphate moieties on hsDNA through electrostatic attraction and stacked on the surface of double stranded hsDNA, which may reduce the binding affinity of MB to hsDNA in the surrounding site. It was indicated that sodium ion might neutralize the negatively charged phosphate backbone of hsDNA, and then weaken the electrostatic attraction between complexes and hsDNA.

[C and N allocation patterns in planted forests and their release patterns during leaf litter decomposition in subalpine area of west Sichuan].

With the planted forest ecosystems of Cercidiphyllum japonicum, Betula utilis, Pinus yunnansinsis, and Picea asperata in subalpine area of west Sichuan as test objects, their total biomass and the C and N contents in soils and tree organs were determined. The results showed that the allocation of C in tree organs had less correlation with the age of the organs, while that of N and C/N ratio had closer relationship with the age. The N content in young organs was higher than that in aged ones, whereas the C/N ratio was higher in aged organs than in young organs, and higher in the leaf litters of needle-leaved forests than in those of broad-leaved forests. There was an obvious enrichment of C and N in the topsoil of test forests. The accumulated amounts of C and N in the whole planted forest ecosystem, including tree, litter, and 0-40 cm soil layer, were 176.75-228.05 t x hm(-2) and 11.06-16.54 t x hm(-2), respectively, and the nutrients allocation ratio between soil-litter and tree was (1.9-3.3):1 for C and (15.6-41.5):1 for N. Needle-leaved forests functioned as a stronger "C-sink" than broad-leaved forests. The decomposition rate of the leaf litters in needle-leaved forests was larger than that in broad-leaved forests, with the turnover rate being 2.2-3.7 years and 3.9-4.2 years, respectively. During the decomposition of leaf litter, the C in all of the four forests released at super-speed, with the turnover rate being 1.9-3.4 years. As for N, it also released at super-speed in C. japonicum and B. utilis forests, with the turnover rate being 1.9-3.2 years, but released at low speed in P. yunnansinsis and P. asperata forests, with the turnover rate being 6.7-8.5 years.

[Effects of leaf litter replacement on soil biological and chemical characteristics in main artificial forests in Qinling Mountains].

Through 2 years leaf litter replacement experiments in 4 typical artificial pure forests Larix kaempferi, Pinus tabulaeformis, Catalpa fargesii, and Quercus aliena var. acuteserrata in Qinling Mountains of China, this paper studied the effects of leaf litter replacement on soil biological and chemical characteristics and the interspecific relationships between different tree species. The results showed that the annual decomposition rate of broad-leaved litter was 33.70% higher than that of needle-leaved litter. The annual decomposition rate of needle-leaved litter increased by 8.35%-12.15% when replaced to broad-leaved forests, whereas that of broad-leaved litter decreased by 5.38%-9.49% when replaced to needle-leaved forests. Leaf litter replacement between needle and broad-leaved forests could increase the contents of soil organic-C and available N, P and K, and the increments were obviously higher in needle-leaved forests (8.70%-35.84%) than in broad-leaved forests (3.73%-10.44%). In needle-leaved forests, the increments with the replacement of C. fargesii litter (24.63%-35.84%) were higher than those with the replacement of Q. aliena var. acuteserrata litter (8.70%-28.15%). Furthermore, the replacement of broad-leaved litter could make the soil pH in needle-leaved forests changed from light-acid to neutral, and increase soil enzyme activities, microbial amounts, and microbial biomass C and N contents. The increments with the replacement of C. fargesii litter were higher than those with the replacement of Q. aliena var. acuteserrata litter. The soil enzyme activities, microbial amounts, and microbial biomass C and N contents in broad-leaved forests after the replacement of needle-leaved litter differed with broadleaved tree species. Q. aliena var. acuteserrata forest had the higher soil enzyme activities and microbial biomass C and N contents, while C. fargesii forest was in adverse. It was suggested that in the control of soil degradation under artificial pure forests, much attention should be paid to the direction of interspecific relationship in mixed forestation and leaf litter replacement.