Abnormal spinal curvature and its influencing factors among middle and high school students in Inner Mongolia Autonomous Region / 中国学校卫生

Objective@#To investigate the incidence of abnormal spinal curvature and related factors among middle school students in the Inner Mongolia Autonomous Region, so as to provide evidence for abnormal spinal curvature prevention and treatment.@*Methods@#By using a random stratified cluster sampling method, 87 908 students of middle and high school students from all 12 counties(districts) were investigated via questionnaires for abnormal spinal curvature and health influencing factors in Inner Mongolia Autonomous Region. Chi square test was used to perform demographic characteristics and univariate analysis, and binary multivariate Logistic regression model was used to screen the risk factors for spinal curvature abnormalities in middle school students.@*Results@#A total of 3 131(3.56%) students with spinal curvature abnormalities were detected, with boys (3.69%) higher than that of girls(3.44%), urban areas (6.15%) higher than that of the suburban counties (2.50%), and high school students ( 4.97 %) higher than that of junior high school(2.73%) students( χ 2=4.01, 702.19, 299.36, P <0.05). The detectable rate of spinal curvature abnormalities increased with grade ( χ 2 trend =309.29, P <0.05). Logistic regression analysis showed that factors influencing abnormal spinal curvature included myopia, overweight, obesity, the frequency of classroom seating arrangements, time spent on homework/reading after school every day, time spent in daytime outdoor activities, self imposed requirements for posture of sitting and standing, phase of studying, gender, and area ( OR =0.53-2.55, P <0.05).@*Conclusion@#Abnormal spinal curvature is strongly correlated to nutritional status, myopia, sitting posture when reading and writing, sedentary time, and time spent in outdoor activities. The collaboration of multiple departments is required to establish anenvironment to protect the spine, early detection and early intervention.

miR­133b affects cell proliferation, invasion and chemosensitivity in renal cell carcinoma by inhibiting the ERK signaling pathway.

Renal cell carcinoma has the highest incidence rate of cancer types in the urinary system. Moreover, microRNAs (miRNA) have been closely associated with numerous types of tumor. The present study aimed to investigate the effects of miRNA (miR)­133b on the proliferation, invasion and chemosensitivity of renal cell carcinoma cells, and to determine whether its mechanism was regulated by the ERK signaling pathway. Both renal cell carcinoma and adjacent healthy tissues from 60 patients, in addition to renal cell carcinoma lines, ACHN, Caki­1, A­498 and 786­O, and 293 cells, were used in this study. miR­133b expression was measured from renal cell carcinoma, adjacent healthy tissues and renal cell carcinoma cell lines by reverse transcription­quantitative PCR. Cells were transfected with miR­133b mimic to achieve miR­133b overexpression. The proliferative, migratory and invasive ability of the cells were evaluated using MTT, wound healing and Matrigel assays, respectively, and flow cytometry was used to detect the apoptotic rate. Following treatment with an ERK inhibitor, U0126, and activator, LM22B­10, western blotting was used to detect the expression of related proteins and the activity of the ERK signaling pathway. The overexpression of miR­133b significantly inhibited cell proliferation, migration and invasion, whilst inducing apoptosis and increasing the drug sensitivity of renal cell carcinoma cells to cisplatin, docetaxel and doxorubicin. The miR­133b mimic also increased the protein expression levels of Bax and decreased the expression levels of matrix metalloproteinase (MMP)­2, MMP­9, ATP­binding cassette subfamily G2, P­glycoprotein, Bcl­2 and proliferating cell nuclear antigen, as well as the phosphorylation of ERK (P<0.05). The administration of the U0216 inhibitor demonstrated similar effects to miR­133b overexpression, and there was no significant difference compared with the miR­133b mimic transfection (P>0.05). However, the overexpression of miR­133b combined with LM22B­10 treatment weakened the anticancer effects of miR­133b mimic transfection (P<0.05). In conclusion, miR­133b overexpression was observed to inhibit the proliferation, migration and invasion of renal cell carcinoma cells and improve chemotherapeutic sensitivity; it was suggested that the mechanism maybe related to the inhibition of ERK1/2 phosphorylation and thus decreased ERK signaling pathway activity.

The effects of nesfatin-1 in the paraventricular nucleus on gastric motility and its potential regulation by the lateral hypothalamic area in rats.

The current study investigated the effects of nesfatin-1 in the hypothalamic paraventricular nucleus (PVN) on gastric motility and the regulation of the lateral hypothalamic area (LHA). Using single unit recordings in the PVN, we show that nesfatin-1 inhibited the majority of the gastric distention (GD)-excitatory neurons and excited more than half of the GD-inhibitory (GD-I) neurons in the PVN, which were weakened by oxytocin receptor antagonist H4928. Gastric motility experiments showed that administration of nesfatin-1 in the PVN decreased gastric motility, which was also partly prevented by H4928. The nesfatin-1 concentration producing a half-maximal response (EC50) in the PVN was lower than the value in the dorsomedial hypothalamic nucleus, while nesfatin-1 in the reuniens thalamic nucleus had no effect on gastric motility. Retrograde tracing and immunofluorescent staining showed that nucleobindin-2/nesfatin-1 and fluorogold double-labeled neurons were observed in the LHA. Electrical LHA stimulation changed the firing rate of GD-responsive neurons in the PVN. Pre-administration of an anti- nucleobindin-2/nesfatin-1 antibody in the PVN strengthened gastric motility and decreased the discharging of the GD-I neurons induced by electrical stimulation of the LHA. These results demonstrate that nesfatin-1 in the PVN could serve as an inhibitory factor to inhibit gastric motility, which might be regulated by the LHA.

Eu-MOFs with 2-(4-carboxyphenyl)imidazo[4,5-f]-1,10-phenanthroline and ditopic carboxylates as coligands: synthesis, structure, high thermostability, and luminescence properties.

Hydrothermal reactions of europium(III) salt with 2-(4-carboxyphenyl)imidazo[4,5-f]-1,10-phenanthroline and dicarboxylic acid as coligands-benzene-1,4-dicarboxylic acid, 4,4'-biphenyldicarboxylic acid, 2,5-dibromoterephthalic acid, and naphthalene-1,4-dicarboxylic acid-lead to four europium fluorescent materials (1-4). Structural analyses reveal that 1-4 have binuclear 3D metal-organic frameworks with different channels, void volumes, and conjugated structures tuned by ditopic carboxylates. There are no latticed and coordinated water molecules occurring in 1-3, while the free water molecules fill in 1D channels of 4. 4' was readily obtained via water removal of 4. Thermal analyses of all compounds show the high thermal stability of the main framework up to 450 °C. Optical studies indicate that 1-4 and 4' show the characteristic red luminescence emission of the Eu(III) ion in the visible regions at room temperature. On the basis of emission spectra, their luminescence lifetimes were determined. In particular, compound 4' shows a longer lifetime (τ = 0.942 ms) and significantly enhanced quantum yield (39%) compared with those of 1 (11%, 0.770 ms), 2 (4%, 0.414 ms), 3 (18%, 0.807 ms), and 4 (26%, 0.858 ms).

Central nesfatin-1 influences the excitability of ghrelin-responsive gastric distension neurons in the arcuate nucleus and reduces gastric motility in rats.

Although the novel satiety peptide nesfatin-1 has been shown to regulate gastric motility, the underlying mechanisms have yet to be elucidated. The study aimed to explore the effects of nesfatin-1 on ghrelin-responsive gastric distension (GD) neurons in the arcuate nucleus (Arc), and potential regulation mechanisms of gastric motility by the paraventricular nucleus (PVN). Single-unit discharges in the Arc were recorded extracellularly, and gastric motility in conscious rats was monitored during the administration of nesfatin-1 to the Arc or electrical stimulation of the PVN. Retrograde tracing and fluo-immunohistochemistry staining were used to determine NUCB2/nesfatin-1 neuronal projections. Nesfatin-1 inhibited most of the ghrelin-responsive GD-excitatory neurons, but excited ghrelin-responsive GD-inhibitory neurons in the Arc. Gastric motility was significantly reduced by nesfatin-1 administration to the Arc in a dose-dependent manner. The firing activity in the Arc and changes to gastric motility were partly reduced by SHU9119, an antagonist of melanocortin 3/4 receptors. Electrical stimulation of PVN excited most of the ghrelin-responsive GD neurons in the Arc and promoted gastric motility. Nonetheless, pretreatment with an anti-NUCB2/nesfatin-1 antibody in the Arc further increased the firing rate of most of the ghrelin-responsive GD-excitatory neurons and decreased the ghrelin-responsive GD-inhibitory neurons following electrical stimulation of the PVN. Gastric motility was enhanced by pretreatment with an anti-NUCB2/nesfatin-1 antibody in the Arc following PVN stimulation. Furthermore, NUCB2/nesfatin-1/fluorogold double-labeled neurons were detected in the PVN. These results suggest that nesfatin-1 could serve as an inhibitory factor in the Arc to regulate gastric motility via the melanocortin pathway. The PVN could be involved in the regulation of the Arc in gastric activity.

Poly[[diaquadi-µ(2)-cyanido-bis-(µ(2)-pyrazine-2-carboxyl-ato)dicopper(I)copper(II)] dihydrate].

In the title compound, {[Cu(II)Cu(I) (2)(C(5)H(3)N(2)O(2))(2)(CN)(2)(H(2)O)(2)]·2H(2)O}(n), the Cu(II) atom lies on an inversion centre and is octa-hedrally coordinated by two N atoms and two O atoms from opposing pyrazine-2-carboxyl-ate (2-pac) ligands and two water O atoms. The Cu(I) atom has a triangular geometry, coordinated by one N atom and one C atom from two bridging cyanide ligands, and another N atom from the 2-pac ligand. The three-dimensional structure features a succession of two-dimensional sheets containing [Cu(CN)](n) chains linked by Cu(2-pac)(2)(H(2)O)(2) groups. The coordinated and free water mol-ecules are involved in an extended three-dimensional hydrogen-bond network with the 2-pac ligands.

Bis[(1-methyl-1H-tetra-zol-5-yl)sulfan-yl]methane.

The mol-ecule of the title compound, C(5)H(8)N(8)S(2), lies on a twofold rotation axis that relates on 1-methyl-tetra-zolyl group to the other; the five-membered rings are twisted by 53.1 (1)°.

Nanoporous lanthanide-carboxylate frameworks based on 5-nitroisophthalic acid.

The reactions of lanthanide nitrates with 5-nitroisophthalic acid (ab. 5-H(2)nip) in DMF and ethanol (1 : 1) mixed solution gave rise to three nanoporous lanthanide polymers, {[Ln(2)(5-nip)(3)(DMF)(4)](DMF)(2)}(n) (Ln = Nd (), Dy (), Ho (), 5-nip = 5-nitroisophthalate). Single-crystal X-ray diffraction analyses reveal that they are isomorphous and feature three-dimensional metal-organic frameworks with two-dimensional intersecting channels occupied by guest DMF molecules constructed from the linkage of dimer Ln(2)C(6)O(12) SBUs and 5-nip ligands. The guest DMF molecules can be reversibly removed from as identified using TGA-DSC and PXRD. The heat of adsorption of the guest-free sample of with DMF was measured with a value of 10.3 kJ mol(-1) by an RD496-III type microcalorimeter. In addition, the photoluminescent property of was investigated.

catena-Poly[[[tetra-aqua-iron(II)]-µ-5,5'-diazenediylditetra-zolido] dihydrate].

In the title compound, {[Fe(C(2)N(10))(H(2)O)(4)]·2H(2)O}(n), the coordin-ation geometry around the Fe(II) atom, which lies on a center of inversion, is distorted octa-hedral, with bonds to four O atoms and two N atoms. The azotetra-zolate ligand displays a bridging coordination mode, forming an infinite zigzag chain. Inter-molecular O-H⋯O and O-H⋯N hydrogen bonding and offset face-to-face π-π stacking inter-actions [centroid-centroid distance = 3.4738 (13) Å] lead to a three-dimensional network.

Low Temperature Heat Capacities and Standard Molar Enthalpy of Formation of 2-Pyrazinecarboxylic Acid (C5H4N2O2)(s).

Low-temperature heat capacities of 2-pyrazinecarboxylic acid (C5H4N2O2)(s) were measured by a precision automated adiabatic calorimeter over the temperature range from 78 to 400 K. A polynomial equation of heat capacities as a function of temperature was fitted by least squares method. Based on the fitted polynomial, the smoothed heat capacities and thermodynamic functions of the compound relative to the standard reference temperature 298.15 K were calculated and tabulated at 10 K intervals. The constant-volume energy of combustion of the compound at T = 298.15 K was measured by a precision rotating-bomb combustion calorimeter to be ΔcU = -(17839.40 ± 7.40) J g-1. The standard molar enthalpy of combustion of the compound was determined to be ΔcH0m = -(2211.39 ± 0.92) KJ mol-1, according to the definition of combustion enthalpy. Finally, the standard molar enthalpy of formation of the compound was calculated to be ΔfH0m = -(327.82 ± 1.13) kJ mol-1 in accordance with Hess law.

Apical ligand substitution, shape recognition, vapor-adsorption phenomenon, and microcalorimetry for a pillared bilayer porous framework that shrinks or expands in crystal-to-crystal manners upon change in the cobalt(II) coordination environment.

A 2D pillared bilayer coordination polymer, [Co(5-NH(2)-bdc)(bpy)(0.5)(H(2)O)] x 2 H(2)O (1; 5-NH(2)-bdc = 5-aminoisophthalate; bpy = 4,4'-bipyridine) has been hydrothermally synthesized and shows a novel microporous host framework with 1D channels and high thermal stability (approximately 400 degrees C). The framework of 1 exhibits reversible single-crystal-to-single-crystal transformations upon removing and rebinding the coordinated waters as well as replacing them with MeOH and EtOH from the solvent. X-ray crystallography reveals that the coordination geometry of Co(II) changes from octahedron to square pyramid, as well as the shrinkage/expansion of pore deformation in respect to the subsequent shear motion of bpy pillars and vice versa. The dehydrated form 2 exhibits a shape recognition ability, which can accommodate linear molecules, such as MeCN and 2-propynyl alcohol, and interesting storage capabilities for oversized MeOH, EtOH, and benzene molecules, concomitant with spongelike dynamic transformation. The microcalorimetric study indicates that the crystalline state-liquid guest exchange and guest inclusion processes (1 superset MeOH or EtOH, 2 superset MeOH, EtOH or MeCN) are feasibly endothermic reactions with the values of molar enthalpy, DeltaH(theta)(m), of +21.38(96), +12.68(85), +25.92(86), +17.03(57), and +14.93(75) kJ mol(-1), respectively.

[Evaluation and analysis of auditory function and its clinical characteristics in low birth weight premature infants.].

OBJECTIVE: To investigate and analyze dynamic changes of auditory function in premature babies with fetal age of less than 37 weeks who were categorized into different birth weight groups and to detect abnormalities of auditory function in these babies and to describe the early development patterns of auditory function in infancy. METHODS: Total of 252 subjects (504 ears) from neonatal ward, neonatal intensive care unit and auditory clinic in Guangzhou Children Hospital, whose fetal age were less than 37 weeks, were included in our study and received auditory function evaluation from January 2004 to February 2008. To investigate the correlation between birth weight and development and abnormality of auditory function in premature babies, all subjects were divided into four groups according to birth weight: 2.5 kg. Each group was further categorized by subject's age on first auditory function evaluation in 0 - 3 months (include 3 months), 3 - 6 months (include 6 months) and above 6 months, respectively. Subjects who were evaluated more than once in different age frame would be grouped into multiple evaluation subgroups. All subjects underwent one or more objective auditory examinations including auditory brainstem response (ABR), distortion product otoacoustic emission (DPOAE), tympanometry and acoustic stapedius reflex. RESULTS: A tendency of decreased wave V threshold of ABR was seen as birth weight increased, while the percentage of subjects with ABR wave V threshold

Diaqua-(5-methyl-pyrazine-2-carboxyl-ato-κN,O)iron(II).

In the neutral title complex, [Fe(C(6)H(5)N(2)O(2))(2)(H(2)O)(2)], the coordination geometry aound the Fe(II) atom, which lies on an inversion centre, is distorted octa-hedral comprising two N atoms and two O atoms from two 5-methyl-pyrazine-2-carboxyl-ate ligands, and two water mol-ecules. The crystal structure is stabilized by a network of O-H⋯O hydrogen bonds, resulting in a two-dimensional supra-molecular structure.

[Two patterns of mediastinal lymph node resection for non-small cell lung cancer of stage IIIA: survival analysis of 219 cases].

BACKGROUND & OBJECTIVE: Correctly dealing with mediastinum lymph nodes during operation is critical to the prognosis of resectable non-small cell lung cancer (NSCLC) of stage IIIA, but the removal extent of mediastinum lymph nodes is controversial. This study was to explore the effects of 2 patterns of mediastinum lymph node resection on long-term survival of stage IIIA NSCLC patients. METHODS: Clinical data of 219 stage IIIA NSCLC patients, underwent complete resection from Jan. 1999 to Jan. 2004 in Xinjiang Tumor Hospital, were reviewed. Of the 219 patients, 109 underwent mediastinal lymph node sampling (LS), and 110 underwent systematic mediastinal lymphadenectomy (SML). Survival statuses of the patients were analyzed by Life table method and Kaplan-Meier method; the prognosis was analyzed with Cox multivariate regression model. RESULTS: The 1-, 3-, and 5-year survival rates were 82%, 28%, 13% in LS group, and 88%, 37%, 16% in SML group. The median survival time was significantly longer in SML group than in LS group (23.5 months vs. 20.0 months, P<0.05). Cox multivariate analysis showed that histopathologic type, metastasis state of mediastinal lymph nodes, mediastinum lymph node resection pattern were prognostic factors of stage IIIA NSCLC patients. CONCLUSION: As compared with LS, SML in radical operation could improve the survival rate of stage IIIA NSCLC patients.

A new high-nitrogen compound [Mn(ATZ)(H2O)4] x 2H2O: synthesis and characterization.

A new high-nitrogen compound [Mn(ATZ)(H(2)O)(4)] x 2H(2)O (ATZ=5,5-azotetrazolate) was synthesized. Crystal structure and elemental, IR and thermal analyses were investigated in the present work. It crystallized in triclinic space group P-1 with lattice parameters a=6.304(2)A, b=7.004(2)A, c=7.921(3)A, alpha=76.114(5) degrees , beta=74.023(5) degrees , gamma=69.254(4) degrees . TG-DTG and DSC measurements are employed to postulate the thermal decomposition mechanism. The thermal decomposition kinetics of the main exothermic reaction was investigated by non-isothermal method and obtained its enthalpy of decomposition and the probable kinetic mechanism. An attempt was made to incorporate the relation between thermal stability and the structure.

[Spectra of rare earth complexes RE(Et2 dtc),3 (phen)].

The ternary solid complexes RE(Et2dtc)3 (phen) (RE=La, Pr, Nd, Sm-Er) were synthesized with sodium diethyldithiocarbamate (NaEt2 dtc x 3H2O), 1,10-phenanthroline (o-phen x H2O) and hydrated lanthanide chlorides in absolute ethanol by improved reported method. IR results revealed that RE3+ coordinated with sulfur atoms of NaEt2 dtc and nitrogen atoms of o-phen. As for UV spectrum of the complexes, energy transfer between o-phen and RE3+ was the primary process, and the main absorption peaks showed a slight red shift compared to that of o-phen; FS spectrum, as a comparison, showed that the complexes Sm (Et2 dtc)3 (phen) and Eu(Et2dtc)3 (phen) have a higher efficiency of intermolecular energy transfer and a stronger fluorescence character.

[FTIR studies of L-threonic acid and its metal compounds].

Highly pure solid compounds, such as L-threonic acid, calcium L-threonate, magnesium L-threonate, manganese L-threonate, cobalt L-threonate, nickel L-theronate, and zinc L-threonate, were prepared, wherein, L-threonic acid was obtained from calcium L-threonate by strong acid type ion exchange process, calcium L-threonate or zinc L-threonate was prepared by alcohol extracting the concentrated filter liquor of the reaction of Vc, H2O2 and CaCO3 or ZnCO3, the reminder of the compounds were synthesized using alcohol extracting the concentrated solution derived from the reaction of L-threonic acid solution, prepared by double decomposition reaction of calcium L-threonate with oxalic acid, and superfluous MgO, MnCO3, Co2(OH)2CO3 and Ni2(OH)2CO3. The compositions of the compounds were determined by chemical and elemental analysis, and these compounds have the formula M(C4H7O5)2.nH2O (M = Ca, Zn, n = 0; M = Mg, Mn, Co, n = 1; M = Ni, n = 2). The purity of the compounds was 99.60% by HPLC. The IR spectra of the complexes were similar with each other but different from that of L-threonic acid. The characteristic absorption peaks of water were not observed in those of calcium L-threonate or zinc L-threonate, which showed that the molecule of water was not involved in the complexes. Further analyses indicate that M2+ in the compounds coordinated to oxygen atom of the carboxy group, while the proton of the carboxyl group was dissociated and the proton belonging to hydroxyl was not M2+ coordinated to L-threonic acid through the sp3 hybrizated fashion. It was assumed that the coordination number of M2+ was 4.

[Spectra of the complexes of zinc salts with AMP].

The complexes of ZnCl2 and ZnSO4 with AMP in molar ratios of 1:1 and 1:2 were prepared through reflux in alcohol. The compositions of the complexes were determined to be Zn(AMP)2Cl2(A) and Zn(AMP)SO4(B) by chemical and elemental analyses. It was identified via IR analysis for the complexes that nitrogen atom of amino group and one of nitrogen atoms of pyrimidine coordinated to Zn2+ in bidentate fashion. Cl- in the complex of A and SO4(2-) in the complex of B participated in the coordination to Zn2+ and some feedback characteristic was found in the bond of N-->Zn2+, which was proved by XPS spectra. Study on 1H NMR for the complexes showed that two ligands joined the coordination to Zn2+ in the complex of A while one ligand did in the complex of B. Based on the above analyses, the structures of the complexes were presumed.