Pulmonary fibrosis (PF) is a major public health issue with limited treatment options. As the active ingredient of the n-butanol extract of Amygdalus mongolica (BUT), amygdalin inhibits PF. However, its mechanisms of action are unclear and need further verification. Therefore, the purpose of the present studies was to investigate the anti-fibrotic effects of BUT on PF by serum metabolomics and the transforming growth factor β (TGF-β) pathway. Sixty male Sprague-Dawley rats were randomly divided into control, untreated PF, prednisone-treated (5 mg/kg), and BUT-treated (1.75, 1.25, 0.75 g/kg) groups, and the respective drugs were administered intragastrically for 21 days. The serum metabolomics profiles were determined by ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS) and metabolism network analysis. The expression of TGF-β1, Smad-3, Smad-7, and α-smooth muscle actin (α-SMA) was measured using a real-time polymerase chain reaction in the lung tissue. BUT significantly alleviated fibrosis by reducing the mRNA expressions of TGF-β1 (from 1.73 to 1.13), Smad-3 (from 2.01 to 1.19), and α-SMA (from 2.14 to 1.19) and increasing that of Smad7 (from 0.17 to 0.62). Twenty-eight potential biomarkers associated with PF were identified. In addition, four key biomarkers were restored to baseline levels following BUT treatment, with the lowest dose showing optimal effect. Furthermore, A. mongolica BUT was found to improve PF by the pentose phosphate pathway and by taurine, hypotaurine, and arachidonic acid metabolism. These findings revealed the mechanism of A. mongolica BUT antifibrotic effects and metabolic activity in PF rats and provided the experimental basis for its clinical application.

SUMMARY: To investigate the correlation between the anatomical morphology of palatal rugae and sex. The study sample consisted of 120 students studying from Shanxi Medical University, of which 60 were females and 60 were males. The digital model of the palatal rugae was obtained by the 3 Shape TRIOS intraoral scanner. And the shapes of palatal rugae were recorded. Association between palatal rugae shape and sex were tested using Chi-square analysis. And logistic regression analysis (LRA) was carried out to calculate the accuracy of gender prediction using rugae shapes. There was a statistically significant difference between males and females in terms of the distribution of wavy and circular palate rugae. The use of logistic regression analysis obtained a sex predictive value of 65 % when all the rugae shapes were analyzed. Digital images of the palatal rugae morphology contribute to more accurate and convenient for data collection and transformation. It was found that rugae patterns can moderately identify the sex of the specific population when multivariate statistics such as LRA is applied. The palatal rugae morphology can be utilized as an assistant measure for sex identification.

RESUMEN: Investigar la correlación entre la morfología anatómica de las rugas palatinas y el sexo. En la muestra de este estudio se incluyeron 120 estudiantes de la Universidad Médica de Shanxi, (60 mujeres y 60 hombres). El modelo digital de las rugas palatinas se obtuvo mediante escáner intraoral 3 Shape TRIOS, y se registraron las formas de las rugas palatinas. La asociación entre la forma de las rugas palatinas y el sexo se evaluó mediante un análisis de Chi-cuadrado; para calcular la precisión de la predicción de sexo se llevó a cabo un análisis de regresión logística (ARL) Se observó una diferencia estadísticamente significativa entre hombres y mujeres en términos de la distribución de las rugas palatinas onduladas y circulares. El uso de análisis de regresión logística obtuvo un valor predictivo de sexo del 65 % cuando se analizaron todas las formas de las rugas. Las imágenes digitales de la morfología de las rugas palatinas contribuyen a una recopilación de datos más precisa. En este análisis se determinó que los patrones de rugas pueden identificar relativamente el sexo de una población específica, cuando se aplican estadísticas multivariadas como ARL. La morfología de las rugas palatinas se puede utilizar como medida de ayuda para la identificación de sexo.

Boron is an essential trace element which plays an important role in process of metabolism and the function of the tissues. However, the effects of boron on the intestinal cells in African ostrich chicks are poorly reported. Therefore, this study was designed to investigate the role of boron on proliferation and apoptosis of the intestinal cells. A total of 36, ten day-old ostrich chicks were randomly divided into six groups and fed on the same basal diet supplemented with 0, 40, 80, 160, 320 and 640 mg/L boric acid in drinking water for 80 days. Proliferatingcell nuclearantigen (PCNA) wasused to test the proliferation indexof intestine in different group byimmunohistochemicalstaining (IHC). Apoptoticcellsofintestinewere detectedbyDutp-biotin nick end labeling (TUNEL) reaction and evaluated by integral optical density (IOD). Results showed that proliferationof intestinal cells significantly increased in groups of 80, 160, 320 and 640 mg/L. TUNEL reaction showed that apoptosis significantly decreased in 80 mg/L groups, while significantly increased in high dose of boron groups (320 and 640 mg/L), especially inepithelium. In conclusion, low dose of boron-supplemented water could promote cell proliferation and depress apoptosis, while high dose of boron could cause intestinal apoptosis and thus we found increased proliferation of intestine cell as a compensatory adaption. These findings may support optimal dosage of boron that could protect the development of ostrich intestine, while high dosage of boron could suppress it, or even has toxic effects on it.

El boro es un elemento esencial que desempeña un importante rol en el proceso del metabolismo y en la función de los tejidos. Sin embargo, existe poca información de los efectos del boro en las células intestinales de polluelos de avestruz Africana. Por lo tanto, este estudio fue diseñado para investigar el papel del boro sobre la proliferación y la apoptosis de las células intestinales. Un total de 36 polluelos de avestruz de diez días se dividieron, aleatoriamente, en seis grupos y se alimentaron con una misma dieta basal suplementada con 0, 40, 80, 160, 320 y 640 mg/L de ácido bórico en agua potable durante 80 días. Se utilizó el antígeno nuclear celular de células en proliferación (PCNA) para probar el índice de proliferación de intestino en diferentes grupos por tinción inmunohistoquímica. Las células apoptóticas del intestino fueron detectadas por dUTP-biotina nick etiquetado para reacción (TUNEL) y evaluadas por la densidad óptica integrada (DOI). Los resultados mostraron que la proliferación de las células intestinales aumentó significativamente en los grupos de 80, 160, 320 y 640 mg /L. La reacción TUNEL mostró que la apoptosis se redujo significativamente en los grupos de 80 mg/L, mientras que el aumento fue significativo en grupos tratados con dosis alta de boro (320 y 640 mg/L), especialmente en el epitelio. En conclusión, la baja dosis de boro en agua suplementada podría promover la proliferación celular y deprimir la apoptosis, mientras que altas dosis de boro podrían provocar apoptosis intestinal y, por lo tanto, se halló una mayor proliferación de las células del intestino como una adaptación compensatoria. Estos hallazgos indican que una dosis óptima de boro podría proteger el desarrollo del intestino del avestruz, mientras que altas dosis de boro podrían suprimirla, o incluso tener efectos tóxicos sobre ella.

Microextração líquido-líquido dispersiva (DLLME) utilizando líquido iônico (IL) como solvente extrator foi desenvolvida com uma nova abordagem para a determinação de quatro pesticidas piretróides em amostras ambientais de água e solo. Cromatografia líquida de alto rendimento com detector de UV (HPLC-UV) foi empregada na análise cromatográfica. Este método é rápido, fácil de operar e ambientalmente correto. O solvente clorado altamente tóxico foi substituído pelo IL hexafluorofosfato de 1-hexil-3-metilimidazólio ([C6MIM][PF6]), para o qual elevados valores de recuperação de extração e fatores de enriquecimento foram obtidos. Os efeitos do volume de IL, tipo e volume do solvente dispersor, adição de sal, pH e tempo de extração foram investigados e otimizados. Nas condições ideais, o método mostrou boa resposta linear com valores de coeficiente de correlação (R²) no intervalo de 0,9943 a 0,9986. Desvio padrão relativo (RSD) variou de 3,9 a 10,1%. Fator de enriquecimento, limite de detecção e recuperação variaram de 260 a 319, de 0,94 a 1,97 µg L-1 e de 89 a 98%, respectivamente. Para amostras de água reais, RSD variou de 3,8 a 10,8%, e recuperação de 83 a 99%. Para análise de amostra de solo, RSD e recuperação variaram de 3,7 a 8,9% e 88 a 98%, respectivamente.

Dispersive liquid-liquid microextraction (DLLME) using ionic liquid (IL) as extraction solvent was developed as a new approach for the determination of four pyrethroid pesticides in environmental water and soil samples. High-performance liquid chromatography with ultraviolet detection (HPLC-UV) was employed on chromatographic analysis. The method is rapid, easy to operate and enviromentally-friendly. The highly toxic chlorinated solvent was replaced by the IL 1-hexyl-3-methylimidazolium hexafluorophosphate ([C6MIM][PF6]), in which high extraction recovery and enrichment factors were obtained. The effects of IL volume, type and volume of disperser solvent, salt addition, pH and extraction time were investigated and optimized. Under optimum conditions, the method showed good linear response with correlation coefficient (R²) values in the range of 0.9943 to 0.9986. Relative standard deviation (RSD) varied from 3.9 to 10.1%. Enrichment factor, limit of detection and recovery ranged from 260 to 319, 0.94 to 1.97 µg L-1 and 89 to 98%, respectively. For real water samples, RSD ranged from 3.8 to 10.8%, and recovery from 83 to 99%. For soil sample analysis, RSD and recovery ranged from 3.7 to 8.9% and 88 to 98, respectively.

To isolate differentially expressed peanut genes responsive to chilling, a suppression subtractive hybridization (SSH) cDNA library was constructed for a chilling tolerant peanut cultivar A4 with mRNAs extracted from the seeds imbibed at 2ºC and 15ºC, respectively, for 24 hrs. A total of 466 cDNA clones were sequenced, from which 193 unique transcripts (73 contigs and 120 singlets) were assembled. Of these unique transcripts, 132 (68.4%) were significantly similar to the sequences in GenBank non-redundant (nr) protein database, which belonged to diverse functional categories including metabolism, signal transduction, stress response, cell defense and transcriptional regulation. The remaining 61 (31.6%) showed no similarity to either hypothetical or known proteins. Six differentially expressed transcripts were further confirmed with real-time quantitative PCR (RT-qPCR).