中国尺蛾亚科三新记录属研究（鳞翅目： 尺蛾科）

本文记述中国尺蛾亚科3新记录属及3新记录种： 羚尺蛾Absala dorcada Swinhoe,双弓尺蛾Calleremites subornata Warren,巨尺蛾Pachista superans (Butler)。总结了每个属、种的形态特征;为羚尺蛾 Absala dorcada Swinhoe和巨尺蛾 Pachista superans (Butler) 指定了选模。     

Neuromedin B and its receptor influence the activity of myometrial primary cells in vitro through regulation of Il6 expression via the Rela/p65 pathway in mice

The neuromedin B receptor (Nmbr) is an important physiological regulator of spontaneous activities and stress responses through different cascades as well as its autocrine and paracrine effects. Previous studies have revealed that neuromedin B (Nmb) and its receptor signal via the Rela (also known as p65)/Il6 pathway in a mouse model of pregnancy. This study investigated the mechanism of Nmbr signaling via the Rela/p65-Il6 pathway and regulation of the concentration of intracellular free calcium ([Ca(2+)](i)) during the onset of labor in primary mouse myometrial cell cultures isolated from mice in term labor. Data demonstrated Nmbr agonist-mediated upregulation of the DNA binding activity of Rela/p65, Il6 expression, and [Ca(2+)](i) in a concentration-dependent manner. Furthermore, a significant correlation was observed between DNA binding activity of Rela/p65 and Il6 expression. Moreover, this up-regulation was blocked by Nmbr and Rela/p65 knockdown, achieved by RNA interference (RNAi) technology. No significant differences were identified in the inhibition of Il6 expression as a result of Nmbr or Rela/p65 knockdown. However, significant differences were observed between the [Ca(2+)](i) in Rela/p65-specific group and that in the Nmbr-specific small interfering RNA (siRNA)-treated groups. These data demonstrated that the Nmb/Nmbr interaction in pregnant myometrial primary cells in vitro predominantly influenced uterine activity through regulation of Il6 expression via the Rela/p65 pathway, although the effects of Nmbr on [Ca(2+)](i) involved several pathways that remain to be elucidated.     

Lysosomal membrane permeabilization is involved in curcumin-induced apoptosis of A549 lung carcinoma cells

We previously reported that curcumin inhibited lung cancer A549 cells growth and promoted cell apoptosis in vitro. In this study, we further examined the apoptosis-related parameters, including lysosomal damage and cathepsin activation, in A549 cells exposed to curcumin. We found that curcumin caused lysosomal membrane permeabilization (LMP) and cytosolic relocation of cathepsin B (cath B) and cathepsin D (cath D). However, only Z-FA-fmk (a cath B inhibitor) but not pepstatin A (a cath D inhibitor) inhibited curcumin-induced cell apoptosis, mitochondrial membrane potential loss, and cytochrome c release. The antioxidant N-acetylcysteine and glutathione attenuated LMP, suggesting that lysosomal destabilization was dependent on the elevation of reactive oxygen species and which precedes mitochondrial dysfunction. These findings indicated a novel pathway for curcumin regulation of ROS-lysosomal-mitochondrial pathway and provided the key mechanism of regulation of LMP in cell apoptosis, which may be exploited for cancer treatment.     

The G protein coupled receptor 3 is involved in cAMP and cGMP signaling and maintenance of meiotic arrest in porcine oocytes

The arrest of meiotic prophase in mammalian oocytes within fully grown follicles is dependent on cyclic adenosine monophosphate (cAMP) regulation. A large part of cAMP is produced by the Gs-linked G-protein-coupled receptor (GPR) pathway. In the present study, we examined whether GPR3 is involved in the maintenance of meiotic arrest in porcine oocytes. Expression and distribution of GPR3 were examined by western blot and immunofluorescence microscopy, respectively. The results showed that GPR3 was expressed at various stages during porcine oocyte maturation. At the germinal vesicle (GV) stage, GPR3 displayed a maximal expression level, and its expression remained stable from pro-metaphase I (MI) to metaphase II (MII). Immunofluorescence staining showed that GPR3 was mainly distributed at the nuclear envelope during the GV stage and localized to the plasma membrane at pro-MI, MI and MII stages. RNA interference (RNAi) was used to knock down the GPR3 expression within oocytes. Injection of small interfering double-stranded RNA (siRNA) targeting GPR3 stimulated meiotic resumption of oocytes. On the other hand, overexpression of GPR3 inhibited meiotic maturation of porcine oocytes, which was caused by increase of cGMP and cAMP levels and inhibition of cyclin B accumulation. Furthermore, incubation of porcine oocytes with the GPR3 ligand sphingosylphosphorylcholine (SPC) inhibited oocyte maturation. We propose that GPR3 is required for maintenance of meiotic arrest in porcine oocytes through pathways involved in the regulation of cAMP and cGMP.     

Cytotoxicity, apoptosis, cellular uptake, cell cycle distribution, and DNA-binding investigation of ruthenium complexes

Three new ruthenium(II) polypyridyl complexes [Ru(bpy)(2)(BHIP)](2+) 1, [Ru(phen)(2)(BHIP)](2+) 2, and [Ru(dip)(2)(BHIP)](2+) 3 were synthesized and characterized. The cytotoxicity of the three complexes was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The apoptosis induced by the complexes was studied by cell morphology and flow cytometry. The results showed that the percentage of apoptotic cells is 7.19%, 75.58%, and 3.51% in the presence of complexes 1, 2, and 3, respectively. The cellular uptakes were also performed and the results indicated that complexes 1, 2, and 3 can enter into the cytoplasm and also into the nucleus. The studies on antiproliferative mechanism showed the induction of S-phase arrest by complexes 1, 2, and 3. DNA-binding constants of these complexes with calf thymus DNA (CT-DNA) were determined to be 1.07 (± 0.47) × 10(5) M(-1) (s = 2.04), 1.21 (± 0.32) × 10(5) M(-1) (s = 1.88), and 2.75 (± 0.27) × 10(5) M(-1) (s = 2.17), respectively. Upon irradiation at 365 nm, complexes 1, 2, and 3 can induce cleavage of pBR322 DNA.     

Prediction of Disease-Related Interactions between MicroRNAs and Environmental Factors Based on a Semi-Supervised Classifier

Accumulated evidence has shown that microRNAs (miRNAs) can functionally interact with a number of environmental factors (EFs) and their interactions critically affect phenotypes and diseases. Therefore, in-silico inference of disease-related miRNA-EF interactions is becoming crucial not only for the understanding of the mechanisms by which miRNAs and EFs contribute to disease, but also for disease diagnosis, treatment, and prognosis. In this paper, we analyzed the human miRNA-EF interaction data and revealed that miRNAs (EFs) with similar functions tend to interact with similar EFs (miRNAs) in the context of a given disease, which suggests a potential way to expand the current relation space of miRNAs, EFs, and diseases. Based on this observation, we further proposed a semi-supervised classifier based method (miREFScan) to predict novel disease-related interactions between miRNAs and EFs. As a result, the leave-one-out cross validation has shown that miREFScan obtained an AUC of 0.9564, indicating that miREFScan has a reliable performance. Moreover, we applied miREFScan to predict acute promyelocytic leukemia-related miRNA-EF interactions. The result shows that forty-nine of the top 1% predictions have been confirmed by experimental literature. In addition, using miREFScan we predicted and publicly released novel miRNA-EF interactions for 97 human diseases. Finally, we believe that miREFScan would be a useful bioinformatic resource for the research about the relationships among miRNAs, EFs, and human diseases.     

大花栀子植物挥发物成分测定及其日变化分析

为探究大花栀子植物挥发物成分组成及其一天内早、中、晚的差异,采用热脱附气质联用技术对其进行香气成分的分析。结果表明:全天从其花朵中共鉴定出62种成分,主要为萜烯类、酯类、醇类物质,且不同时间其成分差异显著,如早、中、晚3个时间段,β-蒎烯相对含量分别为1.93%、1.69%、8.81%,顺式-β-罗勒烯分别为28.22%、4.35%、16.47%。3-蒈烯(3.45%)、异丁子香酚(0.21%)等只在早上检出;月桂烯(0.38%)、伞花烃(2.46%)等只在晚上检出;芳樟醇、金合欢烯等在早上和午间两个时间段相对含量较高,而在晚上却未检测出。从植物VOCs角度结合其日变化动态,为大花栀子园林配置及其综合开发利用提供理论依据。     

濒危植物长叶红砂适应盐胁迫的生理生化机制研究

以濒危盐生植物长叶红砂(Reaumuria trigyna)幼苗为材料,研究了不同浓度NaCl溶液(0、100、200、300和400mmol/L)处理30d对其生长和生理生化指标的影响,以分析长叶红砂的耐盐生理机制。结果表明:(1)100和200mmol/L NaCl处理时,长叶红砂鲜重和干重均显著增加,但随着盐浓度继续增加,长叶红砂幼苗生长受到抑制,且地上部受到的抑制大于根部,显示长叶红砂适宜生长的NaCl浓度是200mmol/L。(2)随NaCl胁迫浓度的升高,长叶红砂的净光合速率(Pn)、蒸腾速率(Tr)和气孔导度(Gs)呈下降趋势,胞间CO2浓度(Ci)呈上升趋势,说明光合速率的下降使利用CO2的能力下降,胞间积累了大量的CO2,且盐处理浓度越高量越大。(3)随NaCl胁迫浓度的升高,长叶红砂幼苗Na+、Cl-含量增加,可溶性糖、脯氨酸、游离氨基酸及可溶性蛋白等有机渗透调节物质的合成增加。研究认为,长叶红砂是通过调节叶片Na+、Cl-以及有机渗透调节物质含量来提高其耐盐能力。     

中国绮夜蛾属Acontia Ochsenheimer分类学修订（鳞翅目：夜蛾科：绮夜蛾亚科）

首次报道尺蛾科泽尺蛾属Zamarada Moore, 1887和超泽尺蛾Z. excisa Hampson, 1891在我国分布,给出了形态描述和特征图。     

NaCl胁迫对花棒叶片光合特性及游离氨基酸代谢的影响

为了解盐胁迫对花棒生理特性的影响,研究了不同浓度NaCl胁迫下花棒叶片的光合气体交换、叶绿素荧光以及游离氨基酸的变化.结果表明:低浓度NaCl胁迫下,花棒叶片的光系统Ⅱ通过耗散过剩激发能,避免了光伤害.此时气孔限制是导致光合速率降低的主要原因.随着NaCl胁迫的加剧,叶片的光保护机制不足以避免过氧化引起的伤害,导致光系统Ⅱ受损.200 mmol·L-1 NaCl处理下,非气孔限制成为抑制光合作用的主要原因.NaCl胁迫下,花棒叶片中主要游离氨基酸的积累与代谢发生变化.低浓度NaCl胁迫时,叶片中的脯氨酸、谷氨酸、天冬氨酸和丙氨酸等主要游离氨基酸含量显著积累;随着NaCl浓度进一步升高,叶片中的天冬氨酸和谷氨酸含量减少,脯氨酸的合成与积累增加.