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951.
通过三氨基三蝶烯与3,4,9,10-苝四羧酸酐(PTCDA)、均苯四甲酸酐(PMDA)、3,3’,4,4’-联苯二酐(BPDA)以及螺环二酐(SBIDA)的缩聚反应分别合成了4种固有微孔聚酰亚胺材料(Trip-PIMs)。采用傅里叶红外光谱(FT-IR)、固体核磁碳谱(Solid-state 13C-NMR)、扫描电子显微镜(SEM)、热重分析(TG)和氮气吸附等测试手段表征了材料的微孔结构和物理化学性能,测试了材料对有机气体和液体的吸附性能。结果表明:三蝶烯结构的引入使材料获得了较高的比表面积,同时具有良好的溶胀特性;对比烷烃,该材料对胺类和苯类具有更高的吸附率;螺环结构的引入能进一步提高材料骨架的溶胀特性,从而提升材料的吸附能力。 相似文献
952.
Ping Liu Qi Wu Yu Tang Zhiguo Zhou Malong Feng 《The American journal of emergency medicine》2018,36(3):470-474
Background
Esmolol may have some potential in treating septic shock and sepsis. However, the results remain controversial. We conduct a systematic review and meta-analysis to explore the efficacy of esmolol in patients with septic shock and sepsis.Methods
PubMed, EMbase, Web of science, EBSCO, and Cochrane library databases are systematically searched. Randomized controlled trials (RCTs) assessing the efficacy of esmolol for septic shock and sepsis are included. Two investigators independently search articles, extract data, and assess the quality of included studies. Meta-analysis is performed using the random-effect model.Results
Five RCTs are included in the meta-analysis. Overall, compared with control intervention in septic patients, esmolol intervention is found to significantly increase survival rate (risk ratio (RR) = 2.06; 95% confidence interval (CI) = 1.52 to 2.79; P = 0.006), decrease heart rate (Standard Mean difference (Std. MD) = ? 2.43; 95% CI = ? 4.13 to ? 0.72; P = 0.005) and TnI (Std. MD = ? 1.91; 95% CI = ? 2.39 to ? 1.43; P < 0.00001), but has no significant impact on mean arterial pressure (MAP) (Std. MD = 0.11; 95% CI = ? 0.21 to 0.44; P = 0.49), central venous pressure (CVP) (Std. MD = ? 0.11; 95% CI = ? 0.50 to 0.28; P = 0.58) and central venous oxygen saturation (ScvO2) (Std. MD = 1.87; 95% CI = ? 1.53 to 5.26; P = 0.28).Conclusions
Esmolol treatment may be able to improve survival rate, and reduce heart rate and TnI, but has no influence on MAP, CVP and ScvO2 in patients with septic shock and sepsis. 相似文献953.
目的:探讨电脑验光和检影验光在儿童散瞳前后验光效果,了解电脑验光仪是否能在儿童中应用.方法:对我院进行验光的500例1000眼屈光不正儿童相关资料进行分析,患儿首先进行电脑验光,然后使用10g/L硫酸阿托品眼用凝胶滴眼,3d后分别进行电脑验光和检影验光,比较两种验光效果.结果:近视性屈光不正电脑验光组球镜度数为2.70±2.75DS、柱镜度数为1.54± 1.10DC,均低于检影验光组(P<0.05);两组轴位差异不显著(P<0.05);远视性屈光不正电脑验光组球镜度数为-2.35±2.18DS、柱镜度数为-1.50±1.15DC,低于检影验光组(P<0.05);两组轴位差异不显著(P>0.05);散瞳前散光度为1.54±1.10D、散光轴为14.38±11.11度;散瞳后电脑验光散光度为1.45±1.21D、散光轴为12.78±10.31度,显著高于检影验光(P<0.05);两种验光方法所测球镜绝对值的差值≤0.50D,占75%(350/500),≤1.00D的占77.4%(387/500),409例柱镜绝对值的差值≤0.50D,占81.8%.结论:儿童验光配镜关乎儿童视觉发育,电脑验光和检影验光均有利弊,且电脑验光不能取代检影验光可将其作为快速验光的辅助工具. 相似文献
954.
目的:研究我国贫困农村地区妇女主任对当地不同卫生机构孕产妇保健服务(医疗设备、医务人员技术水平和态度)的满意度评价及影响其评价的相关因素。方法:自行设计问卷,采取整群分层随机调查方法,选取四川、甘肃和云南3省,14县(区),120个乡镇,993个农村的妇女主任作为调查对象,就其对当地不同卫生机构(村卫生室、乡镇卫生院、县妇幼保健站、县医院)孕产妇保健服务评价进行调查,并基于Ordered Logit模型分析影响村妇女主任评价的因素。结果:在医疗设备和医务人员技术水平方面,卫生机构的级别越高,村妇女主任对其评价越好。在医务人员态度方面,卫生机构越基层,村妇女主任对其评价越好。影响村妇女主任对不同卫生机构医疗设备、医务人员技术水平和态度评价的相关因素包括本村孕产妇保健基本情况、村妇女主任个人特征、村级社会经济情况。结论:农村妇女主任对当地不同卫生机构提供的妇幼保健服务总体较为满意,影响村妇女主任对卫生机构医疗设备、医务人员技术水平和态度评价的相关因素因卫生机构的层级而异。通过提高农村基层卫生机构孕产妇保健服务的医疗设备和技术水平、改善县级卫生机构医疗人员的服务态度、加大农村孕产妇保健服务的供给力度、重点扶持农村妇女主任开展孕产妇保健工作、强化农村妇女主任孕产妇保健知识的宣传和培训以提高农村妇女主任对不同卫生机构的满意程度。 相似文献
955.
Canqing Yu Zumin Shi Jun Lv Huaidong Du Lu Qi Yu Guo Zheng Bian Liang Chang Xuefeng Tang Qilian Jiang Huaiyi Mu Dongxia Pan Junshi Chen Zhengming Chen Liming Li 《Nutrients》2015,7(7):5834-5849
Limited evidence exists for the association between diet pattern and obesity phenotypes among Chinese adults. In the present study, we analyzed the cross-sectional data from 474,192 adults aged 30–79 years from the China Kadoorie Biobank baseline survey. Food consumption was collected by an interviewer-administered questionnaire. Three dietary patterns were extracted by factor analysis combined with cluster analysis. After being adjusted for potential confounders, individuals following a traditional southern dietary pattern had the lowest body mass index (BMI) and waist circumference (WC); the Western/new affluence dietary pattern had the highest BMI; and the traditional northern dietary pattern had the highest WC. Compared to the traditional southern dietary pattern in multivariable adjusted logistic models, individuals following a Western/new affluence dietary pattern had a significantly increased risk of general obesity (prevalence ratio (PR): 1.06, 95% confidence interval (CI): 1.03–1.08) and central obesity (PR: 1.07, 95% CI: 1.06–1.08). The corresponding risks for the traditional northern dietary pattern were 1.05 (1.02–1.09) and 1.17 (1.25–1.18), respectively. In addition, the associations were modified by lifestyle behaviors, and the combined effects with alcohol drinking, tobacco smoking, and physical activity were analyzed. Further prospective studies are needed to elucidate the diet-obesity relationships. 相似文献
956.
Jingjing Ben Xudong Zhu Hanwen Zhang Qi Chen 《British journal of pharmacology》2015,172(23):5523-5530
Class A1 scavenger receptors (SR‐A1) are membrane glycoproteins that can form homotrimers. This receptor was originally defined by its ability to mediate the accumulation of lipids in macrophages. Subsequent studies reveal that SR‐A1 plays critical roles in innate immunity, cell apoptosis and proliferation. This review highlights recent advances in understanding the structure, receptor pathway and regulation of SR‐A1. Although its role in atherosclerosis is disputable, recent discoveries suggest that SR‐A1 function in anti‐inflammatory responses by promoting an M2 macrophage phenotype in cardiovascular diseases. Therefore, SR‐A1 may be a potential target for therapeutic intervention of cardiovascular diseases.
Open in a separate window
Open in a separate windowThese Tables list key protein targets and ligands in this article which are hyperlinked to corresponding entries in http://www.guidetopharmacology.org, the common portal for data from the IUPHAR/BPS Guide to PHARMACOLOGY (Pawson et al., 2014) and are permanently archived in the Concise Guide to PHARMACOLOGY 2013/14 (a,bAlexander et al., 2013a, 2013b).
Scavenger receptors are cell surface receptors that are structurally diverse but they typically recognize many different ligands to participate in diverse biological functions. The functional mechanisms of scavenger receptors include endocytosis, phagocytosis, adhesion and signalling, which ultimately leads to the removal of non‐self‐ or altered self‐targets. There are 10 classes of scavenger receptors according to a unified nomenclature system for scavenger receptors (Prabhudas et al., 2014). Class A scavenger receptors have several structural features in common, including a cytoplasmic tail, a transmembrane domain, a spacer region, a helical coiled coil domain, a collagenous domain and a C‐terminal cysteine‐rich domain (Figure 1). Class A1 scavenger receptor (SR‐A1), also known as SCARA1, CD204 or macrophage scavenger receptor 1, is the prototypical SR‐A molecule and was the first scavenger receptor to be identified (Goldstein et al., 1979; Kodama et al., 1990; Rohrer et al., 1990)Open in a separate windowFigure 1Members of class A scavenger receptor family. The members of class A scavenger receptor family have a similar structure that is composed of a cytoplasmic tail, a transmembrane domain, a spacer region, a helical coiled coil domain, a collagenous domain and a C‐terminal cysteine‐rich domain.SR‐A1 was initially identified by its ability to mediate the formation of foam cells, a characteristic component of atherosclerotic lesions (Goldstein et al., 1979; Kodama et al., 1990; Krieger and Herz, 1994; Bowdish and Gordon, 2009). However, observations from various SR‐A1 gene knockout mouse models have yielded discrepant results concerning its role in the occurrence and development of atherosclerotic lesions (Suzuki et al., 1997; Kuchibhotla et al., 2008; Manning‐Tobin et al., 2009). A role beyond the handling of cholesterol is emerging for SR‐A1 in the pathogenesis of cardiovascular diseases. It not only functions as a phagocytic receptor and an innate immune recognition receptor but also plays an important role in cell apoptosis and cell proliferation. An overview of the recent progress of SR‐A1 structure, signal transduction and its roles in cardiovascular diseases will be provided in this review. 相似文献
Linked Articles
This article is part of a themed section on Chinese Innovation in Cardiovascular Drug Discovery. To view the other articles in this section visit http://dx.doi.org/10.1111/bph.2015.172.issue-23Abbreviations
- acLDL
- acetylated low‐density lipoprotein
- ER
- endoplasmic reticulum
- I/R
- ischaemia/reperfusion
- LTA
- lipoteichoic acid
- MI
- myocardial infarction
- mLDL
- modified low‐density lipoprotein
- oxLDL
- oxidized low‐density lipoprotein
- PRR
- pattern recognition receptor
- RAGE
- receptor for advanced glycated end‐products
- SR‐A1
- class A1 scavenger receptor
- TLR4
- Toll‐like receptor 4
- TRAF6
- TNF receptor‐associated factor 6
TARGETS |
---|
Catalytic receptors a |
Mer receptor tyrosine kinase |
TLR4 |
Enzymes b |
Caspase 3 |
ERK |
JNK |
Mitogen‐activated protein kinase kinase 7 (MKK7) |
p38 |
PI3K |
PKC |
PLC‐γ1 |
LIGANDS |
---|
Amyloid β |
IFN‐γ |
IL‐1 |
IL‐10 |
LPS |
Lysophosphatidylcholine |
Macrophage colony‐stimulating factor (M‐CSF) |
MMP‐9 |
Phorbol ester (PMA) |
Phosphatidylserine |
TGF‐β1 |
TNF‐α |
957.
Chunling Yan Yongjie Yang Kenji Saito Pingwen Xu Chunmei Wang Antentor Othrell Hinton Jr Xiaofeng Yan Qi Wu Qingchun Tong Joel K Elmquist Makoto Fukuda Yong Xu 《British journal of pharmacology》2015,172(14):3510-3521
Background and Purpose
Most forms of human obesity are characterized by impaired leptin sensitivity and, therefore, the effectiveness of anti-obesity leptin therapy in these leptin-resistant obese patients is marginal. Hence, the development of strategies to increase leptin sensitivity is of high priority in the field of obesity research.Experimental Approach
We first examined the effects of co-administration of leptin and meta-chlorophenylpiperazine (mCPP), an agonist of 5-HT2C and 5-HT1B receptors, on energy balance in leptin-resistant diet-induced obese (DIO) mice. We further assessed leptin-induced phosphorylation of the STAT-3 (pSTAT3) in various brain regions of DIO mice pretreated with mCPP or in mice genetically lacking 5-HT2C receptors.Results
Co-administration of mCPP with leptin had an additive effect on reducing body weight in DIO mice. Furthermore, mCPP pretreatment in DIO mice enhanced leptin-induced pSTAT3 in the arcuate nucleus, the ventromedial hypothalamic nucleus, and the ventral premammillary nucleus. Finally, deletion of 5-HT2C receptors significantly blunted leptin-induced pSTAT3 in these same hypothalamic regions.Conclusions and Implications
Our study provides evidence that drugs, which activate 5-HT2C receptors, could function as leptin sensitizers and be used in combination with leptin to provide additional weight loss in DIO.Tables of LinksTARGETS | |
---|---|
GPCRsa | Catalytic receptorsb |
5-HT1B receptor | Leptin receptor |
5-HT2C receptor | Enzymesc |
Melanocortin 4 receptor | JAK2 |
LIGANDS | |
---|---|
5-HT | Leptin |
Agouti-related peptide | Lorcaserin |
Amylin | Meta-chlorophenylpiperazine |
Glycine | Neuropeptide Y |
H2O2 | POMC |
Isoflurane | Sibutramine |
958.
The intramolecular proton-transfer processes of thymine were investigated by the density functional theory method. It is shown that the mutation from keto (T) to enol (T′) form is affected by zeolitic imidazolate framework-8 (ZIF-8) fragments such as single 2-methylimidazole neutral crystals (M), and negatively charged 2-methylimidazole ligands (M−). Results show that with the number (n) of water (w) molecules that assist proton-transfer increasing from 1 to 4, the order of the tautomeric energy barriers (in kcal mol−1) is T-2w (16.3) < T-1w (17.6) < T-3w (17.8) < T-4w (20.5). In the presence of M, the order of energy barrier is MT-2w (16.6) < MT-1w (17.7) < MT-3w (18.9) < MT-4w (20.8). M− has a catalysis effect on the energy barrier and the order is M−T-2w (14.4) < M−T-3w (15.2) < M−T-1w (16.3) < M−T-4w (16.8). The attachment of the M− fragment slightly promotes the proton-transfer processes in some instances. The characterization of the proton-transfer processes is helpful to understand the genotoxicity of ZIF-8 during drug delivery applications.Investigations on whether fragments from decomposed ZIF-8 would affect the intramolecular proton-transfer of thymine by DFT modeling. 相似文献
959.
Jia Liang Liangling Sun Balaji Devakumar Shaoying Wang Qi Sun Heng Guo Bin Li Xiaoyong Huang 《RSC advances》2018,8(48):27144
Double perovskite-based LiLaMgWO6:Mn4+ (LLMW:Mn4+) red phosphors were synthesized by traditional solid-state route under high temperature, and they showed bright far-red emission under excitation of 344 nm. The crystal structure, luminescence performance, internal quantum efficiency, fluorescence decay lifetimes, and thermal stability were investigated in detail. All samples exhibited far-red emissions around 713 nm due to the 2Eg → 4A2g transition of Mn4+ under excitation of near-ultraviolet and blue light, and the optimal doping concentration of Mn4+ was about 0.7 mol%. The CIE chromaticity coordinates of the LLMW:0.7% Mn4+ sample were (0.7253, 0.2746), and they were located at the border of the chromaticity diagram, indicating that the phosphors had high color purity. Furthermore, the internal quantum efficiency of LLMW:0.7% Mn4+ phosphors reached up to 69.1%, which was relatively higher than those of the reported Mn4+-doped red phosphors. Moreover, the sample displayed good thermal stability; the emission intensity of LLMW:0.7% Mn4+ phosphors at 423 K was 49% of the initial value at 303 K, while the activation energy was 0.39 eV. Importantly, there was a broad spectral overlap between the emission band of LLMW:Mn4+ phosphors and the absorption band of phytochrome PFR under near-ultraviolet light. All of these properties and phenomena illustrate that the LLMW:Mn4+ phosphors are potential far-red phosphors for applications in plant cultivation LEDs.Novel Mn4+-activated LiLaMgWO6 far-red emitting double-perovskite phosphors with high photoluminescence efficiency and good thermal stability were developed for applications in plant cultivation LEDs. 相似文献
960.
Yun Zhou Lixin Liu Tao Wu Guolong Yuan Junyu Li Qiujie Ding Fugang Qi Wenjun Zhu Xiaoping OuYang Yuan Wang 《RSC advances》2018,8(48):27073
Highly efficient solar light absorption capabilities and quantum yields in photocatalysts are key to their application in photocatalytic fields. Towards this end, TiO2/InVO4 nanofibers (NFs) have been designed and fabricated successfully by a one-pot electrospinning process. The resulting TiO2/InVO4 NFs display excellent visible-light photocatalytic activity, owing to their prominent visible-light absorption and electron–hole separation properties. Time-resolved transient PL spectroscopy demonstrated that the TiO2/InVO4 NFs display longer emission decay times (22.0 ns) compared with TiO2 NFs (15.5 ns), implying that the heterojunction can remarkably suppress the electron–hole recombination and promote the carrier transfer efficiency. With tailored heterostructure features, TiO2/InVO4 NFs exhibit superior visible-light photodegradation activity, and after 80 min of visible-light irradiation, almost 95% of RhB molecules can be decomposed by TiO2/InVO4 NFs, while only 18% of RhB molecules can be decomposed by pure TiO2 NFs.TiO2/InVO4 nanofibers have been designed and fabricated successfully by one-pot electrospinning process, which display longer carrier lifetime (22 ns) and enhanced visible-light photocatalytic activity. 相似文献