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Postbiotics are health-promoting microbial metabolites delivered as a functional food or a food supplement. They either directly influence signaling pathways of the body or indirectly manipulate metabolism and the composition of intestinal microflora. Cancer is the second leading cause of death worldwide and even though the prognosis of patients is improving, it is still poor in the substantial part of the cases. The preventable nature of cancer and the importance of a complex multi-level approach in anticancer therapy motivate the search for novel avenues of establishing the anticancer environment in the human body. This review summarizes the principal findings demonstrating the usefulness of both natural and synthetic sources of postbotics in the prevention and therapy of cancer. Specifically, the effects of crude cell-free supernatants, the short-chain fatty acid butyrate, lactic acid, hydrogen sulfide, and β-glucans are described. Contradictory roles of postbiotics in healthy and tumor tissues are highlighted. In conclusion, the application of postbiotics is an efficient complementary strategy to combat cancer. 相似文献
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基于高斯回归分析的水稻氮素敏感波段筛选及含量估算 总被引:1,自引:0,他引:1
WANG Jiao-jiao SONG Xiao-yu MEI Xin YANG Gui-jun LI Zhen-hai LI He-li MENG Yang 《光谱学与光谱分析》2021,41(6):1722-1729
水稻氮素含量的准确监测是稻田精准施肥的重要环节,水稻叶片氮素含量发生变化会引起叶片、冠层的光谱发射率发生变化,高光谱遥感是目前作物氮素无损监测的关键技术之一。以2018年-2019年湖北监利两年水稻氮肥试验为基础,分别获取水稻分蘖期、拔节期、孕穗期、扬花期、灌浆期五个生育期水稻叶片和冠层两个尺度的高光谱反射率数据及对应的叶片氮素含量数据,利用单波段原始光谱和一阶导数光谱的相关性分析、高斯过程回归(GPR)等方法筛选水稻全生育期叶片及冠层尺度氮素敏感波段。针对敏感波段,利用单波段回归分析、随机森林(RF)、支持向量回归(SVR)、高斯过程回归-随机森林(GPR-RF)、高斯过程回归-支持向量回归(GPR-SVR)和GPR构建水稻氮素监测模型,并进行精度对比,以确定水稻叶片在各生育期的氮素估算最佳模型。结果表明:GPR筛选的敏感波段符合水稻氮素含量及光谱变化的规律。相同条件下,叶片模型精度整体高于冠层模型。相关性分析模型中,叶片尺度原始光谱模型更好,冠层尺度刚好相反,冠层一阶导数光谱可以减弱稻田背景噪声的影响。其中,叶片最佳模型建模集R2为0.79,验证集R2为0.84;冠层最佳模型建模集R2为0.80,验证集R2为0.77。与相关性回归分析模型相比,机器学习模型受生育期影响小(R2>0.80,NRMSE<10%)。其中,RF比SVR更适合对GPR敏感波段建模,GPR-RF模型可以用1.5%左右的波段达到RF模型使用全部波段的精度。五种方法中,GPR模型对生育期敏感度最低、叶片及冠层尺度效果都很好(R2>0.94,NRMSE<6%)。且与其他四种机器学习方法相比,GPR模型可有效提高冠层氮素含量估算的精度和稳定性(R2增加0.02,NRMSE降低1.2%)。GPR方法可为筛选作物氮素高光谱敏感波段、反演各生育期叶片及冠层氮素含量提供方法参考。 相似文献
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GPR40 受体苯丙酸类激动剂三维定量构效关系研究 总被引:1,自引:0,他引:1
苯丙酸类化合物是G蛋白偶联受体40(GPR40)潜在的生物活性药物。本文基于比较分子力场分析法(Co MFA)和比较分子相似性指数分析法(CoMSIA),分别建立了40个已知活性的GPR40受体苯丙酸类激动剂的三维定量构效关系(3D-QSAR)模型,研究该类激动剂与生物活性之间的关系。CoMFA和CoMSIA模型的交叉验证系数(q~2)分别为0. 527和0. 500,拟合验证系数(r~2)分别为0. 901和0. 860,两个3D-QSAR模型预测值与实验值基本一致,表明模型具有良好的可信度和预测能力。根据两个3D-QSAR模型提供的立体场、静电场、疏水场、氢键供体场和氢键受体场所提供的信息提出优化该类抑制剂结构的药物设计思路,为指导设计更高活性的GPR40激动剂以及GRR40新分子激动活性的预测提供理论依据。 相似文献
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Proteomics analysis of altered proteins in kidney of mice with aristolochic acid nephropathy using the fluorogenic derivatization–liquid chromatography–tandem mass spectrometry method 下载免费PDF全文
《Biomedical chromatography : BMC》2018,32(3)
Aristolochic acid (AA) causes interstitial renal fibrosis, called aristolochic acid nephropathy (AAN). There is no specific indicator for diagnosing AAN, so this study aimed to investigate the biomarkers for AAN using a proteomics method. The C3H/He female mice were given ad libitum AA–distilled water (0.5 mg/kg/day) and distilled water for 56 days in the AA and normal groups, respectively. The AA‐induced proteins in the kidney were investigated using a proteomics study, including fluorogenic derivatization with 7‐chloro‐N‐[2‐(dimethylamino)ethyl]‐2,1,3‐benzoxadiazole‐4‐sulfonamide, followed by high‐performance liquid chromatography analysis and liquid chromatography tandem mass spectrometry with a MASCOT database searching system. There were two altered proteins, thrombospondin type 1 (TSP1) and G protein‐coupled receptor 87 (GPR87), in the kidney of AA‐group mice on day 56. GPR87, a tumorigenesis‐related protein, is reported for the first time in the current study. The renal interstitial fibrosis was certainly induced in the AA‐group mice under histological examination. Based on the results of histological examination and the proteomics study, this model might be applied to AAN studies in the future. TSP1 might be a novel biomarker for AAN, and the further role of GPR87 leading to AA‐induced tumorigenesis should be researched in future studies. 相似文献
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超前探测中探地雷达应用与结果的处理分析 总被引:1,自引:0,他引:1
在隧道施工中,由于地质条件的复杂性和勘察工作的局限性,往往造成地质勘查成果与开挖后的情况不一致,这就要求在隧道施工工程中进行超前跟踪探测,确保隧道施工的安全。本文主要介绍SIR-3000探地雷达系统在郴(州)宁(远)高速公路芒头岭隧道超前预报中的应用概况,并采用空间域滤波和希尔伯特变换等方法对探测结果进行处理,根据处理结果对隧道掌子面前方溶洞、裂隙等地质情况进行预测。隧道后期的开挖情况证明了雷达预测结果的正确性,取得了较好的预测效果,同时也说明了采用空间滤波、希尔伯特变换等处理方法对改进实测数据质量方面的有用性。 相似文献
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Guoxia Ji Qinghua Guo Qidi Xue Ruifang Kong Shiben Wang Kang Lei Renmin Liu Xuekun Wang 《Molecules (Basel, Switzerland)》2021,26(22)
GPR120 is a promising target for the treatment of type 2 diabetes (T2DM), which is activated by free fatty acids (FFAs) and stimulates the release of glucagon-like peptide-1(GLP-1). GLP-1, as an incretin, can enhance glucose-dependent secretion of insulin from pancreatic beta cells and reduce blood glucose. In this study, a series of novel GPR120 agonists were designed and synthesized to improve the stability and hydrophilicity of the phenylpropanoic acid GPR120 agonist TUG-891. Compound 11b showed excellent GPR120 agonistic activity and pharmacokinetic properties, and could reduce the blood glucose of normal mice in a dose-dependent manner. In addition, no hypoglycemic side effects were observed even at a dose of 100 mg/kg. Moreover, 11b showed good anti-hyperglycemic effects in diet-induced obese (DIO) mice. Molecular simulation illustrated that compound 11b could enter the active site of GPR120 and interact with ARG99. Taken together, the results indicate that compound 11b might be a promising drug candidate for the treatment of T2DM. 相似文献
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Sonia Burgaz Concepcin García Claudia Gonzalo-Consuegra Marta Gmez-Almería Francisco Ruiz-Pino Juan Diego Unciti María Gmez-Caas Juan Alcalde Paula Morales Nadine Jagerovic Carmen Rodríguez-Cueto Eva de Lago Eduardo Muoz Javier Fernndez-Ruiz 《Molecules (Basel, Switzerland)》2021,26(24)
Cannabinoids act as pleiotropic compounds exerting, among others, a broad-spectrum of neuroprotective effects. These effects have been investigated in the last years in different preclinical models of neurodegeneration, with the cannabinoid type-1 (CB1) and type-2 (CB2) receptors concentrating an important part of this research. However, the issue has also been extended to additional targets that are also active for cannabinoids, such as the orphan G-protein receptor 55 (GPR55). In the present study, we investigated the neuroprotective potential of VCE-006.1, a chromenopyrazole derivative with biased orthosteric and positive allosteric modulator activity at GPR55, in murine models of two neurodegenerative diseases. First, we proved that VCE-006.1 alone could induce ERK1/2 activation and calcium mobilization, as well as increase cAMP response but only in the presence of lysophosphatidyl inositol. Next, we investigated this compound administered chronically in two neurotoxin-based models of Parkinson’s disease (PD), as well as in some cell-based models. VCE-006.1 was active in reversing the motor defects caused by 6-hydroxydopamine (6-OHDA) in the pole and the cylinder rearing tests, as well as the losses in tyrosine hydroxylase-containing neurons and the elevated glial reactivity detected in the substantia nigra. Similar cytoprotective effects were found in vitro in SH-SY5Y cells exposed to 6-OHDA. We also investigated VCE-006.1 in LPS-lesioned mice with similar beneficial effects, except against glial reactivity and associated inflammatory events, which remained unaltered, a fact confirmed in BV2 cells treated with LPS and VCE-006.1. We also analyzed GPR55 in these in vivo models with no changes in its gene expression, although GPR55 was down-regulated in BV2 cells treated with LPS, which may explain the lack of efficacy of VCE-006.1 in such an assay. Furthermore, we investigated VCE-006.1 in two genetic models of amyotrophic lateral sclerosis (ALS), mutant SOD1, or TDP-43 transgenic mice. Neither the neurological decline nor the deteriorated rotarod performance were prevented with this compound, and the same happened with the elevated microglial and astroglial reactivities, albeit modest spinal motor neuron preservation was achieved in both models. We also analyzed GPR55 in these in vivo models and found no changes in both TDP-43 transgenic and mSOD1 mice. Therefore, our findings support the view that targeting the GPR55 may afford neuroprotection in experimental PD, but not in ALS, thus stressing the specificities for the development of cannabinoid-based therapies in the different neurodegenerative disorders. 相似文献
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