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1.
Int J Mol Sci ; 23(20)2022 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-36293048

RESUMO

Sleep is a fundamental, evolutionarily conserved, plastic behavior that is regulated by circadian and homeostatic mechanisms as well as genetic factors and environmental factors, such as light, humidity, and temperature. Among environmental cues, temperature plays an important role in the regulation of sleep. This review presents an overview of thermoreception in animals and the neural circuits that link this process to sleep. Understanding the influence of temperature on sleep can provide insight into basic physiologic processes that are required for survival and guide strategies to manage sleep disorders.


Assuntos
Ritmo Circadiano , Sono , Animais , Ritmo Circadiano/fisiologia , Temperatura , Sono/fisiologia , Homeostase/fisiologia , Plásticos
2.
Ying Yong Sheng Tai Xue Bao ; 31(11): 3621-3630, 2020 Nov.
Artigo em Chinês | MEDLINE | ID: mdl-33300711

RESUMO

Forests play an important role in terrestrial carbon cycles. The mechanism underlying carbon balance in temperate deciduous broad-leaved forests is not clear. In this study, net ecosystem exchange (NEE) and environmental factors, including air temperature (Ta), soil temperature (Ts), photosynthetically active radiation (PAR), vapor pressure deficit (VPD), soil water content (SWC) and precipitation (P) were continually measured using eddy covariance techniques in 2019 in a deciduous broad-leaved forest in Songshan, Beijing. We analyzed the characteristics of NEE and its response to environmental factors. The results showed that, at diurnal scale, the monthly averaged NEE exhibited a "U" shape curve (i.e., being a carbon sink over daytime while being a carbon source during nighttime) over the growing season. During the non-growing season, NEE was positive (i.e., carbon source) at diurnal scale. At the seasonal scale, NEE exhibited a unimodal curve. The annual cumulative NEE was -111 g C·m-2·a-1. Annual ecosystem respiration was 555 g C·m-2·a-1, while gross ecosystem productivity was 666 g C·m-2·a-1. Carbon sequestration peaked in June, while emission peaked in November. PAR was the dominant factor affecting daytime NEE (NEEd). VPD was the main factor that indirectly affected daytime NEEd, with an optimal VPD value that maximizes daytime NEE around 1-1.5 kPa. Soil temperature was the main factor affecting nighttime NEE (NEEn). SWC was a limiting factor for NEEn. Too high or too low SWC would inhibit NEEn, with an optimal SWC value of 0.28 m3·m-3.


Assuntos
Carbono , Ecossistema , Pequim , Dióxido de Carbono/análise , China , Florestas
3.
Biomater Sci ; 7(4): 1543-1553, 2019 Mar 26.
Artigo em Inglês | MEDLINE | ID: mdl-30681086

RESUMO

Among various polymeric gene delivery systems, peptide-based vectors demonstrate great potential owing to their unique structure and properties, including flexibility; however, there is insufficient molecular understanding of the role and properties of amino acids as building blocks in gene delivery. In this work, we constructed a series of histidine (H)-containing peptide-grafted dextran (D-RxHy) vectors via a simple two-step reaction of dextran with five RxHyC peptides: R7H3C, R5H3C, R5H5C, R3H5C, and R3H7C. The gel electrophoresis study unveiled the DNA-binding ability of H residues. While all D-RxHy vectors possess similarly low cytotoxicity, D-R3H7 exhibited the highest gene transfection efficiency. Interestingly, at the low nitrogen to phosphate (N/P) ratio of 2, D-R3H7 displayed a 6-8-fold higher luciferase expression compared to the gold standard branched PEI (25k). D-R3H7 and D-R5H5 demonstrated favorable cell uptake rates. A chloroquine-treated transfection assay confirmed the key effect of the high buffering capacity of H-rich D-R3H7 on its high gene transfection efficiency, especially at low N/P ratios. The present work unveiled that histidine is critical for both DNA condensation and the accurate control of endosomal escape. The tunable D-RxHy platform not only demonstrates promising potential for therapeutic purposes but can also be used as a tool to elucidate the molecular mechanism of polymer-based transfection.


Assuntos
Dextranos/farmacologia , Técnicas de Transferência de Genes , Peptídeos/farmacologia , Polímeros/farmacologia , Animais , Células COS , Sobrevivência Celular/efeitos dos fármacos , Chlorocebus aethiops , DNA Bacteriano/química , DNA Bacteriano/genética , Dextranos/química , Endossomos/efeitos dos fármacos , Vetores Genéticos/síntese química , Vetores Genéticos/química , Humanos , Células MCF-7 , Peptídeos/química , Plasmídeos/química , Plasmídeos/genética , Polímeros/química
4.
Biomed Pharmacother ; 111: 657-665, 2019 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-30611990

RESUMO

A microRNA (miRNA) is a single-stranded, small and non-coding RNA molecule that contains 20-25 nucleotides. More than 2000 miRNAs have been identified in human genes since the first miRNA was discovered in Caenorhabditis elegans in the early 1990s. miRNAs play a crucial role in various biological processes by regulating gene expression through post-transcriptional mechanisms. The alterations of their levels are associated with various diseases, such as glucometabolic disorder and lipid metabolism disorder. In recent years, miRNAs have been proved to be involved in regulating the functions of pancreatic ß-cells, insulin resistance and other biological behaviors related to glucometabolic disorder and the pathogenesis of diabetes mellitus (DM). This review summarized specific miRNAs, including miRNA-375 (miR-375), miRNA-155 (miR-155), miRNA-21 (miR-21), miRNA-33 (miR-33), the let-7 family and some other miRNAs related to glucometabolic regulation, introduced the obstacles and challenges in miRNA therapy, and discussed the prospect of new treatment methods for glucometabolic disorder.


Assuntos
Glucose/metabolismo , Doenças Metabólicas/tratamento farmacológico , Doenças Metabólicas/metabolismo , MicroRNAs/metabolismo , Animais , Diabetes Mellitus/tratamento farmacológico , Diabetes Mellitus/genética , Diabetes Mellitus/metabolismo , Glucose/genética , Humanos , Hiperglicemia/tratamento farmacológico , Hiperglicemia/genética , Hiperglicemia/metabolismo , Insulina/genética , Insulina/metabolismo , Células Secretoras de Insulina/efeitos dos fármacos , Células Secretoras de Insulina/metabolismo , Doenças Metabólicas/genética , MicroRNAs/administração & dosagem , MicroRNAs/genética
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