Previous studies show that several structures of the house sparrow visual system are metabolically rhythmic, as determined by 2-deoxy[(14)C]glucose (2DG) uptake, and that these metabolic rhythms depend upon rhythmic melatonin in this species. In many species of birds, high affinity binding of 2[(125)I] iodomelatonin is widespread in the brain, especially in visual system structures. The present study asks whether 2DG uptake is similarly rhythmic in the chick brain and whether exogenous melatonin administration affects 2DG uptake. Chicks were injected with 2DG and sacrificed 1 h later. Their brains were removed and processed for 2DG autoradiography. Chicks were injected during the late day with melatonin or saline prior to the 2DG injection and brain processing. We found that the visual suprachiasmatic nucleus showed both daily and circadian differences in 2DG uptake. Six of seven visual structures displayed daily uptake changes, while only two structures showed circadian fluctuations. Melatonin affected daytime 2DG uptake within visual suprachiasmatic nucleus and ectostriatum only. These results indicate that the chick circadian system is involved in the regulation of energy metabolism in the visual system but that the role for pineal melatonin in that regulatory process is a subtle one.
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http://dx.doi.org/10.1016/s0361-9230(01)00753-5 | DOI Listing |
J Mater Chem B
January 2025
Department of Neurology, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, Anhui, P. R. China.
Drug delivery for epilepsy treatment faces enormous challenges, where the sole focus on enhancing the ability of drugs to penetrate the blood-brain barrier (BBB) through ligand modification is insufficient because of the absence of seizure-specific drug accumulation. In this study, an amphipathic drug carrier with a glucose transporter (GLUT)-targeting capability was synthesised by conjugating 2-deoxy-2-amino-D-glucose (2-DG) to the model carrier DSPE-PEG. A 2-DG-modified nano drug delivery system (NDDS) possessing robust stability and favourable biocompatibility was then fabricated using the nanoprecipitation method.
View Article and Find Full Text PDFSTAR Protoc
December 2024
Department of Medicine, College of Medicine, National Taiwan University, Taipei 100, Taiwan. Electronic address:
2-deoxy-D-glucose (2DG) is a glucose analog converted to 2-deoxy-D-glucose-6-phosphate (2DG-6P) by hexokinase in glycolysis. While 2DG commonly measures glucose uptake, 2DG-6P detects glucose utilization. Here, we present a protocol to measure glucose utilization in various tissues after entering a mouse's body using radiolabeled 2DG.
View Article and Find Full Text PDFAm J Mens Health
November 2024
Department of Urology, Zigong Fourth People's Hospital, Zigong, China.
SPC25 is associated with unfavorable outcomes in various cancers, but its role in prostate cancer (PRAD) is unclear. More research is needed on glycolysis and ferroptosis targets in PRAD. Bioinformatics tools were used to analyze SPC25 expression disparities.
View Article and Find Full Text PDFBiomedicines
October 2024
Department of Medical Biology, Kaczkowski Military Institute of Hygiene and Epidemiology, Kozielska 4, 01-163 Warsaw, Poland.
Background: One defining feature of various aggressive cancers, including glioblastoma multiforme (GBM), is glycolysis upregulation, making its inhibition a promising therapeutic approach. One promising compound is 2-deoxy-d-glucose (2-DG), a d-glucose analog with high clinical potential due to its ability to inhibit glycolysis. Upon uptake, 2-DG is phosphorylated by hexokinase to 2-DG-6-phosphate, which inhibits hexokinase and downstream glycolytic enzymes.
View Article and Find Full Text PDFEcotoxicol Environ Saf
October 2024
Research and Development Center for Efficient Utilization of Coastal Bioresources, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, PR China; Laboratory for Marine Biology and Biotechnology, Qingdao Marine Science and Technology Center, Qingdao 266237, PR China; Muping Coastal Environment Research Station, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, PR China. Electronic address:
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