toggle visibility Search & Display Options

Select All    Deselect All
 |   | 
Details
   print
  Records Links
Author Chaves, I.; Pokorny, R.; Byrdin, M.; Hoang, N.; Ritz, T.; Brettel, K.; Essen, L.-O.; van der Horst, G.T.J.; Batschauer, A.; Ahmad, M. url  doi
openurl 
  Title The cryptochromes: blue light photoreceptors in plants and animals Type Journal Article
  Year 2011 Publication Annual Review of Plant Biology Abbreviated Journal Annu Rev Plant Biol  
  Volume 62 Issue Pages (down) 335-364  
  Keywords Adenosine Triphosphate/metabolism; Animals; Cryptochromes/chemistry/classification/*physiology; DNA Repair; Deoxyribodipyrimidine Photo-Lyase/chemistry/classification/physiology; Homing Behavior; Insects/physiology; *Light Signal Transduction; Magnetics; Mice; Oxidation-Reduction; Phosphorylation/physiology; Plants/*metabolism; blue light  
  Abstract Cryptochromes are flavoprotein photoreceptors first identified in Arabidopsis thaliana, where they play key roles in growth and development. Subsequently identified in prokaryotes, archaea, and many eukaryotes, cryptochromes function in the animal circadian clock and are proposed as magnetoreceptors in migratory birds. Cryptochromes are closely structurally related to photolyases, evolutionarily ancient flavoproteins that catalyze light-dependent DNA repair. Here, we review the structural, photochemical, and molecular properties of cry-DASH, plant, and animal cryptochromes in relation to biological signaling mechanisms and uncover common features that may contribute to better understanding the function of cryptochromes in diverse systems including in man.  
  Address Department of Genetics, Erasmus University Medical Center, 3000 CA Rotterdam, The Netherlands. i.chaves@erasmusmc.nl  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1543-5008 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:21526969 Approved no  
  Call Number IDA @ john @ Serial 341  
Permanent link to this record
 

 
Author Morera, A.L.; Abreu, P. url  doi
openurl 
  Title Daytime/night-time and summer/winter melatonin and malondialdehyde rhythms: an inverse relationship Type Journal Article
  Year 2007 Publication Journal of Pineal Research Abbreviated Journal J Pineal Res  
  Volume 43 Issue 3 Pages (down) 313-314  
  Keywords Human Health; Circadian Rhythm/*physiology; Humans; *Light; Malondialdehyde/*metabolism; Melatonin/*metabolism; *Seasons  
  Abstract  
  Address  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 0742-3098 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:17803530 Approved no  
  Call Number LoNNe @ kagoburian @ Serial 784  
Permanent link to this record
 

 
Author Kijlstra, A.; Tian, Y.; Kelly, E.R.; Berendschot, T.T.J.M. url  doi
openurl 
  Title Lutein: more than just a filter for blue light Type Journal Article
  Year 2012 Publication Progress in Retinal and eye Research Abbreviated Journal Prog Retin Eye Res  
  Volume 31 Issue 4 Pages (down) 303-315  
  Keywords Animals; Biological Transport/physiology; Eye/metabolism; Humans; Lutein/chemistry/deficiency/pharmacology/*physiology; Macular Degeneration/etiology/prevention & control; Retinal Diseases/metabolism; Scavenger Receptors, Class B/physiology; blue light  
  Abstract Lutein is concentrated in the primate retina, where together with zeaxanthin it forms the macular pigment. Traditionally lutein is characterized by its blue light filtering and anti-oxidant properties. Eliminating lutein from the diet of experimental animals results in early degenerative signs in the retina while patients with an acquired condition of macular pigment loss (Macular Telangiectasia) show serious visual handicap indicating the importance of macular pigment. Whether lutein intake reduces the risk of age related macular degeneration (AMD) or cataract formation is currently a strong matter of debate and abundant research is carried out to unravel the biological properties of the lutein molecule. SR-B1 has recently been identified as a lutein binding protein in the retina and this same receptor plays a role in the selective uptake in the gut. In the blood lutein is transported via high-density lipoproteins (HDL). Genes controlling SR-B1 and HDL levels predispose to AMD which supports the involvement of cholesterol/lutein transport pathways. Apart from beneficial effects of lutein intake on various visual function tests, recent findings show that lutein can affect immune responses and inflammation. Lutein diminishes the expression of various ocular inflammation models including endotoxin induced uveitis, laser induced choroidal neovascularization, streptozotocin induced diabetes and experimental retinal ischemia and reperfusion. In vitro studies show that lutein suppresses NF kappa-B activation as well as the expression of iNOS and COX-2. Since AMD has features of a chronic low-grade systemic inflammatory response, attention to the exact role of lutein in this disease has shifted from a local effect in the eye towards a possible systemic anti-inflammatory function.  
  Address University Eye Clinic Maastricht, Maastricht, The Netherlands. aize.kijlstra@wur.nl  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1350-9462 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:22465791 Approved no  
  Call Number IDA @ john @ Serial 343  
Permanent link to this record
 

 
Author Reiter, R.J.; Tan, D.X.; Korkmaz, A.; Rosales-Corral, S.A. url  doi
openurl 
  Title Melatonin and stable circadian rhythms optimize maternal, placental and fetal physiology Type Journal Article
  Year 2014 Publication Human Reproduction Update Abbreviated Journal Hum Reprod Update  
  Volume 20 Issue 2 Pages (down) 293-307  
  Keywords Human Health; Animals; Antioxidants/physiology; Biological Clocks/physiology; Circadian Rhythm/*physiology; Female; Fetus/*physiology; Humans; Mammals; Melatonin/biosynthesis/*physiology; Mice; Oxidative Stress/physiology; Parturition/physiology; Placenta/metabolism/*physiology; Pre-Eclampsia/etiology/metabolism; Pregnancy; Uterus/metabolism; circadian rhythms; fetus; melatonin; placenta; pre-eclampsia  
  Abstract BACKGROUND: Research within the last decade has shown melatonin to have previously-unsuspected beneficial actions on the peripheral reproductive organs. Likewise, numerous investigations have documented that stable circadian rhythms are also helpful in maintaining reproductive health. The relationship of melatonin and circadian rhythmicity to maternal and fetal health is summarized in this review. METHODS: Databases were searched for the related published English literature up to 15 May 2013. The search terms used in various combinations included melatonin, circadian rhythms, biological clock, suprachiasmatic nucleus, ovary, pregnancy, uterus, placenta, fetus, pre-eclampsia, intrauterine growth restriction, ischemia-reperfusion, chronodisruption, antioxidants, oxidative stress and free radicals. The results of the studies uncovered are summarized herein. RESULTS: Both melatonin and circadian rhythms impact reproduction, especially during pregnancy. Melatonin is a multifaceted molecule with direct free radical scavenging and indirect antioxidant activities. Melatonin is produced in both the ovary and in the placenta where it protects against molecular mutilation and cellular dysfunction arising from oxidative/nitrosative stress. The placenta, in particular, is often a site of excessive free radical generation due to less than optimal adhesion to the uterine wall, which leads to either persistent hypoxia or intermittent hypoxia and reoxygenation, processes that cause massive free radical generation and organ dysfunction. This may contribute to pre-eclampsia and other disorders which often complicate pregnancy. Melatonin has ameliorated free radical damage to the placenta and to the fetus in experiments using non-human mammals. Likewise, the maintenance of a regular maternal light/dark and sleep/wake cycle is important to stabilize circadian rhythms generated by the maternal central circadian pacemaker, the suprachiasmatic nuclei. Optimal circadian rhythmicity in the mother is important since her circadian clock, either directly or indirectly via the melatonin rhythm, programs the developing master oscillator of the fetus. Experimental studies have shown that disturbed maternal circadian rhythms, referred to as chronodisruption, and perturbed melatonin cycles have negative consequences for the maturing fetal oscillators, which may lead to psychological and behavioral problems in the newborn. To optimize regular circadian rhythms and prevent disturbances of the melatonin cycle during pregnancy, shift work and bright light exposure at night should be avoided, especially during the last trimester of pregnancy. Finally, melatonin synergizes with oxytocin to promote delivery of the fetus. Since blood melatonin levels are normally highest during the dark period, the propensity of childbirth to occur at night may relate to the high levels of melatonin at this time which work in concert with oxytocin to enhance the strength of uterine contractions. CONCLUSIONS: A number of conclusions naturally evolve from the data summarized in this review: (i) melatonin, of both pineal and placental origin, has essential functions in fetal maturation and placenta/uterine homeostasis; (ii) circadian clock genes, which are components of all cells including those in the peripheral reproductive organs, have important roles in reproductive and organismal (fetal and maternal) physiology; (iii) due to the potent antioxidant actions of melatonin, coupled with its virtual absence of toxicity, this indoleamine may have utility in the treatment of pre-eclampsia, intrauterine growth restriction, placental and fetal ischemia/reperfusion, etc. (iv) the propensity for parturition to occur at night may relate to the synergism between the nocturnal increase in melatonin and oxytocin.  
  Address Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USA  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1355-4786 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:24132226 Approved no  
  Call Number LoNNe @ christopher.kyba @ Serial 504  
Permanent link to this record
 

 
Author Smith, M.R.; Revell, V.L.; Eastman, C.I. url  doi
openurl 
  Title Phase advancing the human circadian clock with blue-enriched polychromatic light Type Journal Article
  Year 2009 Publication Sleep Medicine Abbreviated Journal Sleep Med  
  Volume 10 Issue 3 Pages (down) 287-294  
  Keywords Adult; Circadian Rhythm/*radiation effects; Female; Humans; *Light; Lighting/*methods; Male; Melatonin/metabolism; Phototherapy/*methods; Sleep; Wakefulness; Young Adult; blue light; sleep  
  Abstract BACKGROUND: Previous studies have shown that the human circadian system is maximally sensitive to short-wavelength (blue) light. Whether this sensitivity can be utilized to increase the size of phase shifts using light boxes and protocols designed for practical settings is not known. We assessed whether bright polychromatic lamps enriched in the short-wavelength portion of the visible light spectrum could produce larger phase advances than standard bright white lamps. METHODS: Twenty-two healthy young adults received either a bright white or bright blue-enriched 2-h phase advancing light pulse upon awakening on each of four treatment days. On the first treatment day the light pulse began 8h after the dim light melatonin onset (DLMO), on average about 2h before baseline wake time. On each subsequent day, light treatment began 1h earlier than the previous day, and the sleep schedule was also advanced. RESULTS: Phase advances of the DLMO for the blue-enriched (92+/-78 min, n=12) and white groups (76+/-45 min, n=10) were not significantly different. CONCLUSION: Bright blue-enriched polychromatic light is no more effective than standard bright light therapy for phase advancing circadian rhythms at commonly used therapeutic light levels.  
  Address Biological Rhythms Research Laboratory, Rush University Medical Center, Suite 425, 1645 W. Jackson Boulevard, Chicago, IL 60612, USA  
  Corporate Author Thesis  
  Publisher Place of Publication Editor  
  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN 1389-9457 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:18805055; PMCID:PMC2723863 Approved no  
  Call Number IDA @ john @ Serial 289  
Permanent link to this record
Select All    Deselect All
 |   | 
Details
   print

Save Citations:
Export Records: