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Author Liu, Z.; Qian, M.; Tang, X.; Hu, W.; Sun, S.; Li, G.; Zhang, S.; Meng, F.; Cao, X.; Sun, J.; Xu, C.; Tan, B.; Pang, Q.; Zhao, B.; Wang, Z.; Guan, Y.; Ruan, X.; Liu, B. url  doi
openurl 
  Title SIRT7 couples light-driven body temperature cues to hepatic circadian phase coherence and gluconeogenesis Type Journal Article
  Year 2019 Publication Nature Metabolism Abbreviated Journal Nat Metab  
  Volume 1 Issue 11 Pages 1141-1156  
  Keywords Animals  
  Abstract The central pacemaker in the hypothalamic suprachiasmatic nucleus (SCN) synchronizes peripheral oscillators to coordinate physiological and behavioural activities throughout the body. How circadian phase coherence between the SCN and the periphery is controlled is not well understood. Here, we identify hepatic SIRT7 as an early responsive element to light that ensures circadian phase coherence in the mouse liver. The SCN-driven body temperature (BT) oscillation induces rhythmic expression of HSP70, which promotes SIRT7 ubiquitination and proteasomal degradation. Acute temperature challenge dampens the BT oscillation and causes an advanced liver circadian phase. Further, hepatic SIRT7 deacetylates CRY1, promotes its FBXL3-mediated degradation and regulates the hepatic clock and glucose homeostasis. Loss of Sirt7 in mice leads to an advanced liver circadian phase and rapid entrainment of the hepatic clock upon daytime-restricted feeding. These data identify a BT–HSP70–SIRT7–CRY1 axis that couples the mouse hepatic clock to the central pacemaker and ensures circadian phase coherence and glucose homeostasis.  
  Address  
  Corporate Author Thesis  
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  Language Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN (down) 2522-5812 ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number GFZ @ kyba @ Serial 2747  
Permanent link to this record
 

 
Author Anbalagan, M.; Dauchy, R.; Xiang, S.; Robling, A.; Blask, D.; Rowan, B.; Hill, S. url  doi
openurl 
  Title SAT-337 Disruption Of The Circadian Melatonin Signal By Dim Light At Night Promotes Bone-lytic Breast Cancer Metastases Type Journal Article
  Year 2019 Publication Journal of the Endocrine Society Abbreviated Journal  
  Volume 3 Issue Supplement_1 Pages  
  Keywords Animals  
  Abstract Breast cancer metastasis to bone is a major source of morbidity and mortality in women with advanced metastatic breast cancer. Morbidity from metastasis to bone is compounded by the fact that they cannot be surgically removed and can only be treated with chemotherapy and/or radiation therapy. Thus, there is critical need to develop new treatment strategies that kill bone metastatic tumors and reduce osteolytic lesions to improve patient quality of life and extend patient survival. Circadian rhythms are daily cycles of ~24 h that control many if not most physiologic processes and their disruption by exposure to light at night (LAN) or jet lag has been shown to be strongly associated with the development of cancer, particularly breast cancer. We have found that disruption of the anti-cancer circadian hormone melatonin (MLT) by light at night can significantly enhance the metastatic potential in breast cancer cells. Our work supports the report of the International Agency for Research on Cancer that shift work is a “probable human carcinogen” and highlights the association between exposure to light at night and invasive breast cancer. We recently reported that human breast tumor xenografts grown in athymic nude female rats housed in a photoperiod of 12h light at day: 12h dim light at night (dLAN, 0.2 lux – blocks the nighttime circadian MLT signal), display resistance to doxorubicin (Dox). More importantly, tumor growth and drug resistance could be blocked by the administration of Dox in circadian alignment with nocturnal MLT during dLAN. Our recent preliminary studies show that poorly invasive ERα positive MCF-7 breast cancer cells, when injected into the tibia (to mimic bone metastatic disease) of Foxn1nu athymic nude mice (which produce a strong circadian nighttime melatonin signal) housed in a dLAN photoperiod (suppressed nocturnal MLT production) developed full blown breast cancer tumors in bone (P<0.05) that are highly osteolytic (P<0.05). Moreover, patients with metastatic breast cancer are routinely treated with doxorubicin, which itself can promote bone damage. Our studies demonstrate that MLT slows the growth of metastatic breast cancer in bone but that the chrono-therapeutic use of doxorubicin in circadian alignment with melatonin in Foxn1nu mice with tibial breast tumors, reduced tumor growth in bone, reduced bone erosion, and promoted the formation of new bone. Successful use of this chronotherapeutic use of Dox and MLT in clinical trials increasing efficacy in preventing or suppressing breast cancer metastasis to bone while decreasing toxic side effects of doxorubicin would provide a revolutionary advancement in the treatment of bone metastatic breast cancer and decrease the morbidity and mortality associated with breast cancer metastasis to bone.  
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  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN (down) 2472-1972 ISBN Medium  
  Area Expedition Conference  
  Notes Approved no  
  Call Number GFZ @ kyba @ Serial 2433  
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Author Rodríguez Martín, A.; Holmberg, R.; Dann, P.; Chiaradia, A. url  doi
openurl 
  Title Penguin colony attendance under artificial lights for ecotourism Type Journal Article
  Year 2018 Publication Journal of Experimental Zoology. Part A, Ecological and Integrative Physiology Abbreviated Journal J Exp Zool A Ecol Integr Physiol  
  Volume 329 Issue 8-9 Pages 457-464  
  Keywords Animals  
  Abstract Wildlife watching is an emerging ecotourism activity around the world. In Australia and New Zealand, night viewing of little penguins attracts hundreds of thousands of visitors per year. As penguins start coming ashore after sunset, artificial lighting is essential to allow visitors to view them in the dark. This alteration of the nightscape warrants investigation for any potential effects of artificial lighting on penguin behavior. We experimentally tested how penguins respond to different light wavelengths (colors) and intensities to examine effects on the colony attendance behavior at two sites on Phillip Island, Australia. At one site, nocturnal artificial illumination has been used for penguin viewing for decades, whereas at the other site, the only light is from the natural night sky. Light intensity did not affect colony attendance behaviors of penguins at the artificially lit site, probably due to penguin habituation to lights. At the not previously lit site, penguins preferred lit paths over dark paths to reach their nests. Thus, artificial light might enhance penguin vision at night and consequently it might reduce predation risk and energetic costs of locomotion through obstacle and path detection. Although penguins are faithful to their path, they can be drawn to artificial lights at small spatial scale, so light pollution could attract penguins to undesirable lit areas. When artificial lighting is required, we recommend keeping lighting as dim and time-restricted as possible to mitigate any negative effects on the behavior of penguins and their natural habitat.  
  Address Research Department, Phillip Island Nature Parks, Cowes, Victoria, Australia  
  Corporate Author Thesis  
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  Language English Summary Language Original Title  
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  ISSN (down) 2471-5638 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:29603671 Approved no  
  Call Number GFZ @ kyba @ Serial 1834  
Permanent link to this record
 

 
Author Sanders, D.; Gaston, K.J. url  doi
openurl 
  Title How ecological communities respond to artificial light at night Type Journal Article
  Year 2018 Publication Journal of Experimental Zoology. Part A, Ecological and Integrative Physiology Abbreviated Journal J Exp Zool A Ecol Integr Physiol  
  Volume 329 Issue 8-9 Pages 394-400  
  Keywords Ecology  
  Abstract Many ecosystems worldwide are exposed to artificial light at night (ALAN), from streetlights and other sources, and a wide range of organisms has been shown to respond to this anthropogenic pressure. This raises concerns about the consequences for major ecosystem functions and their stability. However, there is limited understanding of how whole ecological communities respond to ALAN, and this cannot be gained simply by making predictions from observed single species physiological, behavioral, or ecological responses. Research needs to include an important building block of ecological communities, namely the interactions between species that drive ecological and evolutionary processes in ecosystems. Here, we summarize current knowledge about community responses to ALAN and illustrate different pathways and their impact on ecosystem functioning and stability. We discuss that documentation of the impact of ALAN on species interaction networks and trait distributions provides useful tools to link changes in community structure to ecosystem functions. Finally, we suggest several approaches to advance research that will link the diverse impact of ALAN to changes in ecosystems.  
  Address Wissenschaftskolleg zu Berlin, Institute for Advanced Study, Berlin, Germany  
  Corporate Author Thesis  
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  Language English Summary Language Original Title  
  Series Editor Series Title Abbreviated Series Title  
  Series Volume Series Issue Edition  
  ISSN (down) 2471-5638 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:29656458 Approved no  
  Call Number GFZ @ kyba @ Serial 1857  
Permanent link to this record
 

 
Author Dimovski, A.M.; Robert, K.A. url  doi
openurl 
  Title Artificial light pollution: Shifting spectral wavelengths to mitigate physiological and health consequences in a nocturnal marsupial mammal Type Journal Article
  Year 2018 Publication Journal of Experimental Zoology. Part A, Ecological and Integrative Physiology Abbreviated Journal J Exp Zool A Ecol Integr Physiol  
  Volume 329 Issue 8-9 Pages 497-505  
  Keywords Animals; Lighting  
  Abstract The focus of sustainable lighting tends to be on reduced CO2 emissions and cost savings, but not on the wider environmental effects. Ironically, the introduction of energy-efficient lighting, such as light emitting diodes (LEDs), may be having a great impact on the health of wildlife. These white LEDs are generated with a high content of short-wavelength 'blue' light. While light of any kind can suppress melatonin and the physiological processes it regulates, these short wavelengths are potent suppressors of melatonin. Here, we manipulated the spectral composition of LED lights and tested their capacity to mitigate the physiological and health consequences associated with their use. We experimentally investigated the impact of white LEDs (peak wavelength 448 nm; mean irradiance 2.87 W/m(2) ), long-wavelength shifted amber LEDs (peak wavelength 605 nm; mean irradiance 2.00 W/m(2) ), and no lighting (irradiance from sky glow < 0.37 x 10(-3) W/m(2) ), on melatonin production, lipid peroxidation, and circulating antioxidant capacity in the tammar wallaby (Macropus eugenii). Night-time melatonin and oxidative status were determined at baseline and again following 10 weeks exposure to light treatments. White LED exposed wallabies had significantly suppressed nocturnal melatonin compared to no light and amber LED exposed wallabies, while there was no difference in lipid peroxidation. Antioxidant capacity declined from baseline to week 10 under all treatments. These results provide further evidence that short-wavelength light at night is a potent suppressor of nocturnal melatonin. Importantly, we also illustrate that shifting the spectral output to longer wavelengths could mitigate these negative physiological impacts.  
  Address Department of Ecology, Environment and Evolution, La Trobe University, Melbourne, Australia  
  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 (down) 2471-5638 ISBN Medium  
  Area Expedition Conference  
  Notes PMID:29722167 Approved no  
  Call Number GFZ @ kyba @ Serial 1888  
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