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1.
Proc Natl Acad Sci U S A ; 119(13): e2118803119, 2022 03 29.
Article in English | MEDLINE | ID: mdl-35312355

ABSTRACT

SignificanceThe function of our biological clock is dependent on environmental light. Rodent studies have shown that there are multiple colors that affect the clock, but indirect measures in humans suggest blue light is key. We performed functional MRI studies in human subjects with unprecedented spatial resolution to investigate color sensitivity of our clock. Here, we show that narrowband blue, green, and orange light were all effective in changing neuronal activity of the clock. While the clock of nocturnal rodents is excited by light, the human clock responds with a decrease in neuronal activity as indicated by a negative BOLD response. The sensitivity of the clock to multiple colors should be integrated in light therapy aimed to strengthen our 24-h rhythms.


Subject(s)
Circadian Clocks , Circadian Rhythm/physiology , Humans , Light , Photobiology , Suprachiasmatic Nucleus/physiology
2.
Physiol Behav ; 139: 351-60, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25446229

ABSTRACT

Animals have circadian clocks that govern their activity pattern, resulting in 24h rhythms in physiology and behaviour. Under laboratory conditions, light is the major external signal that affects temporal patterns in behaviour, and Mus musculus is strictly nocturnal in its behaviour. In the present study we questioned whether under natural conditions, environmental factors other than light affect the temporal profile of mice. In order to test this, we investigated the activity patterns of free-ranging M. musculus in a natural habitat, using sensors and a camera integrated into a recording unit that the mice could freely enter and leave. Our data show that mice have seasonal fluctuations in activity duration (6.7±0.82 h in summer, 11.3±1.80 h in winter). Furthermore, although primarily nocturnal, wild mice also exhibit daytime activity from spring until late autumn. A multivariate analysis revealed that the major factor correlating with increased daytime activity was population activity, defined as the number of visits to the recording site. Day length had a small but significant effect. Further analysis revealed that the relative population activity (compared to the past couple of days) is a better predictor of daytime activity than absolute population activity. Light intensity and temperature did not have a significant effect on daytime activity. The amount of variance explained by external factors is 51.9%, leaving surprisingly little unexplained variance that might be attributed to the internal clock. Our data further indicate that mice determine population activity by comparing a given night with the preceding 2-7 nights, a time frame suggesting a role for olfactory cues. We conclude that relative population activity is a major factor controlling the temporal activity patterns of M. musculus in an unrestricted natural population.


Subject(s)
Animals, Wild/physiology , Circadian Rhythm/physiology , Mice/physiology , Motor Activity/physiology , Social Behavior , Actigraphy , Animals , Light , Multivariate Analysis , Photoperiod , Regression Analysis , Seasons , Temperature , Video Recording
3.
J Proteomics ; 77: 144-53, 2012 Dec 21.
Article in English | MEDLINE | ID: mdl-22842157

ABSTRACT

In order to balance the speed of analytical sample preparation procedures with mass spectrometry (MS)-based clinical proteomics the application of high-throughput robotic systems for body fluid workup is essential. In this paper we describe the implementation of various solid-phase extraction (SPE) sample preparation protocols on two different platforms, namely: 1) Magnetic bead-based SPE of peptides and proteins from body fluids on a Hamilton liquid handling workstation; 2) Cartridge-based SPE on a SPARK Symbiosis system. All SPE protocols were optimized for MS-based proteomics and compared with respect to obtained peptide- and protein profiles. Throughput numbers that were achieved in a 24 hour time frame for the sample workup procedures were more than 700 samples for the magnetic bead-based method and over 1000 samples for the cartridge-based method.


Subject(s)
Blood Proteins/chemistry , Blood Proteins/isolation & purification , Plasma/chemistry , Proteomics/instrumentation , Proteomics/methods , Proteomics/standards , Blood Proteins/metabolism , Female , Humans , Male , Plasma/metabolism , Robotics/instrumentation , Robotics/methods
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