At a rough estimate, the human organism consists of 100 trillion cells. An internal clock, which is based on genetically determined machinery, ticks in every single one of them. The suprachiasmatic nucleus (SCN), which is located in the brain´s hypothalamus, acts as the master clock for most organs and physiological processes. These processes follow a daily individual circadian rhythm, for example the heartbeat, blood pressure, digestion and hormone production. When the body clock is synchronised to switch between day and night on earth, light plays the leading role. Chronobiology is the study of the function of the body clock, as well as its effects on the physiological and pathological processes inside the human body. The information it provides on the effects of night work, jetlag or lack of sunlight during winter, as well as on fluctuations in liver detoxification capacity delivers valuable insights for medical and pharmaceutical research.
Over the past few years, a host of chronobiological study results have been published by leading scientist Dr. Steven Brown and other researchers of the departments for chronobiology and sleep research at the Institute of Pharmacology and Toxicology at the University of Zurich. In many cases there were joint research projects between different laboratories at the university of Zurich, as well as institutes of the Swiss universities in Basel and Geneva, and Berlin Charité or Humboldt University. These projects revealed, among other things, that in the course of our life, our body clock makes us change from "night owl" to "early bird" due to hormonal changes (1). In 2008 evidence was found showing that the circadian period of "early birds" is far shorter than that of "night owls" who have difficulty getting up in the morning (2). A study that was published in 2012 concluded that the circadian rhythm directly influences numerous metabolic processes in the human body, even when the usual daytime activities like sleeping and eating were not taken into consideration. Maybe the saying: "True beauty comes from within" will soon have to be changed into: "True beauty follows the body clock".
Gene expression tests are performed to investigate the mechanism of the body clock on a molecular-biological level. This is done using two Memmert CO2 incubators INCO246med which are set up in the laboratory of the Institute of Pharmacology and Toxicology at Zurich University; a third is used for regular cell cultivation. To visualise the processes in a cell in vitro, researchers use a trick. They use bioluminescence, the ability of insects and other creatures to produce light. The luciferase gene, which is responsible for light production, is transfected under the control of a "clock gene" into the cell which is investigated. This "reporter" makes the cells light up as soon as this gene is activated. The intensity of the light radiation is measured in the CO2 incubators with the help of a robot that moves the ultra-sensitive light sensors over the cells at regular intervals. Other current research projects focus on the signal paths in human skin cells. For example, verifiable evidence of significant differences between mentally ill and healthy people was found (3).
Even minimum light incidence in the CO2 incubator can falsify test results. For this reason, total darkness is an absolute must. The appliances are placed in a separate, air-conditioned, dark room, and even the integrated CO2 sensors were sealed as they emit a small amount of light. What the team at the Institute of Pharmacology and Toxicology at the University of Zurich values particularly highly in the Memmert INCOmed is the possibility to seal off the chamber entirely, as well as the sterilsation function.
This article is essentially based on the explanations and publications provided by the Institute of Pharmacology and Toxicology at the University of Zurich. AtmoSAFE would like to thank Prof. Steven Brown, PhD, as well as Dr. Robert Dallmann, Senior Scientist, for their kind assistance.
Further information and literature: www.pharma.uzh.ch/research/chronobiology/areas/chronobiology/publications.html
Sources:
1 Pagani et al. (2011) Serum factors in older individuals change cellular clock properties
www.pnas.org/content/108/17/7218.full
2 Brown et al. (2008) Molecular insights into human daily behaviour
www.pnas.org/content/105/5/1602.full
3 Gaspar et al. (2014), Human cellular differences in cAMP – CREB signalling correlate with light-dependent melatonin suppression and bi-polar disorder
onlinelibrary.wiley.com/doi/10.1111/ejn.12602/abstract
Dallmann et al. (2012) The human circadian metabolome
www.pnas.org/content/early/2012/01/30/1114410109
