Frequent flyers rejoice: Scientists design way to treat jet lag and other sleeping disorders

Scientists have designed new molecules which can modify the sleep/wake cycle, Paving the way for improved treatments for jet lag and sleep disorders.

PTI May 30, 2016 15:43:25 IST
Frequent flyers rejoice: Scientists design way to treat jet lag and other sleeping disorders

Tokyo: Frequent travellers, rejoice! Scientists have designed new molecules which can modify the sleep/wake cycle, Paving the way for improved treatments for jet lag and sleep disorders. The negative impacts of jet lag and shift work could be significantly reduced if it were possible to reset our 24-hour natural circadian or sleep/wake cycle, researchers said.

Frequent flyers rejoice Scientists design way to treat jet lag and other sleeping disorders

Exhausted travelers rest at an airport. Reuters

Now, scientists from Nagoya University's Institute of Transformative Bio-Molecules (ITbM) in Japan have synthesised molecules that can shorten the circadian period. These molecules act directly on one of our "clock proteins", called CRY, researchers said. Most living organisms, including humans, have a biological clock that resets every 24 hours, regulating functions such as sleep/wake cycles and metabolism. When this cycle is disrupted, like in jet lag, sleep disorders occur, they said.

Long-term sleep loss may affect the cardiovascular, endocrine, immune and nervous systems with severe consequencesincluding hypertension, obesity and mental health disorders, among others. Our biological clock is basically run by four "master regulator" proteins that work in tandem. CLOCK and BMAL1, when combined, promote the production of the proteins PER and CRY.

These proteins, in turn, block CLOCK and BMAL1, thus closing the cycle. This cycle of activation, production and stop/block goes around once a day and is also influenced by a compound called FBXL3, which flags CRY for degradation by cellular enzymes, researchers said. A molecule discovered in 2012, called KL001, lengthens the circadian cycle by competing with FBLX3 for the same spot on the CRY protein, preventing its degradation.

By analysing its structure, researchers prepared compounds that were similar to KL001, thus synthesising the first circadian shortening molecules that target the CRY protein. "We hope we can make further use of synthetic chemistry to make bioactive molecules that can control the circadian rhythm of animals and gain further insight into the circadian clock mechanism, which will surely contribute to medical applications, food production and advances in clock research," said Takashi Yoshimura from ITbM.

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