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Increased levels of the body's own cannabinoids impair embryonic brain development

Date:
July 17, 2014
Source:
Medical University of Vienna
Summary:
The human body produces substances, called endocannabinoids, that work in a similar way to cannabis. These endocannabinoids may not produce a “high”, but are of tremendous importance for the functioning of the neural network in the brain -- especially during the embryonic stage. If this network is interfered with as a result of too many circulating endocannabinoids, the development of the embryonic brain can be impaired. Researchers have now discovered what mechanism underlies the development of this impairment.
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FULL STORY

The human body produces substances, called endocannabinoids, that work in a similar way to cannabis. These endocannabinoids may not produce a "high," but are of tremendous importance for the functioning of the neural network in the brain -- especially during the embryonic stage. If this network is interfered with as a result of too many circulating endocannabinoids, the development of the embryonic brain can be impaired. Researchers at the Medical University of Vienna's Centre for Brain Research have now discovered what mechanism underlies the development of this impairment.

"Stimulation storm" in the brain

The protein "Slit" and its receptor "Robo" (roundabout) are important signaling molecules in the developing brain. Slits can regulate directional guidance of nerve cell processes (called axons), by binding to Robo receptors, directing the formation of embryonic brain circuitry. Researchers at the Medical University of Vienna have now shown that endocannabinoids can regulate Slit and Robo levels in both nerve cells and oligodendrocytes, which support nerve cells, through cannabinoid receptors CB1 and CB2.

This signaling system is important for correct embryonic brain development. If this system goes haywire due to increased levels of endocannabinoids, a kind of "stimulation storm" occurs. "In this case, both Slit and Robo are produced in greater quantities, leading to changes in axonal guidance decisions," explains Erik Keimpema. If the endocannabinoid system is in balance, however, this type of over-stimulation does not occur.

Human relevance

The researchers from MedUni Vienna also found this signalling system, and its regulation by cannabinoids, in human embryonic brains. Since, increased endocannabinoid levels are found in metabolic syndromes such as obesity and insulin resistance, as well as during maternal infections, "it is important to normalize altered endocannabinoid levels during pregnancy to ensure correct embryonic brain development," says the MedUni Vienna researcher. "We have demonstrated that the body's own cannabinoids are able to regulate an important signalling system in the development of embryonic brain circuitry."


Story Source:

Materials provided by Medical University of Vienna. Note: Content may be edited for style and length.


Journal Reference:

  1. Alán Alpár, Giuseppe Tortoriello, Daniela Calvigioni, Micah J. Niphakis, Ivan Milenkovic, Joanne Bakker, Gary A. Cameron, János Hanics, Claudia V. Morris, János Fuzik, Gabor G. Kovacs, Benjamin F. Cravatt, John G. Parnavelas, William D. Andrews, Yasmin L. Hurd, Erik Keimpema, Tibor Harkany. Endocannabinoids modulate cortical development by configuring Slit2/Robo1 signalling. Nature Communications, 2014; 5 DOI: 10.1038/ncomms5421

Cite This Page:

Medical University of Vienna. "Increased levels of the body's own cannabinoids impair embryonic brain development." ScienceDaily. ScienceDaily, 17 July 2014. <www.sciencedaily.com/releases/2014/07/140717094826.htm>.
Medical University of Vienna. (2014, July 17). Increased levels of the body's own cannabinoids impair embryonic brain development. ScienceDaily. Retrieved December 22, 2024 from www.sciencedaily.com/releases/2014/07/140717094826.htm
Medical University of Vienna. "Increased levels of the body's own cannabinoids impair embryonic brain development." ScienceDaily. www.sciencedaily.com/releases/2014/07/140717094826.htm (accessed December 22, 2024).

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