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Mol Psychiatry. 2017 Apr 4. doi: 10.1038/mp.2017.65. [Epub ahead of print]

Blocking human fear memory with the matrix metalloproteinase inhibitor doxycycline.

Bach DR1,2,3, Tzovara A1,2,3, Vunder J1,2.

Author information

1
Division of Clinical Psychiatry Research, Psychiatric Hospital, University of Zurich, Zurich, Switzerland.
2
Neuroscience Centre Zurich, University of Zurich, Zurich, Switzerland.
3
Wellcome Trust Centre for Neuroimaging and Max Planck UCL Centre for Computational Psychiatry and Ageing Research, University College London, London, UK.

Abstract

Learning to predict threat is a fundamental ability of many biological organisms, and a laboratory model for anxiety disorders. Interfering with such memories in humans would be of high clinical relevance. On the basis of studies in cell cultures and slice preparations, it is hypothesised that synaptic remodelling required for threat learning involves the extracellular enzyme matrix metalloproteinase (MMP) 9. However, in vivo evidence for this proposal is lacking. Here we investigate human Pavlovian fear conditioning under the blood-brain barrier crossing MMP inhibitor doxycyline in a pre-registered, randomised, double-blind, placebo-controlled trial. We find that recall of threat memory, measured with fear-potentiated startle 7 days after acquisition, is attenuated by ~60% in individuals who were under doxycycline during acquisition. This threat memory impairment is also reflected in increased behavioural surprise signals to the conditioned stimulus during subsequent re-learning, and already late during initial acquisition. Our findings support an emerging view that extracellular signalling pathways are crucially required for threat memory formation. Furthermore, they suggest novel pharmacological methods for primary prevention and treatment of posttraumatic stress disorder.Molecular Psychiatry advance online publication, 4 April 2017; doi:10.1038/mp.2017.65.

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