Imperial College London

Dipl. Psych. Tobias Buchborn

Faculty of MedicineDepartment of Medicine

Marie Skłodowska-Curie Research Fellow
 
 
 
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Contact

 

+44 (0)20 7594 3205t.buchborn

 
 
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Location

 

Burlington DanesHammersmith Campus

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Summary

 

Summary

  • Tobias Buchborn studied Psychology at the Otto-von-Guericke University in Magdeburg, Germany. In his Diploma thesis, he investigated the behavioural and pharmacodynamic effects of the 5-HT1A/2A agonist LSD on bulbectomised rats, an animal model of depression.
  • Tobias ran his PhD project in Neuroscience at the Institute of Pharmacology and Toxicology in Magdeburg. Here, his research addressed the behavioural and molecular biological correlates of tolerance to serotonergic hallucinogens, with focus on processes of 5-HT2A regulation.
  • Currently, Tobias works as a MSCA Individual Research Fellow at the Department of Medicine, Laboratory for Neuronal Circuit Dynamics, where he applies voltage imaging techniques to investigate the 5-HT2A-glutamatergic corticodynamics of serotonergic hallucinogens.

Further inormation

Publications

  • Buchborn T, Schröder H, Höllt V, Grecksch G (2014). Repeated lysergic acid diethylamide in an animal model of depression: Normalisation of learning behaviour and hippocampal serotonin 5-HT2 signalling.  J. Psychopharmacol., 28, 6, 545-552. doi: 10.1177/0269881114531666.
  • Buchborn T, Schröder H, Dieterich DC, Grecksch G, Höllt V (2015). Tolerance to LSD and DOB induced Shaking behaviour: Differential adaptations of frontocortical 5-HT2A and glutamate receptor binding sites. Behav. Brain Res., 281, 62–68. doi:10.1016/j.bbr.2014.12.014.
  • Buchborn T, Grecksch G, Dieterich DC, Höllt V (2016). Tolerance to lysergic acid diethylamide (LSD): Overview, correlates, and clinical implications. In: Preedy VR (ed.), Neuropathology of Drug Addictions and Substance Misuse, Volume 2: Stimulants, Club and Dissociative Drugs, Hallucinogens, Steroids, Inhalants and International Aspects, 846-858. Academic Press. doi:10.1016/B978-0-12-800212-4.00079-0.