13.05.2022 – Mattias Andréasson defends his PhD
Right: Per and Martin Paucar together with thesis opponent Prof. Claudia Trenkwalder
11.05.2022 – Public defence of Ioannis Mantas
Lunch at lab day
Per Svenningsson named as a member of the Molecular Psychiatry Editorial board
Per Svenningsson is now a board member of the editorial team for Molecular Psychiatry. Visit the following link to see all members: https://www.nature.com/mp/editors/editorial-board
Ceremony Arvid Carlsson Foundation award
Grant from the Aligning Science Across Parkinson’s (ASAP) initiative
Per Svenningsson has been awarded a grant of approximately 1.86 million US dollar for three years, from the Aligning Science Across Parkinson’s (ASAP) initiative for an ambitious, multidisciplinary effort to study how abnormal protein aggregates may spread from the gut to the brain to drive the early stages of Parkinson’s disease. The total award is 8.9 million US dollar grant for three years.
https://news.ki.se/ki-researcher-awarded-186-million-us-dollar-for-parkinsons-disease
Nobel Prize in Physiology or Medicine awarded to David Julius and Ardem Patapoutian for their discoveries of receptors for temperature and touch
As a member of the Nobel Committee, Per Svenningsson was very actively involved with this year’s Nobel Prize in Physiology or Medicine.
Our research on how ketamine prevents depression was published on Molecular Psychiatry
The discovery that the anaesthetic ketamine can help people with severe depression has raised hopes of finding new treatment options for the disease. Researchers at Karolinska Institutet have now identified novel mechanistic insights how the drug exerts its antidepressant effect. The findings have been published in the journal Molecular Psychiatry.
https://news.ki.se/new-findings-on-how-ketamine-prevents-depression
Article published in Molecular Psychiatry
Ji-Seon Seo et al. found that p11 is highly expressed in ependymal cells, and is significantly decreased in patients with MDD, and in two mouse models of depression induced by chronic stress. These results identify a new role and a key molecular determinant for ependymal cell-driven CSF flow in mood disorders.