CR27 NEUROKIN - NEUROKIN SARL (
Benedicte Menn, ph. +33 4 91828178, fax +33 4
91828101, menn@inmed.univ-mrs.fr
Expertise and current research performed: Neurokin is a new start-up
company which develops a new generation of neuroprotectants, kinase inhibitors,
for the treatment and prevention of acute neurological diseases such as stroke
and epilepsy from different families of chemical compounds. Neurokin has an
expertise on neuronal death related to excitotoxicity.Excitotoxicity plays a
central role in neuronal death associated with neurological disorders such as
Parkinson’s, Huntington’s, Alzheimer’s, stroke and epilepsy. Neurokin has
already developped models of excitotoxicity in vitro: mixed neuronal and
hippocampal organotypic cultures, as well as in vivo models of cerebral
ischemia. Neurokin has already collaboration with INSERM (U29,
Facilities/Equipment: Neurokin has a full
access to the INMED’s equipment and facilities including: tissue culture and
surgery rooms, confocal microscopes, animal facilities, and all equipment for
histology (cryostat, vibratome,...) and electrophysiology set.
Personnel involved in the project
Principal investigator: Bénédicte Menn (F), Ph.D. Degree in oncology
and neuroscience. Actual position: Project Leader Neurokin since 2003.
Past position: Post-doctoral fellow (UCSF, Stem Cells Dpt, Alvarez-Buylla lab).
Working in the field since 1997. Research interests are: Excitotoxicity,
neuronal death, stroke, stem cells, signal transduction, neuronal
differentiation
Serge Timsit (M), M.D., Ph. D.
Degree in Neurology and Neuroscience. Actual
position: Neurokin founder, scientific director, and neurologist. Past position: medical
director in bio-tech company; post-doctoral fellow (INSERM U29, Ben-Ari lab).
Working in the field since 1990. Research interests are: stroke,
excitotoxicity, neuronal death, cell cycle, kinase inhibitors. Damien Rei (M). PhD student. Degree in
biology (master). Research interests: epilepsy models, cell cycle. Technician
to be recruited
Recent relevant publications/patents
1.
Menn B. et al. (in preparation). Cell cycle kinases
inhibitors prevent excitotoxic neuronal death in models of epilepsy and stroke.
2.
Timsit S. et al. (1999). Increased cylin D1 in
vulnerable neurons in the hippocampus after ischemia and epilepsy: a modulator
of in vivo programmed cell death ? Eur.
J. Neurosci. 11:263-278.
3.
Menn B. et al. (1998). Differential expression of TrkC
catalytic and noncatalytic isoforms suggests that they act independently or in
association. J Comp Neurol 401:47-64.
4.
Khrestchatisky M., Timsit S. et al. (1996) Neuronal
death and damage repair: roles of protoncogenes and cell cycle-related
proteins. In Pharmacology of Cerebral ischemia (J. Krieglstein, ed.), pp 41-56.
Medpharm Scientific Publishers,
5.
Patent: Timsit et al..:
Method of treating and preventing acute neural lesions with substances that
modulate the expression or function of a protein involved in the cell cycle and
pharmaceutical preparations containing such substances. FR00/03673.