Dr. Paul Greengard's pioneering work in delineating how neurons communicate with one another in the brain earned him the 2000 Nobel Prize in Medicine or Physiology.
Rockefeller University
The Stern Center at The Rockefeller University
Under the direction of Nobel Laureate Dr. Paul Greengard,
the Stern Center at The Rockefeller University has
concentrated their research on discovering why, of the
two major populations of dopamine neurons in the brain,
one is more susceptible to cell death in PD than the
other.
Dr. Greengard’s scientist have created a very sensitive
method for separating these two types of neurons that
has allowed the identification of many differences in
their gene function. This is expected to provide
new drug targets for the treatment of PD. Drugs
that address these targets would have the potential to
arrest disease progression.
They have discovered a major new signaling pathway in
the brain that is based on ribonucleic acid (RNA).
These regulatory RNAs (also called micro RNA) appear to
control the functions of specific genes that are
required for neuronal survival. An understanding
of these RNAs may give us the power to prevent death of
neurons in diseases such as PD.
A further major discovery has been a mechanism in
neurons that regulates the expression of serotonin
receptors. These play a major role in mood and
depression and are indirect targets of most
anti-depressant medications. The regulatory
mechanism was revealed by the discovery of the function
of a protein called “P11.” This information is
expected to usher in a new class of extremely effective
drugs to treat the depression associated with PD.
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Harvard University
At Harvard University’s McLean Hospital,
we support the research of Dr. Ole
Isacson whose research lab, The Stern
Center for Neuroregeneration Research is
using gene therapy to protect the most
vulnerable neurons in PD models.
Through this gene therapy, Dr. Isacson’s
lab was able to protect the most
vulnerable neurons in PD models. Dr.
Isacson’s lab was able to generate
neurons from
dopamine cells that were transplanted.
These scientists also have made
significant progress in studying a
molecule called G-substrate, a
phosphatase inhibitor. In human studies,
they have found that transplanted fetal
neurons can survive in patients for at
least 14 years.
All of these studies demonstrated new
ways to protect and regenerate the
dopamine system that produces the
symptoms of Parkinson’s disease.
IND - The Institute for
Neurodegenerative
Disorders
The MSPRF sponsored
research at the IND is
conducted under the
direction of
Yale Professors Dr. Ken
Marek and Dr. John
Seibyl. This lab
is developing novel
tools for early
detection and monitoring
of Parkinson’s disease
by studying physiologic,
biochemical and
neuroimaging biomarkers
for non-dominergic
manifestations of
Parkinsonism.
The IND has been active
in the expansion of
Amadeus (American and
European Union SPECT
Imaging Consortium) to
continue the application
of rigorous,
standardized
quantitative
neuroimaging technology
in multi-center trials
to improve diagnosis and
evaluate treatments for
Parkinson disease and
related disorders. They
have initiated a
multi-site study to
develop smell testing
and brain imaging as a
potential tool for early
diagnosis of Parkinson
disease.
The IND will continue
its research and
development of new
ligands/biomarkers for
neurodegenerative
disorders for Parkinson
disease, and other
neurological disorders.