WEST LAFAYETTE, Ind. – A Purdue University graduate and a Purdue Research Park of Northwest Indiana (NWI) startup have published a research study inBioorganic & Medicinal Chemistry Letters that identifies a small molecule SERCA activator that may improve memory and cognition.
In the Alzheimer’s disease models, the SERCA activator shows promise in reducing the cellular stress and preventing cell loss in neurons. The molecule corrects cells’ calcium ion balance and represents a new therapeutic strategy for neurodegeneration drug development.
“We have identified a compound that could therapeutically slow or halt Alzheimer’s disease, while also demonstrating its ability to cross the blood brain barrier, provide good bioavailability and cause no identifiable off target effects,” said Katie Krajnak, co-author and graduate of Purdue University Northwest’s Department of Biological Sciences.
Krajnak and Russell Dahl, chief executive officer of Neurodon, LLC, co-published the study “A New Target for Alzheimer’s disease: A Small Molecule SERCA Activator is Neuroprotective in vitro and Improves Memory and Cognition in APP/PS1 Mice” in Bioorganic & Medicinal Chemistry Letters. Read the study here.
“We are interested in neurodegenerative conditions such as Alzheimer’s and Parkinson’s diseases,” Dahl said. “Brain cell loss occurs when the cells’ calcium balance is disrupted. We focus on correcting intracellular calcium handling by developing molecules that target calcium handling proteins, such as SERCA.”
In the study, Dahl and Krajnak explored how a SERCA activator affects neurodegeneration. The team focused on two subjects, memory/cognition and brain cell mass, which are standard in pre-clinical Alzheimer’s studies.
Dahl and Krajnak found that their molecule preserved brain cell mass and boosted memory in the treated subjects. The study details an array of tests, including the water maze test for memory, and illustrates the SERCA activator molecule’s capacity for neuroprotection.
“Our focus is creating molecules that reach their target and act as a protector against cellular injury,” Dahl said. “Currently, there are no drugs approved that actually slow down or halt neurodegeneration. Our ultimate product would accomplish this feat and bring the medicine to clinics.”
In a previous study, the SERCA activator also produced a 60 percent reduction in Alzheimer’s brain plaques, an aftereffect of treatment. The current study further validates these results by proving that the molecule also treats prevalent Alzheimer’s symptoms.
“We could finally have a therapy modifying Alzheimer’s disease,” Krajnak said. “This molecule has the ability to rescue cells from apoptosis, or cell death. Preventing cell death can also prevent further brain atrophy and memory loss accompanying the disease.”
Neurodon is a startup, located in the Purdue Research Park of NWI, working toward discovering neuroprotective drugs. Dahl and his team research treatments to different cell death illnesses, such as Alzheimer’s diseases and amyotrophic lateral sclerosis (ALS).
Next, Neurodon moves forward to preclinical testing and, eventually, to develop an oral pill treating neurodegeneration. To accomplish this goal, the startup needs more researchers and/or partners.
Writer: Kelsey Henry, 765-588-3342, firstname.lastname@example.org
Purdue Research Foundation Contact: Cynthia Sequin, 765-558-3340, email@example.com
Sources: Russell Dahl, firstname.lastname@example.org
Katherine Krajnak, email@example.com
A new target for Alzheimer’s disease: A small molecule SERCA activator is neuroprotective in virto and improves memory and cognition in APP/PS1 mice
Katherine Krajnak, Russell Dahl
Neurodon LLC, 9800 Connecticut Dr. Crown Point, IN 46307, USA
Amongst the cellular cacophony of altered signals in Alzheimer’s disease (AD), disrupted Ca2+ homeostasis and consequential endoplasmic reticulum (ER) stress signals have been recognized as key determinants of neuron fate. This altered Ca2+ state is accompanied by a failing sarco/endoplasmic reticulum Ca2+-ATPase (SERCA) pump, which has been recognized as a causal feature of the underlying disease state. Repair of the Ca2+ dyshomeostasis represents a putative drug target via alleviation of ER stress and rescue of injured neurons, effectively modifying the AD state. Herein, we report a small molecule SERCA activator that rescues brain cells and raises ER Ca2+ in vitro, and shows efficacy in the APP/PS1 double transgenic mouse model of Alzheimer’s disease. These results support SERCA activation as a therapeutic target for AD.