DALLAS - October 4, 2016 - A protein linked to higher risk of Alzheimer's can be removed from the brains of mice without hindering memory and learning, according to a study that addresses whether potential therapeutics targeting this protein would have detrimental side effects.
The study from the Peter O'Donnell Jr. Brain Institute also showed, however, that the protein's absence in other parts of the body hinders brain function as blood cholesterol levels rise. This result substantiates previous research that indicated cardiovascular health affects the brain.
Researchers focused on the removal of apolipoprotein E (ApoE), which in a certain form can support the buildup of toxic plaques in the brains of Alzheimer's patients. Studies elsewhere have sought to determine whether reducing ApoE could be an effective treatment in preventing the disease, but a lingering question has been whether the protein is necessary for healthy brain function.
The study found that mice can maintain their learning and memory when virtually all ApoE is removed from the brain but kept present in the liver to filter cholesterol. Mice that lacked ApoE in both the brain and liver experienced unhealthy cholesterol levels and lost cognitive function.
More research is needed to determine what causes the cardiovascular issues to affect the brain, said Dr. Joachim Herz, the study's Principal Investigator and Professor of Molecular Genetics, Neuroscience, Neurology and Neurotherapeutics at the O'Donnell Brain Institute at UT Southwestern Medical Center.
But the findings, published in The Journal of Neuroscience, add support to the belief that reducing ApoE in the brain could eventually be a viable therapeutic option for treating Alzheimer's.
"This approach still holds potential," said Dr. Herz, holder of the Thomas O. and Cinda Hicks Family Distinguished Chair in Alzheimer's Disease Research and Director of the Center for Translational Neurodegeneration Research.
ApoE has several roles in the body, including transporting cholesterol and related molecules such as β-amyloid that form plaques in the brains of Alzheimer's patients if not properly filtered or removed.
The type of ApoE produced by the ApoE gene determines how effectively the amyloid is removed from the brain. ApoE2 is the most effective, ApoE3 is in the middle and ApoE4 is the most likely to allow for the buildup of amyloid plaques. People whose genes produce ApoE4 are at high risk of developing Alzheimer's.
Studies are ongoing at UT Southwestern and elsewhere to further understand the various effects that ApoE4 removal has on brain and body function.
The latest study was performed by Courtney Lane-Donovan, a Medical Science Training Program student in her final clinical year with her colleagues and co-authors Wen Mai Wong, Dr. Murat S. Durakoglugil, Dr. Catherine R. Wasser, Dr. Shan Jiang, and Dr. Xunde Xian in the Department of Molecular Genetics and the Center for Translational Neurodegeneration Research.
The research was supported with funding from the National Institutes of Health, the American Health Assistance Foundation, the Consortium for Frontotemporal Dementia Research, the Bright Focus Foundation, the Lupe Murchison Foundation, and the Ted Nash Long Life Foundation.
About UT Southwestern Medical Center
UT Southwestern, one of the premier academic medical centers in the nation, integrates pioneering biomedical research with exceptional clinical care and education. The institution's faculty includes many distinguished members, including six who have been awarded Nobel Prizes since 1985. The faculty of almost 2,800 is responsible for groundbreaking medical advances and is committed to translating science-driven research quickly to new clinical treatments. UT Southwestern physicians provide medical care in about 80 specialties to more than 100,000 hospitalized patients and oversee approximately 2.2 million outpatient visits a year.