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ACE Inhibitors found useful for memory preservation in lupus patients

ACE Inhibitors found useful for memory preservation in lupus patients

ACE inhibitors can block the process of microglia (brain cells) activation in mice. This process contributes to memory loss and other cognitive impairments in SLE (systemic lupus erythematosus) patients, and therefore, can be used for memory preservation in such patients.

These are the results of a study published in the Journal of Experimental Medicine. 

Betty Diamond, The Feinstein Institute for Medical Research, Manhasset, New York, and colleagues investigated the mechanism of long-term neuronal dysfunction mediated by transient exposure to antibody. They showed that activated microglia and C1q are critical mediators of neuronal damage.

SLE is a complex autoimmune disease that arises when the body starts to make antibodies that target its own, healthy cells, often specifically recognizing DNA. Patients can suffer from a wide variety of symptoms, but as many as 90% develop neuropsychiatric lupus, which is often characterized by cognitive impairments such as memory loss or confusion.

The researchers found that lupus patients experiencing memory loss often produce antibodies — called DNRAbs — that recognize both DNA and a critical brain protein called the NMDA receptor, NMDAR. Antibodies are usually unable to enter the brain, but, after injury or infection, DNRAbs are thought to gain temporary access to the brain, where they can target neurons expressing NMDAR. This causes the neurons to die or lose the synapses that connect them to neighboring nerve cells, resulting in memory loss or other cognitive defects.

Also Read: Omega-3 and Omega-6 fatty acid intake may affect lupus outcomes

Diamond and colleagues suspected that brain cells called microglia might be responsible for trimming the connections between neurons after exposure to DNRAbs. These cells help clear away the debris of dead and dying neurons and can also remove excessive or unwanted synapses during brain development.

To address the role of microglia in SLE, Diamond and colleagues analyzed mice that produce DNRAbs capable of penetrating the brain and inducing memory loss. The researchers found that microglia are activated when DNRAbs enter the brain and that a protein called C1q attracts microglia to the synapses of neurons targeted by these antibodies. Deleting the C1q protein, or depleting the microglial cells themselves, prevented neurons from losing their synapses after exposure to DNRAbs.

ACE inhibitors such as captopril are a class of drugs used to treat high blood pressure. They are also known to block the activation of microglia. Diamond and colleagues found that captopril treatment protected neurons from DNRAbs and preserved the memory of mice producing these antibodies.

“Our study suggests that ACE inhibitors are a promising class of therapeutics that can easily move into clinical trials aimed at mitigating the cognitive dysfunction associated with neuropsychiatric lupus,” Diamond says.

For further reference log on to 10.1084/jem.20180776

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Source: With inputs from Journal of Experimental Medicine

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