Tag Archives: variant

LSD variant cures depression in mice without making them trip, study finds

An LSD-like drug could treat depression in humans without sending patients on a Magical Mystery Tour, according to a new scientific study.

As the use of hallucinogenic drugs for recreational and therapeutic purposes soared to new heights in the US, scientists discovered new variants that appeared to ease anxiety and depression in rodents without delivering mind-bending side effects, according to a report in the scientific journal Nature.

Scientists had culled the new drug from a library of 75 million molecules that share the unusual structures that affect serotonin release found in drugs like psilocybin, the primary ingredient in magic mushrooms, and lysergic acid diethylamide (LSD).

The researchers were not specifically looking for an antidepressant but soon realized they were on their way to a breakthrough, according to NPR.

Study author Dr. Bryan Roth, a professor of pharmacology at UNC Chapel Hill School of Medicine, recalled a fellow scientist asking, “‘What are we looking for here anyway?’ And I said, ‘Well, if nothing else, we’ll have the world’s greatest psychedelic drugs,’” he told the outlet.

Researchers say the findings could mark a breakthrough in the treatment of using psychedelics as antidepressants.
AFP via Getty Images
The new molecules demonstrated the same antidepressant effect as psilocybin without its mind-bending properties.
AP

As research continued, the team took its lead from other studies that showed psilocybin could rewire the human brain and stave off depression.

The team identified the two “best” and “most potent” properties from its library of molecules and gave them to mice, University of California pharmaceutical chemistry professor Brian Shoichet told the outlet.

“We found our compounds had essentially the same antidepressant activity as psychedelic drugs [but] they had no psychedelic drug-like actions at all,” Roth reportedly said.

Researchers gauged the mental health of a mouse by judging how resilient it is when facing adversity. For example, a depressed mouse would tend to give up quickly when dangled by its tail, but would continue to struggle if under the influence of antidepressants like ketamine or psilocybin, scientists reportedly said.

A man ingests LSD at Woodstock ’94 in Saugerties, New York.
Corbis via Getty Images

Prior observation of mice on LSD found that mice that are tripping twitch their noses. That symptom did not occur when the mice were given the new test drug.

Scientists were hopeful that human depression patients would have the same experience, with some tweaking of the molecules so they wouldn’t increase heart rate and raise blood pressure in the same way LSD does, according to the report.

“Society would like a molecule that you can get prescribed and just take and you don’t need a guided tour for your trip,” Shoichet reportedly said, referencing the rise of psychedelic retreats that provide medical supervision.

Doctors say such an advancement would be a huge breakthrough because the brain rewiring of psychedelics takes hold almost immediately and could last for a year of more, in contrast with slow-acting pharmaceutical antidepressants that need to be taken daily.

A previous breakthrough in the field led to the creation of a hallucination-free variant of ibogaine, a mind-altering drug which is derived from the bark of a tree native to Africa.

“It’s very encouraging to see multiple groups approach this problem in different ways and come up with very similar solutions,” University of California chemical neuroscientist David Olson, who led the ibogaine project, told the outlet.

Read original article here

Common Gene Variant Linked to Mortality

New research may explain why some people with COVID-19 only experience minor, flu-like symptoms and others have severe disease that can result in death.

It may be the most baffling quirk of COVID: While some infected individuals only have minor, flu-like symptoms, in others

“It is clear that age, sex, and certain preconditions such as diabetes increase the risk of detrimental outcomes, but these factors don’t fully explain the spectrum of COVID outcomes,” says Sohail Tavazoie, M.D., Ph.D. He is the Leon Hess Professor, Howard Hughes Medical Institute Faculty Scholar and Head of the Meyer Laboratory of Systems Cancer Biology at The Rockefeller University. “This is the first time that we’ve seen such a common genetic variant associated with COVID mortality.”

A closer look at APOE

In previous research, Tavazoie’s lab studied a gene called APOE that plays a role in cancer metastasis. After discovering that the gene suppresses the spread of melanoma and regulates anti-tumor immune responses, he and his team began looking at its different forms, or alleles, more closely. Although, most people have a form called APOE3, 40% of the population carries at least one copy of the APOE2 or APOE4 variant. People with APOE2 or APOE4 produce proteins that differ from APOE3 protein by one or two

The APOE gene provides instructions for making a protein called apolipoprotein E. This protein combines with lipids (fats) in the body to form molecules called lipoproteins. Lipoproteins package cholesterol and other fats and carrying them through the bloodstream. There are at least three slightly different versions (alleles) of the APOE gene. Each person inherits two APOE alleles, one from each biological parent. The major alleles are called ε2, ε3, and ε4. The most common allele is ε3, which is found in more than half of the general population.

Just one or two amino acids make a difference. Notably, people with APOE4 are at greater risk of developing Alzheimer’s and atherosclerosis. Also, Tavazoie and Benjamin Ostendorf, a postdoctoral fellow in his lab, have demonstrated that APOE4 and APOE2 impact the immune response against melanoma. As the COVID-19 pandemic progressed, Tavazoie and Ostendorf began to wonder whether APOE variants might impact COVID outcomes, as well. “We had looked only at non-infectious diseases,” he says. “But what if APOE variants also made people vulnerable to an infectious agent, like SARS-CoV-2? Could they cause different immune responses against a virus?”

To investigate, Tavazoie and colleagues first exposed more than 300 mice engineered to carry human APOE to a mouse-adapted version of SARS-CoV-2 produced by colleagues Hans-Heinrich Hoffmann and Charles M. Rice. They discovered that mice with APOE4 and APOE2 were more likely to die than those with the more common APOE3 allele. “The results were striking,” says Ostendorf, lead author on the study. “A difference in just one or two amino acids in the APOE gene was sufficient to cause major differences in the survival of mice exhibiting COVID.”

In addition, mice with APOE2 and APOE4 had more virus replicating in their lungs and more signs of inflammation and tissue damage. At the cellular level, the scientists discovered that APOE3 appeared to reduce the amount of virus entering the cell, while animals with the other variants had less potent immune responses to the virus. “Taken together, these results suggest that the APOE genotype impacts COVID outcomes in two ways,” Ostendorf says, “by modulating the immune response and by preventing SARS-CoV-2 from infecting cells.”

Toward clinical practice

The lab next turned to retrospective human studies. In an analysis of 13,000 patients in the UK Biobank, the research team uncovered that individuals with two copies of either APOE4 or APOE2 were more likely to have died of COVID than those with two copies of APOE3. (Approximately 3% of individuals have two copies of APOE2 or APOE4, representing an estimated 230 million people worldwide.)

“The results were striking. A difference in just one or two amino acids in the APOE gene was sufficient to cause major differences in the survival of mice exhibiting COVID.” — Benjamin Ostendorf

Tavazoie emphasizes that there is no evidence that the 40% of individuals carrying only one of these alleles are at increased risk. Furthermore, he says those with two APOE2 or APOE4 alleles are likely at lower risk today than the data indicates. “Vaccination changes the picture,” he explains. “Data in UK Biobank spans the length of the pandemic, and many of the individuals who died early on would likely have been protected had they been vaccinated.”

Moving forward, Tavazoie hopes to see prospective studies on the link between APOE and distinct COVID outcomes. “We’ve taken the first step,” he says. “But to be clinically useful, these results will need to be assessed in prospective human trials that test individuals for their APOE genotypes and account for the availability of vaccination, something that wasn’t available early in the pandemic and would improve COVID outcomes across APOE genotypes.”

If future research confirms a link between APOE and COVID outcomes, clinicians might recommend that individuals with APOE4 or APOE2 be prioritized for vaccinations, boosters, and antiviral therapies. Screening for APOE is fairly routine and inexpensive, and many individuals already know their APOE variants because commercial genetic tests such as 23andMe use it to gauge Alzheimer’s risk. At the same time, Tavazoie cautions that screening for a gene variant linked to Alzheimer’s is not without ethical hurdles, because many people would rather not know whether they are predisposed to an incurable neurodegenerative disease.

For his part, Tavazoie plans to also take a closer look at how APOE interacts with various biological systems. The link between APOE4, Alzheimer’s, and COVID, for instance, raises the possibility that this gene may play a role in the neurocognitive complications that arise in some COVID patients. “We want to better understand the function of APOE by studying how it shapes the behavior of cells in these disparate contexts of cancer, dementia, and now viral infection,” Tavazoie says.

Reference: “Common germline genetic variants of APOE impact COVID-19 mortality” by Benjamin N. Ostendorf, Mira A. Patel, Jana Bilanovic, H.-Heinrich Hoffmann, Sebastian E. Carrasco, Charles M. Rice and Sohail F. Tavazoie, 21 September 2022, Nature.
DOI: 10.1038/s41586-022-05344-2



Read original article here