Scientists have puzzled out why two noted molecules do the things they do.
It's sometimes taken as a hallucinogen – as a club drug called ‘Special K’ – and at high doses, it’s a widely-used anesthetic. Researchers are now figuring out why ketamine also has fast-acting, antidepressant-like effects as well.
This could be a direct target for quick-acting treatments of major depression.
Traditional antidepressants, like Zoloft or Paxil, often take weeks or months to have an effect – a major drawback for treating high-risk individuals. A single low dose of intravenous ketamine, on the other hand, can alleviate major symptoms within hours, with effects lasting up to 2 weeks.
When put in a tub of water, mice considered depressed quickly give up escape attempts and float motionless. Half an hour after receiving a dose of ketamine, mice swim for a longer period of time.
But what goes on in their brains was unclear. Scientists knew that ketamine binds to, and blocks, a receptor in the brain called NMDAR, which triggers its anesthetic effects.
Now, a team led by Lisa Monteggia from University of Texas Southwestern Medical Center found that by blocking NMDARs in mice, the depression lessened.
"We've identified a novel pathway never before linked to any behavior, let alone an antidepressant response," says Monteggia, "that could be a novel drug target."
Drugs that inhibit eEF2 kinase could become antidepressants that work faster than any current medication.
The study was published in Nature this week.
Smokers are, on average, thinner than non-smokers; they also tend to put on weight after they quit. That’s because nicotine decreases appetite. And researchers now show that that’s because nicotine activates a certain group of neurons in the brain.
A team led by Marina Picciotto of Yale focused on one particular nicotine receptor, dubbed α3β4. Mice who received drugs engineered to stimulate only α3β4 receptors were eating less.
In fact, mice who received the drug binding to α3β4 receptors ate half the amount of food as untreated mice in 2 hours after administering the drug. Their body fat dropped 15% to 20% over 30 days.
These nicotine receptors are involved in the fight-or-flight response that occurs when animals encounter a threat: these responded to nicotine in a way that reduced hunger.
Evolutionarily, "the fight-or-flight response is one where you actually want to preserve your energy to do something very important," Picciotto says. "So maybe you don't want to be out there eating while you're supposed to be running away from a tiger."
So smoking remains a leading cause of preventable death, and this study suggests that nicotine-based treatments could help people quit smoking and control their obesity or metabolic disorders.
"Imagine a nicotine-based medicine which could only target those cells which stop eating and not trigger the need for tobacco," Picciotto says.
The study was published in Science last week.
Images: ketamine by Dr. Saudade, nicotine by lydiashiningbrightly via Flickr
This post was originally published on Smartplanet.com