Mapping Ketamine’s Impact on the Brain – Neuroscience News

Summary: A study reveals that repeated use of ketamine leads to structural changes in the brains dopamine system, emphasizing the need for targeted ketamine therapies.

The research suggests that specific brain regions should be addressed to minimize unintended effects on other dopamine areas. Repeated ketamine exposure decreases dopamine neurons linked to mood regulation and increases dopamine neurons related to metabolism and basic functions.

These findings may explain ketamines potential in treating eating disorders and the dissociative behavioral effects observed in users. The study paves the way for improved ketamine applications in clinical settings.

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Source: Columbia University

Ketamine an anesthetic also known for its illicit use as a recreational drug has undergone a thorough reputational rehabilitation in recent years as the medical establishment has begun to recognize its wide-ranging therapeutic effects.

The drug is increasingly used for a range of medical purposes, including as a painkiller alternative to opioids, and as a therapy for treatment-resistant depression.

In a new study published in the journalCell Reports, Columbia biologists and biomedical engineers mapped ketamines effects on the brains of mice, and found that repeated use over extended periods of time leads to widespread structural changes in the brains dopamine system.

The findings bolster the case for developing ketamine therapies that target specific areas of the brain, rather than administering doses that wash the entire brain in ketamine.

Instead of bathing the entire brain in ketamine, as most therapies now do, our whole-brain mapping data indicates that a safer approach would be to target specific parts of the brain with it, so as to minimize unintended effects on other dopamine regions of the brain, Raju Tomer, the senior author of the paper said.

The study found that repeated ketamine exposure leads to a decrease in dopamine neurons in regions of the midbrain that are linked to regulating mood, as well as an increase in dopamine neurons in the hypothalamus, which regulates the bodys basic functions like metabolism and homeostasis.

The former finding, that ketamine decreases dopamine in the midbrain, may indicate why long-term abuse of ketamine could cause users to exhibit similar symptoms to people with schizophrenia, a mood disorder.

The latter finding, that ketamine increases dopamine in the parts of the brain that regulate metabolism, on the other hand, may help explain why it shows promise in treating eating disorders.

The researchers highly-detailed data also enabled them to track how ketamine affects dopamine networks across the brain. They found that ketamine reduced the density of dopamine axons, or nerve fibers, in the areas of the brain responsible for our hearing and vision, while increasing dopamine axons in the brains cognitive centers. These intriguing findings may help explain the dissociative behavioral effects observed in individuals exposed to ketamine.

The restructuring of the brains dopamine system that we see after repeated ketamine use may be linked to cognitive behavioral changes over time, Malika Datta, a co-author of the paper said.

Most studies of ketamines effects on the brain to-date have looked at the effects of acute exposure how one dose affects the brain in the immediate term. For this study, researchers examined repeated daily exposure over the course of up to ten days. Statistically significant alterations to the brains dopamine makeup were only measurably detectable after ten days of daily ketamine use.

The researchers assessed the effects of repeated exposure to the drug at two doses, one dose analogous to the dose used to model depression treatment in mice, and another closer to the dose that induces anesthesia. The drugs effects on dopamine system were visible at both doses.

The study is charting a new technological frontier in how to conduct high-resolution studies of the entire brain, said Yannan Chen, a co-author of the paper. It is the first successful attempt to map changes induced by chronic ketamine exposure at what is known as sub-cellular resolution, in other words, down to the level of seeing ketamines effects on parts of individual cells.

Most sub-cellular studies of ketamines effects conducted to-date have been hypothesis-driven investigations of one area of the brain that researchers have targeted because they believed that it might play an important role in how the brain metabolizes the drug. This study is the first sub-cellular study to examinethe entire brain without first forming such a hypothesis.

Bradley Miller, a Columbia psychiatrist and neuroscientist who focuses on depression, said: Ketamine rapidly resolves depression in many patients with treatment resistant depression, and it is being investigated for longer term use to prevent the relapse of depression.

This study reveals how ketamine rewires the brain with repeated use. This is an essential step for developing targeted treatments that effectively treat depression without some of the unwanted side effects of ketamine.

The research was supported by the National Institutes of Health (NIH) and the National Institute of Mental Health (NIMH). The papers lead authors are Malika Datta and Yannan Chen, who completed their research in Raju Tomers lab at Columbia. Datta is now a postdoctoral fellow at Yale.

This study gives us a deeper brain-wide perspective of how ketamine functions that we hope will contribute to improved uses of this highly promising drug in various clinical settings as well as help minimize its recreational abuse. Morebroadly, the study demonstrates that the same type of neurons located in different brain regions can be affected differently by the same drug, said Tomer.

Author: Christopher Shea Source: Columbia University Contact: Christopher Shea Columbia University Image: The image is credited to Neuroscience News

Original Research: The findings will be published in Cell Reports

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Mapping Ketamine's Impact on the Brain - Neuroscience News

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