Cure for depression?

Gyakuto

Senior Master
Researchers found that a single, carefully administered dose of psilocybin can produce rapid and sustained improvements in individuals with severe treatment-resistant depression, offering new hope when traditional therapies have failed.

The participants had tried at least five prior treatments without any improvement. Then, they received one 25-milligram dose of psilocybin alongside psychological support. Just three weeks after treatment, the changes were hard to deny. Nearly 70 percent of participants experienced a signification reduction in their symptoms, and 42 percent achieved complete remission.

The results indicated that the benefits lasted up to 3 months, suggesting one treatment could have long-term benefits. The treatment was well-tolerated with no serious adverse effects reported, underscoring its potential as a safe alternative for people with limited options.
 
Researchers found that a single, carefully administered dose of psilocybin can produce rapid and sustained improvements in individuals with severe treatment-resistant depression, offering new hope when traditional therapies have failed.

The participants had tried at least five prior treatments without any improvement. Then, they received one 25-milligram dose of psilocybin alongside psychological support. Just three weeks after treatment, the changes were hard to deny. Nearly 70 percent of participants experienced a signification reduction in their symptoms, and 42 percent achieved complete remission.

The results indicated that the benefits lasted up to 3 months, suggesting one treatment could have long-term benefits. The treatment was well-tolerated with no serious adverse effects reported, underscoring its potential as a safe alternative for people with limited options.
So, you will promote a hallucinogenic but worry about ground wheat?
 
Single dose? Wow that is interesting indeed.

Also interesting as 5-HT2A activation suppresses the other serotonin receptors, such as 5-HT1A with is the main normal target in depression, which is why 5-HT2A antagonists enhance SSRI drugs in depression. But I suppose this also indicates how heterogenous depressions are as well?! After all this was for treatment resistance depression, which is indicative of different mechanisms.

I wonder if the "direction" of neuroplastic changes, is effectively in the right direction in this case? Is it coincidental, or does this appear sponteanously as plasticity increases because of the depression itself - self healing??
 
Single dose? Wow that is interesting indeed.

Also interesting as 5-HT2A activation suppresses the other serotonin receptors, such as 5-HT1A with is the main normal target in depression, which is why 5-HT2A antagonists enhance SSRI drugs in depression. But I suppose this also indicates how heterogenous depressions are as well?! After all this was for treatment resistance depression, which is indicative of different mechanisms.

I wonder if the "direction" of neuroplastic changes, is effectively in the right direction in this case? Is it coincidental, or does this appear sponteanously as plasticity increases because of the depression itself - self healing??
For many years, depression was seen as a neurochemical pathology centring on substances such as orexin, serotonin etc. Drugs were developed to modulate their activities which worked very quickly after administeration, within hours sometimes, but the depressive state often took weeks, month or sometimes, never lifted. This didn’t make sense and it was realised that something else was going on. Today, the focus on this biomedical model of depression has shifted away to ‘we don’t really know’. It’s a bit of a shame because the biomedical model of depression took away the ‘blame’ for depression from the sufferer; “You, your parents, your lifestyle etc haven’t facilitated your depression’s onset, it’s your brain chemicals just like if you had a thyroid issue or something”! Now we can’t really say that which can add to the suffering.

True depression is terrible. If psilocybin can cure it or ameliorate it’s symptoms but we don’t understand it’s mechanisms, then so be it, we will work it out. One’s moral beliefs on this substance have no bearing on it, and if you suffered from depression and have moral issues about the cure for it, then go ahead and refuse it, but one shouldn’t impose one’s own values on others (Nancy Reagan has a lot to answer for and has put this branch of research back by decades).
 
For many years, depression was seen as a neurochemical pathology centring on substances such as orexin, serotonin etc. Drugs were developed to modulate their activities which worked very quickly after administeration, within hours sometimes, but the depressive state often took weeks, month or sometimes, never lifted. This didn’t make sense and it was realised that something else was going on. Today, the focus on this biomedical model of depression has shifted away to ‘we don’t really know’. It’s a bit of a shame because the biomedical model of depression took away the ‘blame’ for depression from the sufferer; “You, your parents, your lifestyle etc haven’t facilitated your depression’s onset, it’s your brain chemicals just like if you had a thyroid issue or something”! Now we can’t really say that which can add to the suffering.

True depression is terrible. If psilocybin can cure it or ameliorate it’s symptoms but we don’t understand it’s mechanisms, then so be it, we will work it out. One’s moral beliefs on this substance have no bearing on it, and if you suffered from depression and have moral issues about the cure for it, then go ahead and refuse it, but one shouldn’t impose one’s own values on others (Nancy Reagan has a lot to answer for and has put this branch of research back by decades).
I certainly have no moral issues, that didn't even occur to me. I am just curious to understand. The brain is one of the more interesting systems to understand.

My current impression is that one problem of why some drugs work and some don't in many neuropsychiatric conditions is that what are catogoried into a handful diagnosis, are really very heterogenous conditions. So sometimes the categorisation into a few diagnosis is limiting rather than helping. I believe there are many subcategories of "depression", with different mechanisms, so do find a single cure for 100% of those patients seems unreasonable.
 
I certainly have no moral issues, that didn't even occur to me.
Oh I didn’t mean you, Fungus…you’re a man of science!
I am just curious to understand. The brain is one of the more interesting systems to understand.
If the brain was simple enough to understand, we would be so simple that we couldn’t!
My current impression is that one problem of why some drugs work and some don't in many neuropsychiatric conditions is that what are catogoried into a handful diagnosis, are really very heterogenous conditions. So sometimes the categorisation into a few diagnosis is limiting rather than helping. I believe there are many subcategories of "depression", with different mechanisms, so do find a single cure for 100% of those patients seems unreasonable.
Have you heard of the DSM-V. It categorises all recognised psychiatric conditions according to their core symptoms. It makes for interesting reading.

One other issue with pharmaceutical treatments is the drug doesn’t necessarily bind to the (brain) cell receptor with consistent efficacy (‘lock and key’)They have a range of affinities and individual may have slightly different receptor structures adding to the complexity of predicting drug actions. It’s very complex so when a new drug is developed that has a positive effect, it’s a really big thing (semaglutide is a real miracle despite what some people think).
 
Have you heard of the DSM-V. It categorises all recognised psychiatric conditions according to their core symptoms. It makes for interesting reading.
Yes, I am well aware of that. What I meant is that any same symptom profile (no matter how it is categorised) can have an array of ethiologies. And to choose the right treatment, it is the ethiology that needs to be categorized, not the symptoms; which of course is not always known for many conditions and that is the real problem :rolleyes:

One other issue with pharmaceutical treatments is the drug doesn’t necessarily bind to the (brain) cell receptor with consistent efficacy (‘lock and key’)They have a range of affinities and individual may have slightly different receptor structures adding to the complexity of predicting drug actions. It’s very complex so when a new drug is developed that has a positive effect, it’s a really big thing (semaglutide is a real miracle despite what some people think).
Yes, this seems really complex, which is why it caught my attention, even though I am not primarily into neuroscience. But I am into the process of making models of complex systems per see. And the brain is an excellent model system, that is intuitive in a way.
 
Nancy Reagan?! I remember reading that she used to eat two bananas before bedtime cause it made her sleep well….
Yes, she was key in the ‘war in drugs’ that made all drugs (except alcohol and tobacco… the worst offender) taboo. As a consequence all research on things like psilocybin and other potentially therapeutic drugs was halted. It’s only in recent years that scientific research on psychoactive drugs has recommenced. She was a very stupid woman.
 
Yes, I am well aware of that. What I meant is that any same symptom profile (no matter how it is categorised) can have an array of ethiologies. And to choose the right treatment, it is the ethiology that needs to be categorized, not the symptoms; which of course is not always known for many conditions and that is the real problem :rolleyes:
Perhaps this is why we have a carbon-based psychiatric to use their experiences and observations to make an informed judgement in treatment.
Yes, this seems really complex, which is why it caught my attention, even though I am not primarily into neuroscience. But I am into the process of making models of complex systems per see. And the brain is an excellent model system, that is intuitive in a way.
It’s so complex and I think our understanding of it is misplaced. We need our ‘black body radiation’ moment to usher in a new perspective on its function.
 
It’s so complex and I think our understanding of it is misplaced. We need our ‘black body radiation’ moment to usher in a new perspective on its function.
I have been awaiting a paradigm shift in foundational physics community for 30 years. It is first when you study sufficiently complex systems, that the problem with existing paradigms gets obvious, ie when the very framework for or "understanding" is wrong. But it may take a century to see.
 
Yes, she was key in the ‘war in drugs’ that made all drugs (except alcohol and tobacco… the worst offender) taboo. As a consequence all research on things like psilocybin and other potentially therapeutic drugs was halted. It’s only in recent years that scientific research on psychoactive drugs has recommenced. She was a very stupid woman.
“Just say no!”
 
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