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Greenlighter
Greetings Bluelighters!
Opiate users know the pain of withdrawal, both acutely and post-acutely. It's the latter of these two that I would like to discuss.
I am aware that opiates work because they mimic endorphines. I am also aware that the body produces some pretty badass ones, such as beta-endorphine, which is believed to be roughly 80 times more potent than morphine†. It is my understanding that the brain reacts to chronic opiate use in several ways that are harmful, including:
I have been attempting to recover from these effects using a combination of low-dose buprenorphine, nutrition, exercise, and spirituality. My question is this: will the presence of buprenorphine in my system continue to cause my body to down-regulate my µ receptor level? If so, won't I be desensitized to my own endogenous endorphines, even if I manage to return to the homeostatic level at which they are produced at normal levels?
I would appreciate insight into this matter from those who are more educated about the pharmacological and physiological chemistry involved here.
Sources:
† - http://en.wikipedia.org/wiki/Beta-endorphin
‡ - http://www.ncbi.nlm.nih.gov/pubmed/8097244
Opiate users know the pain of withdrawal, both acutely and post-acutely. It's the latter of these two that I would like to discuss.
I am aware that opiates work because they mimic endorphines. I am also aware that the body produces some pretty badass ones, such as beta-endorphine, which is believed to be roughly 80 times more potent than morphine†. It is my understanding that the brain reacts to chronic opiate use in several ways that are harmful, including:
- Ceasing to produce endogenous endorphines
- Down-regulating receptors to said opiate when production limitation fails to lower syrum levels‡
I have been attempting to recover from these effects using a combination of low-dose buprenorphine, nutrition, exercise, and spirituality. My question is this: will the presence of buprenorphine in my system continue to cause my body to down-regulate my µ receptor level? If so, won't I be desensitized to my own endogenous endorphines, even if I manage to return to the homeostatic level at which they are produced at normal levels?
I would appreciate insight into this matter from those who are more educated about the pharmacological and physiological chemistry involved here.
Sources:
† - http://en.wikipedia.org/wiki/Beta-endorphin
‡ - http://www.ncbi.nlm.nih.gov/pubmed/8097244
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