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Biotech & Biomedical/molecular mechanism of drug addiction/dependence

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Question
Why is buprenorphine less addictive than other opioids (like fentanyl) - is it explainable by its strength of binding to the common receptor, or?

Answer
Hi, Miguel,

Thanks for your question.

Buprenorphine is what is referred to as a partial agonist - i.e. it binds to the receptor but even at its maximum cannot give as much of an effect as a full agonist (such as morphine) - it is, thus, also a partial antagonist (partially inhibits the actions of full agonists).

As addiction is likely to be linked to strength of the effect of the drug, buprenorphine has less effect and, therefore, less addiction.

It is not quite this simple as addiction (as opposed to dependence) is more complex involving memory functions as well.

Hope this helps.

Paul  

Biotech & Biomedical

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Dr.Paul Skett

Expertise

drug metabolism or biotransformation from basic to advanced, hepatocytes from basic to advanced, drug toxicity and side effects, alcohol clearance and levels

Experience

32 years research experience in above areas, 30 years educational experience in University. Retained expert for numerous legal firms dealing with matters of drugs (legal and illegal)and alcohol.

Education/Credentials
B.Sc(Hons) Biochemistry, University of Liverpool, UK
fil.dr. (Medical Chemistry) Karolinska Institute, Stockholm, Sweden

Fellow of the British Pharmacological Society

Fellow of the Higher Education Academy

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