Anti-stress properties of buprenorphine: a better choice for stress-induced relapse to drug addiction
Mohammad Ashraf Ahmad Bidin, Nurul Nazierah Rosman, Maryam Saadah Suhaimi, Syed Mohd Syahmi Syd Mohmad Faudzi, Irna Elina Ridzwan
Abstract
Mohammad Ashraf Ahmad Bidin, Nurul Nazierah Rosman, Maryam Saadah Suhaimi, Syed Mohd Syahmi Syd Mohmad Faudzi, Irna Elina Ridzwan
Abstract
Compared to methadone, buprenorphine has a unique pharmacological profile in which it is a partial agonist at the mu- and NOP, but antagonist at the kappa-opioid receptors. This gives advantage to buprenorphine to have lesser abusive tendency and has ability to reduce relapse to drug taking. Previous studies had shown that stress, which has been linked to relapse, increased the release of dynorphin (an endogenous kappa-opioid receptor agonist) and potentiates the rewarding effects of morphine. In this study, we tested if buprenorphine treatment has ability to block the drug seeking behaviour in mice using a conditioned place preference (CPP) paradigm. Initially, a modified forced-swim test (FST) was conducted for two consecutive days to induce stress by testing for immobility in mice. A significant difference between control and treatment groups (n = 8 for each group, P 0.05) in the time spent for the treatment group (n = 8) during post morphine-conditioning session compared to their baseline, which suggested that buprenorphine has the ability to prevent morphine-seeking behaviour as compared to the control group (n = 8, P < 0.05) . These results suggest the advantage of buprenorphine as therapeutic agent to treat stress-induced relapse in drug addiction.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Compared to methadone, buprenorphine has a unique pharmacological profile in which it is a partial agonist at the mu- and NOP, but antagonist at the kappa-opioid receptors. This gives advantage to buprenorphine to have lesser abusive tendency and has ability to reduce relapse to drug taking. Previous studies had shown that stress, which has been linked to relapse, increased the release of dynorphin (an endogenous kappa-opioid receptor agonist) and potentiates the rewarding effects of morphine. In this study, we tested if buprenorphine treatment has ability to block the drug seeking behaviour in mice using a conditioned place preference (CPP) paradigm. Initially, a modified forced-swim test (FST) was conducted for two consecutive days to induce stress by testing for immobility in mice. A significant difference between control and treatment groups (n = 8 for each group, P 0.05) in the time spent for the treatment group (n = 8) during post morphine-conditioning session compared to their baseline, which suggested that buprenorphine has the ability to prevent morphine-seeking behaviour as compared to the control group (n = 8, P < 0.05) . These results suggest the advantage of buprenorphine as therapeutic agent to treat stress-induced relapse in drug addiction.
Key concepts: Buprenorphine, Morphine, Conditioned place preference, Dynorphin, κ-opioid receptor, Addiction, Agonist, Opioid