Unveiling the therapeutic potential of octreotide in treating morphine dependence

The potential of octreotide (OCT), an octapeptide synthetic somatostatin agonist, to mitigate addiction, specifically morphine dependence, was evaluated in a comprehensive approach involving behavioral, molecular, histological, and docking studies. OCT decreased addiction-related behaviors in Wistar rats previously exposed to morphine, normalizing their exploratory activities and reducing drug-seeking behaviors. Histological assessments revealed octreotide-induced reductions in opioid-induced neuronal damage, suggesting a neuroprotective function. Octreotide's behavioral and histopathological effects were associated with regulation of molecular pathways known to be critical in morphine dependence processes, including TLR4, BDNF, SIRT1, and mTOR. Supplementary docking studies elucidated octreotide's high affinity for addiction-related targets, suggesting that a biological interaction between OCT and players in pathways known to play a role in addiction could be involved in behavioral and cellular effects noted. When our results are taken together, we conclude that OCT could be a promising candidate for opioid dependence treatment and underscore the necessity for further preclinical and clinical investigations.

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Publication Details

Journal
Scientific Reports
Published
2025-08-14
DOI
https://doi.org/10.1038/s41598-025-12761-6
Citations
1
Primary Topic
Pancreatic function and diabetes
Type
article
Field-Weighted Citation Impact
2.01

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article

Unveiling the therapeutic potential of octreotide in treating morphine dependence

Kristi A. Kohlmeier, Mohammad Banazadeh, Mohammad Shabani, Sedigheh Amiri et al.
1 citations
Scientific Reports
Pancreatic function and diabetes
2.01
article

Unveiling the therapeutic potential of octreotide in treating morphine dependence

Kristi A. Kohlmeier, Mohammad Banazadeh, Mohammad Shabani, Sedigheh Amiri, Moazamehosadat Razavinasab, Mohammad Amin Langarizadeh, Amir Hossain Moqaddari, Reyhaneh Naderi, Hamid Forootanfar, Mohammad Navid Ebrahimi, Meysam Ahmadi‐Zeidabadi, Amin Hassanshahi, Zahra Esmaili, Mehran Ilaghi, Zeynab Pirmoradi, Maryam Amiri, Leili Rouhi
article en
1 citations

Abstract

The potential of octreotide (OCT), an octapeptide synthetic somatostatin agonist, to mitigate addiction, specifically morphine dependence, was evaluated in a comprehensive approach involving behavioral, molecular, histological, and docking studies. OCT decreased addiction-related behaviors in Wistar rats previously exposed to morphine, normalizing their exploratory activities and reducing drug-seeking behaviors. Histological assessments revealed octreotide-induced reductions in opioid-induced neuronal damage, suggesting a neuroprotective function. Octreotide's behavioral and histopathological effects were associated with regulation of molecular pathways known to be critical in morphine dependence processes, including TLR4, BDNF, SIRT1, and mTOR. Supplementary docking studies elucidated octreotide's high affinity for addiction-related targets, suggesting that a biological interaction between OCT and players in pathways known to play a role in addiction could be involved in behavioral and cellular effects noted. When our results are taken together, we conclude that OCT could be a promising candidate for opioid dependence treatment and underscore the necessity for further preclinical and clinical investigations.

Scientific ReportsVol. 15(1)
University of Copenhagen (DK), Kerman University of Medical Sciences (IR), University of Saskatchewan (CA), Bam University of Medical Sciences (IR), Shahid Beheshti University (IR), Tehran University of Medical Sciences (IR)
Kerman Neuroscience Research Center, Kerman University of Medical Sciences
Openalex Percentile: Top 13%
Pancreatic function and diabetes
2.01
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