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Updated: Dec 18, 2025

Isolated Pancreatic Islet Treatment and Apoptosis Measurement
Published on: May 2, 2025
Cannabinoids as anti-ROS in aged pancreatic islet cells
Maryam Baeeri1, Mahban Rahimifard1, Seyed Mojtaba Daghighi1
1Toxicology and Diseases Group, Pharmaceutical Sciences Research Center (PSRC), The Institute of Pharmaceutical Sciences (TIPS), Department of Toxicology and Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran.
Aims:
Cannabinoids are the chemical compounds with a high affinity for cannabinoid receptors affecting the central nervous system through the release of neurotransmitters. However, the current knowledge related to the role of such compounds in the regulation of cellular aging is limited. This study aimed to investigate the effect of cannabidiol and tetrahydrocannabinol on the function of aged pancreatic islets.
Main Methods:
The expression of p53, p38, p21, p16, and Glut2 genes and β-galactosidase activity were measured as hallmarks of cell aging applying real-time PCR, ELISA, and immunocytochemistry techniques. Pdx1 protein expression, insulin release, and oxidative stress markers were compared between young and aged rat pancreatic islet cells.
Key Findings:
Upon the treatment of aged pancreatic islets cells with cannabidiol and tetrahydrocannabinol, the expression of p53, p38, p21 and the activity of β-galactosidase were reduced. Cannabidiol and tetrahydrocannabinol increase insulin release, Pdx1, Glut2, and thiol molecules expression, while the oxidative stress parameters were decreased. The enhanced expression of Pdx1 and insulin release in aged pancreatic islet cells reflects the extension of cell healthy aging due to the significant reduction of ROS.
Significance:
This study provides evidence for the involvement of cannabidiol and tetrahydrocannabinol in the oxidation process of cellular aging.
Insights
Cannabidiol and tetrahydrocannabinol reduce cellular aging markers in pancreatic islets. These cannabinoids enhance insulin release and reduce oxidative stress, suggesting a role in healthy cellular aging.
Area of Science:
- Endocrinology
- Cellular Biology
- Pharmacology
Background:
- Cannabinoids interact with cannabinoid receptors, influencing the central nervous system.
- Limited knowledge exists regarding cannabinoids' role in regulating cellular aging.
- Pancreatic islet function is crucial for metabolic health and is susceptible to aging processes.
Purpose of the Study:
- To investigate the effects of cannabidiol (CBD) and tetrahydrocannabinol (THC) on aged pancreatic islet cells.
- To assess the impact of CBD and THC on key markers of cellular aging in pancreatic islets.
- To explore the potential of these cannabinoids in mitigating age-related functional decline in pancreatic islets.
Main Methods:
- Quantitative assessment of aging hallmarks including p53, p38, p21, p16 gene expression, and β-galactosidase activity.
- Utilized real-time PCR, ELISA, and immunocytochemistry for gene and protein expression analysis.
- Compared Pdx1 protein expression, insulin release, and oxidative stress markers in young versus aged rat pancreatic islet cells.
Main Results:
- CBD and THC treatment reduced the expression of aging markers (p53, p38, p21) and β-galactosidase activity in aged pancreatic islets.
- Both cannabinoids significantly increased insulin release, Pdx1, Glut2, and thiol molecule expression.
- A decrease in oxidative stress markers and reactive oxygen species (ROS) was observed, correlating with enhanced Pdx1 expression and insulin release.
Conclusions:
- CBD and THC demonstrate a protective effect against cellular aging in pancreatic islets.
- These cannabinoids promote healthy cellular aging by reducing oxidative stress and improving islet function.
- The findings suggest a potential therapeutic role for CBD and THC in managing age-related metabolic dysfunction.
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