Apoptosis PDGF-A SOD caspase 3 sertoli cell tetrahydrocannabinol zinc

Journal

Endocrine, metabolic & immune disorders drug targets
ISSN: 2212-3873
Titre abrégé: Endocr Metab Immune Disord Drug Targets
Pays: United Arab Emirates
ID NLM: 101269157

Informations de publication

Date de publication:
2023
Historique:
received: 06 09 2022
revised: 24 01 2023
accepted: 24 01 2023
pubmed: 25 3 2023
medline: 25 3 2023
entrez: 24 3 2023
Statut: ppublish

Résumé

Global rise in cannabis abuse during reproductive years has placed a large number of men at risk for the adverse consequences of δ-9-tetrahydrocannabinol (THC), the primary active component of cannabis. It has been reported that THC affects male fertility and causes testicular cell dysfunction and apoptosis. This study aimed to investigate the possible protective role of zinc pretreatment against the toxic effects of THC in cultured mouse Sertoli cells and the underlying mechanism. The Mus Musculus Sertoli cell line (TM4) was cultured, exposed to THC alone (470 μM, 24 h), co-administered with zinc (8 μM, 48 h), and investigated in three groups: control, THC, and THC + zinc. The MTT was performed to evaluate cell viability. TUNEL assay was also applied for the detection of cell apoptosis and a western blot was performed for measuring protein expression levels of Caspase3, Pro-caspase3, SOD, and PDGF-A. THC significantly decreased cell viability (p < 0.001) and expression levels of SOD, PDGF-A, and pro-caspase3 proteins (p < 0.05 for all), whereas increased Sertoli cells apoptosis (p < 0.001) and expression level of cleaved caspase3 protein (p < 0.001). Pretreatment with zinc reversed THC-induced apoptotic and oxidative effects and reduced cleaved caspase3/pro-caspase3 ratio but could not reverse THC-induced reduction of PDGF-A expression level in TM4 cells. The present data suggest that THC induces Sertoli cell damage through a multitarget mechanism. Zinc was reported to protect against THC-induced Sertoli cell damage due to its antiapoptotic and antioxidant activities, indicating its clinical importance against THC-induced testicular toxicity among addicted men.

Sections du résumé

BACKGROUND BACKGROUND
Global rise in cannabis abuse during reproductive years has placed a large number of men at risk for the adverse consequences of δ-9-tetrahydrocannabinol (THC), the primary active component of cannabis. It has been reported that THC affects male fertility and causes testicular cell dysfunction and apoptosis. This study aimed to investigate the possible protective role of zinc pretreatment against the toxic effects of THC in cultured mouse Sertoli cells and the underlying mechanism.
METHODS METHODS
The Mus Musculus Sertoli cell line (TM4) was cultured, exposed to THC alone (470 μM, 24 h), co-administered with zinc (8 μM, 48 h), and investigated in three groups: control, THC, and THC + zinc. The MTT was performed to evaluate cell viability. TUNEL assay was also applied for the detection of cell apoptosis and a western blot was performed for measuring protein expression levels of Caspase3, Pro-caspase3, SOD, and PDGF-A.
RESULTS RESULTS
THC significantly decreased cell viability (p < 0.001) and expression levels of SOD, PDGF-A, and pro-caspase3 proteins (p < 0.05 for all), whereas increased Sertoli cells apoptosis (p < 0.001) and expression level of cleaved caspase3 protein (p < 0.001). Pretreatment with zinc reversed THC-induced apoptotic and oxidative effects and reduced cleaved caspase3/pro-caspase3 ratio but could not reverse THC-induced reduction of PDGF-A expression level in TM4 cells.
CONCLUSION CONCLUSIONS
The present data suggest that THC induces Sertoli cell damage through a multitarget mechanism. Zinc was reported to protect against THC-induced Sertoli cell damage due to its antiapoptotic and antioxidant activities, indicating its clinical importance against THC-induced testicular toxicity among addicted men.

Identifiants

pubmed: 36959135
pii: EMIDDT-EPUB-130307
doi: 10.2174/1871530323666230322092046
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1611-1620

Subventions

Organisme : Urmia University
ID : 10429

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Kimia Ahmadi (K)

Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran.

Fatemeh Asgharzadeh (F)

Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Shadi Mohammadpour-Asl (S)

Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Fatemeh Ayari (F)

Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Fatemeh Rahbar (F)

Student Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Morteza Motazakker (M)

Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.

Shiva Roshan-Milani (S)

Neurophysiology Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.

Amin Abdollahzade Fard (AA)

Department of Physiology, Nephrology and Kidney Transplant Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran.

Classifications MeSH