Curcumin nano-micelle induced testicular toxicity in healthy rats; evidence for oxidative stress and failed homeostatic response by heat shock proteins 70-2a and 90.
8-Hydroxy-2'-Deoxyguanosine
/ metabolism
Animals
Biomarkers
/ metabolism
Catalase
/ metabolism
Curcumin
/ administration & dosage
DNA Damage
/ drug effects
Glutathione
/ metabolism
Glutathione Peroxidase
/ metabolism
HSP70 Heat-Shock Proteins
/ genetics
HSP90 Heat-Shock Proteins
/ genetics
Homeostasis
/ drug effects
Male
Malondialdehyde
/ metabolism
Micelles
Nanoparticles
/ administration & dosage
Oxidation-Reduction
/ drug effects
Oxidative Stress
/ drug effects
Rats, Wistar
Sperm Count
Sperm Motility
/ drug effects
Spermatozoa
/ drug effects
Testis
/ drug effects
Curcumin
HSP70-2a
HSP90
Nano-micelle
Oxidative stress
Spermatogenesis
Journal
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295
Informations de publication
Date de publication:
Oct 2021
Oct 2021
Historique:
received:
09
05
2021
revised:
23
06
2021
accepted:
14
07
2021
pubmed:
27
7
2021
medline:
5
1
2022
entrez:
26
7
2021
Statut:
ppublish
Résumé
This study explores the effect of curcumin nano-micelle (NCMN) on the testicular anti-oxidant status and heat shock proteins (Hsp) 70-2a and Hsp 90 expression. Therefore, 24 male Wistar rats were divided into control, 7.50 mg/kg, 15 mg/kg, and 30 mg/kg of NCMN-received groups. Following 48 days, the testicular total anti-oxidant capacity (TAC), total oxidant status (TOS), malondialdehyde (MDA) and glutathione (GSH), catalase (CAT) and glutathione peroxidase (GPX) activities, immunoreactivity of 8-oxodG, Hsp70-2a and Hsp90 expressions, germ cell's DNA and mRNA damages, the spermatozoa count, motility and DNA integrity were assessed. With no change in the testicular TAC level, the TOS, MDA and GSH contents were increased in the NMC-received groups. However, CAT and GPX activities were decreased. The NCMN suppressed spermatogenesis, increased immunoreactivity of 8-oxodG, stimulated the Hsp70-2a and Hsp90 expressions, and resulted in severe DNA and mRNA damages. Moreover, the NCMN-received animals exhibited remarkable reductions in the spermatozoa count, motility and DNA integrity. In conclusion, chronic and high dose consumption of NCMN initiates OS, and in response to OS, the Hsp70-2a and Hsp90 expression increases. However, considering enhanced DNA and mRNA damages and suppressed spermatogenesis, HSPs over-expression can neither boost the anti-oxidant system nor overcome the NCMN-induced OS-related damages.
Identifiants
pubmed: 34311173
pii: S0753-3322(21)00727-7
doi: 10.1016/j.biopha.2021.111945
pii:
doi:
Substances chimiques
Biomarkers
0
HSP70 Heat-Shock Proteins
0
HSP90 Heat-Shock Proteins
0
Hspa2 protein, rat
0
Micelles
0
Malondialdehyde
4Y8F71G49Q
8-Hydroxy-2'-Deoxyguanosine
88847-89-6
Catalase
EC 1.11.1.6
Glutathione Peroxidase
EC 1.11.1.9
Glutathione
GAN16C9B8O
Curcumin
IT942ZTH98
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
111945Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Masson SAS.. All rights reserved.