Preventive Electroacupuncture Alleviates Oxidative Stress and Inflammation via Keap1/Nrf2/HO-1 Pathway in Rats with Cyclophosphamide-Induced Premature Ovarian Insufficiency

Copyright © 2022 Yang Chen et al..

Electroacupuncture (EA) is a popular therapeutic therapy for premature ovarian insufficiency (POI). However, little has been known about the underlying processes of EA therapy. To investigate the benefit of EA and reveal the mechanism, thirty SD female rats were allocated into the control, model, sham, EA, and GnRHa groups at random. Vaginal smears were used to monitor the rats' estrous cycle. Serum liver and renal function (ALT, AST, BUN, and Cr), sex hormone (FSH, E2, and AMH), oxidative stress markers (SOD, GSH, and MDA), and inflammatory cytokine (IL6, IL1β, and TNFα) levels were measured by enzyme-linked immunosorbent assay (ELISA). Their ovary morphology was observed by hematoxylin-eosin staining. Transmission electron microscope was used to remark the ultrastructure of the granulocytes. Protein and gene expressions of Keap1/Nrf2/HO-1 pathway were detected by western blot and RT-PCR. Compared with the model group, in the EA group, the levels of serum sex hormones recovered to normal levels. Moreover, it reduced oxidative stress in rats, as demonstrated by increased SOD and GSH levels and decreased MDA levels. Meanwhile, Keap1 mRNA and protein expression dropped considerably in the EA group, while the mRNA and protein expressions of Nrf2 and HO-1 increased. We found that preventive EA might rescue rats with CTX-induced ovarian dysfunction. The anti-inflammatory and antioxidative stress properties of EA, which elevated the Keap1/Nrf2/HO-1 signaling pathway, might be the underlying mechanism. Furthermore, as compared to GnRHa, electroacupuncture did not raise the burden of the liver (ALT and AST) or the kidney (BUN and Cr). Electroacupuncture has a meaningful impact and a sufficient level of safety, making it useful for therapeutic setting in POI.

Errataetall:

RetractionIn: Biomed Res Int. 2023 Aug 2;2023:9816950. - PMID 37564145

Medienart:

E-Artikel

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

Zur Gesamtaufnahme - volume:2022

Enthalten in:

BioMed research international - 2022(2022) vom: 26., Seite 6718592

Sprache:

Englisch

Beteiligte Personen:

Chen, Yang [VerfasserIn]
Zhao, Rui [VerfasserIn]
Li, Xiang [VerfasserIn]
Luan, Yun-Peng [VerfasserIn]
Xing, Li-Wei [VerfasserIn]
Zhang, Xiao-Juan [VerfasserIn]
Wang, Jing [VerfasserIn]
Xia, Xiao-Yan [VerfasserIn]
Zhao, Rong [VerfasserIn]

Links:

Volltext

Themen:

8N3DW7272P
Cyclophosphamide
EC 1.15.1.1
Journal Article
KEAP1 protein, human
KEAP1 protein, rat
Kelch-Like ECH-Associated Protein 1
NF-E2-Related Factor 2
RNA, Messenger
Retracted Publication
Superoxide Dismutase

Anmerkungen:

Date Completed 07.09.2022

Date Revised 11.08.2023

published: Electronic-eCollection

RetractionIn: Biomed Res Int. 2023 Aug 2;2023:9816950. - PMID 37564145

Citation Status MEDLINE

doi:

10.1155/2022/6718592

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM345773632