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HERO ID
3066068
Reference Type
Journal Article
Title
N-acetylcysteine Ameliorates the Erectile Dysfunction Caused by Chronic Intermittent Hypoxia in Rats: Partly Involvement of Endoplasmic Reticulum Stress
Author(s)
Zhu, Die; Deng, Yan; Pan, Y; Wang, Z; Yuan, X; Guo, X; Wang, Yu; Liu, H
Year
2015
Is Peer Reviewed?
1
Journal
Urology
ISSN:
0090-4295
EISSN:
1527-9995
Volume
86
Issue
4
Page Numbers
844.e7-844.e14
Language
English
PMID
26206453
DOI
10.1016/j.urology.2015.07.013
Web of Science Id
WOS:000366464300051
Abstract
OBJECTIVE:
To conduct a study using a rodent model of chronic intermittent hypoxia (CIH) to define whether endoplasmic reticulum stress (ERS) is involved in the CIH-induced apoptosis of penile tissue and erectile dysfunction (ED), and whether treatment with N-acetylcysteine (NAC) alleviates pathological variations in corpus cavernosa. Previous work has prompted that CIH acted as the major trigger linking obstructive sleep apnea syndrome and ED.
MATERIALS AND METHODS:
Five-month-old Sprague-Dawley male rats were subjected to 8 hours of intermittent hypoxia per day, with or without NAC for 5 weeks. Erectile function, apoptosis of penile tissue, levels of ERS-associated proapoptotic effectors, and nitric oxide (NO) and nitric oxide synthase (NOS) activity were determined.
RESULTS:
Treatment with NAC inhibited apoptosis of penile tissue, the expressions of ERS-related products: BIP, CHOP, caspase12, and Bax, NO, and endothelial NOS. Administration of NAC before CIH significantly improved the CIH-induced impaired erectile function.
CONCLUSION:
Our results show that pre-CIH NAC administration ameliorates the ED following CIH partly by alleviating CIH-induced ERS and cell apoptosis via regulating the expressions of BIP, CHOP, caspase12, and Bax.
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