Extracorporeal Shockwave Therapy Alleviates Inflammatory Pain by Down-Regulating NLRP3Inflammasome in Experimental Chronic Prostatitis and Chronic Pelvic Pain Syndrome
- Author:
Woong Jin BAE
1
;
Dongho SHIN
;
Jun Jie PIAO
;
Soomin KIM
;
Yong Sun CHOI
;
Bong Hee PARK
;
Hyun Jin JUNG
;
Samuel SORKHI
;
Saager CHAWLA
;
Chung Woon CHEON
;
Dae Up KANG
;
Jong Tae CHOI
;
Sang-Hyuck PARK
;
Sae Woong KIM
;
Mahadevan Raj RAJASEKARAN
Author Information
- Publication Type:Original Article
- From:The World Journal of Men's Health 2024;42(1):157-167
- CountryRepublic of Korea
- Language:English
-
Abstract:
Purpose:To evaluate the anti-inflammatory and antioxidative effects of extracorporeal shockwave therapy (ESWT) on prostatitis and explore the mechanism of alleviating pain.
Materials and Methods:For in vitro testing, RWPE-1 cells were randomly divided into 5 groups: (1) RWPE-1 group (normal control), (2) LPS group (lipopolysaccharide inducing inflammation), (3) 0.1ESWT group (treated by 0.1 mJ/mm2 energy level), (4) 0.2ESWT group (treated by 0.2 mJ/mm2 energy level), and (5) 0.3ESWT group (treated by 0.3 mJ/mm2 energy level). After ESWT was administered, cells and supernatant were collected for ELISA and western blot. For in vivo testing, Sprague-Dawley male rats were randomly divided into 3 groups: (1) normal group, (2) prostatitis group, and (3) ESWT group (n=12 for each). Prostatitis was induced by 17 beta-estradiol and dihydrotestosterone (DHT) administration. Four weeks after ESWT, the pain index was assessed for all groups and prostate tissues were collected for immunohistochemistry, immunofluorescence, apoptosis analysis and, western blot.
Results:Our in vitro studies showed that the optimal energy flux density of ESWT was 0.2 mJ/mm2. In vivo, ESWT ameliorated discomfort in rats with prostatitis and inflammation symptoms were improved. Compared to normal rats, overexpressed NLRP3 inflammasomes triggered apoptosis in rats with prostatitis and this was improved by ESWT. TLR4-NFκB pathway was overactive after experimental prostatitis, compared to normal and ESWT groups, and prostatitis induced alterations in BAX/BAK pathway were inhibited by ESWT.
Conclusions:ESWT improved CP/CPPS by reducing NLRP3 inflammasome and ameliorated apoptosis via inhibiting BAX/BAK pathway in a rat model. TLR4 may play a key role in bonding NLRP3 inflammasome and BAX/BAK pathways. ESWT might be a promising approach for the treatment of CP/CPPS.
