Non-Invasive Radiofrequency Hyperthermia Attenuates HMGB1/TLR4/NF-κB Inflammatory Axis in a Chronic Prostatitis/Chronic Pelvic Pain Syndrome Rat Model

被引:1
作者
Kim, Soomin [1 ,2 ]
Piao, Jun Jie [1 ,2 ]
Bang, Seokhwan [1 ]
Moon, Hyong Woo [1 ]
Cho, Hyuk Jin [1 ]
Ha, U-Syn [1 ]
Hong, Sung-Hoo [1 ]
Lee, Ji Youl [1 ]
Kim, Hae Hoon [3 ]
Kim, Ha Nul [3 ]
Jeon, Kyung-Hwa [4 ]
Rajasekaran, Mahadevan Raj [5 ]
Kim, Sae Woong [1 ,2 ]
Bae, Woong Jin [1 ,2 ,5 ]
机构
[1] Catholic Univ Korea, Dept Urol, Coll Med, Seoul, South Korea
[2] Catholic Univ Korea, Catholic Integrat Med Res Inst, Coll Med, Seoul, South Korea
[3] Dongseo Medicare Co, Seongnam, South Korea
[4] Ehwa Womans Univ, Grad Sch Pharmaceut Sci, Coll Pharm, Seoul, South Korea
[5] Univ Calif San Diego, San Diego Sch Med, Dept Urol, La Jolla, CA 92093 USA
关键词
HMGB1; protein; Hyperthermia; Prostatitis; Toll-like receptor 4; CYTOKINES; HMGB1;
D O I
10.5534/wjmh.230230
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Purpose: The primary goal of this study is to evaluate the effect of the non-invasive radiofrequency hyperthermia (RFHT) device on chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) rat model and investigate the underlying mechanism. Materials and Methods: In this study, Sprague-Dawley rats were randomly distributed into three groups: (1) normal control group, (2) CP/CPPS group, and (3) RFHT group. CP/CPPS rat models were induced by 17 beta-estradiol and dihydrotestosterone for 4 weeks and RFHT was administered for 5 weeks after model establishment. During RFHT administration, core body temperatures were continuously monitored with a rectal probe. After administering RFHT, we assessed pain index for all groups and collected prostate tissues for Western blot analysis, immunofluorescence, and immunohistochemistry. We also collected adjacent organs to the prostate including urinary bladder, testes, and rectum for safety assessment via H&E staining along with a terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling assay. Results: After administering RFHT, pain in rats was significantly alleviated compared to the CP/CPPS group. RFHT reduced high-mobility group box 1 (HMGB1) expression and improved inflammation by downregulating subsequent proinflammatory cytokines through inhibition of the toll-like receptor 4 (TLR4)-nuclear factor kappa B (NF-kappa B) pathway. In prostate-adjacent organs, no significant histological alteration or inflammatory infiltration was detected. The area of cell death also did not increase significantly after RFHT. Conclusions: In conclusion, RFHT demonstrated anti-inflammatory effects by inhibiting the HMGB1-TLR4-NF-kappa B pathway in CP/CPPS rat models. This suggests that RFHT could serve as a safe and promising therapeutic strategy for CP/CPPS.
引用
收藏
页码:855 / 864
页数:10
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