Effects of Huang'e Capsules on type IIIA prostatitis and inflammatory cytokines in the expressed prostatic secretion of the patient.
- Author:
Yang-Fan OU
1
;
Yu-Ru LIANG
1
;
Pan XU
1
;
Wen-Bin HUANG
1
;
Zuo-Gang XIE
1
Author Information
1. Department of Andrology, Wenzhou Hospital of Integrated Chinese and Western Medicine, Wenzhou, Zhejiang 325000, China .
- Publication Type:English Abstract
- Keywords:
Huang'e Capsules;
chronic prostatitis;
inflammatory cytokines;
mechanism
- MeSH:
Humans;
Male;
Prostatitis/metabolism*;
Interleukin-8/metabolism*;
Drugs, Chinese Herbal/therapeutic use*;
Transforming Growth Factor beta1/metabolism*;
Prostate/metabolism*;
Leukocyte Elastase/metabolism*;
Tamsulosin;
Treatment Outcome;
Capsules;
Middle Aged;
Phytotherapy;
Cytokines/metabolism*;
Adult;
Levofloxacin
- From:
National Journal of Andrology
2024;30(12):1135-1140
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the clinical efficacy of Huang'e Capsules in the treatment of type ⅢA chronic prostatitis, and its effects on the levels of the inflammatory cytokines neutrophil elastase (NE), IL-8 and TGF-β1 in the expressed prostatic secretion (EPS) of the patients.
METHODS:We selected 120 patients with type ⅢA chronic prostatitis and randomly assigned them to medication with Huang'e Capsules (the trial group, n = 60) or Levofloxacin and Tamsulosin (the control group, n = 60), both for a course of 4 weeks. We obtained the NIH-CPSI scores and the levels of NE, IL-8 and TGF-β1 in the EPS, and compared them between the two groups before and after treatment.
RESULTS:Totally, 116 of the patients completed the study, 59 in the trial and 57 in the control group. The overall clinical effectiveness was significantly higher in the trial group than in the control (89.8% vs 77.2%, P<0.05). Compared with the baseline, the patients of the trial group showed significant decreases after treatment in the total NIH-CPSI scores (32.5±7.4 vs 13.2±5.1), pain symptom scores (13.7±3.9 vs 4.2±2.3), urination symptom scores (6.9±2.4 vs 5.1±3.2) and quality of life (QOL) scores (8.3±2.7 vs 3.7±1.5) (all P< 0.05), and so did the controls in the total NIH-CPSI scores (30.8±7.8 vs 13.7±3.9), pain symptom scores (14.2±4.1 vs 7.8±2.9), urination symptom scores (7.1±2.7 vs 4.9±3.4) and quality of life (QOL) scores (8.1±2.4 vs 5.6±1.9) (all P< 0.05), and the decreases were even more significant in the trial than in the control group in the pain symptom and QOL scores ( P< 0.05). The patients of the trial group also exhibited a marked reduction after treatment in the contents of NE ([1135.4±321.5] vs [347.6±207.3] ng/L, P< 0.05) and IL-8 ([974.9±231.6] vs [ 431.3±207.2] ng/L, P< 0.05) but an elevation in that of TGF-β1 ([591.0±172.1] vs [1 402.1 ± 221.5] ng/L, P< 0.05) in the EPS, and so did the controls in the levels of NE ([1052.8±280.3] vs [761.1±225.1] ng/L, P<0.05), ([1007.5±287.7] vs [775.7±182.5] ng/L, P< 0.05), ([607.8±201.3] vs [871.3±192.5] ng/L, P< 0.05), with even more significant improvement in the trial than in the control group (P< 0.05).
CONCLUSION:Huang'e Capsules has a significant clinical efficacy and safety in the treatment of type IIIA prostatitis, which can effectively relieve the pain and urination symptoms and improve the levels of the inflammatory cytokines NE, IL-8 and TGF-β1 in the patients.