1.Pancreatic kininogenase improves erectile function in streptozotocin-induced type 2 diabetic rats with erectile dysfunction.
Guo-Tao CHEN ; Bai-Bing YANG ; Jian-Huai CHEN ; Zheng ZHANG ; Lei-Lei ZHU ; He-Song JIANG ; Wen YU ; Yun CHEN ; Yu-Tian DAI
Asian Journal of Andrology 2018;20(5):448-453
Erectile dysfunction (ED) associated with type 2 diabetes is a severe problem that requires effective treatment. Pancreatic kininogenase (PK) has the potential to improve the erectile function of ED patients. This study aims to investigate the effect of PK on erectile function in streptozotocin-induced type 2 diabetic ED rats. To achieve this goal, we divided male Sprague-Dawley rats into five groups. One group was not treated, and the other four groups were treated with saline, sildenafil, PK or sildenafil, and PK, respectively, for 4 weeks after the induction of type 2 diabetic ED. Then, intracavernous pressure under cavernous nerve stimulation was measured, and penile tissue was collected for further study. Endothelial nitric oxide synthase levels, smooth muscle content, endothelium content, cyclic guanosine monophosphate (cGMP) levels in the corpus cavernosum, and neuronal nitric oxide synthase levels in the dorsal penile nerve were measured. Improved erectile function and endothelium and smooth muscle content in the corpus cavernosum were observed in diabetic ED rats. When treating diabetic ED rats with PK and sildenafil at the same time, a better therapeutic effect was achieved. These data demonstrate that intraperitoneal injection of PK can improve erectile function in a rat model of type 2 diabetic ED. With further research on specific mechanisms of erectile function improvement, PK may become a novel treatment for diabetic ED.
Animals
;
Cyclic GMP/metabolism*
;
Diabetes Mellitus, Experimental/physiopathology*
;
Erectile Dysfunction/physiopathology*
;
Kallikreins/therapeutic use*
;
Male
;
Muscle, Smooth, Vascular/physiopathology*
;
Nitric Oxide Synthase Type I/metabolism*
;
Nitric Oxide Synthase Type III/metabolism*
;
Penile Erection/physiology*
;
Penis/metabolism*
;
Rats
;
Rats, Sprague-Dawley
;
Sildenafil Citrate/therapeutic use*
;
Treatment Outcome
;
Urological Agents/therapeutic use*
2.Anti-cicatricial and anti-restenosis effect of verapamil on anterior urethral stricture: A randomized controlled clinical trial.
Ruizhi XUE ; Jintang LIAO ; Ting TIAN ; Zhengyan TANG
Journal of Central South University(Medical Sciences) 2018;43(8):843-851
To evaluate the anti-cicatricial and anti-restenosis effect of verapamil on anterior urethral stricture.
Methods: A total of 32 patients received anterior urethral stricture were enrolled in this study. They were divided into 4 blocks according to the duration of previous urethral operations and dilations. Every block was further randomly divided into an experimental group and a control group. Experimental groups received 2 mL injection of verapamil around the anastomosis site of urethra before and after the surgery (2, 4, 6, 8, and 10 weeks after the surgery), while the control groups only received the anastomosis surgery. After surgery, maximal urinary flow rate (Qmax) was examined for all patients once the catheter was removed. In addition, they were also conducted palpation of urethral scar range. The sum of long transverse diameters of urethral scar was measured, and the narrowest urethral inner diameter was examined. The Qmax was rechecked and the urethral scar range was assessed by penis color Doppler elastography after 12 weeks of surgery. The above 4 indexes were used to evaluate the inhibitory effect of verapamil on urethral scar.
Results: The length of palpated urethral scar in the Block 1 to 4 of the experimental groups was (22.75±1.03), (21.25±0.25), (20.75±1.03), and (20.0±0.58) mm, respectively; and those in the control groups (26.00±0.82), (24.5±1.04), (25.75±1.65), and (28.25±1.75) mm, respectively. The Qmax rates in the Block 1 to 4 of the experimental groups were (11.85±0.77), (11.33±0.81), (10.23±0.26), and (10.35±0.17) mL/s, respectively; and those in the control groups were (10.85±0.39), (10.50±0.76), (10.53±1.00), (12.60±0.39) mL/s, respectively. The Qmax rates in the Block 1 to 4 of the experimental groups were (11.73±0.87), (10.65±0.25), (10.23±0.19), and (10.35±0.29) mL/s, respectively; and those in the control groups were (8.05±0.28), (7.73±0.68), (7.53±0.92), and (9.60±0.32) mL/s, respectively. The narrowest diameters of urethral in the Block 1 to 4 of the experimental groups were (9.00±0.58), (7.50±2.89), (7.00±0.10), and (7.00±0.41) mm, respectively; and those in the control groups were (5.50±0.29), (5.00±0.41), (4.75±0.48), and (6.75±0.48) mm, respectively. The ultrasound strain ratio in the Block 1 to 4 of the experimental groups were 6.10±0.22, 6.10±0.17, 5.10±0.16, and 6.90±0.19, respectively; and those in the control groups were 8.00±0.25, 10.60±0.29, 11.30±0.16, and 8.90±0.33, respectively. Compared with the control groups, the experimental groups displayed smaller urethral scar range, less severe scarring, improved Qmax rates and wider inner diameters (all P<0.05).
Conclusion: Urethral regional injection of verapamil intraoperatively or postoperatively can prevent overgrowth of urethral scar tissues after the transperineal anastomosis surgery, and reduce the tendency of postoperative restenosis of anterior urethral stricture.
Anastomosis, Surgical
;
adverse effects
;
Cicatrix
;
diagnostic imaging
;
drug therapy
;
prevention & control
;
Dilatation
;
adverse effects
;
Humans
;
Male
;
Penis
;
diagnostic imaging
;
Postoperative Complications
;
diagnostic imaging
;
drug therapy
;
prevention & control
;
Secondary Prevention
;
Ultrasonography
;
Urethra
;
diagnostic imaging
;
surgery
;
Urethral Stricture
;
prevention & control
;
surgery
;
Urination
;
Urological Agents
;
therapeutic use
;
Verapamil
;
therapeutic use
3.Effects of different medications with tadalafil on erectile dysfunction in males with primary sexual failure.
Wen-Ji LI ; Ming-Xi XU ; Jian-Hua GUO ; Zhi-Kang CAI ; Yue-Qing JIANG ; Zhong WANG
National Journal of Andrology 2017;23(6):522-526
Objective:
To evaluate the effects of three different medications with tadalafil on erectile dysfunction (ED) in young men with primary sexual failure.
METHODS:
This study included 76 male ED patients aged 21-35 years who had primary sexual failure but normal nocturnal penile tumescence and rigidity and failed to respond to psychotherapy. We randomly assigned them to receive oral tadalafil once daily, on demand, or once-daily + on-demand. After 2-3 months of treatment, we evaluated the effects based on the scores of the patients in the five domains of the International Index of Erectile Function (IIEF-5).
RESULTS:
After medication, all the patients showed significantly increased scores in the four domains of IIEF-5, namely, erectile function, orgasmic function, intercourse satisfaction, and overall satisfaction. The on-demand group achieved even higher scores in erectile and orgasmic functions but a lower score in sexual desire than the once-daily group. However, the patients in the once-daily + on-demand group exhibited more significant improvement than those in the other two in all the five domains.
CONCLUSIONS
Once-daily + on-demand medication with tadalafil can significantly enhance the therapeutic effect on psychogenic ED in young men with primary sexual failure.
Adult
;
Coitus
;
Double-Blind Method
;
Drug Administration Schedule
;
Erectile Dysfunction
;
drug therapy
;
psychology
;
Humans
;
Male
;
Orgasm
;
Patient Satisfaction
;
Penile Erection
;
physiology
;
Tadalafil
;
administration & dosage
;
Treatment Outcome
;
Urological Agents
;
administration & dosage
;
Vasodilator Agents
;
administration & dosage
;
Young Adult
4.Triple acupuncture at the Qugu acupoint as an adjunctive therapy for type-Ⅲ chronic prostatitis: Analysis of short- and long-term clinical effects.
Xiao-Yi ZHANG ; Shao-Bo LUO ; Jin-Ying ZHANG ; Zhe-Cheng MENG
National Journal of Andrology 2017;23(5):464-467
Objective:
To investigate the short- and long-term effects of triple acupuncture at the Qugu acupoint as an adjunctive therapy on type-Ⅲ chronic prostatitis / chronic pelvic pain syndrome (CP/CPPS).
METHODS:
We equally randomized 90 CP/CPPS patients into a control and a treatment group, both treated with Levofloxacin Mesylate Tablets (0.5 g, tid) + Terazosin Hydrochloride Capsules (2 mg qd) for 4 weeks, while the latter group by triple acupuncture at the Qugu acupoint as an adjunctive therapy twice a week at the same time. Then, we followed up all the patients for 4 weeks, recorded the cases, time and rate of recurrence, obtained the scores in National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI), quality of life (QoL) and Zung Depression Scale (ZDS), and compared them between the two groups of patients.
RESULTS:
Compared with the controls, the patients of the treatment group showed significantly decreased NIH-CPSI scores in pain (8.6 ± 2.12 vs 6.2 ± 2.25, P <0.05), micturition (5.8 ± 1.22 vs 3.1 ± 1.10, P <0.05), and QoL (6.0 ± 1.33 vs 3.4 ± 1.71, P <0.05) and ZDS score as well (43.9 ± 4.53 vs 33.6 ± 3.20, P <0.01). The recurrence rate was markedly lower while the recurrence time remarkably longer in the treatment than in the control group (15.56 vs 35.56% and [20.0 ± 2.72] vs [12.5 ± 3.47] d, P <0.05).
CONCLUSIONS
As an adjunctive therapy, triple acupuncture at the Qugu acupoint can evidently ameliorate the clinical symptoms, enhance the curative effect of antibacterials, reduce the recurrence rate, and prolong the recurrence time in the treatment of CP/CPPS.
Acupuncture Points
;
Acupuncture Therapy
;
methods
;
Anti-Bacterial Agents
;
therapeutic use
;
Chronic Disease
;
Chronic Pain
;
therapy
;
Combined Modality Therapy
;
Drug Therapy, Combination
;
methods
;
Humans
;
Levofloxacin
;
therapeutic use
;
Male
;
Pelvic Pain
;
therapy
;
Prazosin
;
analogs & derivatives
;
therapeutic use
;
Prostatitis
;
therapy
;
Quality of Life
;
Recurrence
;
Syndrome
;
United States
;
Urological Agents
;
therapeutic use
5.Saw palmetto fruit extract improves LUTS in type ⅢA prostatitis patients.
Yun-Peng SHAO ; Hao-Liang XUE ; Bai-Xin SHEN ; Liu-Cheng DING ; Zheng-Seng CHEN ; Zhong-Qing WEI
National Journal of Andrology 2017;23(5):417-421
Objective:
To assess the clinical efficacy of the saw palmetto fruit extract (SPFE) in the treatment of lower urinary tract symptoms (LUTS) in patients with type ⅢA prostatitis.
METHODS:
This retrospective study included 54 cases of type ⅢA prostatitis treated in the Outpatient Department of our hospital from January to December 2015. The patients were aged 35.06 ± 5.85 years, with a mean disease course of 3.8 ± 2.1 years, and all received oral medication of SPFE Capsules at the dose of 320 mg qd for 12 weeks. We assessed the therapeutic effects by comparing the NIH-chronic prostatitis symptom indexes (NIH-CPSI), voiding diary, International Prostate Symptom Scores (IPSS), and results of urodynamic examination before and after treatment.
RESULTS:
Compared with the baseline, both NIH-CPSI and IPSS were significantly decreased after medication (27.61 ± 3.76 vs 18.6 ± 5.34, P <0.01; 20.44 ± 4.51 vs 10.96±4.62, P <0.01), and urodynamic examination and voiding diary showed dramatic post-medication improvement in the average urinary flow rate ([8.05±1.42] vs [12.05±2.60] ml/s, P <0.01 ), maximum urinary flow rate ([14.22±1.74] vs [21.32±4.51] ml/s, P <0.01), residual urine volume ([46.15±16.57] vs [14.55±10.21] ml, P <0.01), maximum urethral closure pressure ([76.52±3.53] vs [65.32±4.75] cm H2O, P <0.01), mean urinary volume ([124.63±40.55] vs [285.93±58.68] ml, P <0.01), urination frequency (16.96±4.17 vs 8.96±2.50, P <0.01), and nocturia frequency (8.94±3.23 vs 3.15±1.90, P <0.01). No apparent adverse reactions were observed in any of the patients.
CONCLUSIONS
SPFE Capsules can safely and effectively improve LUTS and thus the quality of life of patients with type ⅢA prostatitis.
Adult
;
Chronic Disease
;
Humans
;
Lower Urinary Tract Symptoms
;
drug therapy
;
etiology
;
Male
;
Plant Extracts
;
therapeutic use
;
Prostatitis
;
complications
;
Quality of Life
;
Retrospective Studies
;
Treatment Outcome
;
Urination
;
Urological Agents
;
therapeutic use
6.Effects of Kudzu Root plus Cinnamon Granules on prostatic hyperplasia in mice.
An-Xi WANG ; Xiao-Yu ZHU ; Ting HUANG ; Jin YANG ; Yi-Dong CHENG ; Yu-Feng XU
National Journal of Andrology 2017;23(4):353-360
Objective:
To explore the effects of Kudzu Root plus Cinnamon Granules (KR+C) on prostatic hyperplasia (PH) in mice.
METHODS:
Sixty 4-week-old Kunming male mice were randomly divided into six groups: blank control, PH model, high-, medium- and low-dose KR+C, and finasteride control. All the mice except those in the blank control group were subcutaneously injected with testosterone propionate (5 mg / [kg·d]) at 7 days after surgical castration. The animals of different groups were treated intragastrically with different doses of KR+C, finasteride, and normal saline respectively for 3 weeks and then sacrificed for weighing of the prostate, calculation of the prostatic index, observation of the morphological changes in the prostate after HE staining, determination of the expressions of FGF2, Ki67 and TGF-β1 by immunohistochemistry, detection of 5α-reductase activity by ELISA, and measurement of the apoptosis index of the prostatic cells by TUNEL.
RESULTS:
Compared with the model controls, the mice of the other groups showed significantly reduced prostatic volume (P <0.05), prostatic index (P <0.05), expressions of FGF2, Ki67 and TGF-β1, and activity of 5 α-reductase (P <0.05), but remarkably increased apoptosis index of the prostatic cells (P <0.05). However, no statistically significant differences were observed in the above parameters between the finasteride control and the three KR+C groups (P>0.05).
CONCLUSIONS
KR+C can reduce the prostatic volume of PH mice by decreasing the activity of 5α- reductase, inhibiting the expressions of FGF2, Ki67 and TGF-β1, and promoting the apoptosis of prostatic cells.
Animals
;
Apoptosis
;
Cholestenone 5 alpha-Reductase
;
metabolism
;
Cinnamomum zeylanicum
;
chemistry
;
Fibroblast Growth Factor 2
;
metabolism
;
Finasteride
;
therapeutic use
;
In Situ Nick-End Labeling
;
Ki-67 Antigen
;
metabolism
;
Male
;
Mice
;
Organ Size
;
Phytotherapy
;
methods
;
Plant Roots
;
chemistry
;
Prostate
;
pathology
;
Prostatic Hyperplasia
;
drug therapy
;
metabolism
;
pathology
;
Pueraria
;
chemistry
;
Random Allocation
;
Testosterone Propionate
;
administration & dosage
;
Transforming Growth Factor beta1
;
metabolism
;
Urological Agents
;
therapeutic use
7.Bushen Daozhuo Granules for type Ⅲ prostatitis: A multicenter randomized controlled clinical trial.
Da-Lin SUN ; Bin CAI ; Bao-Fang JIN ; Guo-Shou XIA ; Zhi-An TANG ; Wen-Tao YANG ; Qiang ZOU ; Guo-Hong SONG ; Jian-Guo LIU ; Hong-le ZHAO ; Ning DAI ; Jia-Hui WANG ; Ya-Long GU ; Ya-Lin ZHAI
National Journal of Andrology 2017;23(2):164-168
Objective:
To study the safety and efficacy of Bushen Daozhuo Granules (BDG) in the treatment of type Ⅲ prostatitis.
METHODS:
This multicenter randomized controlled clinical trial included 478 patients with type Ⅲ prostatitis, 290 in the trial group and 188 as controls, the former treated with BDG at 200 ml bid and the latter with tamsulosin hydrochloride sustainedrelease capsules at 0.2 mg qd, both for 4 weeks. Before treatment, after 4 weeks of medication, and at 4 weeks after drug withdrawal, we obtained the NIH Chronic Prostatitis Symptom Index (NIHCPSI) scores and compared the safety and effectiveness rate between the two groups of patients.
RESULTS:
Compared with the baseline, the NIHCPSI score was markedly decreased in the control group after 4 weeks of medication (21.42 ± 4.02 vs 15.67 ± 3.65, P < 0.05) but showed no statistically significant difference from that at 4 weeks after drug withdrawal (19.03 ± 3.86) (P>0.05), while the NIHCPSI score in the trial group was remarkably lower than the baseline both after 4 weeks of medication and at 4 weeks after drug withdrawal (10.92 ± 2.06 and 12.91 ± 2.64 vs 21.58 ± 3.67, P < 0.05). The trial group exhibited both a higher rate of total effectiveness and safety than the control (P < 0.05).
CONCLUSIONS
BDG is safe and effective for the treatment of type Ⅲ prostatitis.
Capsules
;
Chronic Disease
;
Delayed-Action Preparations
;
Drugs, Chinese Herbal
;
adverse effects
;
therapeutic use
;
Humans
;
Male
;
Prostatitis
;
drug therapy
;
pathology
;
Sulfonamides
;
adverse effects
;
therapeutic use
;
Tamsulosin
;
Treatment Outcome
;
Urological Agents
;
adverse effects
;
therapeutic use
8.Efficacy of Lamiophlomis Rotata Capsule in the treatment of type ⅢB prostatitis.
Zhi-Feng WEI ; Kai ZHOU ; Jie DONG ; Dian FU ; Xiao-Feng XU ; Ping LI ; Wen CHENG ; Zheng-Yu ZHANG
National Journal of Andrology 2017;23(12):1107-1110
Objective:
To study the therapeutic effect of Lamiophlomis Rotata Capsule (LRC) in the treatment of type ⅢB prostatitis.
METHODS:
We randomly divided 225 patients with type ⅢB prostatitis into an experimental group (n =125) and a control group (n =120), the former treated orally with LRC at 3 capsules tid while the latter with tamsulosin hydrochloride sustained-release capsules at 0.2 mg qd, both for 4 weeks. We compared the therapeutic effects between the two groups of patients based on the National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) obtained before, immediately after and at 4 weeks after medication.
RESULTS:
A total of 120 patients completed the treatment in the experimental group, which showed remarkable decreases as compared with the baseline in the pain score (5.30 ± 1.23 vs 14.68 ± 1.51, P<0.05), quality of life (QoL) score (6.46 ± 0.93 vs 8.52 ± 1.05, P<0.05) and total NIH-CPSI score (17.50 ± 2.77 vs 27.99 ± 2.98, P<0.05) after 4 weeks of treatment, but no significant change in the urination symptoms score (7.41 ± 1.16 vs 7.16 ± 1.04, P>0.05). The experimental group achieved even markedly lower scores than the controls in the pain symptom (5.30 ± 1.23 vs 13.67 ± 1.49, P<0.05), QoL (6.46 ± 0.93 vs 7.47 ± 0.88, P<0.05) and total NIH-CPSI (17.50 ± 2.77 vs 25.77 ± 2.01, P<0.05) but a higher urination symptoms score than the latter after medication (7.16 ± 1.04 vs 5.68 ± 1.34, P<0.05). At 4 weeks after drug withdrawal, the experimental group also showed significantly lower scores of the pain symptom (7.23 ± 1.03), QoL (6.58 ± 0.87) and total NIH-CPSI (22.18 ± 2.03) than the baseline (all P<0.05) and those in the control group (14.14 ± 0.98, 8.12 ± 0.72 and 26.89 ± 1.67) (all P<0.05). Apart from dizziness in 2 of the patients, who gave up medication halfway, no other obvious adverse reactions were observed during the experiment.
CONCLUSIONS
Lamiophlomis Rotata Capsule deserves to be recommended for the treatment of type ⅢB prostatitis for its safety and effectiveness in reducing the pain and improving the life quality of the patients.
Capsules
;
Chronic Disease
;
Delayed-Action Preparations
;
Drugs, Chinese Herbal
;
therapeutic use
;
Humans
;
Male
;
Pain Management
;
Prostatitis
;
drug therapy
;
pathology
;
Quality of Life
;
Tamsulosin
;
therapeutic use
;
Urination
;
Urological Agents
;
therapeutic use
9.A dosage regimen of M-receptor blocker after TURP for severe BPH with predominant urine storage symptoms.
Jian-Liang CAI ; Da CHEN ; Yu-Feng SONG ; Jing-Chao HAN ; Jing-Tian XIAO ; Ning-Chen LI ; Ming XIA ; Yan-Qun NA
National Journal of Andrology 2017;23(9):793-797
Objective:
To study the dosage regimen of oral M-receptor blocker following transurethral resection of the prostate (TURP) for severe benign prostate hyperplasia (BPH) with predominant urine storage period symptoms (USPSs) and its clinical effect.
METHODS:
Severe BPH patients with predominant USPSs received oral tolterodine (2 mg q12d or 4 mg qd) 6 hours after TURP for 4 weeks. The medication continued for another 2 weeks in case of recurrence of USPSs or until the 12th week in case of repeated recurrence. Before and at 1, 4, 8 and 12 weeks after TURP, we analyzed the International Prostate Symptoms Score (IPSS), quality of life (QoL) score, maximum urinary flow rate (Qmax), and postvoid residual volume (PVR) of the patients.
RESULTS:
Complete clinical data were collected from 106 cases, of which 33 achieved successful drug withdrawal with no aggravation of USPSs at 4 weeks after TURP, 51 at 6-8 weeks, 13 at 10-12 weeks, and 9 needed medication after 12 weeks. Before and at 1, 4, 8 and 12 weeks after TURP, the total IPSSs were 25.33 ± 3.45, 19.33 ± 3.62, 11.56 ± 2.45, 8.38 ± 2.0 and 7.74 ± 1.87, those in the urine storage period were 11.97 ± 1.53, 10.76 ± 1.82, 6.16 ± 1.22, 4.08 ± 1.19 and 3.91 ± 1.15, those at urine voiding were 9.80 ± 1.60, 5.59 ± 1.45, 3.40 ± 0.92, 2.85 ± 0.71, and 2.61 ± 0.67, and the QoL scores were 4.70 ± 0.78, 3.92 ± 0.75, 2.55 ± 0.74, 1.83 ± 0.72 and 1.66 ± 0.75, respectively, with statistically significant differences between the baseline and the scores at 1 and 4 weeks (P <0.01) but not at 8 or 12 weeks (P >0.05). Qmax and PVR were improved progressively and significantly at 1 and 4 weeks (P <0.01) but not at 8 or 12 weeks (P >0.05).
CONCLUSIONS
Four to eight weeks of oral administration of M-receptor blocker may be an effective dosage regimen for severe BPH with predominant USPSs after TURP.
Administration, Oral
;
Clinical Protocols
;
Drug Administration Schedule
;
Humans
;
Male
;
Muscarinic Antagonists
;
administration & dosage
;
Postoperative Care
;
Prostatic Hyperplasia
;
drug therapy
;
surgery
;
Quality of Life
;
Recurrence
;
Tolterodine Tartrate
;
administration & dosage
;
Transurethral Resection of Prostate
;
Treatment Outcome
;
Urination
;
Urological Agents
;
administration & dosage
10.Effects of Xialiqi Capsules on the expressions of PCNA and caspase-3 in rats withbenign prostatic hyperplasia.
Hong-Cai CAI ; Le-Bin SONG ; Guo-Wei ZHANG ; Xing-Rong QING ; Dun-Sheng MO ; Wei LIU ; Xu-Xin ZHAN ; Yu-Feng HUANG ; Xue-Jun SHANG
National Journal of Andrology 2017;23(8):728-733
Objective:
To explore the effects of Xialiqi Capsules(XLQ) on the expressions of the proliferating cell nuclear antigen (PCNA) and caspase-3 in the prostate tissue of the BPH rat model.
METHODS:
Fifty male SD ratswereequally randomized into groups A (sham operation control), B (BPH model control), C (high-dose XLQ), D (low-dose XLQ), and E (finasteridecontrol) andthe BPH modelswere established by subcutaneous injection of testosterone propionate at 0.5 mg per kilogram of the body weight per day for 30 days after castration. After modeling, the animals in groups A and B were treated intragastricallywith normal saline, while those in C, D, and E with XLQ at 1.20 and 0.61 g per kilogram of the body weight per day or finasterideat 0.8 mg per kilogram of the body weight per day, respectively, all for 30 days. Then,the bilateral prostates were harvestedfrom the rats for calculation of the prostatic index (prostate wet weight/ body weight) and determination of the expressions of PCNA and caspase-3 in the prostate tissue by immunohistochemistry and immunofluorescence staining, respectively.
RESULTS:
The prostate wet weight and prostate index were significantly increased in group B as compared with group A, ([1326±60] vs[471±17] g, P<0.01; [2.89±0.18] vs [1.06±0.06] mg/g, P<0.01), but decreased in groups C ([914±36] g;[2.02±0.08] mg/g), D ([1 099±46]g;[2.39±0.11] mg/g), and E ([817±53] g;[1.83±0.10] mg/g)in comparison with B (P<0.01), with statistically significant differences among groups C, D, and E(P<0.01) and most significantly in E.The PCNA level in the prostate tissue wasremarkably higher in group B than in A, but lower in groups C, D and E than in B. The expression of caspase-3 was down-regulatedin group B as compared with A, but up-regulated in groups C, D and E in comparison with B, most significantly in E.
CONCLUSIONS
Xialiqi Capsules can effectively reduce the prostate wet weight and prostatic index of in rats with BPH by inhibiting the level of PCNA and promoting the expression of caspase-3.
Animals
;
Capsules
;
Caspase 3
;
metabolism
;
Drugs, Chinese Herbal
;
administration & dosage
;
pharmacology
;
Finasteride
;
administration & dosage
;
pharmacology
;
Male
;
Orchiectomy
;
Organ Size
;
drug effects
;
Proliferating Cell Nuclear Antigen
;
metabolism
;
Prostate
;
drug effects
;
metabolism
;
pathology
;
Prostatic Hyperplasia
;
drug therapy
;
metabolism
;
pathology
;
Random Allocation
;
Rats
;
Rats, Sprague-Dawley
;
Urological Agents
;
administration & dosage
;
pharmacology

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