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Benign prostatic hyperplasia (BPH) is an age-related non-neoplastic disease of the prostate gland in men that has become a global health issue in recent years. Due to the side effects of conventional treatment options, attention is now focused on phytotherapeutics for its management. We investigated the possible protective effect of Saccharomyces cerevisiae var. boulardii in a rat model of testosterone propionate (TP) induced BPH. Rats were divided into five groups: Gr. I, untreated control group; Gr. II, TP group; Gr. III, TP + finasteride; Gr. IV, TP + S. cerevisiae var. boulardii; and Gr. V, S. cerevisiae var. boulardii group. Treatments were given daily for 28 days. At the end of the experiment, all rats were weighed and the prostatic indices, prostate specific antigen, serum testosterone concentration as well as the histological and histomorphometric changes were evaluated. Saccharomyces cerevisiae var. boulardii significantly (P <0.05) reduced prostate weight, prostatic index, serum prostate specific antigen, prostatic epithelial thickness and increased luminal diameter. Thus, the results of this study suggest that S. cerevisiae var. boulardii is a potential pharmacological candidate for management of benign prostatic hyperplasia.
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OBJECTIVE@#To study the effects of alcohol administration on benign prostate hyperplasia(BPH) and the reproductive toxicity during development of benign prostate hyperplasia.@*METHODS@#Seventy adult male Kunming mice were randomly divided into seven groups:control (group CON), negative control (group NC, injected subcutaneously with soybean oil, 25 mg/(kg·d), intragastric administration of distilled water, 7.5 ml/(kg·d)), alcohol for 7 and 21 days (group AL7 and AL21, intragastric administration with wine of 50% alcohol, 7.5 ml/(kg·d)), testosterone propionate for 7 and 21 days (group TP7 and TP21, injected subcutaneously with testosterone propionate, 25 mg/(kg·d)), testosterone propionate+alcohol for 7 days (group TP+AL7, injected subcutaneously with testosterone propionate, 25 mg/(kg·d), and intragastric administration with wine of 50% alcohol, 7.5 ml/(kg·d)),10 mice in each groups. Twenty-four hours after the last administration, mice were sacrificed. The indexes of prostate and testis and the parameters of sperm were determined in mice. The levels of free radicals, antioxidation and histopathological changes in testis and prostate were determined.@*RESULTS@#Compared with the control, TP7d group, AL7 and AL21d groups, the prostate coefficient of TP + AL7d group was increased significantly and the quantity and quality of sperm were decreased significantly (0.05).@*CONCLUSIONS@#The typical BPH state could be induced after 7-day treatment of testosterone propionate and alcohol. The testicular and sperm were damaged which enhanced the oxidative stress in reproductive system. The results indicated that alcohol could significantly promote the prostate hyperplasia induced by testosterone propionate in mice.
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Animals , Male , Mice , Plant Extracts , Prostatic Hyperplasia , Testosterone PropionateABSTRACT
OBJECTIVE: To investigate the inhibitory effect and possible mechanisms of puerariae isoflavone(PI) on prostatic hyperplasia induced by testosterone propionate.METHODS: Forty-eight male Wistar rats were randomly divided into six groups according to their body weight including normal control group, model group, 40, 80, 160 mg•kg-1•d-1 PI group, and finasteride positive control group. In addition to the sham operation for rats in the normal control group, the rats in other five groups performed castration surgery. After the restoration, the five groups of rats were subcutaneously injected with testosterone propionate (10 mg•kg-1•d-1) for 10 d to establish a benign prostatic hyperplasia model and then the subcutaneous injection was maintained every 2 d. High, middle and low dose PI groups were intragastrically administered (40, 80, 160 mg•kg-1•d-1) from the second day when the benign prostatic hyperplasia model was successfully constructed. The positive control group was given finasteride (1.0 mg•kg-1•d-1).Rats in normal and model groups were given an equal volume of saline for 28 d. After the last administration, the prostate and seminal vesicles were separated under anesthesia in rats, the wet weight and volume of the prostate and seminal vesicles were measured. The prostate and seminal vesicles index were calculated too. Rat blood was drawn and dihydrotestosterone(DHT) and estradiol (E2) in the serum were measured. Nitric oxide (NO), nitric oxide synthase (NOS), superoxide dismutase (SOD) and malondialdehyde (MDA) levels in prostate tissues were measured. The prostate tissue in each group was randomly selected for HE staining. The pathological structure of the prostate tissue was observed under an optical microscope.RESULTS: Compared with the normal control group, the prostate gland index and seminal vesicle gland index of the model group increased significantly (P<0.01), and the DHT and E2 levels in serum increased significantly (P<0.01). MDA content was increased while NO levels, NOS and SOD activities were significantly decreased (P<0.01). HE staining showed that the size of the prostate gland in the model group was different, there were obvious dilation, hyperplasia and papillary protrusions, and the cavity was full of pink and homogeneous density. The interstitial tissue showed obvious dilations of blood vessels, infiltration of inflammatory cells, and proliferation of fibrous connective tissues. Compared with the model group, the index and volume of prostate and seminal vesicles in the PI and positive control groups were significantly decreased (P<0.05 or P<0.01), and the levels of serum DHT and E2 in the middle and high doses PI groups were significantly lower (P<0.05 or P<0.01). In all treatment groups, MDA content was decreased and NO, NOS, and SOD levels were increased (P<0.05 or P<0.01) except the low-dose PI groups. There was moderately hyperplasia in low-dose PI group, mild prostatic hyperplasia in positive control group and middle-dose PI group, basically no hyperplasia in high-dose PI group.CONCLUSION: PI has a certain inhibitory effect on prostate hyperplasia induced by testosterone propionate, especially in the medium and high dose PI groups. The mechanism may be related to the effects of pueraria isoflavone on antioxidant,free radical scavenging in vivo, increasing NOS activity and increasing NO level.
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Objective To establish and assess a rat model of benign prostatic hyperplasia (BPH) complicated with late-onset hypogonadism (LOH). MethocSs A total of 80 SD rats were randomly divided into 4 groups: control group, BPH complicated withLOH (model) group, BPH group andLOH group, with 20 rats in each group. In the model group, intraperitoneal injection of cyclophosphamide (20 mg/[kg · d]) was continuously administered for 5 days, followed by continuous intraperitoneal injection of testosterone propionate (50 mg/[kg · d]) for 28 days; the rats in the BPH group were treated the same as that in the model group, except with the same volume normal saline instead of cyclophosphamide; in the LOH group with same volume lucca oil instead of testosterone propionate; and in the control group, the rats were treated withsame volumenormal saline instead of cyclophosphamide and lucca oil instead of testosterone propionate. Two days after drug withdraw, serum testosterone was detected andweight loading swimming test, tall suspension test and sexual behavior test were performed. Then prostate weight and pathology were determined after the rats were sacrificed by cervical dislocation. Results The mean prostate indexes of rats in the LOH, model, control and BPH groups were 1. 58 ± 0. 13, 2. 93 ± 0. 19, 2. 33 ± 0. 13 and 3 23 ± 0. 11, respectively; serum testosterone levels were (4. 91 ± 1. 06), (9. 52 ± 1. 02), (12. 59 ± 0. 70) and (19. 69 ± 0. 56) ng/mL, respectively; the tail suspension struggling times were 97. 40 ± 15. 86, 120. 40 ± 14. 06, 223. 83 ± 16. 51, and 235. 29 ± 18. 77, respectively; the weight loading swimming timeswere (74. 27 ± 9. 29), (167. 47 ± 23. 35), (302. 33 ± 30. 10) and (261. 59 ± 35. 13) s, respectively; the times of olfactory sensation were 1. 53 ± 0. 52, 3 07 ± 0. 88, 9. 17 ± 1 30 and 9. 59 ± 1. 12, respectively; themean ride across times were 0. 33 ± 0. 49, 0. 47 ± 0. 52, 2. 11 ± 0. 47 and 2. 29 ± 0. 47, respectively. Statistical analyses showed that there were significant differences among the four groups in mean prostate index, serum testosterone level and tall suspension struggling time (P<0. 05, P<0. 01), in weight loading swimming time and time of olfactory sensation (P<0. 01) except between control group and BPH group, and in mean ride across time (P<0. 01) except between control group and BPH group, andmodel group and LOH group. Conclusion A BPH complicated with LOH rat model was successfully established with intraperitoneal injection of cyclophosphamide and testosterone propionate.
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OBJECTIVE:To compare in vivo and in vitro permeation behaviors of the ethosome gels of testosterone,testoster-one propionate and testosterone undecanoate. METHODS:The ethosome gels of testosterone,testosterone propionate and testoster-one undecanoate were prepared. With cumulative permeating amount and permeation rate as the indexes,Franz diffusion cell and HPLC were employed to compare in vitro permeation behaviors of 3 kinds of ethosome gels in mouse skin. With testosterone patch as the positive control drug, electrochemistry method was adopted to detect the concentration of testosterone in plasma 0,3,6, 9,12,24,36 and 48 h after applying such 3 kinds of ethosome gels on the back of rats,and then pharmacokinetic parameters were calculated with DAS 2.0 software. RESULTS:24 h cumulative permeating amounts of the ethosome gels of testosterone,tes-tosterone propionate and testosterone undecanoate were(234.31±13.8),(175.63±41.1)and(72.60±15.3)μg/cm2,and the per-meation rates were(10.25±1.9),(7.64±1.4)and(2.96±0.8)μg/(cm2·h),respectively. The pharmacokinetic parameters of the above-mentioned three kinds of ethosome gels and the positive control drug were respectively as follows as cmax of(20.19±2.57), (17.50±2.91),(0.23±0.04),(14.97±2.12)ng/ml,t1/2Ka of(2.80±0.45),(3.36±0.59),(4.02±0.62),(4.20±0.71)h,AUC0-48 h of(13.85±1.96),(13.93±2.13),(0.35±0.07),(11.76±2.31)ng·h/ml. CONCLUSIONS:in vivo and in vitro permeation behav-iors of the ethosome gels of testosterone and testosterone propionate are fairly good.
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Objective To investigate the effect of testosterone on mitotic orientation in rat prostate epithelial cells and the relative differential gene expression.Methods Twenty SPF male SD rats were divided into 2 groups at random and then subjected to castration.One group of rats was administrated with testosterone 3.7 mg daily for 30 days and the control group was only injected with olive oil.Microscopic analysis was performed using immunohistochemistry.Differential gene expression analysis was conducted by gene microarray and RT-PCR techniques.Results In the testosterone-adminis-trated group, there was a significant mitosis orientation parallel to the basement membrane.But in the control group, mito-sis orientation was oriented perpendicular to the basement membrane.Using the gene microarray and RT-PCR techniques, the cell proliferation genes such as Ran, Tgm4 and Wnt2 in Wnt signal pathway were up-regulated in the testosterone group.Conversely, suppressor cell proliferation genes such as Dkk3 and Fas were down-regulated.Conclusions Mitotic orientation of prostate epithelia cells is changed after testosterone administration.Wnt signal pathway and AR singling path-way also have an influence on the mitosis orientation and cell proliferation.
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Objective To establish a rat model of polycystic ovary syndrome (PCOS),and to study the changes in glucose metabolism by isotope tracer.Methods Female SD rats aged 21 days were divided into control group and PCOS group (made by means of testosterone propionate and high-fat diet).After 8 weeks of molding,glucose tolerance test and rat tail vein perfusion experiment was conducted,by application of the principle of stable isotope tracer technique,rate of glucose appearance was compared in two groups and thus glucose metabolism was measured.Results Compared with control group,PCOS group showed polycystic ovarian changes and significantly elevated serum testosterone levels.After 8 weeks of molding,fasting blood glucose showed no significant difference,while glucose tolerance was impaired and rate of appearance of 6,6-d2-glucose increased significantly in PCOS rats.Conclusions The testosterone propionate combined with high-fat diet could induce PCOS rat model,and the PCOS rats demonstrated a significant increase of glucose rate of appearance despite of normal blood glucose level.Therefore it is suggested that during the early stage of PCOS,change in the glucose metabolism has appeared,and early intervention may be beneficial.
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Present study was performed to demonstrate the effect of exogenous administration of testosterone propionate on photoperiodic induction of testicular growth and development in brahminy myna (Sturnus pagodarum) and baya weaver (Ploceus philippinus). Two groups of brahminy myna and baya weaver (n=5 each) were exposed to15L:9D (group-I) and 9L:15D (group-II), and received 30 µg of TP bird-1 for 15 days. Then, the photoperiod was reversed; the one receiving15L was exposed to 9L and vice versa. Observations on body mass and testis volume were taken at the beginning and at 15 days interval. In brahminy myna, a significant change in body mass occurred under 9L:15D, transfer to 15L:9D, but not under 15L:9D group, transfer to 9L:15D. Also, testes were stimulated under 15L:9D transferred to 9L:15D, but not under 9L:15D transferred to 15L:9D. In baya weaver, body mass increased under 15L:9D and 9L:15D for first 15 days and was maintained until the end of the experiment. Testes enlarged gradually in both groups (15L:9D and 9L:15D transfer to vice versa), but it regressed in 15L:9D group, transferred to 9L:15D after 45 days. Taken together it appears that body mass response indicates the photoperiodic effect and gonadal response indicates the hormonal effect. Finally results conclude that the photoperiod and circulating testosterone levels feedback on to hypothalamus regulates reproductive cycle in these birds.
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To determine if Butea superba Roxb., a traditional Thai male potency herb, has androgenic activity in 60-day-old male Wistar rats, we measured its effects on the pituitary-testicular axis and sex organs. Intact and orchidectomized adult male rats were subdivided into five groups (10 rats/group): distilled water, Butea superba (BS)-10, BS-50, BS-250, and testosterone propionate (TP). They received 0, 10, 50, and 250 mg·kg body weight-1·day-1 BS in distilled water by gavage and 6 mg·kg body weight-1·day-1 TP sc, respectively, during the 30-day treatment period. Blood was collected every 15 days and luteinizing hormone (LH), follicle-stimulating hormone (FSH) and testosterone were measured. Changes of weight and histological appearance of sex organs were determined at the end of the 30-day treatment and 15-day post-treatment periods. TP treatment reduced serum FSH and LH levels and significantly increased the weight of the seminal vesicles and epididymis, in accordance with histopathological changes, in both intact and orchidectomized rats. No changes in serum testosterone, LH, and FSH levels were observed in any of the intact rats treated with BS, but a significant increase in seminal vesicle weight was observed only in the BS-250 group. Although a significant reduction in serum LH was detected in the BS-50 and BS-250 groups of orchidectomized rats, no significant change in weight or histology of sex organs was observed. Thus, we conclude that B. superba needs endogenous testosterone to work synergistically to stimulate the accessory sex organ of intact animals and can potentially exhibit an LH reduction effect in orchidectomized animals.
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Animals , Male , Rats , Butea/chemistry , Follicle Stimulating Hormone/blood , Luteinizing Hormone/blood , Plant Extracts/pharmacology , Testosterone/blood , Luteinizing Hormone/drug effects , Orchiectomy , Organ Size/drug effects , Pituitary Gland/drug effects , Radioimmunoassay , Rats, Wistar , Seminal Vesicles/drug effects , Testis/drug effects , Testosterone Propionate/pharmacologyABSTRACT
OBJECTIVE:To establish a HPLC method for the content determination of testosterone propionate in testosterone propionate paints.METHODS:The assaying was conducted on a Kromasil C 18 column with methanol-water solution(80∶20)as mobile phase,the detection wavelength was254nm and the flow rate was1.0ml/min.RESULTS:The linear concentration range of the testosterone propionate was100～400mg/ml(r=0.9997)with average recovery rate at98.5%(RSD=0.55%).CONCLUSION:The method is simple,accurate and reproducible,and it can be used for the quality control of testosterone propionate paints.
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15-methyl prostaglandin F2a (PGF2a) in a dose of 0.2 rag/kg B. W.combined with testosterone propionate ( TP ) in a dnse of 25mg/ kg B. W. was better than 15-methyl PGF2a alone in a dope of 0.2mg/ kg B. W. on termination of early pregnancy in rats.The endometriurn necrosis only in the uterine deciduous of rats treated with TP.All the above results show that the combined administration of 15 methyl PGF2a and TP is better than the administration of 15-methyl PGF2a alone. TP can probably strengthen the abortion effect of 15-rnethyl PGF2a.
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Objective: To investigate the effects of cadmium and the protection of testosterone propionate on submandibular gland of male rats.Methods:Thirty-five male adult Wistar rats were randomly divided into three groups: control,Cd and Cd + T group.The cadmium concentrations in submandibular gland were measured by flame mode of atomic absorption spectrophotometry.The morphologic changes of GCT cells were observeded by transmission electron microscopy.The expression of AR was determined by immunohistochemical SABC method and was semi-quantitatively analysed by image analysis.Results:The main ultrastructural changes after Cd treatment included swelling or vacuolation of mitochondria,increase of myelin figures in GCT cells,and swelling of mitochondria in the endothelial cells of peritubular capillaries.The changes above were most prominent at 7~15d,and swelling of the cytoplasm and slight karyolysis were also found.The morphology of GCT cells didn't recovery to normal yet after 30d.On the other hand,the ultrastructural lesions of GCT cells in Cd+T group were gentle.Compared with the control group,the cadmium concentrations in both Cd and Cd+T groups were significantly increased.Although they were lower in Cd+T group than that in Cd group,there was no significant difference between the two groups.The immunoreactivity level of AR in Cd and Cd+T groups decreased after Cd treatment,but it was higher in Cd+T group than that in corresponding Cd group,and had significant difference between them at 3,7,15d.Conclusions: The present results indicate that the earlier ultrastructural damage of GCT is related to the direct action of cadmium.The decrease of androgen and androgen receptor might aggravate the damage at later stages.To some extent,testosterone pretreatment could prevent toxicity of cadmium on submandibular gland.
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Objective:To choose the prescription of the optimum testosterone propionate frost and the production craft conditions.Methods:Take the stability and the external appearance forms of the creams as the index sign to be checked,and carry out the experiment with orthogonal test.With the oil matches each other the ratio,the creams dosage,the way to add the main medicine a variable factor.Results:The superior formulation and craft are A 1B 2C 2 or A 1B 3C 3.Conclusion:The ready frost of testosterone propionate meets the provision of the Chinese Medical Dictionary 2000 on relevant ointments.
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Twenty-five male rats, 26-27 days of age, average weight 61.62 gm. were divided into 4 groups. Rats of each group were injected with subcutaneously every second day 1 mg. one of the following drugs: durabolin, Deca-durabolin or Testosterone propionate, and the last group, as normal control, was uninjected. All rats were sacrificed at 54-55 days of age. The thymus glands were weighed and histological appearances were observed. This study showed that thymic weights of all injected groups were less than that of the control, indicating that all 3 drugs caused the thymus gland to involute faster than normal. In comparing the weight and histological appearances of effect on the thymus gland.
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This study was designed to evaluate the effect of estrogen to the growth of leiomyoma and the mechanism of testosterone propionate action on leiomy-oma.The levels of estrogen receptor in uterine tissud and those of estradiol and progesterone in uterine tissue and plasma were determined in 47 women with leiomyoma.The levels of estrogen receptor and estradiol in leiomyomatous tissues were 37.6?4.0 fmol/mg protein and 401.7?92.6 pg/g tissue,respectively.Both of them were higher than the corresponding levels in normal uterine tissues (P