Inhibitory Effect of Thymoquinone on Testosterone-Induced Benign Prostatic Hyperplasia in Wistar Rats

被引:17
作者
Al-Trad, Bahaa [1 ]
Al-Zoubi, Mazhar [2 ]
Qar, Janti [1 ]
Al-Batayneh, Khalid [1 ]
Hussien, Emad [1 ]
Muhaidat, Riyadh [1 ]
Aljabali, Alaa [3 ]
Alkhateeb, Hakam [2 ]
Al Omari, Ghada [1 ]
机构
[1] Yarmouk Univ, Dept Biol Sci, Irbid, Jordan
[2] Yarmouk Univ, Dept Basic Med Sci, Fac Med, Irbid, Jordan
[3] Yarmouk Univ, Fac Pharm, Irbid, Jordan
关键词
thymoquinone; prostatic hyperplasia; testosterone; Wistar rats; ENDOTHELIAL GROWTH-FACTOR; INFLAMMATION; ANGIOGENESIS; APOPTOSIS; TOXICITY; THERAPY;
D O I
10.1002/ptr.5936
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study addresses the possible protective effects of thymoquinone (TQ) against the development of experimentally-induced benign prostatic hyperplasia (BPH) in Wistar rats. Eighteen adult male rats were divided into three groups; the negative control group (n=6) received vehicle, and two groups received subcutaneous testosterone injection (3mg/kg). Animals receiving testosterone were randomized to untreated BPH group (n=6) and BPH+TQ treated group (n=6, 50mg/kg orally for 14days). Histological changes and the mRNA levels of transforming growth factor-(1) (TGF-(1)) and vascular endothelial growth factor-A (VEGF-A) were analyzed. Additionally, dihydrotestosterone and interleukin-6 (IL-6) serum levels were determined. The presented research shows significant increases in prostate weight/body weight ratio, prostate epithelial thickness, serum IL-6 and dihydrotestosterone levels, and the prostatic expressions of TGF-(1) and VEGF-A in the untreated BPH rats. Histological examination of the prostate tissues in the BPH rats showed an elevated level of proliferation in the stromal area and glandular epithelia with abundant intraluminal papillary folds. However, a reduction in prostate weight/body weight ratio, epithelial hyperplasia, serum IL-6 levels, and the expressions of TGF-(1) and VEGF-A were observed in the BPH+TQ treated rats compared with the untreated BPH rats. The findings support TQ as a useful natural treatment for animal BPH model. Copyright (c) 2017 John Wiley & Sons, Ltd.
引用
收藏
页码:1910 / 1915
页数:6
相关论文
共 35 条
  • [21] Inflammation, apoptosis, and BPH: What is the evidence?
    Novara, G
    Galfano, A
    Boscolo-Berto, R
    Ficarra, V
    Navarrete, RV
    Artibani, W
    [J]. EUROPEAN UROLOGY SUPPLEMENTS, 2006, 5 (04) : 401 - 409
  • [22] Inflammation and endothelial activation in Benign Prostatic Hyperplasia and Prostate Cancer
    Pace, Gianna
    Di Massimo, Caterina
    De Amicis, Daniela
    Vicentini, Carlo
    Ciancarelli, M. Giuliana Tozzi
    [J]. INTERNATIONAL BRAZ J UROL, 2011, 37 (05): : 617 - 622
  • [23] Paramasivam A., 2012, Biomed. Prev. Nutr, V2, P169, DOI [10.1016/j.bionut.2012.03.011, DOI 10.1016/J.BIONUT.2012.03.011]
  • [24] LHRH Antagonist Cetrorelix Reduces Prostate Size and Gene Expression of Proinflammatory Cytokines and Growth Factors in a Rat Model of Benign Prostatic Hyperplasia
    Rick, Ferenc G.
    Schally, Andrew V.
    Block, Norman L.
    Halmos, Gabor
    Perez, Roberto
    Fernandez, Jesus B.
    Vidaurre, Irving
    Szalontay, Luca
    [J]. PROSTATE, 2011, 71 (07) : 736 - 747
  • [25] Pathology of benign prostatic hyperplasia
    Roehrborn, C. G.
    [J]. INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2008, 20 (Suppl 3) : S11 - S18
  • [26] Biomarkers of Systemic Inflammation and Risk of Incident, Symptomatic Benign Prostatic Hyperplasia: Results From the Prostate Cancer Prevention Trial
    Schenk, Jeannette M.
    Kristal, Alan R.
    Neuhouser, Marian L.
    Tangen, Catherine M.
    White, Emily
    Lin, Daniel W.
    Kratz, Mario
    Thompson, Ian M.
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2010, 171 (05) : 571 - 582
  • [27] Histopathological aspects associated with the diagnosis of benign prostatic hyperplasia: Clinical implications
    Sciarra, A
    Voria, G
    Mariotti, G
    Gentile, V
    Pastore, P
    Di Silverio, F
    [J]. UROLOGIA INTERNATIONALIS, 2002, 69 (04) : 253 - 262
  • [28] Adverse Side Effects of 5α-Reductase Inhibitors Therapy: Persistent Diminished Libido and Erectile Dysfunction and Depression in a Subset of Patients
    Traish, Abdulmaged M.
    Hassani, John
    Guay, Andre T.
    Zitzmann, Michael
    Hansen, Michael L.
    [J]. JOURNAL OF SEXUAL MEDICINE, 2011, 8 (03) : 872 - 884
  • [29] Distribution of vascular endothelial growth factor (VEGF) in prostate disease
    Walsh, K
    Sriprasad, S
    Hopster, D
    Codd, J
    Mulvin, D
    [J]. PROSTATE CANCER AND PROSTATIC DISEASES, 2002, 5 (02) : 119 - 122
  • [30] Wang L, 2016, STEM CELL TRANSL MED, V6, P394