Influence of Panax ginseng on Alpha-Adrenergic Receptor of Benign Prostatic Hyperplasia / 대한배뇨장애요실금학회지
International Neurourology Journal
; : 179-186, 2014.
Article
in En
| WPRIM
| ID: wpr-149990
Responsible library:
WPRO
ABSTRACT
PURPOSE: Benign prostatic hyperplasia (BPH) is the most common prostate problem in older men. The present study aimed to investigate the inhibitory effect of Panax ginseng C.A. Meyer (P. ginseng) on a rat model of testosterone-induced BPH. METHODS: The rats were divided into 3 groups (each group, n=10): control, testosterone-induced BPH (20 mg/kg, subcutaneous injection), and P. ginseng (200 mg/kg, orally) groups. After 4 weeks, all animals were sacrificed to examine the blood biochemical profiles, prostate volume, weight, histopathological changes, alpha-1D adrenergic receptor (Adra1d) mRNA expression, and epidermal growth factor receptor (EGFR) and B-cell CLL/lymphoma 2 (BCL2) protein expression. RESULTS: The group treated with P. ginseng showed significantly lesser prostate size and weight than the testosterone-induced BPH group. In addition, P. ginseng decreased the mRNA expression of Adra1d as well as the expression of EGFR and BCL2 in prostate tissue. CONCLUSIONS: These results suggest that P. ginseng may inhibit the alpha-1-adrenergic receptor to suppress the development of BPH.
Key words
Full text:
1
Index:
WPRIM
Main subject:
Prostate
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Prostatic Hyperplasia
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Testosterone
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RNA, Messenger
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B-Lymphocytes
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Receptors, Adrenergic, alpha-1
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Models, Animal
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ErbB Receptors
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Panax
Limits:
Animals
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Humans
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Male
Language:
En
Journal:
International neurourology journal
Year:
2014
Type:
Article