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Korean Ginseng Berry Extract Enhances the Male Steroidogenesis Enzymes In Vitro and In Vivoopen access

Authors
Chung, Hyun JooLee, Sang JunJang, AraLee, Chae EunLee, Da WonMyung, Soon ChulKim, Jin Wook
Issue Date
Apr-2023
Publisher
KOREAN SOC SEXUAL MEDICINE & ANDROLOGY
Keywords
Korean ginseng berry extract; Late-onset hypogonadism; Leydig cell; Medicinal plant; Panax ginseng; CA; Meyer; Steroidogenesis
Citation
WORLD JOURNAL OF MENS HEALTH, v.41, no.2, pp 446 - 459
Pages
14
Journal Title
WORLD JOURNAL OF MENS HEALTH
Volume
41
Number
2
Start Page
446
End Page
459
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/66270
DOI
10.5534/wjmh.220075
ISSN
2287-4208
2287-4690
Abstract
Purpose: Testosterone hormonal replacement is the most commonly prescribed solution for men with reproductive issues; however, this treatment has various drawbacks. Hence, the identification of a natural product that promotes steroidogenesis is urgently needed. Ginseng is a popular traditional medicine. This study aimed to investigate steroidogenic effects of Korean ginseng berry extract (GBE; Panax ginseng C.A. Meyer) in vitro and in vivo. Material and Methods: In vitro model, mouse Leydig cells were treated with varying concentrations of GBE, and the levels of steroidogenesis-related genes and proteins and testosterone were measured using western blotting, qRT-PCR, and enzyme linked immunosorbent assay (ELISA). Similarly, in an in vivo model using lipopolysaccharide-injected C57BL/6J mice, expression of steroidogenesis-related genes and proteins and testosterone levels were analyzed. Additionally, sleep deprivation was used to simulate common life stressors related to late-onset hypogonadism (LOH) and the natural effects of aging. Mice were fed sham or GBE before being subjected to paradoxical sleep deprivation.Results: In vitro, GBE induced steroidogenic effects by increasing the levels of enzymes associated with steroidogenesis, steroidogenic acute regulatory protein (STAR), CYP11A1, and CYP17A1. In vivo, GBE significantly increased mRNA and protein levels of steroidogenic enzymes. Furthermore, the synthetic testosterone levels in mouse Leydig cell supernatants and blood sera were increased. In the sleep deprivation study, mice fed GBE showed increased testosterone production and survival under such stressful conditions. Conclusions: GBE increased mRNA and protein levels of steroidogenesis-related enzymes STAR, CYP11A1, and CYP17A1. These key enzymes induced the increased production of testosterone both in vivo and in vitro. Thus, GBE might be a promising therapeutic or additive nutritional agent for improving men's health by increasing steroidogenesis or improving LOH.
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