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Guilingji capsules enhances erectile function by promoting testosterone-dependent angiogenesis in the corpus
Xujun Yu1, Jingyi Zhang2, Suyun Xu3
1School of Medical and Life Sciences, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.
Guilingji capsules (GLJC) treat erectile dysfunction (ED) by enhancing testosterone utilization and promoting angiogenesis. The treatment involves regulating the FGF2, RICTOR/P-AKT/P-FOXO1 pathway in a testosterone-dependent manner.
Area of Science:
- Traditional Chinese Medicine
- Pharmacology
- Urology
Background:
- Erectile dysfunction (ED) is a prevalent condition affecting male sexual health.
- Guilingji capsules (GLJC) are a traditional Chinese medicine formulation used for treating ED.
- The precise mechanisms underlying GLJC's efficacy in ED remain to be fully elucidated.
Purpose of the Study:
- To explore the potential molecular mechanisms of GLJC in treating ED.
- To identify key targets and pathways involved in GLJC's therapeutic effects on ED.
- To validate these mechanisms through in vivo experiments.
Main Methods:
- Network pharmacology analysis of GLJC components and ED-related targets.
- Molecular docking to assess binding affinity of GLJC components to identified targets.
- In vivo validation using d-galactose-induced aging rat model and orchiectomized rats.
Main Results:
- Network pharmacology identified Androgen receptor (AR) and fibroblast growth factor 2 (FGF2) as key targets.
- Molecular docking confirmed effective binding of GLJC components to AR and FGF2.
- GLJC treatment increased erection frequency, serum free testosterone, and penile AR expression in aged rats.
- GLJC promoted angiogenesis and inhibited penile fibrosis by regulating FGF2, RICTOR/P-AKT/P-FOXO1 signaling.
Conclusions:
- GLJC treats ED by enhancing testosterone utilization and promoting angiogenesis in a testosterone-dependent manner.
- The mechanism involves regulating the FGF2, RICTOR/P-AKT/P-FOXO1 signaling pathway.
- GLJC promotes corpus cavernosum survival and inhibits penile fibrosis, offering a potential therapeutic strategy for ED.
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